Preview

Acta Biomedica Scientifica

Расширенный поиск

Молекулярные механизмы персистенции адгезивно-инвазивных Escherichia coli в организме хозяина

https://doi.org/10.29413/ABS.2026-11.2.8

Аннотация

Адгезивно–инвазивные Escherichia coli (AIEC), которые приобрели способность прикрепляться и проникать внутрь эпителиальных клеток, выживать и размножаться внутри макрофагов, а также провоцировать воспалительный процесс, привлекают особое внимание исследователей в связи с тем, что они рассматриваются в качестве одного из участников патогенеза такого тяжёлого хронического воспалительного заболевания желудочно-кишечного тракта (ЖКТ), как болезнь Крона (БК). AIEC представляют собой филогенетически разнообразную группу бактерий, не имеющую генетических детерминант, характерных для патогенных E. coli, и обладающую уникальной метаболической пластичностью, что позволяет им адаптироваться к различным условиям. В настоящее время, один из ключевых вопросов исследований заключается в том, являются ли AIEC триггером БК или же они лишь адаптируются к уже существующему воспалению, используя его для выживания и размножения на фоне сниженного иммунитета слизистой оболочки и нарушения барьерной функции кишечного эпителия. Отдельный интерес представляет изучение механизмов и причин трансформации комменсальных E. coli в патогенный фенотип AIEC.

Целью данного обзора является систематизация и анализ научных данных о ключевых молекулярных механизмах, обеспечивающих успешную колонизацию AIEC кишечника человека. В работе подробно рассматриваются стратегии AIEC преодолевать слой слизи, механизмы адгезии–инвазии и способность выживать и реплицироваться в макрофагах, пластичность метаболизма, позволяющая утилизировать альтернативные источники углерода, способность к образованию биопленок и устойчивость к антибиотикам и антимикробным пептидам.

Для подготовки использовали обзорные и экспериментальные статьи, доступные в полном формате в базе данных PubMed, с использованием ключевого слова «адгезивно–инвазивные Escherichia coli» (AIEC). В качестве фильтра использовали статьи с 1998 года, когда появились первые публикации о AIEC.

Об авторах

О. В. Побегуц
Федеральный научно-клинический центр физико-химической медицины имени академика Ю.М. Лопухина Федерального медико-биологического агентства
Россия

Побегуц Ольга Владимировна - кандидат биологических наук, старший научный сотрудник лаборатории протеомного анализа.

119435, Москва, Малая Пироговская, д. 1а



А. С. Авшалумов
Федеральный научно-клинический центр физико-химической медицины имени академика Ю.М. Лопухина Федерального медико-биологического агентства
Россия

Авшалумов Александер Сергеевич - лаборант-исследователь лаборатории протеомного анализа.

119435, Москва, Малая Пироговская, д. 1а



М. В. Михайлычева
Федеральный научно-клинический центр физико-химической медицины имени академика Ю.М. Лопухина Федерального медико-биологического агентства
Россия

Михайлычева Мария Валерьевна - лаборант-исследователь лаборатории протеомного анализа.

119435, Москва, Малая Пироговская, д. 1а



А. Ю. Горбачев
Федеральный научно-клинический центр физико-химической медицины имени академика Ю.М. Лопухина Федерального медико-биологического агентства
Россия

Горбачев Алексей Юрьевич - кандидат биологических наук, заведующий лабораторией протеомного анализа.

119435, Москва, Малая Пироговская, д. 1а



Список литературы

1. Torres J, Mehandru S, Colombel J-F, Peyrin-Biroulet L. Crohn’s disease. Lancet. 2017; 389(10080): 1741–1755. doi: 10.1016/S0140-6736(16)31711-1

2. Hugot JP, Chamaillard M, Zouali H, Lesage S, Cézard JP, Belaiche J, et al. Association of NOD2 leucine-rich repeat variants with susceptibility to Crohn’s disease. Nature. 2001; 411(6837): 599–603. doi: 10.1038/35079107

3. Hampe J, Franke A, Rosenstiel P, Till A, Teuber M, Huse K, et al. A genome-wide association scan of nonsynonymous SNPs identifies a susceptibility variant for Crohn disease in ATG16L1. Nat. Genet. 2007; 39(2): 207–211. doi: 10.1038/ng1954

