Multilocus Sequence Typing System forCampylobacter jejuni

ABSTRACT The gram-negative bacterium Campylobacter jejuni has extensive reservoirs in livestock and the environment and is a frequent cause of gastroenteritis in humans. To date, the lack of (i) methods suitable for population genetic analysis and (ii) a universally accepted nomenclature has hindered studies of the epidemiology and population biology of this organism. Here, a multilocus sequence typing (MLST) system for this organism is described, which exploits the genetic variation present in seven housekeeping loci to determine the genetic relationships among isolates. The MLST system was established using 194 C. jejuni isolates of diverse origins, from humans, animals, and the environment. The allelic profiles, or sequence types (STs), of these isolates were deposited on the Internet (http://mlst.zoo.ox.ac.uk ), forming a virtual isolate collection which could be continually expanded. These data indicated that C. jejuni is genetically diverse, with a weakly clonal population structure, and that intra- and interspecies horizontal genetic exchange was common. Of the 155 STs observed, 51 (26% of the isolate collection) were unique, with the remainder of the collection being categorized into 11 lineages or clonal complexes of related STs with between 2 and 56 members. In some cases membership in a given lineage or ST correlated with the possession of a particular Penner HS serotype. Application of this approach to further isolate collections will enable an integrated global picture of C. jejuniepidemiology to be established and will permit more detailed studies of the population genetics of this organism.

[1]  E. J. Feil,et al.  Carried Meningococci in the Czech Republic: a Diverse Recombining Population , 2000, Journal of Clinical Microbiology.

[2]  M. Maiden,et al.  High-throughput sequencing in the population analysis of bacterial pathogens of humans. , 2000, International journal of medical microbiology : IJMM.

[3]  B. Barrell,et al.  The genome sequence of the food-borne pathogen Campylobacter jejuni reveals hypervariable sequences , 2000, Nature.

[4]  T. Wassenaar,et al.  Genotyping of Campylobacterspp , 2000, Applied and Environmental Microbiology.

[5]  M. Maiden,et al.  Multilocus Sequence Typing and Antigen Gene Sequencing in the Investigation of a Meningococcal Disease Outbreak , 1999, Journal of Clinical Microbiology.

[6]  M Achtman,et al.  Yersinia pestis, the cause of plague, is a recently emerged clone of Yersinia pseudotuberculosis. , 1999, Proceedings of the National Academy of Sciences of the United States of America.

[7]  D. Wareing The significance of strain diversity in the epidemiology of Campylobacter jejuni gastrointestinal infections , 1999 .

[8]  M. Maiden,et al.  Population Genetic and Evolutionary Approaches to Analysis ofNeisseria meningitidis Isolates Belonging to the ET-5 Complex , 1999, Journal of bacteriology.

[9]  C. Nicol,et al.  Seasonal variation of Campylobacter types from human cases, veterinary cases, raw chicken, milk and water , 1999, Journal of applied microbiology.

[10]  E. Holmes,et al.  The influence of recombination on the population structure and evolution of the human pathogen Neisseria meningitidis. , 1999, Molecular biology and evolution.

[11]  T. Humphrey,et al.  Presence of campylobacter and salmonella in sand from bathing beaches , 1999, Epidemiology and Infection.

[12]  M. Konkel,et al.  Identification of the enteropathogens Campylobacter jejuni and Campylobacter coli based on the cadF virulence gene and its product. , 1999, Journal of clinical microbiology.

[13]  S. Altekruse,et al.  Campylobacter jejuni--an emerging foodborne pathogen. , 1999, Emerging infectious diseases.

[14]  B. Spratt,et al.  A multilocus sequence typing scheme for Streptococcus pneumoniae: identification of clones associated with serious invasive disease. , 1998, Microbiology.

[15]  J. M. Smith,et al.  Free recombination within Helicobacter pylori. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[16]  D. Wareing,et al.  Associations between Heat-Stable (O) and Heat-Labile (HL) Serogroup Antigens of Campylobacter jejuni: Evidence for Interstrain Relationships within Three O/HL Serovars , 1998, Journal of Clinical Microbiology.

[17]  I. Nachamkin,et al.  Campylobacter Species and Guillain-Barré Syndrome , 1998, Clinical Microbiology Reviews.

[18]  R. Owen,et al.  Subtyping of Campylobacter jejuni Penner heat-stable (HS) serotype 11 isolates from human infections. , 1998, Journal of medical microbiology.

[19]  M. Achtman,et al.  Multilocus sequence typing: a portable approach to the identification of clones within populations of pathogenic microorganisms. , 1998, Proceedings of the National Academy of Sciences of the United States of America.

[20]  Daniel H. Huson,et al.  SplitsTree: analyzing and visualizing evolutionary data , 1998, Bioinform..

[21]  P. Carter,et al.  Evidence for recombination in the flagellin locus of Campylobacter jejuni: implications for the flagellin gene typing scheme , 1997, Journal of clinical microbiology.

[22]  R. Pebody,et al.  Outbreaks of campylobacter infection: rare events for a common pathogen. , 1997, Communicable disease report. CDR review.

[23]  J. Ketley Pathogenesis of enteric infection by Campylobacter. , 1997, Microbiology.

[24]  R Staden,et al.  The staden sequence analysis package , 1996, Molecular biotechnology.

[25]  I. Nachamkin,et al.  Analysis of HL and O serotypes of Campylobacter strains by the flagellin gene typing system , 1996, Journal of clinical microbiology.

[26]  Population Genetics of Bacteria , 1995 .

[27]  J. Cowden,et al.  The Public Health Laboratory Service national case-control study of primary indigenous sporadic cases of campylobacter infection , 1995, Epidemiology and Infection.

[28]  M. B. Skirrow,et al.  Diseases due to Campylobacter, Helicobacter and related bacteria. , 1994, Journal of comparative pathology.

[29]  Sudhir Kumar,et al.  MEGA: Molecular Evolutionary Genetics Analysis software for microcomputers , 1994, Comput. Appl. Biosci..

[30]  J. M. Smith,et al.  How clonal are bacteria? , 1993, Proceedings of the National Academy of Sciences of the United States of America.

[31]  R. Goodacre,et al.  Identification Methods in Applied and Environmental Microbiology , 1992 .

[32]  T. Embley The linear PCR reaction: a simple and robust method for sequencing amplified rRNA genes , 1991, Letters in applied microbiology.

[33]  Christopher G. Dowson,et al.  Localized sex in bacteria , 1991, Nature.

[34]  T. Whittam,et al.  Methods of multilocus enzyme electrophoresis for bacterial population genetics and systematics , 1986, Applied and environmental microbiology.

[35]  G. Ruiz-Palacios,et al.  Pathophysiology of Campylobacter enteritis. , 1986, Microbiological reviews.