期刊论文详细信息
Gut Pathogens
Investigation of motility and biofilm formation by intestinal Campylobacter concisus strains
Hazel M Mitchell1  Nupur Kain1  Karina D Huinao1  Nadeem O Kaakoush1  Peter Lavrencic1 
[1] School of Biotechnology and Biomolecular Sciences, The University of New South Wales, Sydney, NSW, 2052, Australia
关键词: Biofilm;    Mucus;    Viscous;    Adherence;    Motility;    Campylobacter concisus;   
Others  :  821778
DOI  :  10.1186/1757-4749-4-22
 received in 2012-11-26, accepted in 2012-12-13,  发布年份 2012
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【 摘 要 】

Motility helps many pathogens swim through the highly viscous intestinal mucus. Given the differing outcomes of Campylobacter concisus infection, the motility of eight C. concisus strains isolated from patients with Crohn’s disease (n=3), acute (n=3) and chronic (n=1) gastroenteritis and a healthy control (n=1) were compared. Following growth on solid or liquid media the eight strains formed two groups; however, the type of growth medium did not affect motility. In contrast, following growth in viscous liquid medium seven of the eight strains demonstrated significantly decreased motility. In media of increasing viscosities the motility of C. concisus UNSWCD had two marked increases at viscosities of 20.0 and 74.7 centipoises. Determination of the ability of UNSWCD to swim through a viscous medium, adhere to and invade intestinal epithelial cells showed that while adherence levels significantly decreased with increasing viscosity, invasion levels did not significantly change. In contrast, adherence to and invasion of UNSWCD to mucus-producing intestinal cells increased upon accumulation of mucus, as did bacterial aggregation. Given this aggregation, we determined the ability of the eight C. concisus strains to form biofilms, and showed that all strains formed biofilms. In conclusion, the finding that C. concisus strains could be differentiated into two groups based on their motility may suggest that strains with high motility have an increased ability to swim through the intestinal mucus and reach the epithelial layer.

