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THE ROLE OF CAMPYLOBACTER JEJUNI INFECTION IN THE DEVELOPMENT OF GUILLAIN-BARRÉ SYNDROME Cover

THE ROLE OF CAMPYLOBACTER JEJUNI INFECTION IN THE DEVELOPMENT OF GUILLAIN-BARRÉ SYNDROME

Open Access
|Feb 2022

References

  1. Ang C.W., Jacobs B.C., Laman J.D.: The Guillain-Barre’ syndrome: a true case ofmolecular mimicry. Trends Immunol. 25, 6–66 (2004)
  2. Ashgar S.S., Oldfield N.J., Wooldridge K.G., Jones M.A., Irving G.J., Turner D.P., Ala’Aldeen D.A.: CapA, an autotransporter protein of Campylobacter jejuni mediates association with human epithelial cells and colonization of the chicken gut. J. Bacteriol. 189, 1856–1865 (2007)10.1128/JB.01427-06185576917172331
  3. Awad W.A., Hess C., Hess M.: Enteric pathogens and their toxin-induced disruption of the intestinal barrier through alteration of tight junctions in chickens. Toxins, 9(2017)10.3390/toxins9020060533143928208612
  4. Avrain L., Vernozy-Rozand C., Kempf I.: Evidence for natural horizontal transfer of tetO gene between Campylobacter jejunistrains in chickens. J. Appl. Microbiol. 97, 134–140 (2004)
  5. Backert S., Boehm M., Wessler S., Tegtmeyer N i wsp.: Transmigration route of Campylobacter jejuni across polarized intestinal epithelia cells: paracellular, transcellular or both? Cell Commun. Signal. 11, 72–87 (2013)
  6. Bilińka M., Koszewicz M.: Zespół Millera-Fishera z dominującymi zaburzeniami połykania i mowy. Adv. Clin. Exp. Med. 13, 515–519 (2004)
  7. Bolinger H., Kathariou S.: The Current state of macrolide resistance in Campylobacter spp.: Trends and impacts of resistance mechanisms. Appl. Environ. Microbiol. 83, e0046-17 (2017)
  8. Bronnec V., Turo H., Bouju A., Cruveiller S., Rodrigues R., Demnerova K., Tresse O., Haddad N., Zagorec M.: Adhesion, biofilm formation, and genomic features of Campylobacter jejuniBf, an atypical strain able to grow under aerobic conditions. Front. Microbbiol. 7, 1002 (2016)10.3389/fmicb.2016.01002492756327446042
  9. Bronowski C., James C.E., Winstanley C.: Role of environmental survival in transmission of Campylobacter jejuni. FEMS Microbiol. Lett. 356,8–19 (2014)
  10. Caldwell D.B., Wang Y., Lin J.: Development, stability, and molecular mechanisms of macrolide resistance in Campylobacter jejuni. Antimicrob. Agents Chemother. 52, 3947–3954 (2008)10.1128/AAC.00450-08257310018779354
  11. Ó Cróinín T., Backert S.: Host epithelial cell invasion by Campylobacter jejuni: trigger or zipper mechanism? Front. Cell. Infect. Microbiol. 2, 25 (2012)10.3389/fcimb.2012.00025341752722919617
  12. Chandrashekhar K., Kassem I. I., Rajashekara G.: Campylobacter jejuni transducer like proteins: Chemotaxis and beyond. Gut Microbes, 8, 323–334 (2017)10.1080/19490976.2017.1279380557041728080213
  13. Chopra I.: Mode of action of the tetracyclines and the nature of bacterial resistance to them, in The Tetracyclines (w) Handbook of Experimental. red.: Hlavka J.J., Boothe J.H., Springer, Berlin, Germany, 1985, s. 317392.10.1007/978-3-642-70304-1_6
  14. Coker O., Akitoye I., Raphael D., Thomas N., Bolaji A., Kehinde O., Obi L.C.: Human campylobacteriosis in developing countries. Emerg. Infect. Dis. 8, 237–243 (2002)
  15. Day C.J., Semchenko E.A., Korolik V.: Glycoconjugates play a key role in Campylobacter jejuni infection between host and pathogen. Front. Cell. Infect. 2, 1–8 (2012)
