Comparative genomic analysis of Vibrio parahaemolyticus: serotype conversion and virulence

被引:82
作者
Chen, Yuansha [2 ,3 ]
Stine, O. Colin [4 ]
Badger, Jonathan H. [1 ]
Gil, Ana I.
Nair, G. Balakrish [5 ]
Nishibuchi, Mitsuaki [6 ]
Fouts, Derrick E. [1 ]
机构
[1] J Craig Venter Inst, Rockville, MD USA
[2] Univ Florida, Emerging Pathogens Inst, Gainesville, FL USA
[3] Univ Florida, Dept Pathol, Gainesville, FL 32611 USA
[4] Univ Maryland, Sch Med, Baltimore, MD 21201 USA
[5] Natl Inst Cholera & Enter Dis, Kolkata, India
[6] Kyoto Univ, Kyoto, Japan
基金
美国国家卫生研究院;
关键词
THERMOSTABLE DIRECT HEMOLYSIN; III SECRETION SYSTEM; SPECIES LEVEL; GENE TRH; IDENTIFICATION; CHOLERAE; SEQUENCE; STRAINS; O3-K6; PROTEIN;
D O I
10.1186/1471-2164-12-294
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Background: Vibrio parahaemolyticus is a common cause of foodborne disease. Beginning in 1996, a more virulent strain having serotype O3:K6 caused major outbreaks in India and other parts of the world, resulting in the emergence of a pandemic. Other serovariants of this strain emerged during its dissemination and together with the original O3:K6 were termed strains of the pandemic clone. Two genomes, one of this virulent strain and one pre-pandemic strain have been sequenced. We sequenced four additional genomes of V. parahaemolyticus in this study that were isolated from different geographical regions and time points. Comparative genomic analyses of six strains of V. parahaemolyticus isolated from Asia and Peru were performed in order to advance knowledge concerning the evolution of V. parahaemolyticus; specifically, the genetic changes contributing to serotype conversion and virulence. Two pre-pandemic strains and three pandemic strains, isolated from different geographical regions, were serotype O3:K6 and either toxin profiles (tdh+, trh-) or (tdh-, trh+). The sixth pandemic strain sequenced in this study was serotype O4:K68. Results: Genomic analyses revealed that the trh+ and tdh+ strains had different types of pathogenicity islands and mobile elements as well as major structural differences between the tdh pathogenicity islands of the pre-pandemic and pandemic strains. In addition, the results of single nucleotide polymorphism (SNP) analysis showed that 94% of the SNPs between O3:K6 and O4:K68 pandemic isolates were within a 141 kb region surrounding the O- and K-antigen-encoding gene clusters. The "core" genes of V. parahaemolyticus were also compared to those of V. cholerae and V. vulnificus, in order to delineate differences between these three pathogenic species. Approximately one-half (49-59%) of each species' core genes were conserved in all three species, and 14-24% of the core genes were species-specific and in different functional categories. Conclusions: Our data support the idea that the pandemic strains are closely related and that recent South American outbreaks of foodborne disease caused by V. parahaemolyticus are closely linked to outbreaks in India. Serotype conversion from O3:K6 to O4:K68 was likely due to a recombination event involving a region much larger than the O-antigen- and K-antigen-encoding gene clusters. Major differences between pathogenicity islands and mobile elements are also likely driving the evolution of V. parahaemolyticus. In addition, our analyses categorized genes that may be useful in differentiating pathogenic Vibrios at the species level.
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