1. Purpose and Methods
This systematic review of the emerging status of multidrug-resistant (MDR) bacteria and fungi in the Arabian Peninsula was designed to answer the following questions:
Is there a common MDR organism (MDRO) reported in the Arabian Peninsula?
Are there any MDR bacteria and fungi that have emerged in the Arabian Peninsula in the last 10 years?
What are the logical relationships between sets of MDR bacteria and fungi in countries of the Arabian Peninsula?
How many in-depth studies have been conducted on the molecular nature of drug-resistant micro-organisms prevalent in the Arabian Peninsula?
What are the novel antimicrobial strategies developed in the study region?
Is there a high mortality reported due to MDR micro-organisms in the Arabian Peninsula?
To what extent have nanomaterials and nanoparticles been exploited against MDR micro-organisms in the Arabian Peninsula?
This review aims to identify the prevalence and emerging status of multidrug-resistant bacteria and fungi and their associated mortality in nine countries of the Arabian Peninsula: Saudi Arabia, Bahrain, Kuwait, Oman, Qatar, the United Arab Emirates, Jordan, Iraq and Yemen. Published data from the past 10 years were retrieved from PubMed, Scopus and Google Scholar from 2 March 2021 to 8 March 2021. This review was registered with PROSPERO (CRD42021246777). The participants or populations selected from the Arabian Peninsula were Saudi Arabia, Bahrain, Kuwait, Oman, Qatar, the United Arab Emirates, Jordan, Iraq, and Yemen.
Inclusion criteria:
Articles reporting the multidrug-resistant bacteria in the Arabian Peninsula.
Articles reporting multidrug-resistant fungi in the Arabian Peninsula.
Research articles published since 2010 regarding multidrug-resistant micro-organisms in the Arabian Peninsula.
Full-text articles.
Exclusion criteria:
Articles discussing the use of multidrug-resistant bacteria and fungi to screen the antimicrobials in the Arabian Peninsula.
Articles reporting the multidrug-resistant micro-organisms from other than the Arabian Peninsula.
Review articles reporting the multidrug-resistant micro-organisms from the Arabian Peninsula.
Original research articles and case studies of multidrug-resistant bacteria and fungi in the Arabian Peninsula and their associated mortality were considered as articles of interest. A total of 1705 articles (published after 2010) from Scopus and PubMed were thoroughly screened for eligibility, as per the inclusion and exclusion criteria. A total of 382 studies were eligible for inclusion as per PRISMA 2009 (Figure 1; Supplementary Table S1). There were three papers reporting MDR micro-organisms from multiple countries: Article 1 [1]—Bahrain, Saudi Arabia and United Arab Emirates; Article 2 [2]—Saudi Arabia, United Arab Emirates, Oman, Qatar, Bahrain, and Kuwait and Article 3 [3]—Saudi Arabia, Kuwait, Oman and United Arab Emirates.
The most urgent public and animal health problems are increasingly caused by multidrug-resistant (MDR) micro-organisms. This problem is widely shown in bacteria that defy ultimate antibiotics and portend an untreatable future. The Arabian Peninsula has several challenges that stimulate the emergence and spread of multidrug-resistant bacteria. Dealing with these challenges requires the of multiple sectors to successfully control the spread and emergence of antimicrobial resistance. The present review summarises the logical relationship between emerging multidrug resistance organisms and associated mortality in the Arabian Peninsula.
2. Logical Relation between Sets of Multidrug-Resistant (MDR) Microbes
Eighty different species of multidrug-resistant bacteria and fungi were reported in the Arabian Peninsula (Figure 2). MDR Acinetobacter baumannii prevailed in all the nine countries of the Arabian Peninsula and was the most prevalent MDR microbe (Table 1), and was able to survive in hot dry summers and mild wet winters. After A. baumannii, Escherichia coli was the next most prevalent MDR microbe, reported in eight countries of the Arabian Peninsula; it was not reported in Yemen.
MDR Candida auris is a globally emerging fungal pathogen, for which diagnoses and treatments are challenging. The incidence of C. auris in clinical specimens from Kuwait, Saudi Arabia, and United Arab Emirates was reported in 11 articles; 580 strains (Table 1 and Table 2) responsible for 54 deaths (Figure 3, Table 3 and Table 4). A total of 13087 Mycobacterium tuberculosis isolates were reported in the region (Table 5).
2.1. Saudi Arabia
Due to its large area and population, the Kingdom of Saudi Arabia has the most significant number of scientific studies on the subject of MDR organisms among the countries of the Arabian Peninsula. Therefore, it has several obstacles that might promote the emergence and transmissiom of MDR micro-organisms. Eventually, a total of 79 unique MDR microbes were reported (Figure 2). The difficulties of this were overcome due to the successful efforts of different sectors to restrict the growth and establishment of MDR micro-organisms in the country. The active monitoring of the onset and spread of MDR micro-organisms is very important. Many relevant articles were published in research and case studies from Saudi Arabia on MDR bacteria and fungi. The inclusion criteria were applied carefully to all the search results (for articles published after 2010) from Scopus and PubMed. A total of 198 studies, as per PRISMA 2009, were eligible for inclusion (Figure 1; Supplementary Table S1). Three publications reported MDR micro-organisms in more than one country of the Arabian Peninsula: the report by Sonnevend and colleagues [1] in Bahrain, Saudi Arabia and United Arab Emirates; a study by Zowawi and colleagues [2] in Saudi Arabia, United Arab Emirates, Oman, Qatar, Bahrain, and Kuwait and a report by Sonnevend and colleagues [3] in Saudi Arabia, Kuwait, Oman and United Arab Emirates. These reports were considered separately for individual counties and also considered as only three studies in general (Figure 1). One hundred and ninety-eight studies reported various MDR organisms in Saudi Arabia, (Table 2), where there were considerably more MDR organisms compared to the other countries in the Arabian Peninsula.
Saudi Arabia had the highest number of MDR strains reported compared to other countries (Supplementary Table S2): 10972 Escherichia coli, 9829 Mycobacterium tuberculosis, 4092 Klebsiella pneumonia, 3787 Acinetobacter baumannii, 2594 Pseudomonas aeruginosa, 2014 Acinetobacter, 986 Staphylococcus aureus, 927 Klebsiella spp., 812 Enterobacter, 722 Proteus vulgaris, 715 Enterobacteriaceae, 695 Methicillin-resistant Staphylococcus aureus (MRSA) and 553 Enterococcus. Recently, the emergence of 18 Clostridioides difficile and 19 Candida auris were reported [24,317]. Between 2010 and 2021, the top five research papers reported MDR micro-organisms in Saudi Arabia. The first report included A. baumannii 59 isolates from human samples: urine, blood culture [147], respiratory specimens, skin and soft tissue specimens, blood, sterile body fluids [146,224] Biofilm-Formation in Clonally Unrelated Multidrug-Resistant Acinetobacter baumannii Isolates), wound swabs, rectal swabs, and sputum [326]. The second report included 51 E. coli isolates from human and animal samples, the isolates from human samples originated from tissue swabs [327] (the genomic diversity and antimicrobial resistance genes in multidrug-resistant CTX-M-positive isolates of Escherichia coli at a healthcare facility in Jeddah), urine, wound pus, vaginal swabs, blood culture, stools and ear swabs [87]. The isolates from animal samples originated from: chicken [60], camel [77], and minced meat samples [72]. The third report included 36 K. pneumonia isolates from human samples: blood, urine, wound swabs, sputum [40], rectal swabs and suction swabs [216]. The fourth report included 36 P. aeruginosa isolates from human samples: respiratory, urine, surgical, blood culture, genital swabs, eye swabs, ear swabs, burns [234], skin tissue, intra-abdominal fluid, bone tissue [26], wound swabs, sputum, and tracheal swabs [228]. The fifth report included 31 M. tuberculosis isolates from human samples: sputum, tissues and biopsies, abscesses, abdominal fluids, breast fluid, cerebrospinal fluid, urine, knee fluid and synovial fluid [117], wound swabs, ENT swabs, blood, tracheal swabs [130] (Supplementary Table S3).
Saudi Arabia had the highest mortality rate, with 365 patients who died due to MDR microbes (Figure 3A). The top three MDR organisms with the highest mortality rates were A. baumannii, M. tuberculosis and P. aeruginosa. Six MDR organisms were related to mortality: S. epidermidis, A. baumannii, M. tuberculosis, C. auris, P. aeruginosa and Enterobacteriaceae (Table 4). Thus, there were 365 MDR strains associated with death. M. tuberculosis caused the highest level of mortality [27]. The impact of the migrant workers from other countries cannot be understated; in 2017, a Filipino resident of Saudi Arabia was diagnosed with MDR Mycobacterium leprae. The etiologic agent was discovered using metagenomic sequencing a biopsy sample of the patient’s skin [324]. In one of the studies, 105 adult patients admitted to the intensive care unit (ICU) at Aseer Central Hospital in 2014 and 2015 were reviewed retrospectively. The species of Acinetobacter were isolated using specific phenotypes and verified by the automated system, Vitek 2. Of the 105 stains, genus Acinetobacter accounted for A. baumannii 49, A. baumannii complex 19, A. baumannii/haemolyticus 32, A. haemolyticus 4, A. lwoffii 1 [144]. There are well-established studies on electron microscopic structures, which reported both dead and alive multidrug-resistant micro-organisms in Saudi Arabia, using confocal laser scanning micrography [328].
