Introduction
Aedes aegypti, the primary arbovirus vector which carries diseases such as dengue, Zika, and chikungunya, has a wide geographic range and can be found in tropical and subtropical areas all over the world [1, 2]. Even though they are most prevalent in humid tropics and subtropics, mosquitoes also threaten public health in temperate regions [3, 4]. The changes in vector presence and abundance are influenced by weather factors and climate change [5]. This leads the public and scientific community to become more concerned about mosquito-borne diseases due to their rapid geographic distribution and rising disease burden. In 2022, the World Health Organisation (WHO) estimated that 390 million people were infected with the dengue virus annually, with Asia accounting for 70% of those cases. The most concerning aspect is that the number of cases continues to increase annually, with 2019 having the highest number of dengue cases recorded worldwide [6].
Effective vector management techniques and extensive surveillance are essential for attaining and maintaining a decline in dengue-related morbidity as the preventive and vector control strategies attempt to minimise dengue transmission, lower the frequency of illness, and prevent disease outbreaks [7]. Therefore, studies on mosquito-borne diseases play an important role in providing effective, efficient and environmentally proper mosquito control [8]. As a result, a large number of insectary-reared mosquitoes is needed for research, mosquito control programmes and studies which involve genetically modified and disease-resistant mosquitoes. Consequently, blood-feeding is a crucial method to produce insectary-reared mosquitoes, whereby an anautogenous mosquito like Ae. aegypti must consume at least one blood meal from a vertebrate host to successfully produce and lay one clutch of eggs [9].
The blood-feeding of female mosquitoes is an essential part of colonisation as it allows female oocytes to develop and mature [10, 11]. The blood-feeding process consists of four sequential steps, including being attracted to and settling on the host, piercing the host’s skin with a fascicle, sucking blood, and removing the styles [12]. Therefore, the blood-feeding process is one of the most complicated and difficult steps to imitate when rearing mosquitoes in the laboratories.
Traditional methods, such as by using the forearm of an entomologist or willing volunteer, may present risks, for example, if the mosquito colony or person feeding them is unknowingly infected with a pathogen [13, 14]. Besides that, various species of live animals also used for mosquito blood feeding in the laboratory, including birds, mice, hens, rats, guinea pigs, white rabbits, hamsters, sheep, horses, and even humans [15–22]. However, by using anaesthetised live animals for direct blood-feeding in the laboratory has several drawbacks, such as the pain and stress caused by blood-feeding, the high cost of keeping animals in the laboratory, need for a suitable physical environment for animals, and specialised staff to manage these resources [10, 23]. In practice, these approaches also frequently require animal preparation, like removing or shaving off its hair, restraints, sedatives and anesthetics, hence, making the process more complicated [24]. In addition, when it comes to animal usage, bioethics committees urge the application of 3Rs: replacement, reduction and refinement. Also, they suggest the use of artificial blood-feeding systems instead of live animals [25].
As a result, several artificial membrane blood-feeding systems were developed to maintain Ae. aegypti colonies in the laboratory. These ranged from commercial blood feeding devices, such as the Hemotek membrane feeding system [26] that can cost up to £980 to £2510 [27] to more cost-effective techniques [28–31]. Besides being low in cost, this artificial blood-feeding system often uses a membrane to mimic the host skin and is effective for blood-feeding without the requirement for maintaining live hosts. Therefore, to induce mosquitoes to feed on blood by using an artificial blood-feeding system require a few components, such as blood source, membrane, feeder which can hold the blood and heat source [11]. When rearing mosquito vectors in the laboratories, researchers frequently face two challenges, which are the feeding technique and blood source that will significantly provide consistency and success in colony establishment, as well as experimentation [32]. Several studies had demonstrated effective artificial methods for blood-feeding Ae. aegypti in the laboratory settings. However, there is currently a notable gap in research concerning the preferred blood sources of Ae. aegypti and how these sources impact its blood-feeding and fecundity rate.
Therefore, the purpose of this review is to evaluate the data (from peer-reviewed papers) on the use of different blood sources and components in artificial membrane feeding system and their effects on blood-feeding and fecundity rate of Ae. aegypti. These study findings may help various research institutes to look for suitable blood sources that will provide the best growth and reproduction rates for Ae. aegypti species.
Methods
The methodologies used in this scoping review were developed by Joanna Briggs Institute (JBI), and are based on a framework first proposed by Arksey and O’Malley (2005) and refined by Levac et al. (2010) [33–35] According to the JBI structure, six steps should be included in a scoping study to assist authors: (i) formulating a research question, (ii) finding relevant studies, (iii) study selection, (iv) visualising data, (v) combining, summarizing, reporting results and (vi) validating study findings [35]. The following research question was investigated by using population, concept, and context (PCC): In artificial membrane feeding of Ae. aegypti (population), do different types of blood source and component used (concept) affect the blood-feeding and fecundity rate of this species (context)? The PCC framework was selected because it facilitated more detailed and accurate findings. The included studies complied with the following criteria:
Population
Only Aedes aegypti species that had been blood fed by using an artificial membrane feeding system were included irrespective of any countries. Each article was screened to determine if the population met the eligibility requirements. Articles that included other mosquito species with artificial membrane feeding were excluded from this review.
