Phylogenetic relationships of Campylobacter jejuni based on porA sequences

被引:19
作者
Clark, Clifford G. [1 ]
Beeston, Anne [1 ]
Bryden, Louis [1 ]
Wang, Gehua [1 ]
Barton, Connie [1 ]
Cuff, Wilfred [1 ]
Gilmour, Matthew W. [1 ]
Ng, Lai-King [1 ]
机构
[1] Publ Hlth Agcy Canada, Natl Microbiol Lab, Bacteriol & Enter Dis Program, Winnipeg, MB R3E 3R2, Canada
基金
英国惠康基金;
关键词
Campylobacter; porin; major outer membrane protein; phylogenetic analysis;
D O I
10.1139/W06-099
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Campylobacter porins are the dominant major outer membrane protein (MOMP) of these bacteria. They are composed of hypervariable, surface-exposed, peptide loops and membrane-embedded, conserved peptide regions. Porins are functionally important and may also be useful for molecular subtyping methods but have not yet been well characterized. We therefore sequenced the porA gene from 39 Campylobacter isolates, including multilocus sequence type (MLST) reference strains, isolates from patients with the Guillain-Barre syndrome, other clinical isolates, and serotyping reference strains. These were compared with additional sequences available from GenBank. Three distinct porA lineages were observed after phylogenetic analysis. Both Campylobacter coli and Campylobacter jejuni were found with group 3 porA sequences, and this was the only group showing any evidence of recombination among porA genes. There was no recombination between porA genes from C. jejuni groups 1 and 2, suggesting there may be functional constraints on changes at this locus. Most of the amino acid differences among the three groups were present in surface-exposed loops, and dissimilar substitutions were found when groups 1 and 2 MOMP were compared. Different MOMP sequence groups may have different biological or antigenic properties, which in turn may be associated with survival in different environments, host adaptation, or virulence.
引用
收藏
页码:27 / 38
页数:12
相关论文
共 35 条
[1]   Electron microscopy of the major outer membrane protein of Campylobacter jejuni [J].
Amako, K ;
Wai, SN ;
Umeda, A ;
Shigematsu, M ;
Takade, A .
MICROBIOLOGY AND IMMUNOLOGY, 1996, 40 (10) :749-754
[2]   Identification and characterisation of a cytotoxic porin-lipopolysaccharide complex from Campylobacter jejuni [J].
Bacon, DJ ;
Johnson, WM ;
Rodgers, FG .
JOURNAL OF MEDICAL MICROBIOLOGY, 1999, 48 (02) :139-148
[3]   Recent developments in Campylobacter pathogenesis [J].
Bereswill, S ;
Kist, M .
CURRENT OPINION IN INFECTIOUS DISEASES, 2003, 16 (05) :487-491
[4]   CONFORMATIONAL-ANALYSIS OF THE CAMPYLOBACTER-JEJUNI PORIN [J].
BOLLA, JM ;
LORET, E ;
ZALEWSKI, M ;
PAGES, JM .
JOURNAL OF BACTERIOLOGY, 1995, 177 (15) :4266-4271
[5]   Tolerance to self gangliosides is the major factor restricting the antibody response to lipopolysaccharide core oligosaccharides in Campylobacter jejuni strains associated with Guillain-Barre syndrome [J].
Bowes, T ;
Wagner, ER ;
Boffey, J ;
Nicholl, D ;
Cochrane, L ;
Benboubetra, M ;
Conner, J ;
Furukawa, K ;
Furukawa, K ;
Willison, HJ .
INFECTION AND IMMUNITY, 2002, 70 (09) :5008-5018
[6]   MOMP (major outer membrane protein) of Campylobacter jejuni;: a versatile pore-forming protein [J].
Dé, E ;
Jullien, M ;
Labesse, G ;
Pagès, JM ;
Molle, G ;
Bolla, JM .
FEBS LETTERS, 2000, 469 (01) :93-97
[7]  
DEMARTINO L, 1995, J SUBMICR CYTOL PATH, V27, P445
[8]   Multilocus sequence typing system for Campylobacter jejuni [J].
Dingle, KE ;
Colles, FM ;
Wareing, DRA ;
Ure, R ;
Fox, AJ ;
Bolton, FE ;
Bootsma, HJ ;
Willems, RJL ;
Urwin, R ;
Maiden, MCJ .
JOURNAL OF CLINICAL MICROBIOLOGY, 2001, 39 (01) :14-23
[9]   Cytokine pattern in the cerebrospinal fluid from patients with GBS and CIDP [J].
Ferrarini, AM ;
Lolli, F ;
Mata, S ;
Pinto, F ;
Tavolato, B ;
Gallo, P .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 1997, 147 (01) :93-95
[10]   Major structural differences and novel potential virulence mechanisms from the genomes of multiple Campylobacter species [J].
Fouts, DE ;
Mongodin, EF ;
Mandrell, RE ;
Miller, WG ;
Rasko, DA ;
Ravel, J ;
Brinkac, LM ;
DeBoy, RT ;
Parker, CT ;
Daugherty, SC ;
Dodson, RJ ;
Durkin, AS ;
Madupu, R ;
Sullivan, SA ;
Shetty, JU ;
Ayodeji, MA ;
Shvartsbeyn, A ;
Schatz, MC ;
Badger, JH ;
Fraser, CM ;
Nelson, KE .
PLOS BIOLOGY, 2005, 3 (01) :72-85