2.2. Bahrain
The Kingdom of Bahrain had the lowest number of research articles, in contrast to the rest of the Arabian Peninsula’s countries, due to its small area and population. The papers in this review, published between 2010 and 2021 and retrieved from PubMed and Scopus, were thoroughly screened for their eligibility, as per the inclusion and exclusion criteria. Only three studies published on MDR bacteria were included in the final qualitative analysis, as per PRISMA 2009 (Figure 1; Supplementary Table S1). Two studies reported MDR micro-organisms in multiple countries: a study by Sonnevend and colleagues [1] in Bahrain, Saudi Arabia, and the United Arab Emirates; and a study by Zowawi and colleagues [2] in Saudi Arabia, United Arab Emirates, Oman, Qatar, Bahrain, and Kuwait (Figure 1). Two unique MDR microbes were reported: Acinetobacter baumannii and Escherichia coli (Figure 2). Compared to the other countries mentioned in this review, Bahrain had the lowest reported MDR strain (n = 11): eight A. baumannii and three E. coli (Supplementary Table S2). Three E. coli isolates from human specimens were obtained, including urine and tissue swabs [1], and eight A. baumannii isolates, from which human samples of blood, sputum, swab, and urine were collected [2] (Supplementary Table S3). Unlike the mortality rates of the other countries, Bahrain reported no MDR microbial infection-associated deaths (Figure 3A). In one of the scientific articles, researchers screened for the mcr-1 gene of colistin resistant Enterobacteriaceae in Bahrain; the mcr-1 strains were positive and their antibiotic resistance was determined. The mcr-1 gene was found in two E. coli isolates [1]. In the study by Thani, on a urinary tract infection (UTI) cefotaxime resistant E. coli strain, a new DNA fragment was discovered. The DNA sequence was found to be linked to the pathogenicity island III536 locus. Researchers used the Single Genome Specific Primer-PCR (SGSP-PCR) to study the genomic state of the newly identified locus, which was discovered to obtain the antibiotic resistance gene blaCTX m [110]. Bahrain was included in the research on the molecular epidemiology and resistance mechanisms of carbapenem-resistant acinophilic bacteria (CRAB) for the Arabian Peninsula countries; eight A. baumannii isolates were identified in Bahrain hospitals, and OXA-51 was found in all of the isolates. Antibiotic resistance genes were detected using PCR, and clonality was determined using repetitive sequence-based PCR (rep-PCR). The majority (84%) of the isolates in this investigation were related to health exposure. The increased awareness of multidrug-resistant organisms in the Gulf Cooperation Council (GCC) states has significant implications for improving infection control procedures, developing antimicrobial stewardship programs and highlighting the importance of regional active monitoring systems [2].
2.3. Kuwait
The studies, published between 2010 and 2021, from selected databases were evaluated for eligibility, as per the inclusion and exclusion criteria, according to PRISMA 2009. Thirty-eight papers on multidrug-resistant (MDR) micro-organisms were included in the final qualitative analysis (Figure 1; Supplementary Table S1). A total of 22 unique MDR micro-organisms were identified from Kuwait (Figure 2), including the studies that reported MDR micro-organisms in various countries (Figure 1) [2,3]. There were seven publications that reported >100 MDR strains such as: 7138 methicillin-resistant Staphylococcus aureus (MRSA), 1176 Mycobacterium tuberculosis, 561 Candida auris, 410 Acinetobacter baumannii, 302 Staphylococcus aureus, 222 Klebsiella pneumonia and 149 Enterobacteriaceae (Supplementary Table S2). Notably, five studies in Kuwait from 2010 to 2021 revealed MDR micro-organisms. The first study revealed 11 M. tuberculosis, from human samples such as, sputum, pus, tissue biopsy, lymph node and endotracheal secretion, and cerebrospinal [112] samples. The second study found eight isolates of A. baumannii acquired from human urine [198] and swab specimens, sputum, blood [2]. The third study discovered six C. auris human isolates from axilla, groin, anterior nares, vascularline exit sites, the oropharynx, respiratory and urinary tract. The isolates were also taken from environmental samples: rooms, units occupied by all the infected C. auris, colonised patients, medical devices, linen, walls, floors, furniture, doorknobs, bed railings, bedside drawers, toilet faucets, and flush handles [9]. The fourth study observed five isolates of Enterobacteriaceae obtained from blood, urine, wound, and tissue swabs [259]. Finally, the fifth study anlysed four E. coli isolates of human samples derived from blood culture, urine, wounds, and central venous pressure [10]. After Saudi Arabia, Qatar, Jordan, and Iraq, Kuwait has the fifth highest mortality rate, with a total number of 78 non-survivors associated with MDR microbial infection (Figure 3A). Seven articles reported MDR microbial infection associated with mortality. The highest mortality in Kuwait was related to the MDR organism, C. auris, with 37 non-survivor patients, whereas C. auris were the most prominent MDRO in terms of the number of deaths (Table 3).
Healthcare-related pneumonia caused by MDR pathogens poses a significant treatment challenge. The frequency of antibiotic medication leads to inefficient antimicrobial therapy. Jamal and colleagues reported unique MDR organisms: two isolates of Haemophilus influenzae, two isolates of Legionella pneumophila, and one isolate of Moraxella catarrhalis. Critically ill patients with clinically diagnosed respiratory tract infections, hospitalised at Mubarak Al Kabeer Hospital between January and April 2013, were selected for their study. Recently, a rapid-multiplex, PCR-based Unyvero pneumonia application (UPA) assay that aids in early decision making became accessible. The respiratory samples from patients with nosocomial pneumonia included the sputum, bronchoalveolar lavage fluid, and endotracheal secretions [12]. From January to December 2016, a study conducted by Hamza and colleagues revealed a novel pathogen of an MDR micro-organism. All adult patients who had the specified GI procedures, used to estimate surgical site infection (SSI) rates among gastrointestinal surgeries in all Kuwait governmental hospitals, were examined in this study. Eventually, a single isolate of Aeromonas hydrophila was obtained from small bowel (SB) surgery [329].
2.4. Oman
After removing duplications, peer reviewed articles, and non-relevant countries of interest, a total of 42 articles were screened. Thirty-three studies were excluded from further analyses and nine articles fulfilled the inclusion criteria from the published data for MDR organisms from Oman in PubMed (n = 43) and Scopus (n = 36). Seventeen different species of multi-drug-resistant organisms were reported in Oman (Figure 2). Escherichia coli was the most recorded MDRO; this organism was identified five times in the studies (Table 2). Although several MDRO were recorded in this country, the following organisms were reported as the lowest among the collected studies: Pseudomonas aeruginosa, Staphylococcus aureus, Stenotrophomonas maltophilia Citrobacter freundii, Enterobacter asburiae, Enterobacter hormaechei, and Enterobacter ludwigii, Serratia marcescens and Pantoea dispersa. The total number of MDRO strains reported in Oman were as follows: 520 Klebsiella pneumoniae, 224 Acinetobacter baumannii, 78 Escherichia coli, 35 Staphylococcus aureus, 27 Pseudomonas aeruginosa, 25 Stenotrophomonas maltophilia, 8 Enterobacter cloacae, 2 Enterococcus faecium, and 1 Citrobacter freundii, (Supplement Table S2).
In the Oman region, E. coli was the most abundant MDRO, as reported by several studies. The study by Al-Kharousi focused on the microbial features of fresh fruit and vegetables at the market stage, evaluating the impact of antibiotic-resistant enterobacteria transmission. More specifically, this study focused on one of the resistance mechanisms in Enterobacteriaceae that could produce AmpC β-lactamase in cefoxitin-resistant isolates. Fourteen isolates displayed a multi-drug resistance for different classes of enterobacteria. From these different classes, E. coli isolates gained resistance to several types of antibiotics compared to other classes; they displayed the resistance to five antibiotics such as ampicillin, chloramphenicol, kanamycin, nalidixic acid, and tetracycline. Six E. coli isolates were collected from lettuce samples that gained a resistance to multiple antibiotics. Some isolates were phenotypically positive for producing the ampC β-lactamase [257]. Another study focused on the epidemiology of multi-drug-resistant organisms via the site of infection and types of bacteria at Sultan Qaboos University Hospital. Although several MDRO were identified, E. coli was the second most abundant among the isolates. The number of isolates was 60 for E. coli with extended spectrum β-lactamases and 5 for E. coli with a carbapenem resistance, respectively, among the samples from different infection sites, such as the bloodstream, urinary tract, and surgical infection [330]. A study focused on the colistin-resistant Enterobacteriaceae in several countries of the Arabian Peninsula, more specifically, studying the presence of the mcr-1 gene in this class. Four E. coli isolates were MDROs had an mcr-1-positive strain. The E. coli strains such as ST648, ST224, ST68, and ST131 belonged to other countries; none of these strains were from Oman [1]. The focus on identifying Arabian Enterobacteriaceae in the Arabian Peninsula region revealed the presence of strains with New Delhi metallo-beta lactamase (NDM)-7. Four stains showed a multi-drug resistance to NDM-7 E. coli; only one (E. coli ST4107) strain was from Oman Hospital, isolated from a patient’s endotracheal secretion. The blaNDM7 was identified on IncX3-type plasmids. In this study, an association was found between identifying the IncX3 type plasmids and spreading the rare NDM-7 variant in the region [101]. The defined mortality data associated with MDRO was not declared in studies from the last ten years [331,332]. This could be a major limitation of the statistical mortality data from the region; further studies are needed to discover the mortality data, which can be correlated with MDRO. Although several MDROs recorded in Oman were found in other regions in the Arabian Peninsula, few organisms were only found in the Oman region: Pantoea dispersa, Bukholderia cepacian, Enterobacter Hormaechei, and Enterobacter ludwigii (Table 1). Therefore, these MDROs were considered unique to the Oman region since they were able to survive in this region; specific studies are needed to find their prevalence and associated physiology.
