Introduction
In developed countries, allergies, and asthma have become more common in recent years1. Th2 cell activation by an allergen or an antigen is the first step in the development of asthma or allergy. Cytokines including IL-4, IL-5, and IL-13 are released by activated Th2 cells and are crucial mediators of asthmatic or allergic inflammation. Eosinophil infiltration, mast cell degranulation, and elevated IgE concentrations are the hallmarks of asthma2. Even while genetics have a major role in the development of asthma, western lifestyle modifications in food contribute to an increase in asthma symptoms. Symbiotic human gut microbiota is responsible for preserving homeostasis between various tissues 3. The wide spectrum of the gut microbiota is influenced by several factors, and nutrition is crucial in preserving this diversity. Low microbiota-available carbohydrates (MACS) in the Western diet, which also reduces the fiber content, excessive sugar, fat, and cholesterol, lowers microbial diversity and may result in the extinction of bacterial species4. Dysbiosis is caused by the decline of microbial species. Inflammatory diseases like allergies and asthma can be brought on by the dysbiosis of the gut microbiota.5
Ayurveda, Naturopathy, and Yoga were the three primary components of the ancient Indian diet6. According to geography and season, Ayurveda outlined what to eat. It is linked to Indian culture through traditional food (Sadya is a typical dish in Kerala), festival food (Mohan bhog Thali in North India), food served in temples, and seasonal dishes (Badam ka halwa in North India during the winter season). To maintain the nutritious integrity of the food, Indian temples have kept an antiquated cooking technique (cooking in clay pots with ancient grains and lentils). The fundamental tenet of this tradition and ritual is the consumption of wholesome foods that are rich in all the nutrients and shield the body from illness. Naturopathy is a different type of therapy, though, and it places a strong emphasis on eating foods that are fresh, preservative-free, in season, and green. A healthy person should eat a variety of cooked and raw foods, according to naturopathy7. Indian cuisine places a strong emphasis on eating foods raw or uncooked, such as Kusumbari, a dish from Karnataka made of raw vegetables and raw lentils. Naturopathic ideas hold that “food is medicine” and recommend leaving one-fourth of the stomach empty, as advised by yoga. A rigorous yogic diet (no-spice, vegetarian, low-fat diet) for the Satvic guna promotes clarity and tranquillity while being beneficial to the body. Water, some spices, grains, vegetables, legumes, fruits, nuts, fresh milk, and its derivatives (ghee, butter, cream, cheese, and yogurt), as well as unpasteurized and homogenized fresh milk, are examples of such meals8. In this review, we propose that the traditional vegetarian, high-fiber diet of ancient India may enhance gut microbial diversity and lessen asthma symptoms. The aim of this review is to explore the potential of the ancient Indian diet in enhancing gut microbial diversity and increasing the population of beneficial probiotic bacteria, with the potential to alleviate symptoms of asthma.
Materials and methods
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Search Process
A keyword search utilizing the phrases “western diet, beneficial microbiota, asthma, gut microbial dysbiosis, Ancient Indian diet” was conducted electronically through the SCOPUS ,Science Direct PubMed, Web of Science, and PsycINFO databases. Books are also included in the PsycINFO database, which was We included in this narrative review are the RCTS, Systematic reviews, case studies and review article that look at how ancient Indian diet consumption maintain the gut microbial diversity, which may prevent gut microbial dysbiosis. preemptively removed from the search.
Inclusion criteria
Search criteria are divided into two arms the first one includes different full-text research papers including how Indian diet altered gut microbial composition. The second one, we included the full text including how presence of certain gut microbiota can prevents the Asthmatic attack. No limitation was set with regard to study participants as to the effect of Ancient Indian on gut microbiota.
Study selection
To find publications that met the eligibility requirements, the first and second authors separately reviewed each publication's title and abstract using the previously described inclusion criteria. We have included 124 research articles, which is published between 1989 to 2024.
Western diet and asthma
Soft drinks, fried foods, and fast food are all heavy in trans fats, sugar, and salt, and Western diets tend to be low in antioxidants and high in pro-inflammatory foods (omega-6 fatty acids)9. Omega-6 fatty acids obtained through fast food and junk food are converted to arachidonic acid, arachidonic acid acts as a precursor molecule for leukotrienes and prostaglandins (inflammatory mediators).10Antioxidants are lacking when fruits and vegetables aren't consumed frequently. Antioxidants typically neutralize reactive oxygen species (ROS), and antioxidant deprivation causes NF-kB factors to become activated. The Western diet is dominated by highly processed foods, highly refined carbohydrates, high fats, especially high saturated fat, highly processed food and preservatives. According to one study a large increase in the consumption of animal fats ,vegetable oils ,sugar and sweeteners is associated with the development of asthma 11.In patients with asthma, eating a high-fat mixed meal has been demonstrated to raise sputum and neutrophil levels four hours after the meal12. Higher fat and lower fiber intake have been linked to increased eosinophilic airway inflammation in persons with severe asthma 13. A high fat diet activates several genes involved in immune system functions in sputum, including TLR 4, which suggests increased inflammation of the airways 14. Many studies have shown that high salt intake causes all types of asthma. Moreover, a study suggested that low salt intake improves lung function in allergic and exercise-induced asthma15. According to one study, eating a lot of ultra processed food was positively correlated with wheezing and asthma among teenage Brazilians16. Another study discovered that eating more than four servings of processed meat per week, as opposed to fewer than one, is linked to worsening symptoms of asthma 17.
Western diet and the diversity of Gut microbiota
The development of allergic disease depends on homeostasis between epithelial cells, regulatory T cells, and the gut microbiome18. The Western diet is a rich source of simple sugars and fats, increases intracellular prooxidants, and causes changes in the diversity and function of the intestinal microbiota9. 19Changes in the diversity and composition of the microbiota are known as dysbiosis. Lack of fiber in the Western diet reduces the intestinal microbiota population, leads to impaired short-chain fatty acids (SCFA) synthesis, and increases the inflammatory state, leading to chronic metabolic disease. Decreased absorption of SCFA increases the concentration of bicarbonate ions in the large intestine. A higher concentration of bicarbonate ion promotes the increase of pH. A high pH Favors the growth of pathogenic bacteria, while a low pH (5.5) in the ileum and cecum inhibits the growth of pathogenic bacteria (Firmicutes phylum). In mice given a high-fat diet for 12 weeks, there are increases in Rikenellaceae and decreases in Ruminococcaceae20. There were significantly fewer rats in the high-fat diet group than in the normal diet group that had virrucomicrobia, a form of bacteria that is common in the mucosa and which will decrease in high-fat diets, obesity, and other disorders 21. Significant microbial changes, increased susceptibility to microbial stimulation in blood and bone marrow-derived monocytes, and a lack of ileal defense were all brought on by a high-sucrose meal that was ingested for a short time. These findings suggest that even in the presence of a high-sugar diet, there is potential for rapid and significant changes in gut microbial composition and systemic immune response22.
