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BMC microbiology2023; 23(1); 246; doi: 10.1186/s12866-023-02986-8

Gut microbiota changes in horses with Chlamydia.

Abstract: Zoonotic diseases pose a significant threat to public health. Chlamydia, as an intracellular pathogen, can colonize the intestinal tract of humans and animals, changing the gut microbiota. However, only a few studies have evaluated alterations in the gut microbiota of horses infected with Chlamydia. Therefore, this study aimed to investigate gut microbiota and serum biochemical indicators in horses with Chlamydial infection (IG) and healthy horses (HG). Fecal and blood samples were collected from 16 horses (IG: 10; HG: 6) before morning feeding for the determination of gut microbiota and serum biochemical parameters. Results: The results showed that total globulin (GLB), alanine aminotransferase (ALT), and creatine kinase (CK) levels were significantly increased in IG compared with HG. Notably, the gut microbial diversity increased in IG compared with HG. Furthermore, Moraxellaceae and Akkermanisa abundance decreased in IG, while Streptococcus, Treponema, Prevotella, and Paraprevotella abundances (13 genera of bacterial species) increased. Compared with HG, carbohydrate metabolism increased in IG while amino acid metabolism decreased. In addition, the abundance of 18 genera of bacteria was associated with the level of five serum biochemical indicators. Conclusions: In summary, this study elucidated the influence of Chlamydia infection in horses on the gut microbiota, unraveling consequential alterations in its composition and metabolic profile. Therefore, this study improves the understanding of Chlamydia-induced intestinal infections.
Publication Date: 2023-09-02 PubMed ID: 37660043PubMed Central: PMC10474637DOI: 10.1186/s12866-023-02986-8Google Scholar: Lookup
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  • Journal Article

Summary

This research summary has been generated with artificial intelligence and may contain errors and omissions. Refer to the original study to confirm details provided. Submit correction.

The research study explores how Chlamydia infections in horses affect their gut microbiota (the collection of microorganisms living in the gastrointestinal tract), as well as some serological indicators. It finds significant shifts in the gut microbiota and some serum biochemical levels, providing new insights into the impact of Chlamydia-induced gastrointestinal infections in horses.

Study Purpose and Methodology

  • The primary objective of the study was to determine changes in the gut microbiota and serum biochemical indicators in horses with Chlamydia infections compared to healthy horses.
  • Fecal and blood samples were collected from a total of 16 horses – 10 infected with Chlamydia (IG) and 6 healthy (HG).
  • The samples were analysed to identify gut microbiota and measure serum biochemical parameters, specifically total globulin (GLB), alanine aminotransferase (ALT), and creatine kinase (CK) levels.

Key Findings

  • The research found that horses with Chlamydia infection showed significantly increased levels of GLB, ALT, and CK compared to the healthy horses.
  • There was a noticeable rise in gut microbial diversity in the infected horses compared to the healthy ones.
  • Specific bacterial families showed alterations in their percentages with Moraxellaceae and Akkermanisa decreasing and Streptococcus, Treponema, Prevotella, and Paraprevotella (incorporating 13 genera of bacteria) increasing in the infected horses.
  • The study also found notable changes in metabolic activities, with carbohydrate metabolism increasing and amino acid metabolism decreasing in infected horses compared to the healthy ones.
  • An observed correlation between the abundance of 18 genera of bacteria and the levels of five serum biochemical indicators was also found.

Conclusion

  • This research has provided evidence of the transformative effect of Chlamydia infection on the gut microbiota of horses, marked by significant shifts in microbiota composition and metabolic activities.
  • This work contributes to the understanding of Chlamydia’s impact on intestinal infections, which can be valuable for developing future therapeutic strategies to control Chlamydia infections in horses.

Cite This Article

APA
Jin Y, Li W, Ba X, Li Y, Wang Y, Zhang H, Li Z, Zhou J. (2023). Gut microbiota changes in horses with Chlamydia. BMC Microbiol, 23(1), 246. https://doi.org/10.1186/s12866-023-02986-8

Publication

ISSN: 1471-2180
NlmUniqueID: 100966981
Country: England
Language: English
Volume: 23
Issue: 1
Pages: 246
PII: 246