2.5. Qatar
The searching process for the published data of MDRO from Qatar for the last decade resulted in a similar number of research results for both PubMed and Scopus; 54 and 52 studies were found in PubMed and Scopus, respectively. After removing duplicates, peer reviewed articles, and non-relevant countries of interest, a total of 52 articles were screened. Thirty-five were excluded from further analyses. Seventeen articles were screened for full-test article eligibility by screening the title and the abstract (Supplementary Table S1). Twenty-seven different species of multidrug-resistant organisms were reported in Qatar (Figure 2). Escherichia coli was the most recorded MDRO and was identified six times (Table 2). Among the collected studies, there were several MDRO recorded in Qatar; nevertheless, the following organisms were recorded as the lowest: Mycobacterium tuberculosis, Staphylococcus aureus, Streptococcus pneumoniae, Stenotrophomonas maltophilia, Enterobacter cloacae, Salmonella typhi, Vibrio vulnificu, Campylobacter spp., Nocardia crassostreae, Staphylococcus epidermidis, Staphylococcus haemolyticus, Staphylococcus hominis, Enterococcus gallinarum, Chryseobacterium indologenes, Acinetobacter spp., Enterobacter spp., Klebsiella spp., Salmonella spp., Bacteroid spp., Coagulase negative Staphylococci, Streptococci spp., and Enterococcus spp. These organisms were reported once as MDR (Table 2). A total of five MDRO above 100 strains were reported in Qatar: 426 Acinetobacter baumannii, 223 Escherichia coli, 223 Mycobacterium tuberculosis, 178 Pseudomonas aeruginosa, and 134 Streptococcus pneumoniae. Furthermore, six MDR organisms were reported: 73 Campylobacter jejuni, 34 Staphylococcus aureus, 26 Staphylococcus epidermidis, 24 Klebsiella pneumoniae, 23 Vibrio vulnificus and 13 Nocardia crassostreae (Supplementary Table S2).
Overall, Escherichia coli was the most abundant MDRO in Qatar. From the studies in Qatar, six research articles reported Escherichia coli (Table 2), which had the highest reported MDRO in Qatar. Hasan and colleagues studied the case of a patient infected with cytomegalovirus-associated, hemophagocytic lymphohistiocytosis that gained antimicrobial resistance. The patient colonised the multidrug-resistant MDR to Enterococcus faecium, Escherichia coli, and Klebsiella pneumoniae. As a result of the severe multidrug resistance, several infections such as respiratory, urine, and bloodstream infections, developed, causing a threat associated with the HLH patients and obtained MDR organisms. The study reported E. coli type ST410, which was isolated from blood. No specific strain numbers were declared for E. coli in this study. Using a whole-genome sequence, there were different sequence types between the vancomycin-resistant Enterococcus isolates from the urine and blood cultures of patients and the previously colonised patients. These authors found that the resistance mechanisms were acquired in the colonizing strains [333].
In another study, the bacterial infection and resistance patterns of pediatric oncology patients after chemotherapy treatment were analysed for MDRO in the bloodstream; 116 strains of Gram-positive and Gram-negative bacteria were isolated. E. coli was the third most common Gram-negative isolate with seven MDR isolates. Two patients died due to the infection of MDRO Stenotrophomonas maltophilia and E. coli. Unfortunately, no specific strain numbers and names were provided, hence they do not appear in the mortality table (Table 3) [55]. The study by Garcell et al. [78] focused on studying the etiology of surgical site infection in a community hospital in Qatar for a period of three years. Samples were collected and patients with contaminated wounds had the highest number of isolates. Most of the isolates in the surgical site were E. coli and Klebsiella spp.; 12 E. coli beta-lactamase (ESBL) isolates were collected from the infection in the surgical site [78]. The epidemiology of bacteremia at Hamad General Hospital isolated 167 g-positive, and 285 g-negative bacteria over a period of one year. The samples were collected from patients’ blood. Several MDRO were found; nevertheless, E. coli was the most common bloodstream isolate; 97 E. coli were isolated. The intravenous catheterisation blood stream infection was found to be the most common source of bacteraemia. In comparison with the other types of etiologic bacteria, the MDR E. coli ESBL caused the highest number of deaths, and accounted for 14 out of 102 mortalities [7]. Regarding the antibiotic resistance of E. coli in Qatar from food-producing animals, 90 E. coli isolates were reported from poultry farms and tested with several antibiotics. Uncooked food or unsanitary hygiene practices can accelerate the transmission of MDR to humans [75]. Having a statistical mortality on MDR microbial infection in the Arabian Peninsula is important for identifying the mortality caused by the MDRO. Qatar had the second highest number (n = 187) of mortalities compared to the other countries in the Arabian Peninsula, (Figure 3A). In Qatar, four studies reported information on mortalities. Several MDR organisms were recorded as the cause of a patient’s death. Acinetobacter baumannii was recorded as a pathogen associated with mortality in several studies (Table 3). The study by Al Samawi et al. recorded the higest number of deaths caused by Acinetobacter baumannii. The total number of non-survivors was 65 out of 239 patients, and 372 strains were isolated from adult patients samples. The respiratory tract was the most prominant site of A. baumannii infection [6]. (Table 3). Another study reported the same organism and its association with the deaths of 15 patients out of 48. A total of 48 MDR A. baumannii strains were isolated from the patients [4] (Table 3). Another study reported 102 deaths due to the MDR organisms, of which 34 were females. Multiple MDR pathogens caused the death of patients; nevertheless, ESBL and MSSA had the highest-recorded mortality [7] (Table 3). Although several MDRO recorded in Qatar were found in other parts of the Arabian Peninsula, Campylobacter spp., Nacardia crassostreae, Chryseobacteriu indologenes, Acinetobacter spp., Bacteroid spp., coagulase negative staphylococci, and Enterococcus spp. were considered unique to Qatar.
2.6. United Arab Emirates
The search terms related to multidrug resistance resulted in 71 studies from PubMed and 38 studies from Scopus. After removing duplicates, peer reviewed articles, and non-relevant countries of interest, a total of 70 articles were screened. Fifty-one studies were excluded from further analyses and 19 articles were screened for eligibility as full-text articles by screening the abstract. Four full-text articles were eliminated because patients were not from the country of interest. A total of fifteen full-text articles were included in this study (Supplementary Table S1).
Twelve different species of multidrug-resistant organisms were reported in the UAE (Figure 2). Escherichia coli was the most abundant MDRO in the UAE and was reported in six studies (Table 2). Although several MDRO were recorded in this country, the following organisms were reported as the lowest among the collected studies: Pseudomonas aeruginosa, Enterobacter cloacae, Candida auris, Citrobacter freundii, Staphylococcus epidermidis, and Salmonella typhi (Table 2). The total strain numbers of MDROs reported in the UAE were: 1116 Mycobacterium tuberculosis, 73 Enterobacteriaceae, 61 Escherichia coli, 55 Klebsiella pneumoniae, 31 Pseudomonas aeruginosa, 16 Acinetobacter baumannii, 6 methicillin-resistant Staphylococcus aureus, and 1 Stenotrophomonas maltophilia (Supplementary Table S2).
E. coli was the most abundant MDRO in UAE, and the highest reported by several articles. The study by Sonnevend et al. focused on the presence of the mcr-1 gene in colistin resistance to E. coli from several countries in the Arabian Peninsula. Four E. coli strains were isolated in this study; only one strain was from UAE, named ABC149 with the sequence type ST131. This sample was isolated from patients’ blood samples. In the Arabian Peninsula, several multi-resistance isolates contained the mcr-1 gene, which could increase mcr-1-carrying strains in these regions [1]. The impacts of ceftolozane–tazobactam and ceftazidime-avibactam against multidrug-resistant isolates such as Escherichia coli, Klebsiella pneumoniae, and Pseudomonas aeruginosa were studied, and included 60 CRE E. coli from different patient samples such as sputum, blood, urine, tissue, and body fluid samples. The study suggested that ceftolozane–tazobactam and ceftazidime–avibactam could treat most of the infections caused by MDROs [45]. Another study focused on the pattern of uropathogenic resistance to antibiotic prophylaxis in patients infected in the urinary tract. E. coli was the most grown organism with prophylaxis. The number of E. coli isolates was 26, and the majority of them were isolated from urine [97]. The activity of hymenochirin-1B against multidrug-resistant bacteria and immunomodulatory properties were studied [182] such as the E. coli strains, ABC 54 and ABC 85, collected from urine and tracheal aspirate. The study revealed a potential drug development, combined with hymenochirin-1B, against several Gram-positive and Gram-negative bacteria, with low cytotoxicity in humans. The characteristics of E. coli in several counties in the peninsula region revealed the presence of the New Delhi Metallo-beta-lactamase (NDM)-7, four stains showed a multi-drug resistance of NDM-7 E. coli, including two strains (ABC133 and ABC218) from the UAE region of patient’s sputum and wound secretion samples. The blaNDM7 was identified on IncX3 type plasmids and an association was found between IncX3 type plasmids and the transmission of the rare NDM-7 variant in the Middle East [101]. Mortality data were not declared in the studies; which is one of the limitations of such data. Further studies are needed to find the mortality data, which can be correlated with the MDRO. All twelve of the different species of multidrug-resistant organisms reported in the UAE were also reported in other countries in the Arabian Peninsula (Table 1). These organisms were able to survive in other parts of the Arabian Peninsula with hot dry summers and mild wet winters.
2.7. Jordan
The screening of multidrug-resistant micro-organisms from Jordan through the databases PubMed, Scopus, and Google Scholar revealed 136, 92 and 22,400 published articles related to multidrug resistance, respectively. After filtering out review papers and limiting the search results timeline to 2010–2021, thirty-seven articles were screened and six papers were excluded, since their samples were reported from ATCC standard cultures rather than human samples, resulting in a total of 31 full-text articles for final consideration. Jordan reported 11 distinct, multidrug-resistant bacterial species; Escherichia coli was the dominant species with 886 isolates in total, and Acinetobacter had the lowest number of strains reported, with 19 [33]. Out of all countries in the Arabian Peninsula, Jordan is the only country that reported Propionibacterium acnes as a unique multidrug-resistant bacterium. Research articles reported a variety of strains that were isolated from humans, hospital environments, or other sources where meat products and green vegetables could be present [334]. Some articles reported a large number of bacterial strains isolated from the aforementioned sources. For instance: 269 E. coli strains were isolated from broiler chickens [85], another study reported 287 Salmonella enterica isolates from beef cattle [100], while 544 Streptococcus pneumoniae isolates were obtained from humans [268].