Concept
This scoping review focused on the types of blood source and component used in artificial blood-feeding system to blood feed Ae. aegypti. Articles with direct blood-feeding on different types of live animals were excluded.
Context
The reviewers included publications that had reported the effect of the concept on (i) blood- feeding rate [(total number of engorged female mosquitoes / total number of female mosquitoes) x 100] and (ii) fecundity rate (number of eggs laid by female mosquitoes)].
Search strategy
This scoping review did not focus on the method of blood-feeding Aedes mosquitoes, but on studies that contained information on types of blood source and component used in the artificial membrane feeding system. The PubMed, Scopus, and Web of Science (Clarivate Analytics) databases were searched for articles from January 1980 to January 2023. In order to make the review more comprehensive and reliable, backward citation screening was used to find eligible articles from each database and then manually searched for more articles. The keywords were combined with suitable Boolean operators like “AND” and “OR” to search for articles in the electronic databases. In order to make the search more precise, proximity operators, truncation, and wildcards were applied to the keywords for the final search strings.
Eligibility criteria
Only full-text articles in English were taken into consideration in this scoping review, whereby articles from countries that were published in a different language might have been overlooked. Besides that, systematic, scoping or narrative reviews and meta-analyses were excluded as the study only interested in the findings of a single study. In the full-text screening stage, reference lists of all of these “reviews” were looked through to find more primary research on the study topic. Moreover, the searched articles must describe about the mosquito species, study sample size, study design, blood-feeding methodology and parameters measured.
For exclusion criteria, an article was excluded if (i) it was not available in full-text, (ii) it contained only mosquito blood-feeding techniques or methods without reporting any results of different types of blood source or component, and (iii) its intended parameters like blood-feeding rate and egg production were not reported. In addition, literature reviews and articles with inadequate data were also excluded.
Data extraction and data charting
The EndNote version 20 software was used to import all searched articles while duplicate files were deleted. All articles and other data files were safely stored in Google Drive by the reviewer. The studies were chosen independently by three reviewers and any discrepancies were handled in discussions with the team. The articles were evaluated twice, whereby the first screening step was based on the title and abstract of article, followed by the full-text screening step. Then, relevant information was retrieved for analysis by using the Microsoft Excel Spreadsheet. The data extraction sheet included the first author’s name and publication year, title of article, types of blood-feeding used, study design, types of blood source or blood component used, and the key findings.
Results
Description of studies
In the initial search through the three databases, a total of 2,161 articles were identified by the reviewers. After the duplicates (n = 296) were removed, the remaining articles were screened by reading the abstracts and publication titles. Then, the remaining 104 full-text articles were further screened for eligibility. Following the final full-text screening, nine articles were selected for inclusion and seven more articles were included following backward citations from these nine articles, resulting in total of 16 eligible articles. Fig 1 shows a flow diagram of the selection process. The most common reasons for exclusion were that the outcome was not of interest and different mosquito species. Some other exclusion criteria were unrelated objectives, reviews, and experimental studies.
[Figure omitted. See PDF.]
The PRISMA flow diagram shows the search and selection process used during our systematic literature search for this scoping review.
Characteristics of included studies
In the selected studies, different types of artificial blood-feeding technique were used: two used Hemotek membrane feeding system [36, 37], two used Glytube [38, 39], two used metal plate [11, 26] and 10 other studies used a variety of simple and affordable membrane feeding methods, which consisted of different types of membrane, such as the sausage casing membrane [12, 20, 30], and Parafilm M [10, 40, 41]. Besides that, several heating sources for the blood, namely circulating water bath [10, 20, 42, 43], germination mat [11], rice grains [26], vegetable oil bag [40], USB chargeable hand warmer, [44] and microwavable heat pack [45] were also used.
A total of 11 studies from 16 used direct blood-feeding method on live animals, such as mice [12, 36, 38, 39, 41, 44], guinea pigs [10, 30], hamsters [20, 42] and rat [40] as the study control. Furthermore, many blood sources from different vertebrates like guinea pigs, mice, rat, chicken, turkey, pig, sheep, cattle, humans as well as blood components such as whole blood, plasma, blood cells from chicken, turkey, rat, pig, sheep, cow and humans were used in the artificial membrane blood feeding system. Besides that, there were a variety of parameters measured in the selected studies such as blood-feeding rate, fecundity rate, hatching rate, survival rate, oviposition rate, mean time egg to adult, the ratio of indigested blood, pupal emergence rate and yolk deposition. However, only blood-feeding and fecundity rate were included in this review because they were reported in all studies. Table 1 summarises the types of study that were taken into account for the review.
[Figure omitted. See PDF.]
Blood sources
Results from all included studies showed that blood meal sources affected blood-feeding and fecundity rate of Ae. aegypti.
Human blood.
The mean percentage of blood feeding rate from feeding on human blood was, on average, high (mean ± standard deviation) (between 51.3% and 97.33 ± 0.99%) [20, 26, 38] which also resulted in a higher fecundity rate that ranged between 14.85 ± 0.39 and 101.0 ± 21.0 eggs per female mosquito, as compared to other blood meal sources.
Cattle blood.