4. Levine A, Rhodes JM, Lindsay JO, Abreu MT, Kamm MA, Gibson PR, et al. Dietary Guidance for Patients with Inflammatory Bowel Disease from the International Organization for the Study of Inflammatory Bowel Disease. Clin. Gastroenterol. Hepatol. 2020; 8(6): 1381-1392. doi: 10.1016/j.cgh.2020.01.046

5. Walker AW, Sanderson JD, Churcher C, Parkes GC, Hudspith BN, Rayment N, et al. High-throughput clone library analysis of the mucosa-associated microbiota reveals dysbiosis and differences between inflamed and non-inflamed regions of the intestine in inflammatory bowel disease. BMC Microbiol. 2011; 11: 7. doi: 10.1186/1471-2180-11-7

6. López-Siles M, Camprubí-Font C, Gómez Del Pulgar EM, Mir MS, Busquets D, Sanz Y, et al. Prevalence, Abundance, and Virulence of Adherent-Invasive Escherichia coli in Ulcerative Colitis, Colorectal Cancer, and Coeliac Disease Front Immunol. 2022; 13:748839. doi: 10.3389/fimmu.2022.748839

7. Baumgart M, Dogan B, Rishniw M, Weitzman G, Bosworth B, Yantiss R, et al. Culture independent analysis of ileal mucosa reveals a selective increase in invasive Escherichia coli of novel phylogeny relative to depletion of Clostridiales in Crohn’s disease involving the ileum. ISME J. 2007; 1: 403-418. doi: 10.1038/ismej.2007.52

8. Chervy M, Barnich N, Denizot J. Adherent-Invasive E. coli: Update on the Lifestyle of a Troublemaker in Crohn’s Disease. Int J Mol Sci. 2020; 21(10): 3734. doi: 10.3390/ijms21103734

9. Barnich N, Arthur JC, Buisson A, Campbell BJ, Carbonnel F, Chassaing B, et al. Adherent-invasive Escherichia coli in Crohn’s disease: the 25th anniversary Gut. 2026; 75(2): 411-424. doi: 10.1136/gutjnl-2025-335331

10. Nadalian B, Yadegar A, Houri H, Olfatifar M, Shahrokh S, Asadzadeh AH, et al. Prevalence of the pathobiont adherent-invasive Escherichia coli and inflammatory bowel disease: a systematic review and meta-analysis. J Gastroenterol Hepatol. 2021; 36(4): 852–863. doi: 10.1111/jgh.15260

11. Dolatabadi RK, Feizi A, Halaji M, Fazeli H, Adibi P. The prevalence of adherent-invasive Escherichia coli and its association with inflammatory bowel diseases: a systematic review and meta-analysis. Front Med. 2021; 8: 730243. doi: 10.3389/fmed.2021.730243

12. Vazeille E, Buisson A, Bringer M-A, Goutte M, Ouchchane L, Hugot J-P, et al. Monocyte-derived macrophages from Crohn’s disease patients are impaired in the ability to control intracellular adherent-invasive Escherichia coli and exhibit disordered cytokine secretion profile. J Crohns Colitis. 2015; 9(5): 410-20. doi: 10.1093/ecco-jcc/jjv053

13. Strugala V, Dettmar PW, Pearson JP, Thickness and continuity of the adherent colonic mucus barrier in active and quiescent ulcerative colitis and Crohn’s disease. Int. J. Clin. Pract. 2008; 62(5): 762–769. doi: 10.1111/j.1742-1241.2007.01665.x

14. Elatrech I, Marzaiol V, Boukemara H, Bournier O, Neut C, Darfeuille-Michaud A, et al. Escherichia coli LF82 differentially regulates ROS production and mucin expression in intestinal epithelial T84 cells: Implication of NOX1. Inflamm. Bowel Dis. 2015; 21(5): 1018–1026. doi: 10.1097/MIB.0000000000000365

15. Gibold L, Garenaux E, Dalmasso G, Gallucci C, Cia D, Mottet-Auselo B, et al. The Vat-AIEC protease promotes crossing of the intestinal mucus layer by Crohn’s disease-associated Escherichia coli. Cell. Microbiol. 2016; 18(5): 617–631. doi: 10.1111/cmi.12539

16. Sevrin G, Massier S, Chassaing B, Agus A, Delmas J, Denizot J, et al. Adaptation of adherent-invasive E. coli to gut environment: Impact on flagellum expression and bacterial colonization ability. Gut Microbes. 2020; 11(3): 364-380. doi: 10.1080/19490976.2017.1421886