E. coli were the dominant MDR bacteria in 11 research studies. One study isolated 142 E. coli ST131 strains from infants’ faecal samples, of which the majority were ESBL producers. The antimicrobial susceptibility of these strains was tested using the disc diffusion technique [64]. Similarly, Haddadin et al. found 19 and 25 MDR E. coli strains from 70 strains isolated from green vegetables and 68 isolated from infants’ faeces, respectively, after testing them for antibiotic susceptibility. In addition, they found a genetic similarity between the strains isolated from plants and infants, implying the possibility of the circulation of these pathogens between both sources [80]. O1, O2, O25, and O78 avian E. coli serotypes were characterised in a study after their isolation from broiler chickens, in order to study their antimicrobial resistance and the associated risk factors [85]. Another study investigated the cause of urinary tract infections among patients in Jordan. They isolated 262 E. coli strains from urine samples, of which 150 were MDR with a high association with the ST131 clone [96]. In addition, for the purpose of studying the colonisation of E. coli in the intestines, 288 stool samples were collected from infants. From these isolates, 52 were MDR and ESBL producers [104].
It was crucial to include mortality data in this review to observe the number of deaths caused solely by MDR micro-organisms and the root cause of their ability to cause a high mortality in the Arabian Peninsula (Table 4). Regarding mortality data collected from Jordan, several bacterial species contributed to these numbers. Specifically, Almomani et al. reported the deaths of 50 patients (24 males and 26 females) out of 119 patients suffering from pneumoniae caused by using ventilators infected with Acinetobacter baumannii in ICUs. This article reported the highest number of mortalities in Jordan [34] (Table 4). MDR Acinetobacter sepsis cases in neonates were also studied to determine the effect of Colistin; this organism caused two deaths out of twenty-one neonates, averaging 0.6 years of age [33]. Furthermore, there were 457 wound infection cases at a Jordanian hospital that included 395 males and 62 females with a median age of 27 years. These infections were caused by several MDR micro-organisms, including Staphylococcus aureus, E. coli, Klebsiella pneumoniae, Pseudomonas, Enterobacter, Acinetobacter, and Proteus and 37 deaths were reported [32].
2.8. Iraq
The number of final research articles from Iraq (n = 75) was generally higher than those reported from other countries in the Arabian Peninsula, with the exception of Saudi Arabia (n = 198), in PubMed and Scopus, and Google Scholar (Supplementary Table S1) for the keywords “multidrug-resistant”, and “multidrug resistance”. After excluding irrelevant articles, review articles, and limiting the timeline to 2010–2021, 75 research articles were eventually obtained for further analysis. A. baumannii was the dominant species in Iraq, followed by E. coli, with 10 research reports among the 28 different bacterial species reported, including four Staphylococcus species and three Klebsiella species. However, the largest number of strains were from Providencia spp.; 1213 isolates were reported from only two studies [49,261]. Several varieties of bacterial strains were reported from Iraq; these included 1063 S. aureus isolated from humans [15], 142 E. coli isolated from chickens [37], and 1209 Providencia spp. from various sources such as humans, soil, chickens, and wastewater [49]. Iraq is the only country in the Arabian Peninsula that reported the multidrug-resistant Vibrio cholerae, making it unique to this region [316].
A total of 12 research articles reported A. baumannii MDR strains. Metallo ג-lactamases producing A. baumannii caused a nosocomial infection in clinical samples from patients’ sputum, blood, urine, and burn wound swabs, in addition to samples from the environment; 124 strains were acquired from Baghdad hospitals to study their multidrug resistance [189]. A study conducted by Muslim et al. to determine the lectin-producing ability among 51 A. baumannii isolates from a hospital environment and patient samples of the sputum, blood, wounds and urine, revealed 17 lectin producers [183]. In addition, a study isolated 96 A. baumannii from clinical samples of wound and burn infections tested against 16 antimicrobial drugs using the disc diffusion technique, and 84 were found to be MDR [174]. Another article reported carbapenem resistance in 44 A. baumannii isolates from 182 patients who suffered wound infections, samples included swabs from joints, bones, and connective tissues [162]. In addition, the virulence factors of 30 A. baumannii strains from patients with blood infections were determined, implying their ability to cause persistent infections due to harboring plcN and lasB genes [177]. Even though, in general, there were many reports from Iraq, only one article reported mortality data compared to the other countries in the Arabian Peninsula. In 2012, Babakir-Mina et al. reported that, out of 654 burn patients, 98 died due to infections caused by S. aureus, while 556 survived (Table 3). These burn patients were mainly females (381) with a median age of 18 years. The nosocomial infection-causing agent was the methicillin-resistant S. aureus (MRSA), with a total of 1063 isolates from the burn swabs [15]. This study alone does not reflect the total mortality caused by MDR micro-organisms in Iraq. More research must be conducted in order to determine the dominant micro-organisms and the root cause of mortality from such organisms.
2.9. Yemen
Yemen had much fewer search results in PubMed, Scopus, and Google Scholar when the keywords, “multidrug-resistant”, and “multidrug resistance” were used. For instance, there were 19 results from PubMed, 38 from Scopus, and 2269 from Google Scholar; articles from Google Scholar were not included. Many search results showed articles reporting parasitic infections in some regions in Yemen and their multidrug resistances, but these were also not included, in addition to irrelevant and older articles published before 2010. Eventually, only six articles were included from the databases PubMed and Scopus for a final analysis. Yemen reported only four distinct bacterial species dominated by Mycobacterium tuberculosis, with 240 strains from four research articles. The remaining three articles reported A. baumannii, Pseudomonas aeruginosa, and S. aureus. All the bacterial isolates in these articles were from human sources, including 120 strains of M. tuberculosis [115], 60 of S. aureus [270], and 65 of P. aeruginosa [237]. As mentioned, the number of reports from Yemen were generally fewer compared to the other countries studied; three research articles mentioned the isolation of M. tuberculosis from patients residing in tuberculosis (TB) centers in Yemen. For instance, MDR M. tuberculosis were isolated from 115 patients’ sputum samples to evaluate the associated risk factors [17]. In a similar study was conducted by the same author, in which MDR M. tuberculosis involving 135 patients was explored to evaluate health-related risk factors [16]. Furthermore, sputum samples were collected from 170 patients in the National TB Institute of Sana’a and 118 M. tuberculosis isolates were identified [115]. Two articles, both written by Jaber et al., reported mortality data in Yemen [16,17]. The first study reported 14 deaths out of 115 tuberculosis patients (65 males and 50 females), with a median age of 45 years, while being treated in TB centers. All of the isolated M. tuberculosis were resistant to at least two drugs. The other study also reported the isolation of M. tuberculosis from sputum samples. This micro-organism caused 14 deaths out of 80 patients (48 males and 32 females) who were also in TB centers [16]. Mortality data were limited to patients treated in TB centers, extensively focusing on MDR M. tuberculosis per se. More extensive mortality studies must be conducted to investigate the prominent MDR micro-organisms causing substantial death cases in the Arabian Peninsula in general, particularly in Yemen.
3. Methods Used to Detect Multidrug-Resistant Organisms
Various detection methods are used to identify MDR organisms: the disc diffusion method [300,330], Kirby and Bauer method [335], microdilution process [161], PCR with specific primers [336], real-time PCR tests with temperature melting analysis [49], MDR-TB detection [125], E-test for antimicrobial resistance [4,148], automated identification and susceptibility system [330], Growth Indicator Tube system [337] automated Phoenix method [221], matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry (MALDI-TOF MS) [4], GeneXpert assay [338], AcrAB–TolC efflux pump system [36], multiplex PCR for confirming isolates [300,317], multilocus sequence typing [300], sequences of 18S rRNA gene and ITS region for MDR fungi [24], 16S rRNA gene sequencing [317], toxin genes multiplex PCR [317], multiplex real-time quantitative PCR [339], DNA Microarray Detection [84] and whole-genome sequencing [21].
The resistance of antibiotics was established for the A. baumannii isolates 506, 510 and 936 isolated in 2006, 2009 and 2012, respectively. In 2012, 12 unique XDRAB strains were extracted from critical patients with ventilator-associated pneumonia (VAP) using the microdilution process [161]. Minimum Inhibitory Concentration (MICs) were indicated by E-test. A CHROMagar Acinetobacter medium was used to diagnose susceptible and multi-drug-resistant A. baumannii (MDRAB) strain. The updated Hodge test (MHT) and multiplex PCR were used to examine carbapenemase-resistant A. baumannii. The E-test process was used to carry out a synergy test. A recent 3-year evaluation study determined a reduction in the antibiotic resistance in Gram-negative bacteria by the Saudi National Action Plan using commercially available identification cards (VITEK 2 ID-GNB cards) and MDR detection (AST-No. 12 cards) [340]. They found that the rates of antibiotic resistance, extended-spectrum beta-lactamase, and multidrug resistance were reduced over time, indicating that the Saudi National Action Plan was effective. Yassin et al., [299] reported the advent of Candida species resistance and suggested an antifungal sensitivity procedure performed prior to deciding on a treatment regimen. Updated techniques such as sequencing the 18S rRNA gene and ITS region in MDR fungi, 16S rRNA gene sequencing in bacteria, and toxin genes multiplex PCR were also adopted by laboratories in Saudi [24,317]. Whole-genome-sequencing-based MDR identifications were also reported [21]. Improved tools are needed for the diagnosis of MDRO [341,342].