Cattle blood demonstrated a comparable blood-feeding rate which ranged between38.2 ± 21.5% and 90.12 ± 3.10% and egg production between 86.7 ± 7.8 and 162.32 ± 25.94 eggs per female with human blood [11, 26, 40].
Sheep blood.
Even though sheep blood showed a higher blood feeding rate which ranged between 86.7 ± 8.5% to 97%, it negatively affected the number of eggs laid that resulted in a significantly low fecundity rate [10, 20]. Despite of low fecundity rate, sheep blood showed no significant difference in the hatching rate as compared to human blood and direct blood-feeding on hamster [20].
Chicken blood.
Chicken blood showed a slight difference in both blood-feeding and fecundity rate as compared to human blood and direct blood-feeding on mice [26, 39]. Additionally, chicken blood showed a blood-feeding rate of 79.67 ± 0.91% using metal plate with Parafilm-M method [26] while the blood feeding rate was reduced to 45.00 ± 1.35% when using Glytube with Parafilm-M method [39]. Meanwhile, only 12.69 ± 0.28 eggs per female was produced in metal plate method whereas female mosquitoes blood fed using Glytube method produced 66.05 ± 15.11 eggs regardless of their low blood feeding rate.
Guinea pig blood.
According to the findings by Phasomkusolsil et al. (2013), guinea pig blood with 66.7 ± 16.6% of blood-feeding rate showed no significant differences with human blood 67.0 ± 19.9% and it demonstrated a higher fecundity rate as compared to mouse blood and human blood in the study by Farnesi et al., [36].
Pig blood.
Two studies found that the blood-feeding and fecundity rate of pig blood showed no significant differences with the control human blood [37] and direct blood-feeding on mice [12]. Similar findings were also found by Deng et al., (2012) when mini pig blood was used against direct feeding on guinea pigs as control.
Rabbit blood.
Rabbit blood was used in only one study by Dias et al. (2018) [10] whereby the defibrinated and citrated rabbit blood showed no significant differences in blood-feeding and fecundity rate. However, it had a low hatching rate which ranged from 54% to 69%, as compared to the direct blood-feeding on guinea pig.
Expired human blood.
A study by Pothikasikorn et al. (2010) [42] found a small significant difference in the blood-feeding and fecundity rate of Ae. aegypti blood that was fed on expired human blood of between 5 days and 15 days, as compared to the blood-fed mosquitoes on mice. However, the 25-day expired human blood showed a very low blood-feeding rate of 18% and 8.8 eggs per female mosquito.
Blood components
In this review, three studies evaluated the efficiency of blood components in blood-feeding Ae. aegypti by using a membrane blood-feeding system [12, 44, 45].
Whole blood.
According to the findings by Luo (2014) [12], the blood-feeding rate of pig whole blood by using Parafilm-M membrane (92.9%) and cattle collagen sausage-casing membrane (89.7%), pig whole blood added adenosine triphosphate (ATP) (90.7%) and pig plasma added with ATP (91.5%) showed a comparable rate with the control direct blood-feeding on mice (98.0%). Besides blood-feeding rate, the fecundity of per female fed on pig whole blood (49.88 ± 7.92 eggs) shows no significant differences with the fecundity rate fed on mice (58.33 ± 2.56 eggs) but it was higher than those fed on pig plasma (33.88 ± 6.43 eggs). In addition, pig whole blood demonstrated a higher hatching rate (94.10 ± 3.54%) than direct blood-feeding on mice (86.25 ± 4.60%) and pig plasma (77.00 ± 6.51%).
Apart from that, blood components like whole blood, plasma and blood cells from two mammals (humans, rat) and two birds (chicken, turkey) were evaluated for the efficiency in blood feeding Ae. aegypti [44]. Amongst the three blood components, whole blood of all vertebrates was identified as the most preferred blood components by Ae. aegypti in terms of blood-feeding and fecundity rate. Another study by Gonzales et al. (2015) [45], also found the similar findings, whereby bovine whole blood recorded the highest rate in blood-feeding and fecundity followed by bovine serum albumin and bovine serum [45].
Red blood cells, hemoglobin and plasma.
Bovine red blood cells, bovine hemoglobin (Hb), sheep blood cells, chicken and turkey plasma recorded the lowest blood-feeding rate with no eggs produced. On the other hand, chicken and turkey blood cells stimulate more eggs production in Ae. aegypti, whereas human blood cells caused females to lay a few or no eggs [44].
Isoleucine content in blood source.
There was no significant difference in the number of eggs produced per mosquito between females that were artificially fed on low isoleucine human blood (55.8 ± 10.6 eggs) as compared to the high isoleucine human blood (52.0 ± 4.4 eggs). It was similar for females that were fed on human naturally (low isoleucine) with a mean of 84.1 ± 5.3 eggs per female as compared to a chick (high isoleucine) with 83.6 ± 5.4 eggs [43].
Discussion
Several research studies demonstrated that many factors influenced the physiological processes in mosquitoes, such as the species of mosquito [46], body size of species [47], blood meal size [48], amino acids derived from erythrocytes [49], types of artificial blood-feeding systems and synthetic membranes [26, 39], types of blood sources or components [44], and the anticoagulant used to preserve the blood source [50]. It had been discovered that mosquito meals must contain proteins for egg maturation and oogenesis [10, 51–53].