17. Boudeau J, Barnich N, Darfeuille-Michaud A. Type 1 pili-mediated adherence of Escherichia coli strain LF82 isolated from Crohn’s disease is involved in bacterial invasion of intestinal epithelial cells. Mol. Microbiol. 2001; 39(5): 1272–1284. doi: 10.1111/j.1365-2958.2001.02315.x

18. Dreux N, Denizot J, Martinez-Medina M, Mellmann A, Billig M, Kisiela D, et al. Point mutations in FimH adhesin of Crohn’s disease-associated adherent-invasive Escherichia coli enhance intestinal inflammatory response. PLoS Pathog. 2013; 9(1): e1003141. doi: 10.1371/journal.ppat.1003141

19. Barnich N, Carvalho FA, Glasser AL, Darcha C, Jantscheff P Allez M, et al. CEACAM6 acts as a receptor for adherent-invasive E. coli, supporting ileal mucosa colonization in Crohn disease. J. Clin. Investig. 2007; 117(6): 1566–1574. doi: 10.1172/JCI30504

20. Dumych T, Yamakawa N, Sivignon A, Garenaux E, Robakiewicz S, Coddeville B, et al. Oligomannose-Rich Membranes of Dying Intestinal Epithelial Cells Promote Host Colonization by Adherent-Invasive E. coli. Front Microbiol. 2018; 9: 742. doi: 10.3389/fmicb.2018.00742

21. Fargea M, Faure F, Douadi C, Chevarin C, Birer A, Sivignon A, et al. ChiA: a major player in the virulence of Crohn’s disease-associated adherent and invasive Escherichia coli (AIEC). Gut Microbes. 2024; 16(1): 2412667. doi: 10.1080/19490976.2024.2412667

22. Rolhion N, Hofman P, Darfeuille-Michaud A. The endoplasmic reticulum stress response chaperone: Gp96, a host receptor for Crohn disease-associated adherent-invasive Escherichia coli. Gut Microbes. 2011; 2(2): 115–119. doi: 10.4161/gmic.2.2.15725

23. Camprubí-Font C, Ruiz Del Castillo B, Barrabés S, Martínez-Martínez L, Martinez-Medina M. Amino acid substitutions and differential gene expression of outer membrane proteins in adherent-invasive Escherichia coli. Front Microbiol. 2019; 10: 1707. doi: 10.3389/fmicb.2019.01707

24. Elhenawy W, Hordienko S, Gould S, Oberc AM, Tsai CN, Hubbard TP, et al. High-throughput fitness screening and transcriptomics identify a role for a type IV secretion system in the pathogenesis of Crohn’s disease-associated Escherichia coli. Nat Commun. 2021; 12: 2032. doi: 10.1038/s41467-021-22306-w

25. Zou Y, He L, Huang SH. Identification of a surface protein on human brain microvascular endothelial cells as vimentin interacting with Escherichia coli invasion protein IbeA. Biochem Biophys Res Commun. 2006; 351(3): 625–630. doi: 10.1016/j.bbrc.2006.10.091

26. Barnich N, Bringer M-A, Claret L, Darfeuille-Michaud A. Involvement of lipoprotein NlpI in the virulence of adherent invasive Escherichia coli strain LF82 isolated from a patient with Crohn’s disease. Infect Immun. 2004; 72(5): 2484–2493. doi: 10.1128/IAI.72.5.2484-2493.2004

27. Bringer M-A, Rolhion N, Glasser A-L, Darfeuille-Michaud A. The oxidoreductase DsbA plays a key role in the ability of the Crohn’s disease-associated adherent-invasive Escherichia coli strain LF82 to resist macrophage killing. J Bacteriol. 2007; 189(13): 4860–4871. doi: 10.1128/JB.00233-07

28. Rolhion N, Barnich N, Claret L, Darfeuille-Michaud A. Strong decrease in invasive ability and outer membrane vesicle release in Crohn’s disease-associated adherent-invasive Escherichia coli strain LF82 with the yfgL gene deleted. J Bacteriol. 2005; 187(7): 2286-2296. doi: 10.1128/JB.187.7.2286-2296.2005

29. Nadalian B, Nadalian B, Reza Zali M, Yadegar A. Outer Membrane Vesicles Derived from Adherent-Invasive Escherichia coli Induce Inflammatory Response and Alter the Gene Expression of Junction-Associated Proteins in Human Intestinal Epithelial Cells Can. J Infect Dis Med Microbiol. 2024; 2024: 2701675. doi: 10.1155/2024/2701675

