Kim Hye-Jin, Cho Jae-Chang
Institute of Environmental Sciences and Department of Environmental Sciences, Hankuk University of Foreign Studies, Yong-In, Korea.
Solana Informatics, San Diego, CA, United States of America.
PLoS One. 2015 Nov 23;10(11):e0142657. doi: 10.1371/journal.pone.0142657. eCollection 2015.
The genetic diversity and population structure of Vibrio vulnificus isolates from Korea and Taiwan were investigated using PCR-based assays targeting putative virulence-related genes and multilocus sequence typing (MLST). BOX-PCR genomic fingerprinting identified 52 unique genotypes in 84 environmental and clinical V. vulnificus isolates. The majority (> 50%) of strains had pathogenic genotypes for all loci tested; moreover, many environmental strains had pathogenic genotypes. Although significant (p < 0.05) inter-relationships among the genotypes were observed, the association between genotype and strain source (environmental or clinical) was not significant, indicating that genotypic characteristics alone are not sufficient to predict the isolation source or the virulence of a given V. vulnificus strain and vice versa. MLST revealed 23-35 allelic types per locus analyzed, resulting in a total of 44 unique sequence types (STs). Two major monophyletic groups (lineages A and B) corresponding to the two known lineages of V. vulnificus were observed; lineage A had six STs that were exclusively environmental, whereas lineage B had STs from both environmental and clinical sources. Pathogenic and nonpathogenic genotypes predominated in MLST lineages B and A, respectively. In addition, V. vulnificus was shown to be in linkage disequilibrium (p < 0.05), although two different recombination tests (PHI and Sawyer's tests) detected significant evidence of recombination. Tajima's D test also indicated that V. vulnificus might be comprised of recently sub-divided lineages. These results suggested that the two lineages revealed by MLST correspond to two distinct ecotypes of V. vulnificus.
利用针对假定毒力相关基因的基于PCR的检测方法和多位点序列分型(MLST),对来自韩国和台湾的创伤弧菌分离株的遗传多样性和种群结构进行了研究。BOX-PCR基因组指纹图谱在84株环境和临床创伤弧菌分离株中鉴定出52种独特的基因型。大多数(>50%)菌株在所有测试位点都具有致病基因型;此外,许多环境菌株也具有致病基因型。虽然观察到基因型之间存在显著(p<0.05)的相互关系,但基因型与菌株来源(环境或临床)之间的关联并不显著,这表明仅基因型特征不足以预测特定创伤弧菌菌株的分离来源或毒力,反之亦然。MLST显示每个分析位点有23 - 35个等位基因类型,总共产生44种独特的序列类型(STs)。观察到两个主要的单系群(谱系A和B),对应于创伤弧菌的两个已知谱系;谱系A有6个仅为环境来源的STs,而谱系B有来自环境和临床来源的STs。致病和非致病基因型分别在MLST谱系B和A中占主导地位。此外,尽管两种不同的重组测试(PHI和索耶测试)检测到显著的重组证据,但创伤弧菌显示出连锁不平衡(p<0.05)。 Tajima's D测试还表明,创伤弧菌可能由最近细分的谱系组成。这些结果表明,MLST揭示的两个谱系对应于创伤弧菌的两种不同生态型。