Researcher Affiliations

Jin, Youshun
  • State Key Laboratory for Animal Disease Control and Prevention, Key Laboratory of Veterinary Public Health of Agriculture Ministry Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730046, China.
  • State Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou Veterinary Research Institute, Lanzhou University, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China.
Li, Wei
  • State Key Laboratory for Animal Disease Control and Prevention, Key Laboratory of Veterinary Public Health of Agriculture Ministry Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730046, China.
Ba, Xuli
  • State Key Laboratory for Animal Disease Control and Prevention, Key Laboratory of Veterinary Public Health of Agriculture Ministry Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730046, China.
  • State Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou Veterinary Research Institute, Lanzhou University, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China.
Li, Yunhui
  • Animal Pathology Laboratory, College of Veterinary Medicine, Northwest A&F University, Xianyang, 712100, China.
Wang, Yanyan
  • State Key Laboratory for Animal Disease Control and Prevention, Key Laboratory of Veterinary Public Health of Agriculture Ministry Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730046, China.
Zhang, Huaiyu
  • Animal Pathology Laboratory, College of Veterinary Medicine, Northwest A&F University, Xianyang, 712100, China.
Li, Zhaocai
  • State Key Laboratory for Animal Disease Control and Prevention, Key Laboratory of Veterinary Public Health of Agriculture Ministry Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730046, China.
Zhou, Jizhang
  • State Key Laboratory for Animal Disease Control and Prevention, Key Laboratory of Veterinary Public Health of Agriculture Ministry Lanzhou Veterinary Research Institute, Chinese Academy of Agricultural Sciences, Lanzhou, 730046, China. zhoujz@lzu.edu.cn.
  • State Key Laboratory for Animal Disease Control and Prevention, College of Veterinary Medicine, Lanzhou Veterinary Research Institute, Lanzhou University, Chinese Academy of Agricultural Sciences, Lanzhou, 730000, China. zhoujz@lzu.edu.cn.

MeSH Terms

  • Humans
  • Animals
  • Horses
  • Gastrointestinal Microbiome
  • Chlamydia
  • Chlamydia Infections / veterinary
  • Zoonoses
  • Bacteroidetes

Grant Funding

  • 2022YFC2304000 / National Key Research and Development Program of China

Conflict of Interest Statement

The authors have no conflicts of interest.