30. Abdelhalim KA, Uzel A, Gülşen Ünal N. Virulence determinants and genetic diversity of adherent-invasive Escherichia coli (AIEC) strains isolated from patients with Crohn’s disease. Microb Pathog. 2020; 145: 104233. doi: 10.1016/j.micpath.2020.104233

31. Larabi A, Dalmasso G, Delmas J, Barnich N, Nguyen HT. Exosomes transfer miRNAs from cell-to-cell to inhibit autophagy during infection with Crohn’s disease-associated adherent-invasive E. coli. Gut Microbes. 2020; 11(6): 1677-1694. doi: 10.1080/19490976.2020.1771985

32. Dalmasso G, Nguyen HTT, Faïs T, Massier S, Barnich N, Delmas J, et al. Crohn’s disease-associated adherent-invasive Escherichia coli manipulate host autophagy by impairing SUMOylation. Cells. 2019; 8(1): 35. doi: 10.3390/cells8010035

33. Carrière J, Bretin A, Darfeuille-Michaud A, Barnich N, Nguyen HTT. Exosomes Released from Cells Infected with Crohn’s Disease-associated Adherent-Invasive Escherichia coli Activate Host Innate Immune Responses and Enhance Bacterial Intracellular Replication. Inflamm Bowel Dis. 2016; 22(3): 516-28. doi: 10.1097/MIB.0000000000000635

34. Michielan A, D’Incà R. Intestinal Permeability in Inflammatory Bowel Disease: Pathogenesis, Clinical Evaluation, and Therapy of Leaky Gut. Mediators Inflamm. 2015; 2015: 628157. doi: 10.1155/2015/628157

35. Wine E, Ossa JC, Gray-Owen SD, Sherman PM. Adherent-invasive Escherichia coli, strain LF82 disrupts apical junctional complexes in polarized epithelia. BMC Microbiol. 2009; 9: 180. doi: 10.1186/1471-2180-9-180

36. Denizot J, Sivignon A, Barreau F, Barreau F, Darcha C, Chan HFC, et al. Adherent-invasive Escherichia coli induces claudin-2 expression and barrier defect in CEABAC10 mice and Crohnʼs disease patients. Inflammatory Bowel Diseases. 2012; 18(2): 294-304. doi: 10.1002/ibd.21787

37. Glasser AL, Boudeau J, Barnich N, Perruchot MH, Colombel JF, Darfeuille-Michaud A. Adherent invasive Escherichia coli strains from patients with Crohn’s disease survive and replicate within macrophages without inducing host cell death. Infect. Immun. 2001; 69(9): 5529-5537. doi: 10.1128/IAI.69.9.5529-5537.2001

38. Bringer MA, Billard E, Glasser A-L, Colombel J-F, Darfeuille-Michaud A. Replication of Crohn’s disease-associated AIEC within macrophages is dependent on TNF-α secretion. Lab. Investig. 2012; 92(3): 411–419. doi: 10.1038/labinvest.2011.156

39. Palmela C, Chevarin C, Xu Zh, Torres J, Sevrin G, Hirten R, et al. Adherent-invasive Escherichia coli in inflammatory bowel disease. Gut. 2018; 67(3): 574-587. doi: 10.1136/gutjnl-2017-314903

40. Pobeguts OV, Ladygina VG, Evsyutina DV, Eremeev AV, Zubov AI, Matyushkina DS, et al. Propionate Induces Virulent Properties of Crohn’s Disease-Associated Escherichia coli. Front Microbiol. 2020; 11: 1460. doi: 10.3389/fmicb.2020.01460

41. Demarre G, Prudent V, Schenk H, Rousseau E, Bringer M-A, Barnich N, et al. The Crohn’s disease-associated Escherichia coli strain LF82 relies on SOS and stringent responses to survive, multiply and tolerate antibiotics within macrophages. PLoS Pathog. 2019; 15(11): e1008123. doi: 10.1371/journal.ppat.1008123

42. Prudent V, Demarre G, Vaseil E, Veri M, Kenech’Du N, Ravet A, et al. Crohn’s disease bacterial strain LF82 gathers biofilm communities to protect itself from phagolysosomal attack. Commun Biol. 2021; 4: 627. doi: 10.1038/s42003-021-02161-7