  16. Dimachkie M.M., Barohn R.J.: Guillain-Barré syndrome and variants. Neurol. Clin. 31, 491–510 (2013)
  17. Engberg J., Aarestrup F. M., Taylor D.E., Gerner-Smidt P., Nachamkin I.: Quinolone and macrolide resistance in Campylobacter jejuni and C. coli: Resistance mechanisms and trends in human isolates. Emerg. Infect. Dis. 7, 24–34 (2001)
  18. Epps S.V.R., Harvey R.B., Hume M.E., Phillips T.D., Anderson R.C., Nisbet D.J.: Foodborne Campylobacter: Infections, Metabolism, Pathogenesis and Reservoirs. Int. J. Environ. Res. Public Health,10, 6292–6304 (2013)10.3390/ijerph10126292388111424287853
  19. Esson D., Grant A.J. i wsp.: Identyfication and initial characterisation of a protein involved in Campylobacter jejuni cell shape. Mirobial Pathogenesis, 104, 202–211 (2017)10.1016/j.micpath.2017.01.042533591828131954
  20. Faber E., Gripp E., Maurischat S, Kaspers B., Tedin K., Menz S., Zuraw A., Kershaw O., Yang I., Rautenschlein S., Josenhansa C.: Novel immunomodulatory Flagellin-Like Protein FlaC in Campy lobacter jejuni and other Campylobacterales. mSphere. 1, 1–24 (2015)
  21. Flanagan R.C., Neal-McKinney J.M., Dhillon A.S., Miller W.G., Konkel M.E.: Examination of Campylobacter jejuni putative adhesins leads to the identification of a new protein, designated FlpA, required for chicken colonization. Infect. Immun. 77, 2399–2407 (2009)10.1128/IAI.01266-08268732819349427
  22. Friis C., Wassenaar T.M., Javed M.A., Snipen L., Lagesen K., Hallin P.F., Newell D.G., Toszeghy M., Ridley A., Manning G., Ussery D.W.: Genomic characterization of Campylobacter jejunistrain M. PLoS One, 5, e12253 (2010)10.1371/journal.pone.0012253292872720865039
  23. Gibreel A. and Taylor D.E.: Macrolide resistance in Campylobacter jejuni and Campylobacter coli. J. Antimic. Chemother. 58, 243–255 (2006)
  24. Guerry P., Monterino M.A. i wsp.: Campylobacter polysaccharide capsules: virulence and vaccines. Front. Cell. Infect. Microbiol. 2, 1–11 (2012)
  25. Han a Zifeng, Willer T., Li L., Pielsticker C., Rychlik I., Velge P., Kaspers B., Rautenschleina S.: Influence of the gut Microbiota composition on Campylobacter jejuni colonization in chickens. Infect. Immun. 85, 11e00380 (2017)10.1128/IAI.00380-17564901328808158
  26. Hermans D., van Deun K., Martel A., van Immerseel F., Messens W., Heyndrickx M., Haesebrouck F., Pasmans F.: Colonization factors of Campylobacter jejuni in the chicken gut. Vet. Res. 42, 82 (2011)10.1186/1297-9716-42-82315673321714866
  27. Hofreuter D.: Defining the metabolic requirements for the growth and colonization capacity of Campylobacter jejuni. Front. Cell. Infect Microbiol. 4, 137 (2014)10.3389/fcimb.2014.00137417842525325018
  28. Horrocks S.M., Anderson R.C., Nisbet D.J., Ricke S.C.: Incidence and ecology of Campylobacter jejuni and coli in animals. Anaerobe,15, 18–25 (2009)10.1016/j.anaerobe.2008.09.00118849005
  29. Ikeda N., Karlyshev A.V.: Putative mechanisms and biological role of coccoid form formation in Campylobacter jejuni. Eur. J. Microbiol. Immunol. 1, 41–49 (2012)
  30. Ilyas A.A., Mithen F.A., Chen Z.W., Cook S.D.: Search for antibodies to neutral glycolipids in sera of patients with Guillain-Barré syndrome. J. Neurol. Sci. 102, 67–75 (1992)