Ae. aegypti prefers mammalian blood [54] selectively human blood [26], even under the availability of other blood sources [55]. However, a previous study which used blood-feeding Ae. aegypti revealed that avian blood resulted in higher egg production than mammalian blood [56]. Contrarily, Suleman and Shirin (1981) [57] found that mammalian blood increased fertility more than avian blood in Culex quinquefasciatus. Therefore, from all studies included in this review, human whole blood-fed mosquitoes showed higher blood-feeding, fecundity and hatching rates as compared to other blood sources or components. However, there are a number of ethical and safety concerns with the use of human blood for insectary colony management. Human blood is also in short supply due to lack of donors, whereby human blood preserved in blood banks is primarily used for medical emergencies instead of insectary experiments. Apart from that, the use of live animals such as mice [12, 36, 38, 39, 41, 44], hamsters [20, 42], guinea pigs [10, 30], and rats [40] in direct blood feeding of Ae. aegypti also gives good blood-feeding and fecundity rates. However, the use of animals in these insectary experiments poses several challenges, including in maintaining the resources, which is costly and labour-intensive, and thus requires approval from animal ethics committee [10]. Therefore, various membrane blood feeding systems were developed, and suitable blood sources or components are required as a blood meal source.
Several studies were conducted to investigate the variation in fertility of mosquitoes after feeding on various hosts, as reviewed by Lyimo and Ferguson (2009) [58]. Subsequent research revealed that this variation was caused by different levels of amino acids in different vertebrate blood sources, whereby some amino acids are limiting factors for egg formation while others enhance the vitellogenesis in mosquitoes [59, 60]. A study by Kaczmarek et al. (2021) [50] found that artificially sheep blood-fed mosquitoes showed significantly higher levels of free fatty acid content in the cuticle of Ae. aegypti as compared to human blood-fed mosquitoes [50]. As a result, the artificially sheep blood-fed mosquitoes showed a reduction in fecundity rate, which might be related to increased transport and buildup of free fatty acids in the cuticle. So, these modifications in the mosquitoes’ body might eventually disrupt the fertility and sensitivity of these insects towards chemical substances like insecticide.
Besides that, a study by Harrington et al. (2001) [43] showed that low isoleucine human blood might increase the energy stores as well as the physiological processes in Ae. aegypti instead of high isoleucine rodent blood or avian blood. However, the differences in energy stores were less noticeable when the females were artificially given human blood with or without isoleucine added. This indicated that a low isoleucine level in human blood might not be the only component which helps energy reserves build up [43].
Bovine whole blood and pig whole blood showed no significant difference in blood-feeding rate as compared to the controls [12, 37, 45]. It was also found that Ae. aegypti fed on bovine whole blood, serum and bovine serum albumin (BSA) produced a greater number of eggs per female as compared to those fed on red blood cells (RBCs) or hemoglobin (Hb), which resulted in no eggs. In contrast, Luo (2014) [12] found that Ae. aegypti’s fecundity rate was considerably reduced when fed with pig plasma as compared to pig whole blood. This was because if sedimentation took place in whole blood during blood-feeding of Ae. aegypti on artificial feeding system, it might result in fewer eggs as they might consume plasma rather than whole blood [12]. Therefore, bovine whole blood and pig whole blood can routinely be obtained from a nearby slaughterhouse and stored in the refrigerator for a period of time, depending on the anticoagulant used [26, 61]. However, this strategy is not practical for certain institutions that are located far from the slaughterhouse.
Apart from that, frozen citrated bovine blood that can be purchased from grocery stores was also successfully used to establish Ae. aegypti colonies with a higher fecundity rate, whereby the frozen bovine blood was thawed before use [11]. This frozen bovine blood can be stored for up to one year in the freezer, which will be a good option for research institutes which are located far from the slaughterhouse [11]. In addition, expired human blood can be obtained from blood banks or hospitals, whereby it has been successfully utilised in the blood-feeding of Ae. aegypti [23, 42, 62]. It is proposed that, Ae. aegypti may be fed on human blood that has been stored for up to 10 days past its expiration date [42]. Furthermore, the previous study revealed that fresh blood had no advantages over preserved human blood as long as the red blood cell lysis does not occur during collection and preservation.
In addition, the types of artificial blood-feeding system have been proven to influence the blood feeding rate and egg production of Ae. aegypti as the use of chicken blood in a metal plate with Parafilm-M resulted in a higher blood-feeding rate and lower egg production than Glytube with Parafilm-M [26, 39]. Likewise, the selection of synthetic membranes used in artificial blood-feeding systems also plays a significant role in mosquito blood feeding, whereby citrated bovine blood that used a metal plate with polytetrafluoroethylene (PTFE) showed a higher blood feeding and fecundity rate than metal plate with Parafilm-M [11]. Therefore, a further detailed review is needed to include all other factors that could affect the blood feeding and fecundity rate in membrane-feeding Ae. aegypti.
Consequently, from this scoping review, it is concluded that bovine whole blood and pig whole blood could be suggested as a suitable blood source in membrane feeding, followed by guinea pig blood in mosquito colonisation. However, other factors such as types of artificial feeding system, heat sources, synthetic membranes, duration of blood feeding, as well as the anticoagulant used play a vital role in selecting a suitable blood meal source. It is hoped that this scoping review provides a framework for future research that is looking for suitable blood meal sources or components to be used in artificial blood feeding systems.