Clostridium is a pathogenic bacterium belonging to the genus Firmicutes that causes excessive inflammation and increases the number of pathogenic immune cells leading to asthma 23.The abundance of the genera Lachnospira, Veillonella and Faecalibacterium (phylum Firmicutes) increases the risk of asthma during the first 100 days of life24. If the pH value of the large intestine is increased, butyrate-producing bacteria (Faecalibacterium, Roseburia, and Eubacterium phylum) decrease and the population of acetate- and propionate-producing bacteria (Bacteroidetes phylum) increases. High pH also Favors the growth of harmful microorganisms (inflammatory endotoxin from lipopolysaccharide producers) and oxygen-resistant microorganisms that damage the intestinal epithelial lining25. Higher populations ofHaemophilus and Moraxella are associated with severe airway obstruction and airway neutrophilia 26.Staphylococcuscontains various endotoxin-like proteases, such as SPLS, which binds to protease-activated receptors on epithelial cells and stimulate secretion of the cytokine-like IL-33 and TSLP, which induces Th2 cell activation leading to asthma27. People on a long-term western diet (rich in animal protein, the nutrient choline and saturated fat) have a high diversity ofBacteroides bacteria and a low concentration of Prevotella28 . However, refined carbohydrates (bran and non-fibrous grains) are consumed in the Western world, including bread, white pasta, starch, sucrose and fructose syrup. High sugar intake increases the population ofEnterobacteriaceae and reduces Lactobacilliassociated with both intestinal and brain inflammation in rodents29.
Concept of Ancient Indian Balanced Diet
The Indian diet shows its uniqueness due to its diversity, history, geography, immigrants, and complexity. The country's diversity has not only shaped its social and political status in today's world, but it has also influenced food culture across the continent. The beauty of traditional Indian food is not only that it is versatile, but also has great nutritional value30. From North India to South India, the tradition of combining grains and legumes provides all the essential amino acids and other macro and micronutrients. Typically, an Indian would eat Khichidi (rice, lentils, vegetables, and ghee), Dalia (crushed wheat, vegetables, and ghee), Dosa (rice, lentils, and butter or ghee), Idly (rice and lentils), and Samber (lentils, vegetables, oil, tamarind with spices), as well as chutney (typically peanut chutney, pudina (peppermint leaf) , Upma (crushed whole grains with vegetables and Hindi), Khij (finger millet khichdi), Roti with ghee (Bajara roti, Makka ki roti), North Indian thali (Dal, Roti, vegetable curries, ghee or curd), South Indian thali (Rice, Samber, Rasam, vegetable curry, ghee), Rajama chawal (broad grain rice), Kadi chawal (curd, gramme flour, and spices), chole bature (wheat flour and horse gram). According to Indian custom, a meal made out of grains, lentils, vegetables, fruits, spices, nuts, oil, milk, and buttermilk with ghee or butter makes the food more compact. Indian cuisine is a type of balanced diet that includes every essential nutrient, and this diet is currently acknowledged as a lacto-vegetarian diet31. It includes all of the macronutrients (carbohydrates, proteins, and fats), fiber, MUFA, PUFA, antioxidants (vitamins C, E, A, and K), and prevents inflammation32. Green leaves of the plant are a rich source of phytochemicals, fibres, and minerals with great anti-inflammatory and antibacterial effects, coupled with edible flowers33.
Every meal should balance the six primary tastes (sweet, salty, sour, bitter, pungent, and astringent), according to Ayurveda 34. Starting with the meal from Kerala, Sadya, it has each of the six flavors35. Every traditional Indian dish, not just those from Kerala, is rich in all flavours and provides a balanced combination of carbs, proteins, fats, vitamins, minerals, and phytochemicals.
Result
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Discussion
The body receives all the macro and micronutrients from the traditional Indian practise of eating dishes with all the flavours (sweet, sour, bitter, salty, and spicy) in one meal. It is not a part of Indian cuisine culture to eat canned food, processed food, or fried food. Fresh, thoroughly cooked, and balanced food is required. The Indian diet is full of anti-inflammatory and antioxidant foods that protect the body's symbiotic microbial variety and prevent the growth of harmful microbes.101
Dietary fibres and prebiotics
: Grains, fruits, vegetables, legumes, leaves, edible flowers and nuts are all sources of fibre. Consuming greater amounts of fibre promotes the growth of Bifidobacterium and Lactobacillus species. Resistant starch and whole grain barley can also increase the number of lactic acid bacteria, including Ruminococcus, Eubacterium rectste and Roseburia. Bifidobacteriumand Lactobacilli play a protective role against pathogenic bacteria and maintain intestinal permeability36,102. Dietary fiber acts as a substrate for intestinal bacterial metabolism and SCFAs as an end product of metabolism103. The main SCFAs are acetate and propionate (used as substrates for metabolism of lipids, glucose and cholesterol) and butyrate (which plays a key role in immunoregulation and maintenance of tissue barrier function), which act as energy substrates for intestinal epithelial cells104. Curd is rich in Lactobacillus bacteria. Bioactive compounds such as hydrogen peroxide and reuterin produced by Lactobacillus bacteria inhibit the growth of pathogenic bacteria, especially E. coli, Bacillusand Staphylococcus aureus54.
Phytochemicals
In contrary, Phytochemicals are noncaloric plant compounds found in grains, legumes, fruits, vegetables, nuts, and spices105. Phytochemicals include polyphenols and derivatives, carotenoids and thiol sulfides, mainly anti-inflammatory, antibiotic and antioxidant. Polyphenols are the most versatile phytochemicals, which are mainly divided into four different types. Flavonoids, phenolic acids, stibenoids (resveratrol), lignans106,107 . Fruits such as grapes, blueberries, sweet soap, mango and citrus fruits, vegetables, herbs, microalgae, herbs, seeds, grains are good sources of polyphenols104. Polyphenols have been shown to increase the number of Bifidobacterium and Lactobacillus species. The reduction of pathogenic Clostridium perfringi and Clostridium histolyticum is probably due to the consumption of polyphenols 45. Ingestion of mango peel and pulp increases Lactobacillus, Bifidobacterium, Akkermansia, Faecalibacteriumanddecreases Clostridium leptum74. Curcumin is a good source of polyphenols, which significantly increases the number of Prevotellaceae, Bacteroidaceae and Rickenellaceae bacteria (Shen et al., 2017). The addition of garlic to the diet increases the number of Lachnospiraceae and Allobaculum and has a bactericidal effect on some bacterial species, including Escherichia coli, Salmonellatyphimurium and Neisseria gonorrhoeae52,53,73. Essential oil of cinnamon inhibits opportunistic pathogenic bacteria including Streptococcus, Staphylococcus, Enterococcus and Pseudomonas aeruginosa 64. The polyphenol in the ginger supplement was able to increase SCFA production by increasing the abundance of SCFA-producing species such as Allobaculumand Bifidobacterium and reducing Clostridia 59. Almond phytochemicals increase Clostridium, Roseburia ,Lachnospira decrease Oscillospira, Parabacteroides, Allistipes, Butyricimonas, Bifidobacterium57 . Phytochemicals in walnuts increase the diversity of Faecalibacterium, Clostridium, Roseburia, Dialister, Coprococcus, Bifidobacterium and decrease Oscillospira, Ruminococcus and Ruminococcus 58.