  31. Ilyas A.A., Mithen F.A., Dalakas M.C., Chen Z.W., Cook S.D.: Antibodies to acidic glycolipids in Guillain-Barre syndrome and chronic inflammatory demyelinating polyneuropathy. J. Neurol. Sci. 107, 111–121 (1992)
  32. Indikova I., Humphrey T.J., Hilbert F.: Survival with a helping hand: Campylobacter and microbiota. Front. Microbiol. 6, 1266 (2015)10.3389/fmicb.2015.01266463742026617600
  33. Iovine N. M.: Resistance mechanisms in Campylobacter jejuni. Virulence,4, 230–240 (2013)10.4161/viru.23753371198123406779
  34. Jannsen R., Krogfelt K.A, Cawthraw S.A., van pelt W., Wagenaar J.A., Owen R.J.: Host-pathogen interactions in Campylobacter infections: the host perspective. Clin.Microbiol. Rev. 21, 505–518 (2008)
  35. John D.A., Williams L.K., Kanamarlapudi V., Humphrey T.J., Wilkinson T.S.: The bacterial species. Campylobacter jejuniinduce diverse innate immune responses in human and avian intestinal epithelial cells. Front. Microbiol. 8, 1840 (2017)10.3389/fmicb.2017.01840562687729033908
  36. Johnson T.J., Shank J.M., Johnson J.G.: Current and potential treatments for reducing Campylobacter colonization in animal hosts and disease in humans. Front. Microbiol. 8, 1–14 (2017)
  37. Kaakoush N.O., Castańo-Rodríguez N., Mitchell H.M., Mana S.M.: Global epidemiology of Campylobacter infection. Clin. Microbiol. Rev. 28, 687–720 (2015)
  38. Kaakoush N.O., Mitchell H. M.: Campylobacter concisus – new player in intestinal disease. Front.Cell. Infect. Microiol. 2, 1–12 (2012)
  39. Kimoto. K., Koga M., Hirata K., Takahashi M., Li J., Gilbert M., Yuki N.: Relationship of bacterial strains to clinical syndromes of Campylobacter– associated neuropathies. Neurology. 67, 1837–1843 (2006)10.1212/01.wnl.0000244468.22377.6b17130419
  40. Kobierecka P.A., Jagusztyn-Krynicka E.K. i wsp.: In vitro characteristics of Lactobacillus spp. strains isolated from the chicken digestive tract and their role in the inhibition of Campylobactercolonization. Microbiol. Open. 6, 1–15 (2017)
  41. Koga M., Takahashi M., Masuda M., Hirata K., Yuki N.: Campylobacter gene polymorphism as a determinant of clinical features of Guillain-Barre syndrome. Neurology, 65, 1376–1381 (2005)10.1212/01.wnl.0000176914.70893.1416162859
  42. Koga M., Yuki N., Takahashi M., Saito K., Hirata K.: Close association of IgA anti-gangloside antibodies with antecedent Campylobacter jejuni infection in Guillain-Barre and Fisher’s syndromes. J. Neuroimmunol. 81, 138–143 (1998)10.1016/S0165-5728(97)00168-9
  43. Kurtkiewicz A.: Kampylobakteriozy u ludzi i zwierząt. Życie Weterynaryjne, 83, 285–288 (2008)
  44. Mahajan S., Rodgeres F.G.: Isolation, characterization, and host-cell-binding properties of a cytotoxin from Campylobacter jejuni. J. Clin. Microiol. 28, 1314–1320 (1990)
  45. Melo R.T., Mendonça E.P., Monteiro G.P., Siqueira M.C.: Intrinsic and extrinsic aspects on Campylobacter jejuni biofilms. Front. Microbiol. 8, 1–15 (2017)
  46. Miller C.E., Rock J.D., Ridley K.A., Williams P.H., Ketley J.M.: Utilization of lactoferrin-bound and transferrin-bound iron by Campylobacter jejuni. J. Bacteriol. 190, 1900–1911 (2008)10.1128/JB.01761-07225886418203832
  47. Mohan V.: The role of probiotics inthe inhibition of Campylobacter jejuni colonization and virulence attenuation. Eur. J. Clin. Microbiol. Infect. Dis. 34, 1503–1513 (2015)