43. Yao T, Liu X, Li D, Huang Y, Yang W, Liu R, et al. Two-component system RstAB promotes the pathogenicity of adherent-invasive Escherichia coli in response to acidic conditions within macrophages. Gut Microbes. 2024: 16(1): 2356642. doi: 10.1080/19490976.2024.2356642

44. Ellermann M, Huh EY, Liu B, Carroll IM, Tamayo R, Sartor RS. Adherent-Invasive Escherichia coli Production of Cellulose Influences Iron-Induced Bacterial Aggregation, Phagocytosis, and Induction of Colitis. Infect Immun. 2015; 83(10): 4068-80. doi: 10.1128/IAI.00904-15

45. Ormsby MJ, Johnson SA, Carpena N, Meikle LM, Goldstone RJ, McIntosh A, et al. Propionic Acid Promotes the Virulent Phenotype of Crohn’s Disease-Associated Adherent-Invasive Escherichia coli. Cell Rep. 2020; 30(7): 2297-2305.e5. doi: 10.1016/j.celrep.2020.01.078

46. Chassaing B, Garénaux E, Carriere J, Rolhion N, Guérardel Y, Barnich N, et al. Analysis of the σE regulon in Crohn’s disease-associated Escherichia coli revealed involvement of the waaWVL operon in biofilm formation. J Bacteriol. 2015; 197(8): 1451-65. doi: 10.1128/JB.02499-14

47. Martinez-Medina M, Strozzi F, Ruiz Del Castillo B, Serrano-Morillas N, Ferrer Bustins N, Martínez-Martínez L. Antimicrobial resistance profiles of adherent invasive Escherichia coli show increased resistance to β-lactams. Antibiotics. 2020; 9(5): 251. doi: 10.3390/antibiotics9050251

48. Fanelli G, Pasqua M, Colonna B, Prosseda G, Grossi M. Expression profile of multidrug resist efflux pumps during intracellular life of attached-patient-patients Escherichia coli strain LF82. Front Microbiol. 2020; 11: 1935. doi: 10.3389/fmicb.2020.01935

49. McPhee JB, Small CL, Reid-Yu SA, Brannon JR, Le Moual H, Coombes BK. Host Defense Peptide Resistance Contributes to Colonization and Maximal Intestinal Pathology by Crohn’s Disease-Associated Adherent-Invasive Escherichia coli. Infect. Immun. 2014; 82: 3383-3393. doi: 10.1128/IAI.01888-14

50. Conway T, Cohen PS. Commensal and Pathogenic Escherichia coli Metabolism in the Gut. Microbiol Spectr. 2015; 3(3): 10.1128/microbiolspec.MBP-0006-2014. doi: 10.1128/microbiolspec.MBP-0006-2014

51. Viladomiu M, Kivolowitz C, Abdulhamid A, Dogan B, Victorio D, Castellanos J. IgA-coated E. coli enriched in Crohn’s disease spondyloarthritis promote TH17-dependent inflammation. Sci Transl Med. 2017; 9(376): eaaf9655. doi: 10.1126/scitranslmed.aaf9655

52. McCafferty DM. Peroxynitrite and inflammatory bowel disease. Gut. 2000; 46(3): 436-9. doi: 10.1136/gut.46.3.436

53. Kitamoto S, Alteri CJ, Rodrigues M, Nagao-Kitamoto H, Sugihara K, Himpsl SD, et al. Dietary l-serine confers a competitive fitness advantage to Enterobacteriaceae in the inflamed gut. Nat Microbiol. 2020; 5(1): 116-125. doi: 10.1038/s4156

54. Rakitina DV, Manolov AI, Kanygina AV, Garushyants SK, Baikova JP, Alexeev DG, et al. Genome analysis of E. coli isolated from Crohn’s disease patients. BMC Genomics. 2017; 18(1): 544. doi: 10.1186/s12864-017-3917-x

55. Viladomiu M, Metz ML, Lima SF, Jin W-B, Chou L, Guo C-J, et al. Adherent-invasive E. coli metabolism of propanediol in Crohn’s disease regulates phagocytes to drive intestinal inflammation. Cell Host Microbe. 2021; 29: 607–619.e8. doi: 10.1016/j.chom.2021.01.002