Plant based fat and milk-based fat
Indians consume vegetable fat and milk-based fat (ghee), which comes mainly obtained from grains, oilseeds, nuts, vegetables and milk. Plant fats are low-fat diets that contain mono- and polyunsaturated fats and alter gut microbial composition by increasing the Bacteroidetes: Firmicutes ratio. Coconut oil is characterized by the presence of both medium and long chain fatty acids and an increased abundance of beneficial bacteria such asLactobacillus, AllobaculumandBifidobacterium species46. Ghee is rich in medium-chain fatty acids and MUFA, the MUFA-enriched diet induced Bifidobacteriaceae, Lactobacillus, Bacteroidetes, Ruminococcaceae and reduced the growth of Firmicutes and Proteobacteria52,53,108.
Plant-based protein and milk-based protein
The protein in peas increased Bifidobacterium and Lactobacillus populations and increases intestinal SCFA levels. Pea protein has an inhibitory effect on pathogenic C. perfingens and Bacteroides fragilis species 45. Casein is a milk protein that can increase the communities of Lactobacilliand Bifidobacterium and reduce the abundance of Staphylococci and Streptococci55,56.
Vitamins
Vitamins, including vitamin K and vitamin B complexes (biotin, cobalamin, folate, nicotinic acid, pantothenic acid, pyridoxine, riboflavin, thiamine) participate in bacterial metabolism, few of them are synthesized in the intestine microbiota 109However, a study reported that carotenoids such as black fluo-lutein increased Bifidobacterium and Lactobacillusspp and decreased Bacteroides spp and Clostridium spp populations39.110 An abundance of vitamin A in the diet may cause Clostridium to grow while Enterococcus and Bacteroides decrease. Kids who don't get enough vitamin A in their diets have less diverse gut microbiomes and more Enterococcus in their excrement 111.Lactobacillus species could become much more prevalent in a mouse model if vitamin A was given112. The delivery of retinoic acid, a physiologically active metabolite of vitamin A, was shown in this study to significantly boost the number of Lactobacillus spp. during a norovirus infection.
The authors postulated that the presence of Lactobacillus in the gut was partially responsible for naro virus suppression after Lactobacillus demonstrated antiviral activity against the norovirus in an in vitro model. Additionally, it was demonstrated that the treatment of retinoic acid raised the number of Allobaculum, Aggregatibacter, Bifidobacterium, Dialister,and Enhydrobacter 113,114. The colonization of Bacteroides thetaiotaomicrons in the gut of an experimental gnotobiotic mouse model was reported to be enhanced by vitamin B12 administration 115. A small group of free-living people with stable cystic fibrosis were assessed, and the results showed that vitamin C intake was negatively correlated with Bacteroidetes and negatively co-related with Firmicutes and its lower taxa116. An investigation on early-weaned pigs revealed the antioxidant potential of vitamin C in scavenging free radicals, repairing the gut microbiota microenvironment, and raising the numbers of Lactobacillus and Bifidobacterium in the gut 117.
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Ancient Indian diet on Asthmatic bacteria
The Indian diet is a low-fat, plant-based diet that is rich in all micro- and macronutrients and has a significant impact on gut microbial diversity. The density of the food ensures antioxidant, antimicrobial and anti-inflammatory effects on pathogenic asthmatic bacteria and increases the diversity of antiasthmatic bacteria. A plant-based diet increases the diversity of Bacteroidetes, Actinobacteria, Prevotella, Bifidobacterium, Lactobacillus, Ruminococcus, Roseburia, Lactobacillus, Lachnospira, Akkermansia and reduces the risk of asthma by stimulating the production of SCFAs. SCFAs bind to a G protein-coupled receptor on the surface of naïve CD4+T cells. In turn, the SCFA-GPR 43 complex promotes acetylation of the T reg transcription factor. Increase T reg differentiation and suppress pathogenic immune cells. Bifidobacterium infantis can increase the number of CD4+, CD25+, FoxP3+ cells in the spleen .CD4+, CD25+ T cells can suppress the activation and proliferation of other CD4+ and CD8+ cells in an antigen-nonspecific manner and reduce the incidence of asthma118. Lactobacillus species have also been shown to increase FoxP3 expression by CD25 cells. in vitro. Supplementation with Lactobacillus reuteri increases Treg in splenocytes and developed key features of asthmatic reactions and methacholine hyperreactivity . Consumption of probiotic bacteria such as Lactobacilli/Casei/Lactis/acidophilus and Bifidobacteria bifidium/lactis reduced allergic diseases42. Prebiotic consumption at a very early age increases the abundance of Firmicutes and Actinobacteria, as well as the proliferation of CD Treg cells and cecal butyrate concentration. Oral administration of Bifidobacterium lactis or Lactobacillus rhamnosus to newborn mice suppressed all aspects of the asthma phenotype 119.
Bacteroides fragilis is sufficient to induce the expression of a specific subset of IL-10-producing CD4+, CD25+, Fox P3+, Treg cells. Bacteria such as Lactobacillus and Helicobacter pylori have been reported to be protective against asthma 120.Antigenic peptide of Akkermansia causes the activation of T cell and increases the peripheral T reg population121. Lachnospirapromotes the T reg cell differention 24Traditional Indian food shows antimicrobial activity against Clostridium, E. coli, Staphylococcus, Haemophilus, Moraxella and Neisseria. The above-mentioned facts are supported by the studies which demonstrated that Haemophilusinfluenza,Streptococcus Pneumoniae, and Moraxella cause respiratory diseases and asthma risk in children 55.Higher concentration of Clostridium increases the concentration of fecal IgE level in asthmatic children ,promotes inflammation and increases the incidence of asthma23.Staphylococcus aureus produces exotoxin serine protease like (SPLS),which promotes the development of eosinophilic asthma 122.Higher population of Haemophilusand Moraxella increases the incidence of childhood asthma 123.Pseudomonas aeruginosa having a protein flagellin increases secretion of IL-6 and IL-8 ,which act as a neutrophil chemoattractant 124.
