期刊论文详细信息
BMC Microbiology
Variation of chemosensory receptor content of Campylobacter jejuni strains and modulation of receptor gene expression under different in vivo and in vitro growth conditions
Victoria Korolik2  Evgeny A Semchenko2  Serena K Day1  Greg Tram2  Rebecca M King2  Lucy K Shewell2  Lauren E Hartley-Tassell2  Christopher J Day2 
[1] Department of Microbiology, Pathology Queensland, Gold Coast Hospital, Southport, Australia;Institute for Glycomics, Griffith University Gold Coast Campus, Griffith University, Griffith, Australia
关键词: Transducer-like proteins;    Campylobacter;    Chemotaxis receptor;   
Others  :  1221843
DOI  :  10.1186/1471-2180-12-128
 received in 2012-03-21, accepted in 2012-06-29,  发布年份 2012
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【 摘 要 】

Background

Chemotaxis is crucial for the colonisation/infection of hosts with Campylobacter jejuni. Central to chemotaxis are the group A chemotaxis genes that are responsible for sensing the external environment. The distribution of group A chemoreceptor genes, as found in the C. jejuni sequenced strains, tlp1-4, 7, 10 and 11 were determined in 33 clinical human and avian isolates.

Results

Group A tlp gene content varied among the strains with genes encoding tlp1 (aspartate receptor, ccaA) and tlp7 present in all strains tested, where as tlp11 was present in only one of our international collection clinical isolates, C. jejuni 520, but was more prevalent (9/13) in the freshly isolated clinical stains from patients who required hospitalisation due to C. jejuni infection (GCH1-17). Relative expression levels of the group A tlp genes were also determined in C. jejuni reference strains NCTC 11168-GS, 11168-O and 81116 using cells grown in vitro at 37°C, 42°C and maintained at room temperature and with cells isolated directly from murine and avian hosts by immune magnetic separation without subsequent culture. Gene expression of tlp genes was varied based on strain, growth conditions and in vivo isolation source. Tlp1, although the most conserved, showed the lowest and most varied mRNA expression and protein production under laboratory conditions. Tlp7 was highly expressed at most conditions tested, and gene expression was not influenced by the tlp7 gene encoding a full length protein or one expressed as separate periplasmic and cytoplasmic domains.

Conclusion

We have shown that chemosensory receptor set variation exists among C. jejuni strains, but is not dependent on the isolation source.