Candida auris is an emerging fungal pathogen with multidrug resistance, causing nosocomial infections and invasive deaths [336]. A trustworthy diagnostic approach, such as using the 18S rRNA gene and ITS region against MDR fungi, is urgently needed [24]. C. auris is often mistaken for numerous other yeast species by phenotypic identification platforms [336]. In this work, PCR and real-time PCR tests were used for identifying C. auris and related species: Candida duobushaemulonii, Candida haemulonii and Candida lusitaniae. Targeted rDNA nucleotide region sequences, C. auris-specific, primers-based PCR or real-time PCR experiments followed by electrophoresis or temperature melting analysis, respectively, were performed using a panel of 140 clinical fungus isolates [336]. The findings of the tests completely corroborated the findings of the DNA sequencing. These genetic techniques address the current phenotypical shortcomings in the identification of C. auris and its associated species. The present MDR-TB outbreak is the result of decades of neglecting significant infectious diseases, a lack of national prevention program services, slow case identification, and inadequate treatment in high-burden countries [113]. The clinical results were vastly enhanced by optimizing care regimes along with the quick detection of DST in first- and second-line medications. The prognosis of MDR-TB was further strengthened by the recent advancements in MDR-TB detection and an intensive empirical management of patients with multiple medications during the initial period of treatment. However, laboratory funding, which is essential for the effective diagnosis of patients with MDR-TB, was largely insufficient. The rapid and cost-effective cultivation of DST systems of M. tuberculosis strains must be strengthened.
A pilot study from Hamad Medical Corporation (HMC), supported carbapenem resistance in randomly selected clinical isolates of multidrug-resistant Acinetobacter baumannii [4]. The research results were used to analyse carbapenemasal in all of the isolated MDR A. baumannii through molecular techniques. Matrix-assisted laser desorption/ionisation time-of-flight mass spectrometry verified the identification of MDR isolates, which was verified and validated by E-test antibiotic tolerance. Real-time PCR was used to explore the molecular nature of carbapenemases (blaOXA-23, blaOXA-24, blaOXA-58, blaNDM). The phylogenetic study on the partial sequence of CsuE and blaOXA-51 genes confirmed the epidemiological relationship between the isolates. The 48 isolates were resistant to most antibiotics, including meropenem, imipenems, ciprofloxacin, levofloxacin, amicacin, gentamicin, and most β-lactam; yet they were susceptible to colistin. The MDR A. baumannii production of OXA-23 carbapenemase in Qatar was described in detail by Rolain [4]. The effect of a 1 and 2 h exposure to low-frequency magnetic fields (0.3 and 0.42 mT) on Pseudomonas aeruginosa resulted in a reduced resistance and increased drug susceptibility [225]. This increase was often linked to the temperature of the environment and the duration of the exposure. Antibiotic resistance in Iraq was conferred on Escherichia coli by the AcrAB–TolC efflux pump system [36], which contributed to poor patient results.
Another study examined 177 chicken samples using the ISO 10272-2006 procedure to isolate Campylobacter spp. A multiplex PCR was used for the confirmation and labelling of the isolates [300]. The disc diffusion method was used to assess the isolates’ antimicrobial resistance, and multilocus sequence typing was used to genotype the isolates. There were three distinct sequence types in ten C. coli isolates, but seven different sequence types in ten C. jejuni isolates. Many of the isolates tested were resistant to ciprofloxacin but not to imipenem, and they were multidrug-resistant to five or more antimicrobials. A retrospective analysis of MDRO data from January to December 2012 used the disc diffusion method to verify antibiotic susceptibility analysis, and an automated identification and susceptibility system was used to recognise and analyse species [330]. Increasing patterns in the prevalence rates of MDRO patients and MDRO isolates were discovered during the study [330]. The study by Al Shamahy et al. examined septic-resistant organisms in the neonatal unit at Al-Thawra Hospital, Sana’a, Yemen and offered an empirical treatment approach [335]. One hundred and fifty-eight neonates, aged 0 to 28 days, were recruited in the study. Blood samples were collected from each neonate, then the samples were cultivated, and, subsequently, antimicrobial susceptibility testing was performed using the Kirby and Bauer method [335].
4. Antimicrobial Resistance Profiles Used for Treating Multidrug-Resistant Organisms
Combining low-frequency magnetic fields with a wide range of antibiotics helped to reduce P. aeruginosa tolerance [225]. The physical parameters of LF-MF, such as strength and exposure duration, influenced the reduction in bacterial resistance and provided a potentially noninvasive and fast treatment option for burn victims [225]. Peptide B1 had a broad-spectrum behaviour against the strains examined in the study by Tell et al. [343]. The concentrations used to destroy microbial cells ranged from 10 to 20 M. B1 had a lower toxicity against mammalian cells and a lower probability of causing hemolysis [343]. Domperidone is an important ArcB inhibitor, a well-known and secure over-the-counter antiemetic [36]. Domperidone reversed the antibiotic tolerance of levofloxacin and ciprofloxacin in MDR E. coli stains and was more effective than the recognised efflux pomp-inhibitor reserpine. It was also able to improve every impact on the sensitive strains of antibiotics. This finding suggests that a combination of antibiotics and domperidone may be utilised to handle multi-drug-resistant E. coli bacteria in the clinic [36]. Multidrug-resistant pneumonia in the health sector offers an important treatment challenge [12]. A Unyvero Pneumonia Application (UPA) quick PCR multiplex test helps to make prompt decisions. UPA was assessed for its successful detection in nosocomial pneumonia of the etiologic pathogen and for resistance indicators. This test also investigated the impact on acute nosocomial pneumonia. The appropriate specimens were treated by UPA according to the manufacturer’s methods, along with conventional cultivation techniques. The results indicated that a multiplex PCR-based test was capable of reliably diagnosing the etiological agents of NP and MDR, as well as resistance indicators. This could allow doctors to make early antibiotic modifications [12]. The analysis of E. faecalis genomes was performed by means of multilocus sequence typing. ST179 and ST16 were the most common STs in clonal complex 16 in Saudi patients (CC16). MDR isolates were approximately 96% (n = 149). There was nearly no coverage of the antibiotics quinupristin/dalfopristine, clindamycin, and erythromycin, but there were elevated levels of streptomycin, gentamycin and ciprophloxacin, which were observed to be under-optimal. Low vancomycin, linezolid and ampicillin resistance were found and suggested for treating E. faecalis infection [292]. Alqasim [57] discovered the frequency of β-lactamases produced by E. coli. They analysed the transportation of these isolates by suspicious antibiotic patterns at phenotypic and genotypic levels. A total of 100 E. coli urine isolates were collected at a tertiary health facility in Riyadh from January 2018 to March 2018. All antimicrobial isolates were tested for susceptibility. The synthesis of ESBL was separated in phenotypic and genotypic phases by double disc synergy testing and a polymerase chain response. A variety of ESBL variations were identified using DNA sequencing. Of the 100 E. coli isolates, 67 were associated with the phenotype of MDR. All isolates were tolerant to all the antibiotics that were used, which were all vulnerable to imipenemia. There were 33 phenotypic and genotypical isolates of ESBLs the in 100 isolates of E. coli. For all ESBL-positive E. coli isolates, CTX m was an ESBL (31/33 isolates; 93.94 percent). In all CTX m carriage isolates, the CTX-M-15 variant was included. The multiple ESBL carriage of 15–33 isolates (45.45%) was detected, with 11 (33.30%) ESBL isolates, compared to four isolates (12.12%) with three ESBLs. A vast range of forefront antibiotics were found by our study, which were frequently utilised for the treatment of UTI patients with a high antimicrobial toleration of E. coli that generated ESBL. Among the E. coli urinary isolates, the most common CTX m variants also had a high incidence of ESBL channels. This is a serious concern and needs to be investigated further to find better treatment options.
M. morganii isolates were highly resistant to many antibacterial agents and classified as MDR bacteria from Bahrain [315], all of which had ESBL. The antibiotics, meropenem and imipenem, were very effective against the M morganii isolates. In Jordan, 31 percent of S. aureus were multidrug-resistant (MDR) among the S. aureus isolates from wound samples [247]; however, they were vulnerable to chloramphenicol, linezolid, nitrofurantoin, rifampicin, and teicoplanin (>80%). In Qatar, a pulsed-field gel electrophoresis analysis of P. aeruginosa isolates from cystic fibrosis patients indicated a strong degree of resemblance, indicating a unique adaptation of these clones to cystic fibrosis-affected lungs. The non-cystic fibrosis, hospitalised cluster had a distinct clonal root with localised clustering and potential hospital-acquired P. aeruginosa infections [221]. A. baumannii isolates from Al-Thawra University hospital in Yemen were immune to almost all antibiotics examined, with a high minimum inhibitory concentrations of imipenem, amikacin, and ciprofloxacin [168]. All three A. baumannii strains were positive for the modified Hodge test, and no inhibition was observed on the activity of β-lactamases. The naturally occurring blaOXA-51-like gene, and the carbapenemase-encoding blaOXA-23-like gene, were observed in all three isolates and detected with 16S rRNA methylase armA gene. A search for aminuglycoside enzymes (AMEs)-producing genes identified the presence of acetyltransferase aac (6-Ib) in one A. baumannii isolate. Fluoroquinolone resistance-associated GyrA genes with one Ser83Leu variation were observed in all of the isolates. A multilocus sequence typing demonstrated that all the isolates were sequence type 2 [168]. A case study in pediatric patients from Saudi Arabia with combined immunodeficiency syndrome, reported treating pneumonia caused by multidrug-resistant P. aeruginosa using ceftolozane/tazobactam, which was recommended only for adult patients (>18 years) [241]. Peptide (AamAP1-Lysine) antibiotic (chloramphenicol, levofloxacin, rifampicin, ampicillin and erythromycin) combinations proved a strong synergistic activity, causing a 64-fold reduction in multidrug-resistant bacteria [344]. Colistin was effective and safe for treating MDR Acinetobacter neonatal sepsis in neonatal units in Amman, Jordan [33].