56. Ormsby MJ, Logan M, Johnson SA, McIntosh A, Fallata G, Papadopoulou R, et al. Inflammation associated ethanolamine facilitates infection by Crohn’s disease-linked adherent-invasive Escherichia coli. Ebio Medicine. 2019; 43: 325–332. doi: 10.1016/j.ebiom.2019.03.071

57. Zhang S, Morgan X, Dogan B, Martin F-P, Strickler S, Oka A, et al. Mucosal metabolites fuel the growth and virulence of E. coli. JCI Insight. 2022; 7: e157013. doi: 10.1172/jci.insight.157013

58. Pobeguts OV, Galyamina MA, Mikhalchik EV, Kovalchuk SI, Smirnov IP, Lee AV, et al. The Role of Propionate-Induced Rearrangement of Membrane Proteins in the Formation of the Virulent Phenotype of Crohn’s Disease-Associated Adherent-Invasive Escherichia coli. Int J Mol Sci. 2024; 25(18): 10118. doi: 10.3390/ijms251810118

59. Tong L-C, Wang Y, Wang Z-B, Liu W-Y, Sun S, Li L, et al. Propionate Ameliorates Dextran Sodium Sulfate-Induced Colitis by Improving Intestinal Barrier Function and Reducing Inflammation and Oxidative Stress. Front Pharmacol. 2016; 7: 253. doi: 10.3389/fphar.2016.00253

60. Agus A, Richard D, Faïs T, Vazeille E, Chervy M, Bonnin V, et al. Propionate catabolism by CD-associated adherent-invasive E. coli counteracts its anti-inflammatory effect. Gut Microbes. 2021; 13: 1-18. doi: 10.1080/19490976.2020.1839318

61. Sistrunk JR, Nickerson KP, Chanin RB, Rasko DA, Faherty CS. Survival of the Fittest: How Bacterial Pathogens Utilize Bile to Enhance Infection. Clin. Microbiol. Rev. 2016; 29(4): 819-836. doi: 10.1128/CMR.00031-16

62. Delmas J, Gibold L, Faïs T, Batista S, Leremboure M, Sinel C, et al. Metabolic Adaptation of Adherent-Invasive Escherichia coli to Exposure to Bile Salts. Sci. Rep. 2019; 9: 2175. doi: 10.1038/s41598-019-38628-1

63. Klumpp J, Fuchs TM. Identification of novel genes in genomic islands that contribute to Salmonella typhimurium replication in macrophages. Microbiology. 2007; 153: 1207-1220. doi: 10.1099/mic.0.2006/004747-0

64. Camprubí-Font C, Martinez-Medina M. Why the discovery of adherent-invasive Escherichia coli molecular markers is so challenging? World J Biol Chem. 2020; 11(1): 1-13. doi: 10.4331/wjbc.v11.i1.1

65. Céspedes S, Saitz W, Canto FD, Fuente M, Quera R, Hermoso M, et al. Genetic Diversity and Virulence Determinants of Escherichia coli Strains Isolated from Patients with Crohn’s Disease in Spain and Chile. Front Microbiol. 2017; 8: 639. doi: 10.3389/fmicb.2017.00639

66. Camprubí-Font C, Ewers C, Lopez-Siles M, Martinez-Medina M. Genetic and Phenotypic Features to Screen for Putative Adherent-Invasive Escherichia coli. Front Microbiol. 2019; 10: 108. doi: 10.3389/fmicb.2019.00108

67. Vazeille E, Chassaing B, Buisson A, Dubois A, de Vallée A, Billard E, et al. GipA Factor Supports Colonization of Peyer’s Patches by Crohn’s Disease-associated Escherichia Coli. Inflamm. Bowel Dis. 2016; 22: 68-81. doi: 10.1097/MIB.0000000000000609

68. Dogan B, Belcher-Timme HF, Dogan EI, Jiang ZD, DuPont HL, Snyder N, et al. Evaluation of Escherichia coli pathotypes associated with irritable bowel syndrome. FEMS Microbiol Lett. 2018; 365(22). doi: 10.1093/femsle/fny249

69. Deshpande NP, Wilkins MR, Mitchell HM, Kaakoush NO. Novel genetic markers define a subgroup of pathogenic Escherichia coli strains belonging to the B2 phylogenetic group. FEMS Microbiol Lett. 2015; 362(22): fnv193. doi: 10.1093/femsle/fnv193