References

This article includes 55 references
  1. Petersen E, Petrosillo N, Koopmans M. Emerging infections-an increasingly important topic: review by the Emerging Infections Task Force.. Clin Microbiol Infect 2018 Apr;24(4):369-375.
    doi: 10.1016/j.cmi.2017.10.035pmc: PMC7129920pubmed: 29155018google scholar: lookup
  2. Acharya KP, Acharya N, Phuyal S, Upadhyaya M, Lasee S. One-health approach: A best possible way to control rabies.. One Health 2020 Dec;10:100161.
  3. Gebreyes WA, Dupouy-Camet J, Newport MJ, Oliveira CJ, Schlesinger LS, Saif YM, Kariuki S, Saif LJ, Saville W, Wittum T, Hoet A, Quessy S, Kazwala R, Tekola B, Shryock T, Bisesi M, Patchanee P, Boonmar S, King LJ. The global one health paradigm: challenges and opportunities for tackling infectious diseases at the human, animal, and environment interface in low-resource settings.. PLoS Negl Trop Dis 2014;8(11):e3257.
  4. Chakraborty C, Bhattacharya M, Nandi SS, Mohapatra RK, Dhama K, Agoramoorthy G. Appearance and re-appearance of zoonotic disease during the pandemic period: long-term monitoring and analysis of zoonosis is crucial to confirm the animal origin of SARS-CoV-2 and monkeypox virus.. Vet Q 2022 Jun 7;42(1):119-124.
  5. Vorimore F, Hölzer M, Liebler-Tenorio EM, Barf LM, Delannoy S, Vittecoq M, Wedlarski R, Lécu A, Scharf S, Blanchard Y, Fach P, Hsia RC, Bavoil PM, Rosselló-Móra R, Laroucau K, Sachse K. Evidence for the existence of a new genus Chlamydiifrater gen. nov. inside the family Chlamydiaceae with two new species isolated from flamingo (Phoenicopterus roseus): Chlamydiifrater phoenicopteri sp. nov. and Chlamydiifrater volucris sp. nov.. Syst Appl Microbiol 2021 Jul;44(4):126200.
    pubmed: 34298369doi: 10.1016/j.syapm.2021.126200google scholar: lookup
  6. Cheong HC, Lee CYQ, Cheok YY, Tan GMY, Looi CY, Wong WF. Chlamydiaceae: Diseases in Primary Hosts and Zoonosis.. Microorganisms 2019 May 24;7(5).
  7. Elwell C, Mirrashidi K, Engel J. Chlamydia cell biology and pathogenesis.. Nat Rev Microbiol 2016 Jun;14(6):385-400.
    doi: 10.1038/nrmicro.2016.30pmc: PMC4886739pubmed: 27108705google scholar: lookup
  8. Ravichandran K, Anbazhagan S, Karthik K, Angappan M, Dhayananth B. A comprehensive review on avian chlamydiosis: a neglected zoonotic disease.. Trop Anim Health Prod 2021 Jul 27;53(4):414.
    doi: 10.1007/s11250-021-02859-0pmc: PMC8313243pubmed: 34312716google scholar: lookup
  9. Polkinghorne A, Greub G. A new equine and zoonotic threat emerges from an old avian pathogen, Chlamydia psittaci.. Clin Microbiol Infect 2017 Oct;23(10):693-694.
    doi: 10.1016/j.cmi.2017.05.025pubmed: 28583739google scholar: lookup
  10. Turin L, Surini S, Wheelhouse N, Rocchi MS. Recent advances and public health implications for environmental exposure to Chlamydia abortus: from enzootic to zoonotic disease.. Vet Res 2022 May 31;53(1):37.
    doi: 10.1186/s13567-022-01052-xpmc: PMC9152823pubmed: 35642008google scholar: lookup
  11. Gautam J, Krawiec C. Chlamydia pneumonia. 2020.
  12. Zhong G. Chlamydia overcomes multiple gastrointestinal barriers to achieve long-lasting colonization.. Trends Microbiol 2021 Nov;29(11):1004-1012.
    doi: 10.1016/j.tim.2021.03.011pmc: PMC8510992pubmed: 33865675google scholar: lookup
  13. He C, Xu Y, Huo Z, Wang J, Jia T, Li XD, Zhong G. Regulation of Chlamydia spreading from the small intestine to the large intestine via an immunological barrier.. Immunol Cell Biol 2021 Jul;99(6):611-621.
    doi: 10.1111/imcb.12446pubmed: 33565158google scholar: lookup
  14. Gacesa R, Kurilshikov A, Vich Vila A, Sinha T, Klaassen MAY, Bolte LA, Andreu-Sánchez S, Chen L, Collij V, Hu S, Dekens JAM, Lenters VC, Björk JR, Swarte JC, Swertz MA, Jansen BH, Gelderloos-Arends J, Jankipersadsing S, Hofker M, Vermeulen RCH, Sanna S, Harmsen HJM, Wijmenga C, Fu J, Zhernakova A, Weersma RK. Environmental factors shaping the gut microbiome in a Dutch population.. Nature 2022 Apr;604(7907):732-739.