5. Mining Natural and Novel Antimicrobials against MDR
The antibacterial activities against the most common multidrug resistance micro-organisms associated with skin infections, were assayed using aqueous and ethanol extracts from five native medicinal plants, most of which showed an antibacterial and antifungal activity, with the highest activity found in the aqueous extract of Arum discoridis [345]. The experiments that characterised and measured the effect of honey on P. aeruginosa quorum sensing networks revealed that low concentrations of honey decreased the expression of exotoxin A (ETA), las and rhl glucons, as well as the corresponding virulence factors through the interruption of the quorum sensing system [346,347]. Edible plants (Gundelie tournefortii L. and Pimpinella anisum L.) and the propolis of Apis mellifera [348] were also considered as options for inhibiting the growth of MDR in combination with antibiotics [69]. Lavender essential oil used against carbapenemase-producing K. pneumonia [349], extracts of Lawsania inermiss, Portulaca oleracea used against Candida albicans [350], and Trachyspermum ammi extracts mediated the green production of metal-nanoparticles against MDR Listeria monocytogenes and Serratia marcescens [351] and were reported as suitable for the identification of novel antimicrobial agents against selective MDROs.
Ultrashort antimicrobial peptides (novel pentapeptide, UP-5) had a strong to moderate efficacy against MDRO, with a low toxicity when used in conjunction with traditional antimicrobials [352]. Alyteserin-2a, a cationic α-helical peptide recovered from the skin secretions of Alytes obstetricans, showed an efficient activity against multidrug-resistant Acinetobacter baumannii and Stenothrophomonas maltophilia [172]. Cuminaldehyde, a key antibacterial ingredient of Calligonum comosum essential oil, was reported to have an antibacterial activity against MDROs in a study from the United Arab Emirates [353]. Actinomycetes, specifically Streptomyces, Nocardiopsis sp., and MK MSt033 were discovered to have an antimicrobial activity against a variety of MDROs [354]. Many peptides were tested against MDR Acinetobacter baumannii [355,356,357]. Terminalia chebula, Terminalia bellirica, and Phyllanthus emblica plants, traditionally used for treating microbial infections were tested against MDR bacteria and fungi [358].
Buffalo milk lactoperoxidase against S. enterica and L. monocytogenes [359]; colistin against MDR Acinetobacter [33]; lactic acid bacteria from raw camel milk [360]; peptides, including hybrid peptides and ultrashort peptides [343,344,352]; ultrashort antimicrobial peptide nanoparticles [356]; Isatin-benzoazine molecular hybrids [361]; chemical derivatives [362,363,364,365]; extracts of Matricaria aurea [366]; extracts of Nepeta deflersiana [223]; Saudi scorpion venoms [367]; artemisinin extract [368]; biocidal polymers [369]; microtubule depolymerizing agents [370]; ozonated water [250]; and marine Streptomyces sp [371] against MDRO were all tested in the study region. Nanomaterials, nanoparticles and nanoformulations [351,356,358,372,373], as well as silver nanomaterials derived from marine Streptomyces [374] were also tested against the growth of multidrug-resistant micro-organisms. Further studies are needed to understand the molecular mechanisms and future possibilities of identifying pharmaceutically active compounds with potential medicinal applications.
6. Conclusions and Future Perspectives
The active surveillance and constant preventive efforts to control MDR infections and associated diseases can improve healthcare facilities and the socio-economic status of patients [375]. Specifically, MDR E. coli is predominantly associated with urinary tract infections in pregnancy [54,61,102]. The emergence of multi drug-resistant Candida albicans is prevalent among pregnant and non-pregnant women with vaginitis [299]. Listeria monocytogenes from patients with spontaneous abortions [310] and multidrug-resistant clinical Enterococcus faecalis from pregnant women [292] highlight the need for more precautions and constant monitoring, with the appropriate identification of MDR and susceptibility tests prior to medication. The development of a candidate vaccine and the early diagnosis of MDR infection shall be a better option for protection against MDR infection. The most prevalent multidrug-resistant Escherichia coli, Mycobacterium tuberculosis, Acinetobacter baumannii, Klebsiella pneumoniae, Pseudomonas aeruginosa, Staphylococcus aureus, Acinetobacter, Enterobacteriaceae, Providencia spp., Streptococcus pneumoniae, methicillin-resistant Staphylococcus aureus (MRSA), Klebsiella spp., Enterobacter, Proteus vulgaris, Candida auris and Enterococcus in the Arabian Peninsula must be diagnosed accurately and rapidly using advanced molecular techniques by developing region-specific diagnostic tools. The control of infections by using specificity detecting systems is an important protection method against MDRO. One study develops a direct detecting system for Candida auris by using a novel multiplex real-time quantitative PCR that has a high degree of specificity in detecting different species-level of Candida [339]. However, in healthcare settings, more detection methods are needed to detect MDRO strains within the species in clinical samples; allowing a reduction in the evolving MDRO pathogenic species. The Arabian Peninsula is rich in religious traditions. Notably, every year, more than 10,000,000 pilgrims visit Saudi Arabia to perform the Umrah and Hajj. Multidrug-resistant Streptococcus pneumoniae [376], Acinetobacter baumannii, Escherichia coli [377], Salmonella enterica [308], and Mycobacterium tuberculosis [378] is observed among the pilgrims; however, it is relatively very low compared to the total number of pilgrims, which indicates the successful surveillance and management of these micro-organisms. International guidelines and recommendations can be implemented for the management and complete prevention of MDRO, such as guidelines for MDRO regarding mass gathering events. Networking MDRO research strategies are mandatory among the countries of the Arabian Peninsula to fight against the risk of MDRO infection and death. This research can enhance the sharing of information, overcome the limited data availability, and identify molecular and physiological mechanisms behind multidrug resistance. MDR co-infection with SARS-CoV-2 among COVID-19 patients shall also be considered to reduce the disease burden [379,380]. This review uncovered the huge requirement for developing novel, safe, and sustainable antimicrobials from natural and other resources to fight against MDRO. Food process parameters and the overuse of antimicrobials require active surveillance to reduce resistance modulators. The present cumulative observations will be informative for effective planning, designing preventive strategies, and prioritizing research goals to achieve MDRO-free zones.
J.F.B., A.S.R., B.S., G.A., N.B.A. and S.A. conceived and designed the research; A.S.R., B.S. and G.A. performed the literature search and screening; J.F.B., N.B.A. and S.A. validated the final articles; J.F.B., A.S.R., B.S. and G.A. analysed and wrote the paper with the contributions of N.B.A. and S.A. All authors have read and agreed to the published version of the manuscript.
This research received no external funding.
Not applicable.
Not applicable.
All data are available upon reasonable request from the corresponding author.
The authors thank the Dean, Institute for Research and Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, Dammam, Saudi Arabia for her continuous support and encouragement. We thank The Deanship of Library Affairs from the Imam Abdulrahman Bin Faisal University for their support.
The authors declare no conflict of interest.
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![View Image - Figure 1. PRISMA 2009 flow diagram for the selection of articles reporting multi drug-resistant micro-organisms from the Arabian Peninsula, since 2010. * There were three papers reporting MDR micro-organisms in multiple countries [1]: Bahrain, Saudi Arabia and United Arab Emirates; [2]: Saudi Arabia, United Arab Emirates, Oman, Qatar, Bahrain, and Kuwait; [3]: Saudi Arabia, Kuwait, Oman and United Arab Emirates. # Google scholar not considered. Country-wise data for the number of articles from various databases are presented in Supplementary Table S1.](https://media.proquest.com/media/hms/THUM/2/EQHbL?_a=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&_s=lc9EZJeUX5qlY0S4mK5LaYsdQ9Y%3D "View Image - Figure 1. PRISMA 2009 flow diagram for the selection of articles reporting multi drug-resistant micro-organisms from the Arabian Peninsula, since 2010. * There were three papers reporting MDR micro-organisms in multiple countries [1]: Bahrain, Saudi Arabia and United Arab Emirates; [2]: Saudi Arabia, United Arab Emirates, Oman, Qatar, Bahrain, and Kuwait; [3]: Saudi Arabia, Kuwait, Oman and United Arab Emirates. # Google scholar not considered. Country-wise data for the number of articles from various databases are presented in Supplementary Table S1.")
Enlarge this image.Figure 1. PRISMA 2009 flow diagram for the selection of articles reporting multi drug-resistant micro-organisms from the Arabian Peninsula, since 2010. * There were three papers reporting MDR micro-organisms in multiple countries [1]: Bahrain, Saudi Arabia and United Arab Emirates; [2]: Saudi Arabia, United Arab Emirates, Oman, Qatar, Bahrain, and Kuwait; [3]: Saudi Arabia, Kuwait, Oman and United Arab Emirates. # Google scholar not considered. Country-wise data for the number of articles from various databases are presented in Supplementary Table S1.
Enlarge this image.Figure 2. List of multidrug-resistant bacteria and fungi reported in Arabian Peninsula. Numbers in the doughnut indicate the number of multidrug-resistant organisms reported in the respective countries of the Arabian Peninsula. MRSA: Methicillin-resistant Staphylococcus aureus.
Enlarge this image.Figure 3. (A) Multidrug-resistant microbial associated mortality reported in the Arabian Peninsula. (B) Dark red line indicates linear trend line of annual mortality due to multidrug-resistant microbial infection. (C) Number of deaths reported due to specific MDR microbial infection in Arabian Peninsula. Map in blue color indicate the country wise mortality due to Acinetobacter baumannii. (D) Percentage mortality due to MDR microbes. Gender information were not reported on the mortality in certain articles. UAE: United Arab Emirates.
