Rapid identification of Salmonella enterica serovars Typhi and Salmonella enterica serovars Paratyphi A from chicken meat

被引:0
|
作者
Raharjo, D. [1 ,2 ]
Yulistiani, R. [3 ,4 ]
Setyarini, W. [2 ]
Arizandy, R. Y. [2 ]
Prayoga, W. [5 ]
Shirakawa, T. [6 ]
机构
[1] Airlangga Univ, Fac Vet Med, Vet Publ Hlth Lab, Surabaya 60115, Indonesia
[2] Airlangga Univ, Inst Trop Dis, Gastroenteritis & Salmonellosis Lab, Surabaya 60115, Indonesia
[3] Univ Pembangunan Nas Vet Jawa Timur, Fac Engn, Dept Food Technol, Jalan Rungkut Madya Gunung Anyar, Surabaya 60294, Indonesia
[4] Sebelas Maret Univ UNS, Grad Sch Program, JalanIr Sutami36A, Kentingan 57126, Surakarta, Indonesia
[5] Airlangga Univ, Salmonella Res Ctr, Anim Biosafety, Level 3, Surabaya 60115, Indonesia
[6] Kobe Univ, Grad Sch Sci Technol & Innovat, Kobe, Hyogo, Japan
关键词
PCR;
D O I
10.1088/1757-899X/633/1/012003
中图分类号
TS2 [食品工业];
学科分类号
0832 ;
摘要
Rapid diagnosis of pathogenic bacteria in food is closely related to safety. We modified a Culture-based methods for Salmonella sp. which rapidly identified Salmonella enterica serovars Typhi and Salmonella enterica serovars Paratyphi A from chicken meat samples. The World Health Organization method consists of six steps of the test, sequentially pre-enrichment, selective enrichment, selective diagnostic isolation, pick presumptive Salmonella colonies, biochemical and serological confirmation. Modifications made at three stages of pick presumptive Salmonella colonies, biochemical confirmation and serological confirmation into a single stage of molecular testing to detect genes rfbE and, using tyv and prt primer. In summary, from 120 samples, the modified technique successfully identified 39 (32.5%) Salmonella enterica serovars Typhi and one Salmonella enterica serovars Paratyphi A (0,83%) compare with 13 (10.8%) and negative result with conventional protocol. The modified were faster and more sensitive than conventional techniques.
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页数:5
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