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Conclusion
People are demonstrating their preference for fast food and canned goods as the world becomes more westernised. Inflammation and other chronic disorders like asthma are brought on by a fast-paced lifestyle, stress, and modern cuisine. A balanced, nutrient-rich diet (heavy in fibre, antioxidants, anti-inflammatory, and probiotic foods) and ancient Indian cooking techniques are being used today. Bacteria in the human digestive tract are significantly influenced by the ancient Indian diet. It promotes the growth of symbiotic helpful bacteria while inhibiting the growth of harmful bacteria that take advantage of opportunities. Consuming a traditional Indian cuisine may conserve gut microbial variety, populations, and avoid the extinction of helpful microbial species (dysbiosis), according to our hypothesis. The ancient Indian cuisine is high in fibre, which boosts the population of bacteria that produce SCFAs. A high SCFA content lowers the absorption of bicarbonate ions and raises the pH of the GI tract. Pathogenic bacteria cannot infect a person when the pH is acidic. In several animal models, dietary change decreases airway hyperresponsiveness, lung inflammation, and enhances gut microbial diversity.
Acknowledgement
We sincerely acknowledge all the faculties of the Department of microbiology, Bharathidasan University, Trichy for their concomitant support.
Funding sources
No financial support was received for the preparation of this manuscript.
Conflict of Interest
We hereby declare that there is no conflict of interest among the authors for both conceptualization and preparation of the manuscript
Authors contribution
Ms. Monalisa Das: -Conceptualization, Methodology, data analysis, writing draft preparation
Dr. Nooruddin Thajuddin: -Visualization, Supervision
Dr. Sanjib Kumar Patra: -Writing, Reviewing, Editing, Investigation
Ms. Megha Pundir: -Software, Validation
Data Availability Statement
Not applicable
Ethics Approval statement
As it is a review article there is no need of ethical statement
Future direction
Till date, no direct research has been done to investigate the impact of the ancient Indian diet on the gut flora of humans.Future research in this field may shed light for a deeper comprehension.
Strachan DP. Hay fever, hygiene, and household size. Br Med J. 1989;299(6710). doi:10.1136/bmj.299.6710.1259
Rangasamy T, Guo J, Mitzner WA, et al. Disruption of Nrf2 enhances susceptibility to severe airway inflammation and asthma in mice. Journal of Experimental Medicine. 2005;202(1). doi:10.1084/jem.20050538
Schroeder BO, Fredrik Backhed. Signals from the gut microbiota to distant organs in physiology and disease. Nat Med. 2016;22(10):1079-1089.
Sonnenburg ED, Smits SA, Tikhonov M, Higginbottom SK, Wingreen NS, Sonnenburg JL. Diet-induced extinctions in the gut microbiota compound over generations. Nature. 2016;529(7585). doi:10.1038/nature16504
Chung KF. Airway microbial dysbiosis in asthmatic patients: A target for prevention and treatment? Journal of Allergy and Clinical Immunology. 2017;139(4). doi:10.1016/j.jaci.2017.02.004
Samanta AK, Kolte AP, Senani S, Sridhar M, Jayapal N. Prebiotics in ancient Indian diets. Curr Sci. 2011;101(1).
Oberg EB, Bradley RD, Allen J, McCrory MA. CAM: Naturopathic dietary interventions for patients with Type 2 diabetes. Complement Ther Clin Pract. 2011;17(3). doi:10.1016/j.ctcp.2011.02.007
Das M, Pundir M, Nayak P, Patra S, Thajuddin N. Yogic diet on gut microbial diversity in asthma. Yoga Mimamsa. 2023;55(01):58-66.
Monteiro CA, Moubarac JC, Cannon G, Ng SW, Popkin B. Ultra-processed products are becoming dominant in the global food system. Obesity Reviews. 2013;14(S2). doi:10.1111/obr.12107
Agus A, Planchais J, Sokol H. Gut Microbiota Regulation of Tryptophan Metabolism in Health and Disease. Cell Host Microbe. 2018;23(6):716-724. doi:10.1016/J.CHOM.2018.05.003
Ahmed A, Elbushra A, Salih O. Food consumption patterns and trends in the Gulf Cooperation Council. Pak J Nutr. 2019;18:623-636.
Wood LG, Garg ML, Gibson PG. A high-fat challenge increases airway inflammation and impairs bronchodilator recovery in asthma. Journal of Allergy and Clinical Immunology. 2011;127(5). doi:10.1016/j.jaci.2011.01.036
Berthon BS, MacDonald-Wicks LK, Gibson PG, Wood LG. Investigation of the association between dietary intake, disease severity and airway inflammation in asthma. Respirology. 2013;18(3). doi:10.1111/resp.12015
Li Q, Baines KJ, Gibson PG, Wood LG. Changes in expression of genes regulating airway inflammation following a high-fat mixed meal in asthmatics. Nutrients. 2016;8(1). doi:10.3390/nu8010030
López-Otín C, Blasco MA, Partridge L, Serrano M, Kroemer G. The hallmarks of aging. Cell. 2013;153(6). doi:10.1016/j.cell.2013.05.039
Melo B, Rezende L, Machado P, Gouveia N, Levy R. Associations of ultra-processed food and drink products with asthma and wheezing among Brazilian adolescents. Pediatric Allergy and Immunology. 2018;29(5). doi:10.1111/pai.12911
Li Z, Rava M, Bédard A, et al. Cured meat intake is associated with worsening asthma symptoms. Thorax. 2017;72(3). doi:10.1136/thoraxjnl-2016-208375
O’Toole PW, Jeffery IB. Gut microbiota and aging. Science (1979). 2015;350(6265). doi:10.1126/science.aac8469
Martínez Leo EE, Acevedo Fernández JJ, Segura Campos MR. Biopeptides with antioxidant and anti-inflammatory potential in the prevention and treatment of diabesity disease. Biomedicine and Pharmacotherapy. 2016;83. doi:10.1016/j.biopha.2016.07.051
Daniel H, Moghaddas Gholami A, Berry D, et al. High-fat diet alters gut microbiota physiology in mice Microbe-microbe and microbe-host interactions. ISME J. 2014;8.
Sharaf LK, Sharma M, Chandel D, Shukla G. Prophylactic intervention of probiotics (L. acidophilus, L. rhamnosus GG) and celecoxib modulate Bax-mediated apoptosis in 1, 2-dimethylhydrazine-induced experimental colon carcinogenesis. BMC Cancer. 2018;18(1):1-13.
