The phenotypic and genotypic characterization of Enterobacter sakazakii strains from infant formula milk

被引:21
|
作者
Ye, Y. [1 ,2 ,3 ]
Wu, Q. [1 ]
Xu, X. [1 ]
Yang, X. [1 ]
Dong, X. [1 ,2 ]
Zhang, J. [1 ]
机构
[1] Guangdong Inst Microbiol, Guangdong Prov Key Lab Microbiol Culture Collect, Guangzhou 510070, Guangdong, Peoples R China
[2] Chinese Acad Sci, S China Sea Inst Oceanol, Guangzhou 510301, Guangdong, Peoples R China
[3] Hefei Univ Technol, Sch Biotechnol & Food Engn, Hefei 230009, Peoples R China
关键词
Enterobacter sakazakii; enterobacterial repetitive intergenic consensus (ERIC)-PCR; random amplified polymorphic DNA (RAPD)-PCR; antibiotic resistance test; DUBLINENSIS SP-NOV; NEONATAL MENINGITIS; GENETIC DIVERSITY; FOOD; PCR; INFECTION; OUTBREAK; PROPOSAL; GENUS; COLI;
D O I
10.3168/jds.2009-2662
中图分类号
S8 [畜牧、 动物医学、狩猎、蚕、蜂];
学科分类号
0905 ;
摘要
Enterobacter sakazakii is an emerging foodborne pathogen associated with severe diseases in neonates. Infant formula milk (IFM) has been identified as one of the major contaminated sources and a transmission vehicle. To determine the phenotypic and genotypic characterization of this pathogen, 22 E. sakazakii strains isolated from IFM by an FDA-recommended method and PCR on the a-glucosidase gene were subtyped by random amplified polymorphic DNA (RAPD)-PCR, enterobacterial repetitive intergenic consensus (ERIC)-PCR, and antibiotic resistance patterns. At a similarity threshold of 80%, 16 ERIC-PCR fingerprint types were identified with a discriminatory power (D) of 0.933, and 18 RAPD-PCR types were identified with D of 0.973. Resistance to 9 antibiotics tested by disk diffusion assay revealed 6 antibiotic resistance patterns with D of 0.749. The comparison of characterization indicated that RAPD-PCR and ERIC-PCR have high discriminatory power showing genetic diversity of E. sakazakii isolates, and ERIC-PCR patterns showed a closer correlation than RAPD-PCR patterns to phenotypic characterization and the brands of IFM. Overall, the ERIC-PCR typing method could be used for tracing sources of E. sakazakii isolates in the food chain.
引用
收藏
页码:2315 / 2320
页数:6
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