    doi: 10.1038/s41586-022-04567-7pubmed: 35418674google scholar: lookup
  15. de Vos WM, Tilg H, Van Hul M, Cani PD. Gut microbiome and health: mechanistic insights.. Gut 2022 May;71(5):1020-1032.
    doi: 10.1136/gutjnl-2021-326789pmc: PMC8995832pubmed: 35105664google scholar: lookup
  16. Dwyer RM. Equine zoonoses: consequences of horse-human interactions. Zoonoses-Infections Affecting Humans and Animals: Focus on Public Health Aspects 2014:643 – 57.
  17. Clark A, Sallé G, Ballan V, Reigner F, Meynadier A, Cortet J, Koch C, Riou M, Blanchard A, Mach N. Strongyle Infection and Gut Microbiota: Profiling of Resistant and Susceptible Horses Over a Grazing Season.. Front Physiol 2018;9:272.
    doi: 10.3389/fphys.2018.00272pmc: PMC5871743pubmed: 29618989google scholar: lookup
  18. Akter R, El-Hage CM, Sansom FM, Carrick J, Devlin JM, Legione AR. Metagenomic investigation of potential abortigenic pathogens in foetal tissues from Australian horses.. BMC Genomics 2021 Oct 2;22(1):713.
    doi: 10.1186/s12864-021-08010-5pmc: PMC8487468pubmed: 34600470google scholar: lookup
  19. Costa MC, Arroyo LG, Allen-Vercoe E, Stämpfli HR, Kim PT, Sturgeon A, Weese JS. Comparison of the fecal microbiota of healthy horses and horses with colitis by high throughput sequencing of the V3-V5 region of the 16S rRNA gene.. PLoS One 2012;7(7):e41484.
  20. Kong CY, Zhu J, Lu JJ, Xu ZH. Clinical characteristics of Chlamydia psittaci pneumonia.. Chin Med J (Engl) 2021 Jan 5;134(3):353-355.
  21. Zhang A, Xia X, Yuan X, Liu Y, Niu H, Zhang Y, Liang J. Severe Chlamydia psittaci Pneumonia Complicated by Rhabdomyolysis: A Case Series.. Infect Drug Resist 2022;15:873-881.
    pmc: PMC8910519pubmed: 35281577doi: 10.2147/idr.s355024google scholar: lookup
  22. Datta B, Njau F, Thalmann J, Haller H, Wagner AD. Differential infection outcome of Chlamydia trachomatis in human blood monocytes and monocyte-derived dendritic cells.. BMC Microbiol 2014 Aug 14;14:209.
    doi: 10.1186/s12866-014-0209-3pmc: PMC4236547pubmed: 25123797google scholar: lookup
  23. Cheong HC, Lee CYQ, Cheok YY, Shankar EM, Sabet NS, Tan GMY, Movahed E, Yeow TC, Sulaiman S, Wong WF, Looi CY, Gupta R, Hassan J, Arulanandam B, AbuBakar S. CPAF, HSP60 and MOMP antigens elicit pro-inflammatory cytokines production in the peripheral blood mononuclear cells from genital Chlamydia trachomatis-infected patients.. Immunobiology 2019 Jan;224(1):34-41.
    doi: 10.1016/j.imbio.2018.10.010pubmed: 30477893google scholar: lookup
  24. Brunham RC, Rey-Ladino J. Immunology of Chlamydia infection: implications for a Chlamydia trachomatis vaccine.. Nat Rev Immunol 2005 Feb;5(2):149-61.
    doi: 10.1038/nri1551pubmed: 15688042google scholar: lookup
  25. Brinkworth AJ, Wildung MR, Carabeo RA. Genomewide Transcriptional Responses of Iron-Starved Chlamydia trachomatis Reveal Prioritization of Metabolic Precursor Synthesis over Protein Translation.. mSystems 2018 Jan-Feb;3(1).
    doi: 10.1128/mSystems.00184-17pmc: PMC5811630pubmed: 29468197google scholar: lookup
  26. Baird MF, Graham SM, Baker JS, Bickerstaff GF. Creatine-kinase- and exercise-related muscle damage implications for muscle performance and recovery.. J Nutr Metab 2012;2012:960363.
    pmc: PMC3263635pubmed: 22288008doi: 10.1155/2012/960363google scholar: lookup
  27. Cheok YY, Lee CYQ, Cheong HC, Looi CY, Wong WF. Chronic Inflammatory Diseases at Secondary Sites Ensuing Urogenital or Pulmonary Chlamydia Infections.. Microorganisms 2020 Jan 17;8(1).
  28. Fassarella M, Blaak EE, Penders J, Nauta A, Smidt H, Zoetendal EG. Gut microbiome stability and resilience: elucidating the response to perturbations in order to modulate gut health.. Gut 2021 Mar;70(3):595-605.
    doi: 10.1136/gutjnl-2020-321747pubmed: 33051190google scholar: lookup