  48. Moran. A.P., Annuk H., Prendergast M.M.: Antibodies induced by ganglioside-mimicking Campylobacter jejuni lipooligosaccharides recognise epitopes at the nodes of Ranvier. J. Neuro-immunol. 165, 179–185 (2005)10.1016/j.jneuroim.2005.04.01315993494
  49. Nachamkin, I., Szymanski, M.C., Blaser, J.M.: Campylobacter. 3-cia ed.; ASM Press: Washington DC, USA (2008)10.1128/9781555815554
  50. Nothaft H., Szymański C.M. i wsp.: Engineering the Campylobacter jejuni N-glycan to create an effective chicken vaccine. Scientific Reports, 6, 26511 (2016)10.1038/srep26511487952127221144
  51. Nyati K.K., Nyati R.: Role of Campylobacter jejuni Infection in the Pathogenesis of Guillain-Barré Syndrome: An Update. Biomed. Res. Int. 852195 (2013)10.1155/2013/852195375543024000328
  52. Nyati K.K., Prasad K.N.: Role of cytokines and Toll-Like receptors in the immunopathogenesis of Guillain-Barré syndrome. Mediators Inflamm. 758639, DOI:10.1155/2014/758639 (2014)10.1155/2014/758639418994725614713
  53. Palyada K.,Threadgill D. and Stintzi A.: Iron acquisition and regulationin Campylobacter jejuni. J. Bacteriol. 186, 4714–4729 (2004)
  54. Phongsisay V.: The immunobiology of Campylobacter jejuni: innate immunity and autoimmune diseases. Immunobiol. 221, 535–543 (2015)10.1016/j.imbio.2015.12.00526709064
  55. Prendergastm M., Moran A.P.: Lipooligosaccharidies in the development of Guillain-Barre’s syndrome and Miller Fisher syndrome forms of acute inflammatory peripheral. Neuropathies J. Endotoxin Res. 6, 341–359 (2000)
  56. Ridley K.A., Rock J.D., Li Y., Ketley J.M.: Hem eutilizationin Campylobacter jejuni. J. Bacteriol. 188, 7862–7875 (2006)10.1128/JB.00994-06163629916980451
  57. Rokosz-Chudziak N., Rastawicki W.: Wybrane mechanizmy chorobotwórczości pałeczek Campylobacter jejuni. Med. Dośw. Mikrobiol. 66, 47–58 (2014)
  58. Sait-Cyr M.J., Guyard-Nicodeme M., Messaoudi S., Chemaly M., Cappelier J.M., Dousset X., Haddad N.: Recent advanced in screening of anti-Campylobacter activity in priobiotics for use in poultry. Front. Microiol. 7, 1–22 (2016)
  59. Saxena A.: Probiotics as a potential alternative for relieving peripheral neurophaties: a case for Guillain-Barre’s syndrome. Front. Microbiol. 6, 1497 (2015)10.3389/fmicb.2015.01497470375626779152
  60. Shu X.M., Cai F.C., Zhang X.P.: Carbohydrate mimicry of Campylobacter jejuni lipooligosaccharide is critical for the induction of anti-GM1 antibody and neuropathy. Muscle Nerve, 33, 225–231 (2006)10.1002/mus.2045716270308
  61. Silva J., Leite D., Fernandes M., Mena C., Gibbs P.A., Teixeira P.: Campylobacter spp. as a foodborne pathogen: a review. Front. Microbiol. 2, 200 (2011)10.3389/fmicb.2011.00200318064321991264
  62. Sofka D., Pfeifer A., Paulsen P., Hilbert F.: Changes with in the intestinal flora of broilers by colonisation with Campylobacter jejuni. Berl. Munch. Tierarztl.Wochenschr. 128, 104–110 (2015)
  63. Stahl M., Vallance B.A.: Insights into Campylobacter jejuni colonization of the mammalian intestinal tract using a novel mouse model of infection. Gut Microbe. 6, 143–148 (2015)10.1080/19490976.2015.1016691461536225831043
  64. Szymanski C.M. and Gaynor E.C.: How a sugary bug gets through the day. Recent developments in understanding fundamental processes impacting Campylobacter jejuni pathogenesis. Gut Microbe,3, 135–144 (2012)10.4161/gmic.19488337094622555465