70. Camprubí-Font C, Lopez-Siles M, Ferrer-Guixeras M, Niubó-Carulla L, Abellà-Ametller C, Garcia-Gil LJ, et al. Comparative genomics reveals new single-nucleotide polymorphisms that can assist in identification of adherent-invasive Escherichia coli. Sci Rep. 2018; 8: 2695. doi: 10.1038/s41598-018-20843-x

71. Camprubí-Font C, Bustamante P, Vidal RM, O’Brien CL, Barnich N, Martinez-Medina M. Study of a classification algorithm for AIEC identification in geographically distinct E. coli strains. Sci Rep. 2020; 10: 8094. doi: 10.1038/s41598-020-64894-5

72. Elhenawy W, Tsai CN, Coombes BK. Host-Specific Adaptive Diversification of Crohn’s Disease-Associated Adherent-Invasive Escherichia coli. Cell Host Microbe. 2019; 25(2): 301-312.e5. doi: 10.1016/j.chom.2018.12.010

73. Imai J, Kitamoto S, Sugihara K, Nagao-Kitamoto H, Hayashi A, Morhardt TL, et al. Flagellin-mediated activation of IL-33-ST2 signaling by a pathobiont promotes intestinal fibrosis. Mucosal Immunol. 2019; 12: 632–643. doi: 10.1038/s41385-019-0138-4

74. Small CLN, Reid-Yu SA, McPhee JB, Coombes BK, Small C-LN, Reid-Yu SA, et al. Persistent infection with Crohn’s disease-associated adherent-invasive Escherichia coli leads to chronic inflammation and intestinal fibrosis. Nat Commun. 2013; 4: 1957. doi: 10.1038/ncomms2957

75. Small CL, Xing L, McPhee JB, Law HT, Coombes BK. Acute infectious gastroenteritis potentiates a Crohn’s Disease pathobiont to fuel ongoing inflammation in the post-infectious period. PLoS Pathog. 2016; 12: e1005907. doi: 10.1371/journal.ppat.1005907

76. Трусов Н.В., Побегуц О.В., Галямина М.А., Смирнов И.П., и др. Способность адгезивно-инвазивной Escherichia coli от пациента с болезнью Крона колонизировать и вызывать воспаление в кишечнике мышей. Вопросы питания. 2025; 9495): 42–60. doi: 10.33029/0042-8833-2025-94-5-42-60

77. Bustamante P, Vidal R. Repertoire and Diversity of Toxin—Antitoxin Systems of Crohn’s Disease-Associated Adherent-Invasive Escherichia coli. New Insight of T His Emergent E. coli Pathotype. Front. Microbiol. 2020; 11: 807. doi: 10.3389/fmicb.2020.00807

78. Guan J, Chen Y, Goh Y-X, Wang M, Tai C, Deng Z, et al. TADB 3.0: An Updated Database of Bacterial Toxin-Antitoxin Loci and Associated Mobile Genetic Elements. Nucleic Acids Res. 2024; 52: D784-D790. doi: 10.1093/NAR/GKAD962

79. Równicki M, Lasek R, Trylska J, Bartosik D. Targeting Type II Toxin–Antitoxin Systems as Antibacterial Strategies. Toxins. 2020; 12: 568. doi: 10.3390/toxins12090568

80. Bustamante P, Ramos-Corominas M, Martinez-Medina M. Contribution of Toxin-Antitoxin Systems to Adherent-Invasive E. coli Pathogenesis. Microorganisms. 2024; 12(6): 1158. doi: 10.3390/microorganisms12061158


Рецензия

Для цитирования:


Побегуц О.В., Авшалумов А.С., Михайлычева М.В., Горбачев А.Ю. Молекулярные механизмы персистенции адгезивно-инвазивных Escherichia coli в организме хозяина. Acta Biomedica Scientifica. 2026;11(2):72-86. https://doi.org/10.29413/ABS.2026-11.2.8

For citation:


Pobeguts O.V., Avshalumov A.S., Mikhailycheva M.V., Gorbachev A.Yu. Molecular mechanisms of persistence of adherent-invasive Escherichia coli in the host organism. Acta Biomedica Scientifica. 2026;11(2):72-86. (In Russ.) https://doi.org/10.29413/ABS.2026-11.2.8

Просмотров: 308

JATS XML


Creative Commons License
Контент доступен под лицензией Creative Commons Attribution 4.0 License.


ISSN 2541-9420 (Print)
ISSN 2587-9596 (Online)