Rajaruban S, Fedorak R, Zalasky A, et al. A77 CONSUMPTION OF REFINED SUGAR RAPIDLY DECREASES MICROBIAL DIVERSITY AND ENHANCES SYSTEMIC RESPONSE TO MICROBIAL STIMULI. J Can Assoc Gastroenterol. 2019;2(Supplement_2). doi:10.1093/jcag/gwz006.076
Chiu CY, Chan YL, Tsai MH, Wang CJ, Chiang MH, Chiu CC. Gut microbial dysbiosis is associated with allergen-specific IgE responses in young children with airway allergies. World Allergy Organization Journal. 2019;12(3). doi:10.1016/j.waojou.2019.100021
Arrieta MC, Stiemsma LT, Dimitriu PA, et al. Early infancy microbial and metabolic alterations affect risk of childhood asthma. American Association for the Advancement of Science. 2015;7(307):307-152.
Chakraborti CK. New-found link between microbiota and obesity. World J Gastrointest Pathophysiol. 2015;6(4). doi:10.4291/wjgp.v6.i4.110
Taylor SL, Leong LE, Choo JM, et al. Inflammatory phenotypes in patients with severe asthma are associated with distinct airway microbiology. Journal of Allergy and Clinical Immunology. 2018;141(1):94-103.
Krysko O, Teufelberger A, Van Nevel S, Krysko D V., Bachert C. Protease/antiprotease network in allergy: The role of Staphylococcus aureus protease-like proteins. Allergy: European Journal of Allergy and Clinical Immunology. 2019;74(11). doi:10.1111/all.13783
Hamr SC, Wang B, Swartz TD, Duca FA. Does nutrient sensing determine how we “see” food? Curr Diab Rep. 2015;15:1-10.
Statovci D, Aguilera M, MacSharry J, Melgar S. The impact of western diet and nutrients on the microbiota and immune response at mucosal interfaces. Front Immunol. 2017;8(JUL). doi:10.3389/fimmu.2017.00838
Srinivas T. Exploring Indian culture through food. Education about Asia. 2011;16(03):38-41.
Agrawal S, Millett CJ, Dhillon PK, Subramanian S, Ebrahim S. Type of vegetarian diet, obesity and diabetes in adult Indian population. Nutr J. 2014;13(1). doi:10.1186/1475-2891-13-89
Shridhar K, Dhillon PK, Bowen L, et al. Nutritional profile of Indian vegetarian diets – The Indian Migration Study (IMS). Nutr J. 2014;13(1). doi:10.1186/1475-2891-13-55
Bhat RS, Al-Daihan S. Phytochemical constituents and antibacterial activity of some green leafy vegetables. Asian Pac J Trop Biomed. 2014;4(3). doi:10.1016/S2221-1691(14)60230-6
Chopra A, Doiphode V V. Ayurvedic medicine: Core concept, therapeutic principles, and current relevance. Medical Clinics of North America. 2002;86(1). doi:10.1016/S0025-7125(03)00073-7
Unnithan AK. Gastronomy Of Kerala Community: Ethnic Nutritional Value Of Onam Sadya. Think India Journal. 2019;22(14):5447-5459.
Tomova A, Bukovsky I, Rembert E, et al. The effects of vegetarian and vegan diets on gut microbiota. Front Nutr. 2019;6. doi:10.3389/fnut.2019.00047
Zhang X, Dong L, Jia X, et al. Bound phenolics ensure the antihyperglycemic effect of rice bran dietary fiber in db/db mice via activating the insulin signaling pathway in skeletal muscle and altering gut. J Agric Food Chem. 2020;68(15):4387-4398.
Nealon NJ, Worcester CR, Ryan EP. Lactobacillus paracasei metabolism of rice bran reveals metabolome associated with Salmonella Typhimurium growth reduction. J Appl Microbiol. 2017;122(6). doi:10.1111/jam.13459
Rizzello CG, Lorusso A, Montemurro M, Gobbetti M. Use of sourdough made with quinoa (Chenopodium quinoa) flour and autochthonous selected lactic acid bacteria for enhancing the nutritional, textural and sensory features of white bread. Food Microbiol. 2016;56. doi:10.1016/j.fm.2015.11.018
Murtaza N, Baboota RK, Jagtap S, et al. Finger millet bran supplementation alleviates obesity-induced oxidative stress, inflammation and gut microbial derangements in high-fat diet-fed mice. British Journal of Nutrition. 2014;112(9). doi:10.1017/S0007114514002396
Wu T, Gao Y, Hao J, et al. Lycopene, amaranth, and sorghum red pigments counteract obesity and modulate the gut microbiota in high-fat diet fed C57BL/6 mice. J Funct Foods. 2019;60. doi:10.1016/j.jff.2019.103437
Olguin-Calderon D., JL González-Escobar, J. L. RV, R. DAE, Leon-Rodriguez D, de la Rosa APB. Modulation of caecal microbiome in obese mice associated with administration of amaranth or soybean protein isolates. Pol J Food Nutr Sci. 2019;69(1).
Han J, Zhang R, Muheyati D, Lv MX, Aikebaier W, Peng BX. The Effect of Chickpea Dietary Fiber on Lipid Metabolism and Gut Microbiota in High-Fat Diet-Induced Hyperlipidemia in Rats. J Med Food. 2021;24(2). doi:10.1089/jmf.2020.4800
Nakatani A, Li X, Miyamoto J, et al. Dietary mung bean protein reduces high-fat diet-induced weight gain by modulating host bile acid metabolism in a gut microbiota-dependent manner. Biochem Biophys Res Commun. 2018;501(4):955-961.
Singh RK, Chang HW, Yan D, et al. Influence of diet on the gut microbiome and implications for human health. J Transl Med. 2017;15(1):1-17.
Djurasevic S, Bojic S, Nikolic B, et al. Beneficial effect of virgin coconut oil on alloxan-induced diabetes and microbiota composition in rats. Plant Foods for Human Nutrition. 2018;73:295-301.
Sung MM, Kim TT, Denou E, et al. Improved glucose homeostasis in obese mice treated with resveratrol is associated with alterations in the gut microbiome. Diabetes. 2017;66(2). doi:10.2337/db16-0680
Liu BL, Chiang PS. Production of hydrolysate with antioxidative activity and functional properties by enzymatic hydrolysis of defatted sesame (Sesamum indicum L.). International Journal of Applied Science and Engineering. 2008;6(2):73-83.
Kaliannan K, Wang B, Li XY, Kim KJ, Kang JX. A host-microbiome interaction mediates the opposing effects of omega-6 and omega-3 fatty acids on metabolic endotoxemia. Sci Rep. 2015;5. doi:10.1038/srep11276
Onishi JC, Campbell S, Moreau M, et al. Bacterial communities in the small intestine respond differently to those in the caecum and colon in mice fed low- and high-fat diets. Microbiology (United Kingdom). 2017;163(8). doi:10.1099/mic.0.000496
Prieto I, Hidalgo M, Segarra AB, et al. Influence of a diet enriched with virgin olive oil or butter on mouse gut microbiota and its correlation to physiological and biochemical parameters related to metabolic syndrome. PLoS One. 2018;13(1). doi:10.1371/journal.pone.0190368
Zhou S, Wang Y, Jacoby JJ, Jiang Y, Zhang Y, Yu LL. Effects of medium-and long-chain triacylglycerols on lipid metabolism and gut microbiota composition in C57BL/6J mice. J Agric Food Chem. 2017;65(31):6599-6607.