  65. Wang Y., Sun S., Zhu J., Cui L., Zhang H.L.: Biomarkers of Guillain-Barre’s syndrome: Some recent progres, more still to be explored. Mediaors Inflamm. 5640098 (2015)10.1155/2015/564098458835126451079
  66. Watson A.E., Sandu P., Gundogdu O., Mills D.C., Inglis N.F., Manson E., Imrie L., Bajaj-Elliott M., Wren B.W., Smith David G.E., Dorrella N.: Campylobacter jejuni outer membrane vesicles play an important role in bacterial interactions with human intestinal epithelial cells. Infect. Immun. 80, 4089–4098 (2012)
  67. Wieczorek K., Osek J. Antimicrobial resistance mechanisms among Campylobacter. Biomed. Res. Int. 340605, DOI: 10.1155/ 2013/340605 (2013)10.1155/2013/340605370720623865047
  68. Xiang S.l., Zhong M., Cai F.C., Deng B., Zhang X.P.: The sialic acid residue i a crucial component of Campylobacter jejuni lipo-oligosaccharide ganglioside mimicry in the induction Guillain-Barre’s syndrome. J. Neuroimmunol. 174, 126–132 (2006)10.1016/j.jneuroim.2006.02.00916567003
  69. Xu F., Zeng X., Haigh R.D., Ketley J.M., Lin J.: Identification and characterization of a new ferric enterobactin receptor CfrB in Campylobacter. J. Bacteriol. 192, 4425–4435 (2010)10.1128/JB.00478-10293737920585060
  70. Yu R.K., Usuki S., Ariga T. Ganglioside molecular mimicry and its pathological roles in Guillain-Barre’ syndrome and related diseases. Infect. Immun. 74, 6517–6527 (2006)10.1128/IAI.00967-06169809216966405
  71. Yuki N. Guillain-Barre syndrome and anti-ganglioside antibodies a clinician scientist’s journey. Proc. Jpn. Acad., Ser. B. Phys Biol. Sci. 88, 299–326 (2012)10.2183/pjab.88.299342268522850724
  72. Yuki N.: Pathogenesis of Guillain-Barre and Miller Fisher syndromes subsequent to Campylobacter jejuni enteritis. Jpn. J. Infect. Dis. 2, 99–105 (1999)
  73. Yuki N, Hartung H.: Guillain-Barr’e Syndrome. New Engl. J. Med. 336, 294–304 (2012)
  74. Yuki N., Koga M.: Bacterial infections in Guillain-Barre and Fisher syndromes. Curr. Opin. Neurol. 19, 451–457 (1995)
  75. Yuki N., Odaka M.: Ganglioside mimicry as cause of Guillain-Barre’s syndrome. Curr. Opin. Neurol. 18, 557–561 (2005)
  76. Zang T., Dong J., Lu Q., Luo Q., Wen G., LiuG., Shao H.: Genotypic diversity, antymicrobial resistance and biofilm-forming abilities of Campylobacter isolated from chicken in Central China. Gut Pathogens, 9, 1–10 (2017)
  77. Zhang X.P., Gilbert M., Yuki N.,Cao F., Li J., Liu h., Lii Q., Meng F., Zhang J.: Association of anti GT1a antibodies with an outbreak of Guillain-Barre’s syndrome and analysis of gangliside mimicry in an associated Campylobacter jejuni strain. PLoS One,10, e0131730 (2015)10.1371/journal.pone.0131730451013026197476
DOI: https://doi.org/10.21307/PM-2018.57.3.260 | Journal eISSN: 2545-3149 | Journal ISSN: 0079-4252
Language: English, Polish
Page range: 260 - 269
Submitted on: Apr 1, 2017
Accepted on: May 1, 2018
Published on: Feb 26, 2022
Published by: Polish Society of Microbiologists
In partnership with: Paradigm Publishing Services
Publication frequency: 4 issues per year

© 2022 Maria Walencka, Agnieszka Matusiak, Magdalena Chmiela, published by Polish Society of Microbiologists
This work is licensed under the Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 License.