  29. Garber A, Hastie P, Murray JA. Factors Influencing Equine Gut Microbiota: Current Knowledge.. J Equine Vet Sci 2020 May;88:102943.
    doi: 10.1016/j.jevs.2020.102943pubmed: 32303307google scholar: lookup
  30. Edwards VL, Smith SB, McComb EJ, Tamarelle J, Ma B, Humphrys MS, Gajer P, Gwilliam K, Schaefer AM, Lai SK, Terplan M, Mark KS, Brotman RM, Forney LJ, Bavoil PM, Ravel J. The Cervicovaginal Microbiota-Host Interaction Modulates Chlamydia trachomatis Infection.. mBio 2019 Aug 13;10(4).
    doi: 10.1128/mBio.01548-19pmc: PMC6692509pubmed: 31409678google scholar: lookup
  31. Filardo S, Di Pietro M, Tranquilli G, Latino MA, Recine N, Porpora MG, Sessa R. Selected Immunological Mediators and Cervical Microbial Signatures in Women with Chlamydia trachomatis Infection.. mSystems 2019 Jun 4;4(4).
    doi: 10.1128/mSystems.00094-19pmc: PMC6550367pubmed: 31164450google scholar: lookup
  32. Xie G, Hu Q, Cao X, Wu W, Dai P, Guo W, Wang O, Wei L, Ren R, Li Y. Clinical identification and microbiota analysis of Chlamydia psittaci- and Chlamydia abortus- pneumonia by metagenomic next-generation sequencing.. Front Cell Infect Microbiol 2023;13:1157540.
    pmc: PMC10331293pubmed: 37434780doi: 10.3389/fcimb.2023.1157540google scholar: lookup
  33. Wen X, Luo S, Lv D, Jia C, Zhou X, Zhai Q, Xi L, Yang C. Variations in the fecal microbiota and their functions of Thoroughbred, Mongolian, and Hybrid horses.. Front Vet Sci 2022;9:920080.
    doi: 10.3389/fvets.2022.920080pmc: PMC9366519pubmed: 35968025google scholar: lookup
  34. Brüssow H. Problems with the concept of gut microbiota dysbiosis.. Microb Biotechnol 2020 Mar;13(2):423-434.
    doi: 10.1111/1751-7915.13479pmc: PMC7017827pubmed: 31448542google scholar: lookup
  35. Guo J, Cui G, Huang W, Zheng Z, Li T, Gao G, Huang Z, Zhan Y, Ding S, Liu S, Yu Z, Ren Z. Alterations in the human oral microbiota in systemic lupus erythematosus.. J Transl Med 2023 Feb 8;21(1):95.
    doi: 10.1186/s12967-023-03892-3pmc: PMC9905765pubmed: 36755319google scholar: lookup
  36. Fettweis JM, Serrano MG, Brooks JP, Edwards DJ, Girerd PH, Parikh HI, Huang B, Arodz TJ, Edupuganti L, Glascock AL, Xu J, Jimenez NR, Vivadelli SC, Fong SS, Sheth NU, Jean S, Lee V, Bokhari YA, Lara AM, Mistry SD, Duckworth RA 3rd, Bradley SP, Koparde VN, Orenda XV, Milton SH, Rozycki SK, Matveyev AV, Wright ML, Huzurbazar SV, Jackson EM, Smirnova E, Korlach J, Tsai YC, Dickinson MR, Brooks JL, Drake JI, Chaffin DO, Sexton AL, Gravett MG, Rubens CE, Wijesooriya NR, Hendricks-Muñoz KD, Jefferson KK, Strauss JF 3rd, Buck GA. The vaginal microbiome and preterm birth.. Nat Med 2019 Jun;25(6):1012-1021.
    doi: 10.1038/s41591-019-0450-2pmc: PMC6750801pubmed: 31142849google scholar: lookup
  37. Sack A, Oladunni FS, Gonchigoo B, Chambers TM, Gray GC. Zoonotic Diseases from Horses: A Systematic Review.. Vector Borne Zoonotic Dis 2020 Jul;20(7):484-495.
    doi: 10.1089/vbz.2019.2541pmc: PMC7339018pubmed: 32077811google scholar: lookup
  38. Park T, Cheong H, Yoon J, Kim A, Yun Y, Unno T. Comparison of the Fecal Microbiota of Horses with Intestinal Disease and Their Healthy Counterparts.. Vet Sci 2021 Jun 17;8(6).
    doi: 10.3390/vetsci8060113pmc: PMC8234941pubmed: 34204317google scholar: lookup
  39. Mahowald MA, Rey FE, Seedorf H, Turnbaugh PJ, Fulton RS, Wollam A, Shah N, Wang C, Magrini V, Wilson RK, Cantarel BL, Coutinho PM, Henrissat B, Crock LW, Russell A, Verberkmoes NC, Hettich RL, Gordon JI. Characterizing a model human gut microbiota composed of members of its two dominant bacterial phyla.. Proc Natl Acad Sci U S A 2009 Apr 7;106(14):5859-64.
    doi: 10.1073/pnas.0901529106pmc: PMC2660063pubmed: 19321416google scholar: lookup
  40. Rey FE, Faith JJ, Bain J, Muehlbauer MJ, Stevens RD, Newgard CB, Gordon JI. Dissecting the in vivo metabolic potential of two human gut acetogens.. J Biol Chem 2010 Jul 16;285(29):22082-90.