Limitations
This scoping review lies in the restriction to a limited number of databases, namely PubMed, Scopus, and Web of Science, for the identification and retrieval of relevant literature. This selective approach may have resulted in the inadvertent exclusion of valuable studies from other databases that could have contributed diverse viewpoints and a more comprehensive understanding of the blood sources preferred by Ae. aegypti. Additionally, only two parameters, namely blood-feeding and fecundity rate were considered within the scope of the included studies. This was because only these two common parameters were evaluated amongst all the 16 included studies. By limiting the assessment to these specific parameters there exists the possibility of neglecting other equally relevant parameters that are influenced by the blood sources and blood components fed by Ae. aegypti.
Conclusions
This scoping review summarised the effects of different types of blood source and component on Ae. aegypti. It explores the impact on the blood-feeding and fecundity rates of Ae. aegypti. In this review, 16 eligible studies found that the blood-feeding and fecundity rates of Ae. aegypti were influenced by the types of blood source or component taken by the species. Therefore, bovine whole blood and pig whole blood showed a comparable blood-feeding and fecundity rate with human blood, followed by guinea pig’s blood. Besides that, the findings of this review showed that sheep blood was not suitable for use in membrane feeding as it decreased the fecundity rate of Ae. aegypti. The findings of this review will be useful to find suitable blood sources and components in blood-feeding Ae. aegypti which will certainly provide the best growth and reproduction rates that play a significant role in establishing mosquito colonies in studies related to medical entomology.
Supporting information
S1 Table. Listed initial papers assessed for eligibility.
https://doi.org/10.1371/journal.pone.0295961.s001
(XLSX)
S1 Checklist. Preferred Reporting Items for Systematic reviews and Meta-Analyses extension for Scoping Reviews (PRISMA-ScR) checklist.
https://doi.org/10.1371/journal.pone.0295961.s002
(DOCX)
Acknowledgments
We would like to express our gratitude to the editors and reviewers for reviewing and commenting on the manuscript. We also acknowledge the support we received from the Department of Parasitology and Medical Entomology and the Faculty of Medicine, UKM. We are grateful for the help and insights we received from Mohd Farihan Md Yatim and the rest of our research team.
Citation: Suresh Y, Azil AH, Abdullah SR (2024) A scoping review on the use of different blood sources and components in the artificial membrane feeding system and its effects on blood-feeding and fecundity rate of Aedes aegypti. PLoS ONE 19(1): e0295961. https://doi.org/10.1371/journal.pone.0295961
About the Authors:
Yuvaraahnee Suresh
Roles: Writing – original draft, Writing – review & editing
Affiliation: Department of Parasitology and Medical Entomology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Cheras, Kuala Lumpur, Malaysia
ORICD: https://orcid.org/0009-0004-4365-1783
Aishah Hani Azil
Roles: Writing – review & editing
E-mail: [email protected]
Affiliation: Department of Parasitology and Medical Entomology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Cheras, Kuala Lumpur, Malaysia
Syamsa Rizal Abdullah
Roles: Writing – review & editing
Affiliation: Department of Parasitology and Medical Entomology, Faculty of Medicine, Universiti Kebangsaan Malaysia, Cheras, Kuala Lumpur, Malaysia
[/RAW_REF_TEXT]
[/RAW_REF_TEXT]
[/RAW_REF_TEXT]
1. Bhatt S, Gething PW, Brady OJ, Messina JP, Farlow AW, Moyes CL, et al. The global distribution and burden of dengue. Nature. 2013;496(7446):504–7. pmid:23563266
2. Hahn MB, Eisen RJ, Eisen L, Boegler KA, Moore CG, McAllister J, et al. Reported distribution of Aedes (stegomyia) aegypti and Aedes (stegomyia) albopictus in the United States, 1995–2016 (diptera: Culicidae). Journal of Medical Entomology. 2016;53(5):1169–75.doi.org/10.1093/jme/tjw072
3. Huang Y-JS, Higgs S, Vanlandingham DL. Emergence and re-emergence of mosquito-borne arboviruses. Current Opinion in Virology. 2019;34:104–9. pmid:30743191
4. Franklinos LH, Jones KE, Redding DW, Abubakar I. The effect of global change on mosquito-borne disease. The Lancet Infectious Diseases. 2019;19(9):e302–e12. pmid:31227327
5. Brugueras S, Fernández-Martínez B, Martínez-de la Puente J, Figuerola J, Porro TM, Rius C, et al. Environmental drivers, climate change and emergent diseases transmitted by mosquitoes and their vectors in southern Europe: A systematic review. Environmental Research. 2020;191:110038. pmid:32810503
6. WHO. Dengue and severe dengue. 2022. https://www.who.int/health-topics/dengue
7. WHO. Global strategy for dengue prevention and control 2012–2020. 2012. https://www.researchgate.net/publication/248707025_Global_Strategy_for_Dengue