Bindels LB, Delzenne NM, Cani PD, Walter J. Opinion: Towards a more comprehensive concept for prebiotics. Nat Rev Gastroenterol Hepatol. 2015;12(5). doi:10.1038/nrgastro.2015.47
Sarkar S, Misra A. Bio-preservation of milk and milk products. Indian Food Industry. 2001;20(4):74-77.
Hooper L V., Littman DR, Macpherson AJ. Interactions between the microbiota and the immune system. Science (1979). 2012;336(6086). doi:10.1126/science.1223490
Hancock REW, Haney EF, Gill EE. The immunology of host defence peptides: Beyond antimicrobial activity. Nat Rev Immunol. 2016;16(5). doi:10.1038/nri.2016.29
Holscher HD, Taylor AM, Swanson KS, Novotny JA, Baer DJ. Almond consumption and processing affects the composition of the gastrointestinal microbiota of healthy adult men and women: a randomized controlled trial. Nutrients. 2018;10(2):126.
Holscher HD, Guetterman HM, Swanson KS, et al. Walnut consumption alters the gastrointestinal microbiota, microbially derived secondary bile acids, and health markers in healthy adults: a randomized controlled trial. J Nutr. 2018;148(06):861-867.
Wang J, Wang P, Li D, Hu X, Chen F. Beneficial effects of ginger on prevention of obesity through modulation of gut microbiota in mice. Eur J Nutr. 2020;59:699-718.
Author C, Abu Sayeed M, Abbas Ali M, Mahbub Alam N, Sarmina Yeasmin M, Mohal Khan A. Antimicrobial Screening of Different Extracts of Piper longum Linn. Res J Agric Biol Sci. 2007;3(6).
Di Meo F, Margarucci S, Galderisi U, Crispi S, Peluso G. Curcumin, gut microbiota, and neuroprotection. Nutrients. 2019;11(10). doi:10.3390/nu11102426
Jagetia GC,, Aggarwal BB. “Spicing up” of the immune system by curcumin. J Clin Immunol. Published online 2007:19-35.
Shen L, Liu L, Ji HF. Regulative effects of curcumin spice administration on gut microbiota and its pharmacological implications. Food Nutr Res. 2017;61. doi:10.1080/16546628.2017.1361780
Unlu M, Ergene E, Unlu GV, Zeytinoglu HS, Vural N. Composition, antimicrobial activity and in vitro cytotoxicity of essential oil from Cinnamomum zeylanicum Blume (Lauraceae). Food and Chemical Toxicology. 2010;48(11). doi:10.1016/j.fct.2010.09.001
Kandhare AD, Bodhankar SL, Singh V, Mohan V, Thakurdesai PA. Anti-asthmatic effects of type-A procyanidine polyphenols from cinnamon bark in ovalbumin-induced airway hyperresponsiveness in laboratory animals. Biomedicine and Aging Pathology. 2013;3(1). doi:10.1016/j.biomag.2013.01.003
Kumar P, Patra AK, Mandal GP, Samanta I, Pradhan S. Effect of black cumin seeds on growth performance, nutrient utilization, immunity, gut health and nitrogen excretion in broiler chickens. J Sci Food Agric. 2017;97(11):3742-3751.
Xu J, Liu T, Li Y, et al. Jamun (Eugenia jambolana Lam.) Fruit Extract Prevents Obesity by Modulating the Gut Microbiome in High-Fat-Diet-Fed Mice. Mol Nutr Food Res. 2019;63(9). doi:10.1002/MNFR.201801307
Xu J, Liu T, Li Y, et al. Jamun (Eugenia jambolana Lam.) fruit extract prevents obesity by modulating the gut microbiome in high-fat-diet-fed mice. Mol Nutr Food Res. 2017;97(11):3742-3751.
Li Y, Bai D, Lu Y, et al. The crude guava polysaccharides ameliorate high-fat diet-induced obesity in mice via reshaping gut microbiota. Int J Biol Macromol. 2022;213:234-246.
Gheisari HR, Amiri F, Zolghadri Y. Antioxidant and antimicrobial activity of Iranian Bael (Aegle marmelos) fruit against some food pathogens. Int J Curr Pharm Res. 2011;3(3):85-88.
Gong Y, Dong R, Gao X, et al. Neohesperidin prevents colorectal tumorigenesis by altering the gut microbiota. Pharmacol Res. 2019;148:104460.
Zhang J, Yang G, Wen Y, et al. Intestinal microbiota are involved in the immunomodulatory activities of longan polysaccharide. Mol Nutr Food Res. 2017;61(11). doi:10.1002/mnfr.201700466
Zhang X, Zhao Y, Xu J, et al. Modulation of gut microbiota by berberine and metformin during the treatment of high-fat diet-induced obesity in rats. Sci Rep. 2015;5(1):14405.
Barnes RC, Kim H, Fang C, et al. Body Mass Index as a Determinant of Systemic Exposure to Gallotannin Metabolites during 6-Week Consumption of Mango (Mangifera indica L.) and Modulation of Intestinal Microbiota in Lean and Obese Individuals. Mol Nutr Food Res. 2019;63(2). doi:10.1002/mnfr.201800512
Gutiérrez-Sarmiento W, Sáyago-Ayerdi SG, Goñi I, et al. Changes in intestinal microbiota and predicted metabolic pathways during colonic fermentation of mango (Mangifera indica L.)—based bar indigestible fraction. Nutrients. 2020;12(3). doi:10.3390/nu12030683
Deehan EC, Yang C, Perez-Muñoz ME, et al. Precision Microbiome Modulation with Discrete Dietary Fiber Structures Directs Short-Chain Fatty Acid Production. Cell Host Microbe. 2020;27(3). doi:10.1016/j.chom.2020.01.006
Saxby S, Tipton L, Lee C, et al. Prebiotic Potential of Taro (Colocasia esculenta) to Modulate Gut Bacteria Composition and Short Chain Fatty Acid Production. Curr Dev Nutr. 2020;4. doi:10.1093/cdn/nzaa062_039
Louis P, Flint HJ. Formation of propionate and butyrate by the human colonic microbiota}. Environ Microbiol. 2017;19(01):29-41.
Prabha R, Ramachandra B, Shankar P. Effect of vegetable extract as bifidogenic agents on the growth of wild strains of bifidobacteria. J Pharmacogn Phytochem. 2021;10(06):279-282.