Logical relation between sets of multidrug-resistant bacteria and fungi in countries of Arabian Peninsula.
| Countries | Number of MDRO | Multidrug-Resistant Micro-Organism(s) |
|---|---|---|
| Bahrain, Iraq, Jordan, Kuwait, Oman, Qatar, Saudi Arabia, United Arab Emirates, Yemen | 1 | Acinetobacter baumannii |
| Bahrain, Iraq, Jordan, Kuwait, Oman, Qatar, Saudi Arabia, United Arab Emirates | 1 | Escherichia coli |
| Iraq, Jordan, Kuwait, Oman, Qatar, Saudi Arabia, United Arab Emirates, Yemen, | 3 | Mycobacterium tuberculosis, Staphylococcus aureus, Pseudomonas aeruginosa |
| Iraq, Kuwait, Oman, Qatar, Saudi Arabia, United Arab Emirates | 1 | Klebsiella pneumoniae |
| Kuwait, Oman, Qatar, Saudi Arabia, United Arab Emirates | 2 | Enterobacter cloacae, Stenotrophomonas maltophilia |
| Iraq, Kuwait, Oman, Qatar, Saudi Arabia | 1 | Enterococcus faecium |
| Iraq, Jordan, Kuwait, Qatar, Saudi Arabia | 1 | Streptococcus pneumoniae |
| Iraq, Jordan, Kuwait, Saudi Arabia | 1 | Salmonella enterica |
| Iraq, Qatar, Saudi Arabia, United Arab Emirates | 1 | Salmonella typhi |
| Kuwait, Saudi Arabia, United Arab Emirates | 1 | Candida auris |
| Iraq, Kuwait, Saudi Arabia, Oman | 3 | Serratia marcescens, Proteus mirabilis, Klebsiella oxytoca |
| Iraq, Saudi Arabia, United Arab Emirates, Oman | 1 | Citrobacter freundii |
| Iraq, Jordan, United Arab Emirates, Qatar | 1 | Staphylococcus epidermis |
| Kuwait, Saudi Arabia | 1 | Candida glabrata |
| Oman, Saudi Arabia | 1 | Pantoea agglomerans |
| Qatar, Saudi Arabia | 1 | Vibrio vulnificus |
| Iraq, Saudi Arabia | 6 | Klebsiella aerogenes, Morganella morganii, Citrobacter koseri, Pantoea spp., Providencia spp., Staphylococcus saprophyticus |
| Iraq, Saudi Arabia, Qatar | Staphylococcus haemolyticus | |
| Kuwait, | 1 | Enterococcus gallinarum |
| Iraq, Jordan | 2 | Listeria monocytogenes, Campylobacter jejuni |
| Saudi Arabia, Qatar | 4 | Staphylococcus hominis, Klebsiella spp., Salmonella spp., Streptococcus spp. |
| Iraq, Qatar | 1 | Enterobacter spp. |
| Saudi Arabia | 53 | Staphylococcus capitis, Staphylococcus caprae, Acinetobacter calcoaceticus baumannii, Pseudomonas, Bacillus subtilis, Leuconostoc mesenteroides, Candida albicans, Staphylococcus epidermidis, Proteus vulgaris, Proteus sp., Bacillus cereus, Lactobacillus plantarum, Bipolaris oryzae, Methicillin-resistant Staphylococcus aureus, Bacillus tequilensis, Staphylococcus, Enterococcus, Staphylococcus saccharolyticus, Leclercia adecarboxylata, Shigella flexnari, Staphylococcus spp., Pantoea eucrina, Enterobacteriaceae, Citrobacter youngae, Staphylococcus petrasii, Lactococcus garvieae, Escherichia fergusonii, Caldimonas manganoxidans, Chryseobacterium gleum, Citrobacter sp., Providencia stuartii, Vancomycin-resistant Enterococcus, Mycobacterium leprae, Clostridium spp., Stenotrophomonus maltophilia, Enterococcus faecalis, Acinetobacter, Non-typhoidal Salmonella, Enterobacter aerogenes, Acinetobacter lwoffii, A. baumannii complex, A. baumannii/haemolyticus, Acinetobacter haemolyticus, Pseudomonas luteola, Serratia fonticola, Penicillin-resistant Streptococcus pyogenes, Bacillus spp., Serratia spp., Candida spp. |
| Kuwait | 5 | Legionella pneumophila, Aeromonas hydrophila, Moraxella catarrhalis, Prevotella spp., Haemophilus influenzae |
| Oman | 5 | Pantoea dispersa, Burkholderia cepacia, Enterobacter asburiae, Enterobacter hormaechei Enterobacter ludwigii |
| Qatar | 7 | Campylobacter spp., Nocardia crassostreae, Chryseobacterium indologenes, Acinetobacter spp., Bacteroid spp., Coagulase negative Staphylococci, Enterococcus spp. |
| Jordan | 1 | Propionibacterium acnes |
| Iraq | 1 | Vibrio cholerae |
Total number of studies that reported the MDR microbe in countries of the Arabian Peninsula.
| S. No | MDR Microbe | Saudi Arabia | Bahrain | Kuwait | Oman | Qatar | United Arab Emirates | Jordan | Iraq | Yemen | Total Number of Reports * |
|---|---|---|---|---|---|---|---|---|---|---|---|
| 1 | Acinetobacter baumannii | 59 | 1 | 8 | 2 | 2 | 5 | 6 | 12 | 1 | 96 # |
| 2 | Escherichia coli | 51 | 2 | 4 | 5 | 6 | 6 | 11 | 10 | 94 | |
| 3 | Mycobacterium tuberculosis | 31 | 11 | 2 | 1 | 2 | 1 | 6 | 4 | 58 | |
| 4 | Klebsiella pneumoniae | 36 | 3 | 4 | 4 | 4 | 7 | 58 | |||
| 5 | Pseudomonas aeruginosa | 36 | 4 | 1 | 4 | 1 | 1 | 9 | 1 | 57 | |
| 6 | Staphylococcus aureus | 16 | 4 | 1 | 1 | 2 | 5 | 5 | 1 | 35 | |
| 7 | Acinetobacter | 14 | 2 | 16 | |||||||
| 8 | Streptococcus pneumoniae | 7 | 1 | 1 | 2 | 1 | 12 | ||||
| 9 | Stenotrophomonas maltophilia | 7 | 1 | 1 | 2 | 11 | |||||
| 10 | Enterobacter cloacae | 6 | 1 | 2 | 1 | 1 | 11 | ||||
| 11 | Candida auris | 4 | 6 | 1 | 11 | ||||||
| 12 | Enterobacteriaceae | 6 | 5 | 11 | |||||||
| 13 | MRSA | 11 | 11 | ||||||||
| 14 | Stenotrophomonus maltophilia | 6 | 1 | 10 | |||||||
| 15 | Salmonella enterica | 2 | 1 | 2 | 4 | 9 | |||||
| 16 | Proteus mirabilis | 8 | 1 | 9 | |||||||
| 17 | Serratia marcescens | 3 | 3 | 1 | 2 | 8 | |||||
| 18 | Enterococcus faecalis | 8 | 8 | ||||||||
| 19 | Citrobacter freundii | 4 | 1 | 1 | 1 | 7 | |||||
| 20 | Enterococcus faecium | 6 | 6 | ||||||||
| 21 | Klebsiella oxytoca | 2 | 2 | 2 | 6 | ||||||
| 22 | Listeria monocytogenes | 2 | 3 | 5 | |||||||
| 23 | Morganella morganii | 4 | 1 | 5 | |||||||
| 24 | Staphylococcus epidermidis | 3 | 1 | 1 | 1 | 5 | |||||
| 25 | Salmonella spp. | 4 | 1 | 1 | 5 | ||||||
| 26 | Klebsiella spp. | 4 | 1 | 1 | 5 | ||||||
| 27 | Candida spp. | 4 | 1 | 5 | |||||||
| 28 | Streptococcus spp. | 2 | 3 | 1 | 5 | ||||||
| 29 | Enterobacter | 4 | 1 | 5 | |||||||
| 30 | Enterococcus | 3 | 2 | 5 | |||||||
| 31 | Staphylococcus spp. | 5 | 5 | ||||||||
| 32 | Salmonella typhi | 2 | 1 | 1 | 1 | 5 | |||||
| 33 | Enterobacter aerogenes | 5 | 5 | ||||||||
| 34 | Staphylococcus hominis | 4 | 1 | 4 | |||||||
| 35 | Candida albicans | 4 | 4 | ||||||||
| 36 | Non-typhoidal Salmonella | 2 | 2 | 4 | |||||||
| 37 | Citrobacter koseri | 2 | 1 | 4 | |||||||
| 38 | Klebsiella aerogenes | 4 | 4 | ||||||||
| 39 | Enterococcus faecalis/faecium | 1 | 1 | 1 | 3 | ||||||
| 40 | Providencia spp. | 1 | 2 | 3 | |||||||
| 41 | Pantoea spp. | 1 | 2 | 3 | |||||||
| 42 | Providencia stuartii | 3 | 3 | ||||||||
| 43 | Acinetobacter lwoffii | 3 | 3 | ||||||||
| 44 | Serratia spp. | 3 | 3 | ||||||||
| 45 | Campylobacter jejuni | 1 | 1 | 2 | |||||||
| 46 | Staphylococcus (MRSA) | 2 | 2 | ||||||||
| 47 | Proteus sp. | 1 | 1 | 2 | |||||||
| 48 | Candida glabrata | 1 | 1 | 2 | |||||||
| 49 | Pantoea agglomerans | 1 | 1 | 2 | |||||||
| 50 | Bacillus subtilis | 2 | 2 | ||||||||
| 51 | Staphylococcus capitis | 2 | 2 | ||||||||
| 52 | Staphylococcus saprophyticus | 2 | 2 |
* MDR organisms reported more than once in the countries of Arabian Peninsula are listed: # includes Acinetobacter calcoaceticus baumannii = 2, A. baumannii complex = 1 and A. baumannii/haemolyticus = 1. MRSA: methicillin-resistant Staphylococcus aureus.
