Genetic Analysis of the Cronobacter sakazakii O4 to O7 O-Antigen Gene Clusters and Development of a PCR Assay for Identification of All C. sakazakii O Serotypes

被引:57
作者
Sun, Yamin [1 ,2 ,3 ]
Wang, Min [1 ,2 ,3 ]
Wang, Quan [1 ,2 ,3 ]
Cao, Boyang [1 ,2 ,3 ]
He, Xin [1 ,2 ,3 ]
Li, Kun [1 ,2 ,3 ]
Feng, Lu [1 ,2 ,3 ]
Wang, Lei [1 ,2 ,3 ,4 ]
机构
[1] Nankai Univ, Minist Educ, Key Lab Mol Microbiol & Technol, Tianjin 300071, Peoples R China
[2] Nankai Univ, TEDA, TEDA Sch Biol Sci & Biotechnol, Tianjin 300071, Peoples R China
[3] TEDA, Tianjin Key Lab Microbial Funct Gen, Tianjin, Peoples R China
[4] TEDA, Tianjin Biochip Corp, Tianjin, Peoples R China
基金
高等学校博士学科点专项科研基金; 中国国家自然科学基金;
关键词
ENTERICA SEROVAR TYPHIMURIUM; RHAMNOSE SYNTHESIS PATHWAY; ESCHERICHIA-COLI O157; DUBLINENSIS SP-NOV; ENTEROBACTER-SAKAZAKII; SALMONELLA-ENTERICA; FUNCTIONAL-CHARACTERIZATION; SHIGELLA-FLEXNERI; SEQUENCE; LIPOPOLYSACCHARIDE;
D O I
10.1128/AEM.07825-11
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
The Gram-negative bacterium Cronobacter sakazakii is an emerging food-borne pathogen that causes severe invasive infections in neonates. Variation in the O-antigen lipopolysaccharide in the outer membrane provides the basis for Gram-negative bacteria serotyping. The O-antigen serotyping scheme for C. sakazakii, which includes seven serotypes (O1 to O7), has been recently established, and the O-antigen gene clusters and specific primers for three C. sakazakii serotypes (O1, O2, and O3) have been characterized. In this study, the C. sakazakii O4, O5, O6, and O7 O-antigen gene clusters were sequenced, and gene functions were predicted on the basis of homology. C. sakazakii 04 shared a similar O-antigen gene cluster with Escherichia coli O103. The general features and anomalies of all seven C. sakazakii O-antigen gene clusters were evaluated and the relationship between O-antigen structures and their gene clusters were investigated. Serotype-specific genes for O4 to O7 were identified, and a molecular serotyping method for all C. sakazakii O serotypes, a multiplex PCR assay, was developed by screening against 136 strains of C. sakazakii and closely related species. The sensitivity of PCR-based serotyping method was determined to be 0.01 ng of genomic DNA and 10(3) CFU of each strain/ml. This study completes the elucidation of C. sakazakii O-antigen genetics and provides a molecular method suitable for the identification of C. sakazakii O1 to O7 strains.
引用
收藏
页码:3966 / 3974
页数:9
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