【 授权许可】

   
2012 Day et al.; licensee BioMed Central Ltd.

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【 参考文献 】
  • [1]Friedman C, Neimann J, Wegener H, Tauxe R: Epidemiology of Campylobacter jejuni infections in the United States and other industrialized nations. In Campylobacter. 2nd edition. Edited by Nachamkin I, Blaser M. ASM Press, Washington DC; 2000:121-138.
  • [2]Oosterom J, Butzler J: Campylobacter: pathogenicity and significance in foods. Int J Food Microbiol 1991, 12:1-8.
  • [3]Young KT, Davis LM, DiRita VJ: Campylobacter jejuni: molecular biology and pathogenesis. Nat Rev Microbiol 2007, 5:665-679.
  • [4]Josenhans C, Suerbaum S: The role of motility as a virulence factor in bacteria. Int J Med Microbiol 2002, 291(8):605-616.
  • [5]Marchant J, Wren B, Ketley J: Exploiting genome sequence: predictions for mechanisms of Campylobacter chemotaxis. Trends Microbiol 2002, 10(4):155-159.
  • [6]Korolik V, Ketley JM: Chemosensory signal transduction pathway of Campylobacter jejuni. In Campylobacter. third edition. Edited by Nachamkin I, Symanski C, Blaser MJ. ASM Press, Washington, DC; 2008:351-366.
  • [7]Hartley-Tassell LE, Shewell LK, Day CJ, Wilson JC, Sandhu R, Ketley JM, Korolik V: Identification and characterization of the aspartate chemosensory receptor of Campylobacter jejuni. Mol Microbiol 2009.
  • [8]Tareen AM, Dasti JI, Zautner AE, Gross U, Lugert R: Campylobacter jejuni proteins Cj0952c and Cj0951c affect chemotactic behaviour towards formic acid and are important for invasion of host cells. Microbiology 2010, 156(Pt 10):3123-3135.
  • [9]Lane M, Lloyd A, Markyvech T, Hagan E, Mobley H: Uropathogenic Escherichia coli strains generally lack functional Trg and Tap chemoreceptors found in the majority of E. coli strains residing in the gut. J Bacteriol 2006, 188:5618-5625.
  • [10]Zautner AE, Herrmann S, Corso J, Tareen AM, Alter T, Gross U: Epidemiological association of different Campylobacter jejuni groups with metabolism-associated genetic markers. Appl Environ Microbiol 2011, 77(7):2359-2365.
  • [11]Gaynor EC, Cawthraw S, Manning G, MacKichan JK, Falkow S, Newell DG: The Genome-Sequenced Variant of Campylobacter jejuni NCTC 11168 and the Original Clonal Clinical Isolate Differ Markedly in Colonization, Gene Expression, and Virulence-Associated Phenotypes. J Bacteriol 2004, 186(2):503-517.
  • [12]Day CJ, Tiralongo J, Hartnell RD, Logue CA, Wilson JC, von Itzstein M, Korolik V: Differential carbohydrate recognition by Campylobacter jejuni strain 11168: influences of temperature and growth conditions. PLoS One 2009, 4(3):e4927.
  • [13]Blaser MJ, Cody HJ: Methods for isolating Campylobacter jejuni from low-turbidity water. Appl Environ Microbiol 1986, 51(2):312-315.
  • [14]Craun GF, Brunkard JM, Yoder JS, Roberts VA, Carpenter J, Wade T, Calderon RL, Roberts JM, Beach MJ, Roy SL: Causes of outbreaks associated with drinking water in the United States from 1971 to 2006. Clin Microbiol Rev 2010, 23(3):507-528.
  • [15]Kemp R, Leatherbarrow AJ, Williams NJ, Hart CA, Clough HE, Turner J, Wright EJ, French NP: Prevalence and genetic diversity of Campylobacter spp. in environmental water samples from a 100-square-kilometer predominantly dairy farming area. Appl Environ Microbiol 2005, 71(4):1876-1882.
  • [16]Newell DG, McBride H, Saunders F, Dehele Y, Pearson AD: The virulence of clinical and environmental isolates of Campylobacter jejuni. J Hyg (Lond) 1985, 94(1):45-54.
  • [17]Guccione E, Leon-Kempis Mdel R, Pearson BM, Hitchin E, Mulholland F, van Diemen PM, Stevens MP, Kelly DJ: Amino acid-dependent growth of Campylobacter jejuni: key roles for aspartase (AspA) under microaerobic and oxygen-limited conditions and identification of AspB (Cj0762), essential for growth on glutamate. Mol Microbiol 2008, 69(1):77-93.
  • [18]Leon-Kempis Mdel R, Guccione E, Mulholland F, Williamson MP, Kelly DJ: The Campylobacter jejuni PEB1a adhesin is an aspartate/glutamate-binding protein of an ABC transporter essential for microaerobic growth on dicarboxylic amino acids. Mol Microbiol 2006, 60(5):1262-1275.
  • [19]Hazelbauer GL, Engstrom P, Harayama S: Methyl-accepting chemotaxis protein III and transducer gene trg. J Bacteriol 1981, 145(1):43-49.
  • [20]Blaser M, Perez G, Smith P, Patton C, Tenover F, Lastovica A, Wang W: Extraintestinal Campylobacter jejuni and Campylobacter coli infections: host factors and strain characteristics. J Infect Dis 1986, 153(3):552-559.
  • [21]King RM, Day CJ, Hartley LE, Connerton IF, Tiralongo J, McGuckin MA, Korolik V: Carbohydrate binding and gene expression by in vitro and in vivo propagated Campylobacter jejuni after Immunomagnetic Separation. J Basic Microbiol 2012. In Press
  • [22]Ringoir DD, Szylo D, Korolik V: Comparison of 2-day-old and 14-day-old chicken colonization models for Campylobacter jejuni. FEMS Immunol Med Microbiol 2007, 49(1):155-158.
  • [23]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(8):2313-2324.
  • [24]Parkhill J, Wren BW, Mungall K, Ketley JM, Churcher C, Basham D, Chillingworth T, Davies RM, Feltwell T, Holroyd S, et al.: The genome sequence of the food-borne pathogen Campylobacter jejuni reveals hypervariable sequences. Nature 2000, 403(6770):665-668.
  • [25]Eyers M, Chapelle S, Van Camp G, Goossens H, Wachter RD: Discrimination among thermophilic Campylobacter species by polymerase chain reaction amplification of 23 S rRNA gene fragments. J Clin Microbiol 1994, 32(6):1623.
  • [26]Sambrook J, Fritsch EF, Maniatis T: Molecular cloning: a laboratory manual. 2nd edition. Cold Spring Harbor Laboratory Press, Cold Spring Harbor, N.Y; 1989.
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