【 授权许可】

   
2012 Lavrencic et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Moore JE, Corcoran D, Dooley JS, Fanning S, Lucey B, Matsuda M, McDowell DA, Megraud F, Millar BC, O’Mahony R, O’Riordan L, O’Rourke M, Rao JR, Rooney PJ, Sails A, Whyte P: Campylobacter. Vet Res 2005, 36:351-382.
  • [2]Gorkiewicz G, Feierl G, Zechner R, Zechner EL: Transmission of Campylobacter hyointestinalis from a pig to a human. J Clin Microbiol 2002, 40:2601-2605.
  • [3]Kaakoush NO, Mitchell HM: Campylobacter concisus - a New player in intestinal disease. Front Cell Infect Microbiol 2012, 2:4.
  • [4]Nielsen HL, Ejlertsen T, Engberg J, Nielsen H: High incidence of Campylobacter concisus in gastroenteritis in North Jutland, Denmark: a population-based study. Clin Microbiol Infect 2012.
  • [5]Kaakoush NO, Deshpande NP, Wilkins MR, Tan CG, Burgos-Portugal JA, Raftery MJ, Day AS, Lemberg DA, Mitchell H: The pathogenic potential of Campylobacter concisus strains associated with chronic intestinal diseases. PLoS One 2011, 6:e29045.
  • [6]Vandamme P, Falsen E, Pot B, Hoste B, Kersters K, De Ley J: Identification of EF group 22 campylobacters from gastroenteritis cases as Campylobacter concisus. J Clin Microbiol 1989, 27:1775-1781.
  • [7]Nielsen HL, Engberg J, Ejlertsen T, Bucker R, Nielsen H: Short-term and medium-term clinical outcomes of Campylobacter concisus infection. Clin Microbiol Infect 2012, 18:E459-E465.
  • [8]Ramos HC, Rumbo M, Sirard JC: Bacterial flagellins: mediators of pathogenicity and host immune responses in mucosa. Trends Microbiol 2004, 12:509-517.
  • [9]Szymanski CM, King M, Haardt M, Armstrong GD: Campylobacter jejuni motility and invasion of Caco-2 cells. Infect Immun 1995, 63:4295-4300.
  • [10]Lee A, O’Rourke JL, Barrington PJ, Trust TJ: Mucus colonization as a determinant of pathogenicity in intestinal infection by Campylobacter jejuni: a mouse cecal model. Infect Immun 1986, 51:536-546.
  • [11]Yao R, Burr DH, Doig P, Trust TJ, Niu H, Guerry P: Isolation of motile and non-motile insertional mutants of Campylobacter jejuni: the role of motility in adherence and invasion of eukaryotic cells. Mol Microbiol 1994, 14:883-893.
  • [12]Man SM, Kaakoush NO, Leach ST, Nahidi L, Lu HK, Norman J, Day AS, Zhang L, Mitchell HM: Host attachment, invasion, and stimulation of proinflammatory cytokines by Campylobacter concisus and other non-Campylobacter jejuni Campylobacter species. J Infect Dis 2010, 202:1855-1865.
  • [13]Guerry P, Ewing CP, Schirm M, Lorenzo M, Kelly J, Pattarini D, Majam G, Thibault P, Logan S: Changes in flagellin glycosylation affect Campylobacter autoagglutination and virulence. Mol Microbiol 2006, 60:299-311.
  • [14]Joshua GW, Guthrie-Irons C, Karlyshev AV, Wren BW: Biofilm formation in Campylobacter jejuni. Microbiology 2006, 152:387-396.
  • [15]Jensen PO, Givskov M, Bjarnsholt T, Moser C: The immune system vs. Pseudomonas aeruginosa biofilms. FEMS Immunol Med Microbiol 2010, 59:292-305.
  • [16]Gunther NW, Chen CY: The biofilm forming potential of bacterial species in the genus Campylobacter. Food Microbiol 2009, 26:44-51.
  • [17]Goon S, Kelly JF, Logan SM, Ewing CP, Guerry P: Pseudaminic acid, the major modification on Campylobacter flagellin, is synthesized via the Cj1293 gene. Mol Microbiol 2003, 50:659-671.
  • [18]Golden NJ, Acheson DW: Identification of motility and autoagglutination Campylobacter jejuni mutants by random transposon mutagenesis. Infect Immun 2002, 70:1761-1771.
  • [19]Kaakoush NO, Deshpande NP, Wilkins MR, Raftery MJ, Janitz K, Mitchell H: Comparative analyses of Campylobacter concisus strains reveal the genome of the reference strain BAA-1457 is not representative of the species. Gut Pathog 2011, 3:15. BioMed Central Full Text
  • [20]Schneider WR, Doetsch RN: Effect of viscosity on bacterial motility. J Bacteriol 1974, 117:696-701.
  • [21]Atuma C, Strugala V, Allen A, Holm L: The adherent gastrointestinal mucus gel layer: thickness and physical state in vivo. Am J Physiol Gastrointest Liver Physiol 2001, 280:G922-G929.
  • [22]Corazziari ES: Intestinal mucus barrier in normal and inflamed colon. J Pediatr Gastroenterol Nutr 2009, 48(Suppl 2):S54-S55.
  • [23]Shigematsu M, Umeda A, Fujimoto S, Amako K: Spirochaete-like swimming mode of Campylobacter jejuni in a viscous environment. J Med Microbiol 1998, 47:521-526.
  • [24]van Klinken BJ, Oussoren E, Weenink JJ, Strous GJ, Buller HA, Dekker J, Einerhand AW: The human intestinal cell lines Caco-2 and LS174T as models to study cell-type specific mucin expression. Glycoconj J 1996, 13:757-768.
  • [25]Hugdahl MB, Beery JT, Doyle MP: Chemotactic behavior of Campylobacter jejuni. Infect Immun 1988, 56:1560-1566.
  • [26]McAuley JL, Linden SK, Png CW, King RM, Pennington HL, Gendler SJ, Florin TH, Hill GR, Korolik V, McGuckin MA: MUC1 cell surface mucin is a critical element of the mucosal barrier to infection. J Clin Invest 2007, 117:2313-2324.
  • [27]Tu QV, McGuckin MA, Mendz GL: Campylobacter jejuni response to human mucin MUC2: modulation of colonization and pathogenicity determinants. J Med Microbiol 2008, 57:795-802.
  • [28]Kaakoush NO, Man SM, Lamb S, Raftery MJ, Wilkins MR, Kovach Z, Mitchell H: The secretome of Campylobacter concisus. FEBS J 2010, 277:1606-1617.
  • [29]Donlan RM: Biofilms: microbial life on surfaces. Emerg Infect Dis 2002, 8:881-890.
  • [30]Reuter M, Mallett A, Pearson BM, van Vliet AH: Biofilm formation by Campylobacter jejuni is increased under aerobic conditions. Appl Environ Microbiol 2010, 76:2122-2128.
  • [31]Anderson GG, Palermo JJ, Schilling JD, Roth R, Heuser J, Hultgren SJ: Intracellular bacterial biofilm-like pods in urinary tract infections. Science 2003, 301:105-107.
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