8. Tabachnick WJ. Research contributing to improvements in controlling Florida’s mosquitoes and mosquito-borne diseases. Insects. 2016;7(4):50. pmid:27690112
9. Clements AN. The biology of mosquitoes. Volume 1: Development, nutrition and reproduction: Chapman & Hall; 1992. doi.org/10.1017/S0007485300034830
10. Dias LdS, Bauzer LGSdR, Lima JBP. Artificial blood feeding for Culicidae colony maintenance in laboratories: does the blood source condition matter? Revista do Instituto de Medicina Tropical de São Paulo. 2018;60. pmid:30231167
11. Tyler-Julian K, Darrisaw C, Lloyd A, Hoel D. The use of frozen, food-grade blood to successfully maintain colonies of four species of mosquitoes (Diptera: Culicidae). Journal of Insect Science. 2021;21(3):1. pmid:33940606
12. Luo YP. A novel multiple membrane blood‐feeding system for investigating and maintaining Aedes aegypti and Aedes albopictus mosquitoes. Journal of Vector Ecology. 2014;39(2):271–7. pmid:25424255
13. Alves FP, Gil LHS, Marrelli MT, Ribolla PE, Camargo EP, Da Silva LHP. Asymptomatic carriers of Plasmodium spp. as infection source for malaria vector mosquitoes in the Brazilian Amazon. Journal of Medical Entomology. 2005;42(5):777–9. pmid:16363160
14. Duong V, Lambrechts L, Paul RE, Ly S, Lay RS, Long KC, et al. Asymptomatic humans transmit dengue virus to mosquitoes. Proceedings of the National Academy of Sciences. 2015;112(47):14688–93. pmid:26553981
15. Edman JD, Webber LA, Schmid AA. Effect of host defenses on the feeding pattern of Culex nigripalpus when offered a choice of blood sources. The Journal of Parasitology. 1974:874–83. doi.org/10.2307/3278923 pmid:4430956
16. Kweka EJ, Mwang’onde BJ, Lyaruu L, Tenu F, Mahande AM. Effect of different hosts on feeding patterns and mortality of mosquitoes (Diptera: Culicidae) and their implications on parasite transmission. Journal of Global Infectious Diseases. 2010;2(2):121. pmid:20606966
17. Waage J, Nondo J. Host behaviour and mosquito feeding success: an experimental study. Transactions of the Royal Society of Tropical Medicine and Hygiene. 1982;76(1):119–22. pmid:7080144
18. Braks M, Juliano S, Lounibos L. Superior reproductive success on human blood without sugar is not limited to highly anthropophilic mosquito species. Medical and Veterinary Entomology. 2006;20(1):53–9. pmid:16608490
19. Bishop A, Gilchrist BM. Experiments upon the feeding of Aedes aegypti through animal membranes with a view to applying this method to the chemotherapy of malaria. Parasitology. 1946;37(1–2):85–100. doi.org/10.1017/S0031182000013202
20. Phasomkusolsil S, Tawong J, Monkanna N, Pantuwatana K, Damdangdee N, Khongtak W, et al. Maintenance of mosquito vectors: effects of blood source on feeding, survival, fecundity, and egg hatching rates. Journal of Vector Ecology. 2013;38(1):38–45. pmid:23701605
21. Rodhain J, Pons C, Vandenbranden J, Bequaert J. Contribution towards the transmission mechanism of trypanosomes by glossines. Archiv fur Schiffs-und Tropenhygiene. 1912;16(21):732–9.
22. Costanzo K, Schelble S, Jerz K, Keenan M. The effect of photoperiod on life history and blood‐feeding activity in Aedes albopictus and Aedes aegypti (Diptera: Culicidae). Journal of Vector Ecology. 2015;40(1):164–71. doi.org/10.1111/jvec.12146
23. Kasap H, Alptekin D, Kasap M, Güzel AI, Lüleyap U. Artificial bloodfeeding of Anopheles sacharovi on a membrane apparatus. Journal of the American Mosquito Control Association. 2003;19(4):367–70. pmid:14710738.
24. Faber PA, Dorai AJ, Chown SL. A standardised low-cost membrane blood-feeder for Aedes aegypti made using common laboratory materials. PeerJ. 2022;10:e14247. pmid:36325181
25. Russell WMS, Burch RL. The principles of humane experimental technique: Methuen; 1959. doi.org/10.5694/j.1326-5377.1960.tb73127.x
26. Gunathilaka N, Ranathunge T, Udayanga L, Abeyewickreme W. Efficacy of blood sources and artificial blood feeding methods in rearing of Aedes aegypti (Diptera: Culicidae) for sterile insect technique and incompatible insect technique approaches in Sri Lanka. BioMed Research International. 2017;2017. doi.org/10.1155/2017/3196924
27. Hemotek . Price list 2022. 2022. p. http://hemotek.co.uk/price-list-2018/.
28. Rutledge L, Ward R, Gould D. Studies on the feeding response of mosquitoes to nutritive solutions in a new membrane feeder. Mosq News. 1964;24(4):407–9. https://www.biodiversitylibrary.org
29. Alto BW, Lounibos LP, Juliano SA. Age-dependent bloodfeeding of Aedes aegypti and Aedes albopictus on artificial and living hosts. Journal of the American Mosquito Control Association. 2003;19(4):347–52. https://www.biodiversitylibrary.org pmid:14710735
30. Deng L, Koou S, Png A, Ng L, Lam-Phua S. A novel mosquito feeding system for routine blood-feeding of Aedes aegypti and Aedes albopictus. Trop Biomed. 2012;29(1):169–74. pmid:22543617.
