Chan Kamfai, Elhanafi Driss, Kathariou Sophia
Department of Food Science, North Carolina State University, Raleigh, North Carolina 27695-7624, USA.
Foodborne Pathog Dis. 2008 Aug;5(4):387-98. doi: 10.1089/fpd.2008.0113.
Previous multilocus sequence typing studies of Campylobacter coli from meat animals identified an unusual cluster of strains, primarily from turkeys, termed "cluster II" and characterized by the presence of the C. jejuni aspA103 allele. To characterize the extent of genomic input from C. jejuni in the aspA region of cluster II C. coli, we sequenced the 6.1 kb genomic region upstream of and including aspA from two turkey-derived cluster II strains (C. coli 6979 and C. coli 7474, of ST-1150 and ST-1161, respectively), as well as from a turkey-derived multidrug-resistant strain (C. coli 6818) representing a major sequence type (ST-1101) outside of cluster II. A gene encoding a putative CRP-family transcriptional regulator (CCO0137) was present in C. coli 6818 and the reference strain C. coli RM2228, whose genome has been sequenced, but not in either cluster II strain evaluated. This gene was also absent from C. jejuni NCTC 11168 and C. jejuni RM1221. Moreover, single nucleotide polymorphism (SNP) analysis revealed that in both cluster II strains, genes encoding subunit II of cytochrome d ubiquinol oxidase (cydB) and a putative aspartate racemase (Cj0085c) harbored numerous C. jejuni-specific SNPs. Interestingly, genes encoding subunit I of cytochrome d ubiquinol oxidase (cydA), uracil-DNA glycosylase (ung), and aspartate ammonia-lyase (aspA) harbored C. coli-specific SNPs in certain portions but C. jejuni-specific SNPs in others, suggesting that these were hybrid genes with C. jejuni-derived segments. Analysis of a ung mutant in C. coli 7474 indicated that the putative hybrid ung of this cluster II strain was functional. Our data suggest the occurrence of recombination events that resulted in genomic import of DNA from C. jejuni in the region between cydA and aspA in cluster II strains of C. coli.
先前对来自动物肉类的空肠弯曲菌进行的多位点序列分型研究,鉴定出了一组不寻常的菌株群,主要来自火鸡,称为“群集II”,其特征是存在空肠弯曲菌aspA103等位基因。为了表征空肠弯曲菌在群集II型空肠弯曲菌aspA区域的基因组输入程度,我们对来自两只火鸡的群集II型菌株(分别为ST-1150的空肠弯曲菌6979和ST-1161的空肠弯曲菌7474)以及来自一只火鸡的多药耐药菌株(空肠弯曲菌6818,代表群集II之外的主要序列类型(ST-1101))的aspA上游6.1 kb基因组区域(包括aspA)进行了测序。编码假定的CRP家族转录调节因子(CCO0137)的基因存在于空肠弯曲菌6818和已测序基因组的参考菌株空肠弯曲菌RM2228中,但在所评估的两个群集II型菌株中均不存在。该基因在空肠弯曲菌NCTC 11168和空肠弯曲菌RM1221中也不存在。此外,单核苷酸多态性(SNP)分析表明,在两个群集II型菌株中,编码细胞色素d泛醇氧化酶亚基II(cydB)和假定的天冬氨酸消旋酶(Cj0085c)的基因含有大量空肠弯曲菌特异性SNP。有趣的是,编码细胞色素d泛醇氧化酶亚基I(cydA)、尿嘧啶-DNA糖基化酶(ung)和天冬氨酸氨裂解酶(aspA)的基因在某些部分含有空肠弯曲菌特异性SNP,而在其他部分含有空肠弯曲菌特异性SNP,这表明这些是含有空肠弯曲菌衍生片段的杂交基因。对空肠弯曲菌7474中的ung突变体进行分析表明,该群集II型菌株假定的杂交ung是有功能的。我们的数据表明发生了重组事件,导致在空肠弯曲菌群集II型菌株的cydA和aspA之间的区域中,有空肠弯曲菌的DNA基因组输入。