    doi: 10.1074/jbc.M110.117713pmc: PMC2903421pubmed: 20444704google scholar: lookup
  41. Fan Q, Wanapat M, Yan T, Hou F. Altitude influences microbial diversity and herbage fermentation in the rumen of yaks.. BMC Microbiol 2020 Dec 4;20(1):370.
    doi: 10.1186/s12866-020-02054-5pmc: PMC7718673pubmed: 33276718google scholar: lookup
  42. Fei Y, Wang Y, Pang Y, Wang W, Zhu D, Xie M, Lan S, Wang Z. Xylooligosaccharide Modulates Gut Microbiota and Alleviates Colonic Inflammation Caused by High Fat Diet Induced Obesity.. Front Physiol 2019;10:1601.
    doi: 10.3389/fphys.2019.01601pmc: PMC6987399pubmed: 32038285google scholar: lookup
  43. Yu X, Wang L, Zheng X, Wen Y, Zhang Z, Fan L, Zhou Q, Yang X, Xue B, Lin Y. Moraxella occupied the largest proportion in the nasal microbiome in healthy children, which potential protect them from COVID-19.. Microb Pathog 2022 Sep;170:105685.
  44. Holman DB, Yang W, Alexander TW. Antibiotic treatment in feedlot cattle: a longitudinal study of the effect of oxytetracycline and tulathromycin on the fecal and nasopharyngeal microbiota.. Microbiome 2019 Jun 5;7(1):86.
    doi: 10.1186/s40168-019-0696-4pmc: PMC6549328pubmed: 31167657google scholar: lookup
  45. Qiu H, Gao H, Yu F, Xiao B, Li X, Cai B, Ge L, Lu Y, Wan Z, Wang Y, Xia T, Wang A, Zhang S. Perinatal exposure to low-level PBDE-47 programs gut microbiota, host metabolism and neurobehavior in adult rats: An integrated analysis.. Sci Total Environ 2022 Jun 15;825:154150.
  46. Zhang T, Li Q, Cheng L, Buch H, Zhang F. Akkermansia muciniphila is a promising probiotic.. Microb Biotechnol 2019 Nov;12(6):1109-1125.
    doi: 10.1111/1751-7915.13410pmc: PMC6801136pubmed: 31006995google scholar: lookup
  47. Zhang T, Ji X, Lu G, Zhang F. The potential of Akkermansia muciniphila in inflammatory bowel disease.. Appl Microbiol Biotechnol 2021 Aug;105(14-15):5785-5794.
    doi: 10.1007/s00253-021-11453-1pubmed: 34312713google scholar: lookup
  48. Martin R, Nauta AJ, Ben Amor K, Knippels LM, Knol J, Garssen J. Early life: gut microbiota and immune development in infancy.. Benef Microbes 2010 Nov;1(4):367-82.
    doi: 10.3920/BM2010.0027pubmed: 21831776google scholar: lookup
  49. Payling L, Fraser K, Loveday S, Sims I, Roy N, McNabb W. The effects of carbohydrate structure on the composition and functionality of the human gut microbiota. Trends Food Sci Tech 2020;97:233–48.
  50. Goyal P, Rajala MS. Reprogramming of glucose metabolism in virus infected cells.. Mol Cell Biochem 2023 Nov;478(11):2409-2418.
    pmc: PMC9884135pubmed: 36709223doi: 10.1007/s11010-023-04669-4google scholar: lookup
  51. Zhang P, Pan S, Yuan S, Shang Y, Shu H. Abnormal glucose metabolism in virus associated sepsis.. Front Cell Infect Microbiol 2023;13:1120769.
    pmc: PMC10130199pubmed: 37124033doi: 10.3389/fcimb.2023.1120769google scholar: lookup
  52. Darville T, Hiltke TJ. Pathogenesis of genital tract disease due to Chlamydia trachomatis.. J Infect Dis 2010 Jun 15;201 Suppl 2(Suppl 2):S114-25.
    doi: 10.1086/652397pmc: PMC3150527pubmed: 20524234google scholar: lookup
  53. Redgrove KA, McLaughlin EA. The Role of the Immune Response in Chlamydia trachomatis Infection of the Male Genital Tract: A Double-Edged Sword.. Front Immunol 2014;5:534.
    doi: 10.3389/fimmu.2014.00534pmc: PMC4209867pubmed: 25386180google scholar: lookup
  54. Chen Y, Yu CY, Deng WM. The role of pro-inflammatory cytokines in lipid metabolism of metabolic diseases.. Int Rev Immunol 2019;38(6):249-266.
    pubmed: 31353985doi: 10.1080/08830185.2019.1645138google scholar: lookup
  55. Lackey DE, Olefsky JM. Regulation of metabolism by the innate immune system.. Nat Rev Endocrinol 2016 Jan;12(1):15-28.
    doi: 10.1038/nrendo.2015.189pubmed: 26553134google scholar: lookup

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