31. Carvalho DO, Nimmo D, Naish N, McKemey AR, Gray P, Wilke AB, et al. Mass production of genetically modified Aedes aegypti for field releases in Brazil. JoVE (Journal of Visualized Experiments). 2014(83):e3579. pmid:24430003
32. Turell MJ. Reduced Rift Valley fever virus infection rates in mosquitoes associated with pledget feedings. The American journal of tropical medicine and hygiene. 1988;39(6):597–602. pmid:3207178
33. Arksey H, O’Malley L. Scoping studies: towards a methodological framework. International journal of social research methodology. 2005;8(1):19–32. doi.org/10.1080/1364557032000119616
34. Levac D, Colquhoun H, O’Brien KK. Scoping studies: advancing the methodology. Implementation science. 2010;5(1):1–9. pmid:20854677
35. Peters MD, Godfrey CM, McInerney P, Soares CB, Khalil H, Parker D. The Joanna Briggs Institute reviewers’ manual 2015: methodology for JBI scoping reviews. 2015.
36. Farnesi LC, Carvalho FD, Lacerda APC, Moreira LA, Bruno RV. The influence of different sources of blood meals on the physiology of Aedes aegypti harboring Wolbachia wMel: mouse blood as an alternative for mosquito rearing. Parasit Vectors. 2021;14(1):21. pmid:33407798
37. Paris V, Cottingham E, Ross PA, Axford JK, Hoffmann AA. Effects of alternative blood sources on Wolbachia infected Aedes aegypti females within and across generations. Insects. 2018;9(4):140. pmid:30314399
38. Costa-da-Silva AL, Navarrete FR, Salvador FS, Karina-Costa M, Ioshino RS, Azevedo DS, et al. Glytube: A Conical Tube and Parafilm M-Based Method as a Simplified Device to Artificially Blood-Feed the Dengue Vector Mosquito, Aedes aegypti. PLoS ONE. 2013;8(1). pmid:23342010
39. de Almeida Costa K, Garcia Rosário IN, Eiras ÁE, da Silva IM. Artificial bloodfeeder glytube: Evaluating different types of membranes and blood sources for feeding aedes aegypti and aedes albopictus. Journal of the American Mosquito Control Association. 2020;36(4):233–9. pmid:33647107
40. Finlayson C, Saingamsook J, Somboon P. A simple and affordable membrane-feeding method for Aedes aegpyti and Anopheles minimus (Diptera: Culicidae). Acta Tropica. 2015;152:245–51. pmid:26440474
41. Sri-In C, Weng S-C, Shiao S-H, Tu W-C. A simplified method for blood feeding, oral infection, and saliva collection of the dengue vector mosquitoes. PloS one. 2020;15(5):e0233618. pmid:32469954
42. Pothikasikorn J, Boonplueang R, Suebsaeng C, Khaengraeng R, Chareonviriyaphap T. Feeding response of Aedes aegypti and Anopheles dirus (Diptera: Culicidae) using out‐of‐date human blood in a membrane feeding apparatus. Journal of Vector Ecology. 2010;35(1):149–55. pmid:20618661
43. Harrington LC, Edman JD, Scott TW. Why do female Aedes aegypti (Diptera: Culicidae) feed preferentially and frequently on human blood? Journal of medical entomology. 2001;38(3):411–22. pmid:11372967
44. Harrison RE, Brown MR, Strand MR. Whole blood and blood components from vertebrates differentially affect egg formation in three species of anautogenous mosquitoes. Parasites & vectors. 2021;14:1–19. pmid:33627180
45. Gonzales KK, Tsujimoto H, Hansen IA. Blood serum and BSA, but neither red blood cells nor hemoglobin can support vitellogenesis and egg production in the dengue vector Aedes aegypti. PeerJ. 2015;3:e938. pmid:26020000
46. Briegel H. Fecundity, metabolism, and body size in Anopheles (Diptera: Culicidae), vectors of malaria. Journal of medical entomology. 1990;27(5):839–50. pmid:2231621
47. Blackmore MS, Lord CC. The relationship between size and fecundity in Aedes albopictus. Journal of Vector Ecology: Journal of the Society for Vector Ecology. 2000;25(2):212–7. pmid:11217219.
48. Roitberg BD, Gordon I. Does the Anopheles blood meal-fecundity curve, curve? Journal of vector ecology: journal of the Society for Vector Ecology. 2005;30(1):83–6. pmid:16007959.