Nissen L, Cattivelli A, Casciano F, Gianotti A, Tagliazucchi D. Roasting and frying modulate the phenolic profile of dark purple eggplant and differently change the colon microbiota and phenolic metabolites after in vitro digestion and fermentation in a gut model. Food Research International. 2022;160. doi:10.1016/j.foodres.2022.111702
Liu G, Liang L, Yu G, Li Q. Pumpkin polysaccharide modifies the gut microbiota during alleviation of type 2 diabetes in rats. Int J Biol Macromol. 2018;115:711-717.
Päivärinta E, Niku M, Maukonen J, et al. Changes in intestinal immunity, gut microbiota, and expression of energy metabolism–related genes explain adenoma growth in bilberry and cloudberry-fed ApcMin mice. Nutrition Research. 2016;36(11). doi:10.1016/j.nutres.2016.10.003
Hemanta MR, Mane VK, Bhagwat A. Analysis of traditional food additive kolakhar for its physico-chemical parameters and antimicrobial activity. J Food Process Technol. 2014;387:5-11.
Valcheva R, Hotte N, Gillevet P, Sikaroodi M, Thiessen A, Madsen KL. Soluble dextrin fibers alter the intestinal microbiota and reduce proinflammatory cytokine secretion in male IL-10-deficient mice. Journal of Nutrition. 2015;145(9). doi:10.3945/jn.114.207738
Elabd EMY, Morsy SM, Elmalt HA. Investigating of Moringa oleifera role on gut microbiota composition and inflammation associated with obesity following high fat diet feeding. Open Access Maced J Med Sci. 2018;6(8):1359.
Elvira-Torales LI, Periago MJ, González-Barrio R, et al. Spinach consumption ameliorates the gut microbiota and dislipaemia in rats with diet-induced non-alcoholic fatty liver disease (NAFLD). Food Funct. 2019;10(4). doi:10.1039/c8fo01630e
Li Y, Cui Y, Lu F, et al. Beneficial effects of a chlorophyll-rich spinach extract supplementation on prevention of obesity and modulation of gut microbiota in high-fat diet-fed mice. J Funct Foods. 2019;60:103436.
Maiyo Z, Ngure R, Matasyoh J, Chepkorir R. Phytochemical constituents and antimicrobial activity of leaf extracts of three Amaranthus plant species. Afr J Biotechnol. 2010;9(21):3178-3182.
Cordonnier C, Le Bihan G, Emond-Rheault JG, Garrivier A, Harel J, Jubelin G. Vitamin B12 uptake by the gut commensal bacteria Bacteroides thetaiotaomicron limits the production of shiga toxin by enterohemorrhagic Escherichia coli. Toxins (Basel). 2016;8(1):14.
Pandey S, Gupta RK. Screening of nutritional, phytochemical, antioxidant and antibacterial activity of Chenopodium album (Bathua). Journal of Pharmacognosy and Phytochemistry JPP. 2014;1(33).
Oteiza P, Fraga CG, Mills D, Taft D. Flavonoids and the gastrointestinal tract: Local and systemic effects. Mol Aspects Med. 2018;61:41-49.
Olalye MT, Rocha JBT. Commonly used tropical medicinal plants exhibt distinct in vitro antioxidant activities against hepatotoxins in rat liver. Experimental and Toxicologic Pathology}. 2007;58(06):433-438.
Holscher HD, Bauer LL, Gourineni V, Pelkman CL, Fahey GC, Swanson KS. Agave inulin supplementation affects the fecal microbiota of healthy adults participating in a randomized, double-blind, placebo-controlled, crossover trial. Journal of Nutrition. 2015;145(9). doi:10.3945/jn.115.217331
Walker AW, Ince J, Duncan SH, et al. Dominant and diet-responsive groups of bacteria within the human colonic microbiota. ISME Journal. 2011;5(2). doi:10.1038/ismej.2010.118
Pontifex MG, Connell E, Le Gall G, et al. Saffron extract (Safr’InsideTM) improves anxiety related behaviour in a mouse model of low-grade inflammation through the modulation of the microbiota and gut derived metabolites. Food Funct. 2022;13(23). doi:10.1039/d2fo02739a
China R, Mukherjee S, Sen S, et al. Antimicrobial activity of Sesbania grandiflora flower polyphenol extracts on some pathogenic bacteria and growth stimulatory effect on the probiotic organism Lactobacillus acidophilus. Microbiol Res. 2012;167(8). doi:10.1016/j.micres.2012.04.003
Muruganantham N, Solomon S, Senthamilselvi M. Antimicrobial activity of Cucurbita maxima flowers (Pumpkin). Journal of Pharmacognosy and Phytochemistry . 2016;5(1).
Sitthiya K, Devkota L, Sadiq MB, Anal AK. Extraction and characterization of proteins from banana (Musa Sapientum L) flower and evaluation of antimicrobial activities. J Food Sci Technol. 2018;55(2). doi:10.1007/s13197-017-2975-z
Kulshrestha PK, Mishra AK, Pal VK, Pandey S, Tripathi D, Yadav P. The antimicrobial activity of bahunia variegata linn. Flower extract (Methanolic). Asian Journal of Pharmaceutical and Clinical Research. 2011;4(SUPPL. 1).
Singh P, Junnarkar A, Reddi G, Singh K. Azadirachta indica neuro psychopharmacological and anti-microbial studies. Fitoterapia. 1987;58(4):233-248.
Shondelmyer K, Knight R, Sanivarapu A, Ogino S, Vanamala JKP. Focus: Nutrition and Food Science: Ancient Thali Diet: Gut Microbiota, Immunity, and Health. Yale J Biol Med. 2018;91(2).
Slavin J. Fiber and prebiotics: Mechanisms and health benefits. Nutrients. 2013;5(4). doi:10.3390/nu5041417
Graf D, Di Cagno R, Fåk F, et al. Contribution of diet to the composition of the human gut microbiota. Microb Ecol Health Dis. 2015;26(0). doi:10.3402/mehd.v26.26164
Rinninella E, Cintoni M, Raoul P, et al. Food components and dietary habits: Keys for a healthy gut microbiota composition. Nutrients. 2019;11(10). doi:10.3390/nu11102393
Gallagher EJ, LeRoith D, Karnieli E. The Metabolic Syndrome-from Insulin Resistance to Obesity and Diabetes. Medical Clinics of North America. 2011;95(5). doi:10.1016/j.mcna.2011.06.001
Medina-Remón A, Casas R, Tressserra-Rimbau A, et al. Polyphenol intake from a Mediterranean diet decreases inflammatory biomarkers related to atherosclerosis: a substudy of the PREDIMED trial. Br J Clin Pharmacol. 2017;83(1). doi:10.1111/bcp.12986
Xu J, Liu T, Li Y, et al. Jamun (Eugenia jambolana Lam.) fruit extract prevents obesity by modulating the gut microbiome in high-fat-diet-fed mice}. Mol Nutr Food Res. 2019;63(9):1801307.