Reports of mortality caused by MDR microbial infection from Qatar, Kuwait, Iraq and Yemen.
| Country | Qatar | Qatar | Qatar | Qatar | Kuwait | Kuwait | Kuwait | Kuwait | Kuwait | Kuwait | Kuwait | Iraq | Yemen | Yemen |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| MDR/Reference | [ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
| Total cases | 48 | 10 | 239 | 452 | 61 | 71 | 14 | 15 | 49 | 11 | 1430 | 654 | 115 | 80 |
| Median age years | 48 | 43 | 49.1 | 45.98 | 58 | 59.5 | 63.9 | 56.6 | 55.6 | 49.8 | 57.5 | 18 | 45 | 45 |
| Gender F | 1 | 57 | 159 | 19 | 24 | 5 | 6 | 15 | 6 | 730 | 381 | 50 | 32 | |
| Gender M | 9 | 182 | 293 | 42 | 47 | 9 | 9 | 34 | 5 | 700 | 273 | 65 | 48 | |
| No. of Discharged patients | 5 | 174 | 350 | 34 | 6 | 46 | 9 | 1415 | 556 | 101 | 66 | |||
| Total number of non-survivors | 15 | 5 | 65 | 102 | 4 | 37 | 9 | 8 | 3 | 2 | 15 | 98 | 14 | 14 |
| Number of non-survivors F | 35 | 2 | 3 | 3 | 1 | |||||||||
| Number of non-survivors M | 5 | 67 | 2 | 6 | 5 | 1 | ||||||||
| Multiple MDR pathogens | 102 | 9 | 3 | 2 | 15 | |||||||||
| Acinetobacter baumannii | 15 | 65 | ||||||||||||
| Pseudomonas aeruginosa | ||||||||||||||
| Staphylococcus aureus | 98 | |||||||||||||
| Mycobacterium tuberculosis | 14 | 14 | ||||||||||||
| Escherichia coli | ||||||||||||||
| Klebsiella pneumoniae | 5 | |||||||||||||
| Staphylococcus epidermidis | ||||||||||||||
| Enterobacteria | ||||||||||||||
| Candida auris | 37 | 8 | ||||||||||||
| Acinetobacter | ||||||||||||||
| Enterobacteriaceae | ||||||||||||||
| Proteus sp. | ||||||||||||||
| Salmonella typhi | 1 | |||||||||||||
| Salmonella enterica | 1 |
Reports of mortality caused by MDR microbial infection from Saudi Arabia and Jordan.
| Country | Saudi Arabia | Saudi Arabia | Saudi Arabia | Saudi Arabia | Saudi Arabia | Saudi Arabia | Saudi Arabia | Saudi Arabia | Saudi Arabia | Saudi Arabia | Saudi Arabia | Saudi Arabia | Saudi Arabia | Saudi Arabia | Jordan | Jordan | Jordan | Jordan |
|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|---|
| MDR/Reference | [ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
[ |
| Total cases | 49 | 83 | 60 | 71 | 2 | 90 | 5 | 7 | 19 | 713 | 86 | 3 | 38 | 146 | 457 | 21 | 119 | 56 |
| Median age years | newborn | 50 | 50.4 | 37.5 | 73.5 | 59.9 | 63.6 | 63 | 57 | 37 | 56 | 43 | 60.5 | 47.3 | 27 | 0.6 | 55.5 | 53.4 |
| Gender F | 11 | 23 | 0 | 32 | 1 | 10 | 294 | 31 | 3 | 14 | 42 | 62 | 64 | 22 | ||||
| Gender M | 18 | 37 | 48 | 2 | 58 | 5 | 6 | 9 | 419 | 55 | 24 | 104 | 395 | 55 | 34 | |||
| No. of Discharged patients | 26 | 30 | 34 | 47 | 2 | 198 | 19 | 69 | 30 | |||||||||
| Total number of non-survivors | 3 | 31 | 54 | 7 | 2 | 54 | 3 | 3 | 4 | 110 | 39 | 1 | 13 | 41 | 37 | 2 | 50 | 26 |
| Number of non-survivors F | 0 | 34 | 14 | 1 | 26 | 12 | ||||||||||||
| Number of non-survivors M | 3 | 76 | 25 | 24 | 14 | |||||||||||||
| Multiple MDR pathogens | 31 | 39 | 41 | 37 | ||||||||||||||
| Acinetobacter baumannii | 54 | 50 | 26 | |||||||||||||||
| Pseudomonas aeruginosa | 54 | 4 | ||||||||||||||||
| Staphylococcus aureus | ||||||||||||||||||
| Mycobacterium tuberculosis | 7 | 110 | ||||||||||||||||
| Escherichia coli | ||||||||||||||||||
| K. pneumoniae | ||||||||||||||||||
| Staphylococcus epidermidis | 3 | |||||||||||||||||
| Enterobacteria | ||||||||||||||||||
| Candida auris | 2 | 3 | 3 | 1 | ||||||||||||||
| Acinetobacter | 2 | |||||||||||||||||
| Enterobacteriaceae | 13 | |||||||||||||||||
| Proteus sp. | ||||||||||||||||||
| Salmonella typhi | ||||||||||||||||||
| Salmonella Enteritidis |
Number of multi drug-resistant strains reported in the Arabian Peninsula. Details of the number of strains are presented in the
| MDRO | Total Strain | Reference |
|---|---|---|
| Escherichia coli | 13254 | [ |
| Mycobacterium tuberculosis | 13087 | [ |
| Acinetobacter baumannii | 5600 | [ |
| Klebsiella pneumoniae | 5480 | [ |
| Pseudomonas aeruginosa | 3445 | [ |
| Staphylococcus aureus | 3133 | [ |
| Acinetobacter | 2033 | [ |
| Enterobacteriaceae | 1411 | [ |
| Providencia spp. | 1216 | [ |
| Streptococcus pneumoniae | 1077 | [ |
| Methicillin-resistant Staphylococcus aureus (MRSA) | 1000 | [ |
| Klebsiella spp. | 927 | [ |
| Enterobacter | 815 | [ |
| Proteus vulgaris | 722 | [ |
| Candida auris | 580 | [ |
| Enterococcus | 553 | [ |
| Pseudomonas spp. | 481 | [ |
| Klebsiella oxytoca | 434 | [ |
| Salmonella enterica | 413 | [ |
| Serratia marcescens | 289 | [ |
| Stenotrophomonus maltophilia | 257 | [ |
| Enterococcus faecalis | 256 | [ |
| Vancomycin resistant Enterococcus (VRE) | 255 | [ |
| Non-typhoidal Salmonella | 248 | [ |
| Vibrio vulnificus | 234 | [ |
| Salmonella typhi | 231 | [ |
| Proteus sp. | 220 | [ |
| Candida spp. | 180 | [ |
| Stenotrophomonas maltophilia | 149 | [ |
| Proteus mirabilis | 137 | [ |
| Campylobacter jejuni | 125 | [ |
| Arcobacter butzleri | 100 | [ |
| Pantoea spp. | 99 | [ |
| salmonella spp. | 85 | [ |
| Listeria monocytogenes | 83 | [ |
| Staphylococcus spp. | 78 | [ |
| Bacillus spp. | 77 | [ |
| Citrobacter freundii | 66 | [ |
| Serratia spp. | 66 | [ |
| Staphylococcus epidermidis | 59 | [ |
| Enterobacter cloacae | 54 | [ |
| Morganella morganii | 54 | [ |
| Citrobacter spp. | 54 | [ |
| Enterobacter aerogenes | 40 | [ |
| A. baumannii/haemolyticus | 32 | [ |
| Streptococcus spp. | 23 | [ |
| Vibrio vulnificus | 23 | [ |
| Staphylococcus saprophyticus | 20 | [ |
| Arcobacter cryaerophilus | 20 | [ |
| Vibrio cholerae | 20 | [ |
| A. baumannii complex | 19 | [ |
| Clostridioides difficile | 18 | [ |
| Enterococcus faecium | 17 | [ |
| Salmonella Enteritidies | 15 | [ |
| Prevotella spp. | 14 | [ |
| Nocardia crassostreae | 13 | [ |
| Candida albicans | 11 | [ |
| Staphylococcus hominis | 11 | [ |
| Acinetobacter lwoffii | 11 | [ |
| Providencia stuartii | 10 | [ |
| Acinetobacter calcoaceticus baumannii | 10 | [ |
| Citrobacter koseri | 9 | [ |
| Pseudomonas luteola | 9 | [ |
| Pantoea agglomerans | 9 | [ |
| Staphylococcus capitis | 4 | [ |
| Acinetobacter haemolyticus | 4 | [ |
| Serratia fonticola | 4 | [ |
| Candida glabrata | 2 | [ |
| methicillin-resistant Staphylococcus epidermidis (MRSE) | 1 | [ |
| penicillin-resistant Streptococcus pyogenes | 1 | [ |
| Leclercia adecarboxylata | 1 | [ |
| Mycobacterium leprae | 1 | [ |
| Chryseobacterium gleum | 1 | [ |
| Enterococcus gallinarum | 1 | [ |
| Klebsiella oxytoca | 1 | [ |
Supplementary Materials
The following are available online at
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; Alia Saeed Rasdan 2 ; Sonbol, Bayan 2 ; Alhamid, Galyah 2 ; Almandil, Noor B 3
; Sayed AbdulAzeez 4
1 Department of Epidemic Diseases Research, Institute for Research and Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, Dammam 31441, Saudi Arabia;
2 Department of Epidemic Diseases Research, Institute for Research and Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, Dammam 31441, Saudi Arabia;
3 Department of Clinical Pharmacy Research, Institute for Research and Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, Dammam 31441, Saudi Arabia;
4 Department of Genetic Research, Institute for Research and Medical Consultations (IRMC), Imam Abdulrahman Bin Faisal University, Dammam 31441, Saudi Arabia;