49. Hurd H. Manipulation of medically important insect vectors by their parasites. Annual review of entomology. 2003;48(1):141–61. pmid:12414739
50. Kaczmarek A, Wrońska AK, Boguś MI, Kazek M, Gliniewicz A, Mikulak E, et al. The type of blood used to feed Aedes aegypti females affects their cuticular and internal free fatty acid (FFA) profiles. PLoS One. 2021;16(4):e0251100. pmid:33930098
51. Uchida K, Oda T, Matsuoka H, Moribayashi A, Ohmori D, Eshita Y, et al. Induction of oogenesis in mosquitoes (Diptera: Culicidae) by infusion of the hemocoel with amino acids. Journal of medical entomology. 2001;38(4):572–5. pmid:11476338
52. Attardo GM, Hansen IA, Shiao S-H, Raikhel AS. Identification of two cationic amino acid transporters required for nutritional signaling during mosquito reproduction. Journal of Experimental Biology. 2006;209(16):3071–8. pmid:16888056
53. Lea AO, Dimond JB, DeLong DM. Role of diet in egg development by mosquitoes (Aedes aegypti). Science. 1956;123(3203):890–1. pmid:13324108
54. Turell MJ, Dohm DJ, Sardelis MR, O’guinn ML, Andreadis TG, Blow JA. An update on the potential of North American mosquitoes (Diptera: Culicidae) to transmit West Nile virus. Journal of medical entomology. 2005;42(1):57–62. pmid:15691009
55. Saifur RG, Dieng H, Hassan AA, Salmah MRC, Satho T, Miake F, et al. Changing domesticity of Aedes aegypti in northern peninsular Malaysia: reproductive consequences and potential epidemiological implications. PLoS One. 2012;7(2):e30919. doi.org/10.1371/journal.pone.0030919
56. Bennett GF. The influence of the blood meal type on the fecundity of Aedes (Stegomyia) aegypti L.(Diptera: Culicidae). Canadian journal of zoology. 1970;48(3):539–43. pmid:5448824
57. Suleman M, Shirin M. Comparison of the Reproductive Capacity of Culex quinquefasciatus Say fed on Cold and Warm-blooded Vertebrates. Pakistan journal of zoology. 1981.
58. Lyimo IN, Ferguson HM. Ecological and evolutionary determinants of host species choice in mosquito vectors. Trends in parasitology. 2009;25(4):189–96. pmid:19269900
59. Dimond J, Lea A, Hahnert W, DeLong D. The Amino Acids Required for Egg Production in Aedes aegypti1. The Canadian Entomologist. 1956;88(2):57–62. doi.org/10.4039/Ent8857-2
60. Spielman A, Wong J. Dietary factors stimulating oogenesis in Aedes aegypti. The Biological bulletin. 1974;147(2):433–42. pmid:4441563
61. Bailey DL, Dame DA, Munroe WL, Thomas JA. Colony maintenance of Anopheles albimanus Wiedemann by feeding preserved blood through natural membrane. Mosq News. 1978;38:403–8.
62. Nasirian H, Ladonni H. Artificial bloodfeeding of Anopheles stephensi on a membrane apparatus with human whole blood. Journal of the American Mosquito Control Association. 2006;22(1):54–6. pmid:16646322
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer
© 2024 Suresh et al. This is an open access article distributed under the terms of the Creative Commons Attribution License: http://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
Abstract
In some laboratories, mosquitoes’ direct blood-feeding on live animals has been replaced with various membrane blood-feeding systems. The selection of blood meal sources used in membrane feeding is crucial in vector mass rearing as it influences the mosquitoes’ development and reproductive fitness. Therefore, this scoping review aimed to evaluate the existing literature on the use of different blood sources and components in artificial membrane feeding systems and their effects on blood-feeding and the fecundity rate of Ae. aegypti. A literature review search was conducted by using PubMed, Scopus, and Web of Science databases according to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA-ScR). The EndNote version 20 software was used to import all searched articles. Relevant information was retrieved for analysis into a Microsoft Excel Spreadsheet. A total of 104 full-text articles were assessed for eligibility criteria, whereby the articles should include the comparison between different types of blood source by using the membrane feeding systems. Only 16 articles were finally included in the analysis. Several studies had reported that human blood was superior in blood-feeding Ae. aegypti as compared to sheep blood which resulted in lower fecundity due to accumulation of free fatty acids (FFA) in the cuticles. In contrast, cattle whole blood and pig whole blood showed no significant differences in the blood-feeding and fecundity rate as compared to human blood. This review also indicated that bovine whole blood and pig whole blood enhanced Ae. aegypti’s vitellogenesis and egg production as compared to plasma and blood cells. In addition, human blood of up to 10 days after the expiration date could still be used to establish Ae. aegypti colonies with good blood-feeding rates and number of eggs produced. Thus, future studies must consider the importance of selecting suitable blood sources and components for membrane blood feeding especially in mosquito colonisation and control measure studies.
You have requested "on-the-fly" machine translation of selected content from our databases. This functionality is provided solely for your convenience and is in no way intended to replace human translation. Show full disclaimer
Neither ProQuest nor its licensors make any representations or warranties with respect to the translations. The translations are automatically generated "AS IS" and "AS AVAILABLE" and are not retained in our systems. PROQUEST AND ITS LICENSORS SPECIFICALLY DISCLAIM ANY AND ALL EXPRESS OR IMPLIED WARRANTIES, INCLUDING WITHOUT LIMITATION, ANY WARRANTIES FOR AVAILABILITY, ACCURACY, TIMELINESS, COMPLETENESS, NON-INFRINGMENT, MERCHANTABILITY OR FITNESS FOR A PARTICULAR PURPOSE. Your use of the translations is subject to all use restrictions contained in your Electronic Products License Agreement and by using the translation functionality you agree to forgo any and all claims against ProQuest or its licensors for your use of the translation functionality and any output derived there from. Hide full disclaimer