An J, Lee H, Lee S, et al. Modulation of pro-inflammatory and anti-inflammatory cytokines in the fat by an aloe gel-based formula, qdmc, is correlated with altered gut microbiota. Immune Netw. 2021;21(2). doi:10.4110/in.2021.21.e15
Rowland I, Gibson G, Heinken A, et al. Gut microbiota functions: metabolism of nutrients and other food components. Eur J Nutr. 2018;57(1). doi:10.1007/S00394-017-1445-8
Molan AL, Liu Z, Plimmer G. Evaluation of the effect of blackcurrant products on gut microbiota and on markers of risk for colon cancer in humans. Phytotherapy Research. 2014;28(3). doi:10.1002/ptr.5009
Lv Z, Wang Y, Yang T, et al. Vitamin A deficiency impacts the structural segregation of gut microbiota in children with persistent diarrhea. J Clin Biochem Nutr. 2016;59(2). doi:10.3164/jcbn.15-148
Hibberd MC, Wu M, Rodionov DA, et al. The effects of micronutrient deficiencies on bacterial species from the human gut microbiota. Sci Transl Med. 2017;9(390). doi:10.1126/scitranslmed.aal4069
Lee H, Ko GP. Antiviral effect of Vitamin A on norovirus infection via modulation of the gut microbiome. Sci Rep. 2016;6. doi:10.1038/srep25835
Lee H, Ko G. New perspectives regarding the antiviral effect of vitamin A on norovirus using modulation of gut microbiota. Gut Microbes. 2017;8(6). doi:10.1080/19490976.2017.1353842
Degnan PH, Barry NA, Mok KC, Taga ME, Goodman AL. Human gut microbes use multiple transporters to distinguish vitamin B 12 analogs and compete in the gut. Cell Host Microbe. 2014;15(1). doi:10.1016/j.chom.2013.12.007
Li L, Krause L, Somerset S. Associations between micronutrient intakes and gut microbiota in a group of adults with cystic fibrosis. Clinical Nutrition. 2017;36(4). doi:10.1016/j.clnu.2016.06.029
Xu J, Xu C, Chen X, et al. Regulation of an antioxidant blend on intestinal redox status and major microbiota in early weaned piglets. Nutrition. 2014;30(5). doi:10.1016/j.nut.2013.10.018
Kursar M, Bonhagen K, Fensterle J, et al. Regulatory CD4+CD25+ T cells restrict memory CD8+ T cell responses. Journal of Experimental Medicine. 2002;196(12). doi:10.1084/jem.20011347
Forsythe P, Inman MD, Bienenstock J. Oral treatment with live Lactobacillus reuteri inhibits the allergic airway response in mice. Am J Respir Crit Care Med. 2007;175(06):561-569.
Hansel TT, Johnston SL, Openshaw PJ. Microbes and mucosal immune responses in asthma. The Lancet. 2013;381(9869). doi:10.1016/S0140-6736(12)62202-8
Kuczma MP, Szurek EA, Cebula A, et al. Self and microbiota-derived epitopes induce CD4+ T cell anergy and conversion into CD4+Foxp3+ regulatory cells. Mucosal Immunol. 2021;14(2). doi:10.1038/s41385-020-00349-4
Stentzel S, Teufelberger A, Nordengrün M, et al. Staphylococcal serine protease–like proteins are pacemakers of allergic airway reactions to Staphylococcus aureus. Journal of Allergy and Clinical Immunology. 2017;139(2):492-500.e8. doi:10.1016/J.JACI.2016.03.045
Teo SM, Mok D, Pham K, et al. The infant nasopharyngeal microbiome impacts severity of lower respiratory infection and risk of asthma development. Cell Host Microbe. 2015;17(05):704-715.
Nakamoto K, Watanabe M, Sada M, et al. Pseudomonas aeruginosa-derived flagellin stimulates IL-6 and IL-8 production in human bronchial epithelial cells: A potential mechanism for progression and exacerbation of COPD. Exp Lung Res. 2019;45(8). doi:10.1080/01902148.2019.1665147
Monalisa Das1; Nooruddin Thajuddin1; Sanjib Patra2 and Megha Pundir2
1Department of Microbiology; Bharathidasan University; Tiruchirappalli; Tamil Nādu; India.
2Department of Yoga; Central University of Rajasthan; Ajmer; Rajasthan India.
Corresponding Author E-mail: [email protected]
Monalisa Das1; Nooruddin Thajuddin1; Sanjib Patra2 and Megha Pundir2
1Department of Microbiology; Bharathidasan University; Tiruchirappalli; Tamil Nādu; India.
2Department of Yoga; Central University of Rajasthan; Ajmer; Rajasthan India.
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Abstract
Modernization, a stressful lifestyle, attachment to a Western diet, and the use of preserved and processed foods lead to a loss of homeostasis of intestinal microbial diversity. The use of refined flour and refined sugar, which lack of micro biota-accessible carbohydrates (MAC), means dietary fiber high salt consumption, and saturated fats in fried and packaged foods cause gut microbiota dysbiosis. Microbial dysbiosis caused by high fat, salt, and lack of fiber causes several metabolic diseases, including asthma.
The objective of the study is to develop a hypothetic model that “Ancient Indian diet” which is inspired by thousands of years of Indian science, including Yoga, Ayurveda, and Naturopathy may maintain the diversity of the gut microbiota and may inhibits the asthmatic symptoms by enhancing the growth of antiasthmatic bacteria.
A keyword search utilizing the phrases "western diet, beneficial microbiota, asthma, gut microbial dysbiosis, Ancient Indian diet" was conducted electronically search through the SCOPUS ,Science Direct ,PubMed, Web of Science, and PsycINFO databases. Search criteria are divided into two arms the first one includes different full-text research papers including how Indian diet altered gut microbial composition. The second one, we included the full text including how presence of certain gut microbiota can prevents the asthmatic attack. To find publications that met the eligibility requirements, the first and third authors separately reviewed each publication's title and abstract using the previously described inclusion criteria. We have included 124 research articles, which is published between 1989 to 2024.
A plant-based ancient Indian diet increases the diversity of Bacteroidetes, Actinobacteria, Prevotella, Bifidobacterium, Lactobacillus, Ruminococcus, Roseburia, Lactobacillus, Lachnospira, Akkermansia and shows inhibitory effects against Clostridium, E. coli, Staphylococcus, Haemophilus, Moraxella and Neisseria.
The ancient Indian diet a low-fat lacto-vegetarian diet maintains gut microbiota homeostasis, and suppresses the growth of pathogenic asthmatic bacteria and promotes the growth of beneficial asthmatic bacteria.
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