Molecular Epidemiology of Nontyphoidal Salmonella in Poultry and Poultry Products in India: Implications for Human Health

被引:36
|
作者
Saravanan, Sellappan [1 ]
Purushothaman, Venketaraman [2 ]
Murthy, Thippichettypalayam Ramasamy Gopala Krishna [1 ]
Sukumar, Kuppannan [3 ]
Srinivasan, Palani [1 ]
Gowthaman, Vasudevan [1 ]
Balusamy, Mohan [1 ]
Atterbury, Robert [4 ]
Kuchipudi, Suresh V. [4 ]
机构
[1] Tamil Nadu Vet & Anim Sci Univ, Poultry Dis Diag & Surveillance Lab, Namakkal 637002, Tamil Nadu, India
[2] Tamil Nadu Vet & Anim Sci Univ, Ctr Anim Hlth Studies, Madhavarum Milk Colony, Chennai 6000051, Tamil Nadu, India
[3] Tamil Nadu Vet & Anim Sci Univ, Dept Vet Microbiol, Vet Coll & Res Inst, Namakkal 637002, Tamil Nadu, India
[4] Univ Nottingham, Sch Vet Med & Sci, Loughborough LE12 5RD, Leics, England
关键词
Isolation; Identification; NTS; Zoonotic Salmonella; Genetic diversity; Poultry products; India; FIELD GEL-ELECTROPHORESIS; TANDEM REPEAT ANALYSIS; GENETIC DIVERSITY; ENTERITIDIS; IDENTIFICATION; INFECTION; RESISTANCE; GALLINARUM; SEQUENCE; RFBS;
D O I
10.1007/s12088-015-0530-z
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
Human infections with non-typhoidal Salmonella (NTS) serovars are increasingly becoming a threat to human health globally. While all motile Salmonellae have zoonotic potential, Salmonella Enteritidis and Salmonella Typhimurium are most commonly associated with human disease, for which poultry are a major source. Despite the increasing number of human NTS infections, the epidemiology of NTS in poultry in India has not been fully understood. Hence, as a first step, we carried out epidemiological analysis to establish the incidence of NTS in poultry to evaluate the risk to human health. A total of 1215 samples (including poultry meat, tissues, egg and environmental samples) were collected from 154 commercial layer farms from southern India and screened for NTS. Following identification by cultural and biochemical methods, Salmonella isolates were further characterized by multiplex PCR, allele-specific PCR, enterobacterial repetitive intergenic consensus (ERIC) PCR and pulse field gel electrophoresis (PFGE). In the present study, 21/1215 (1.73 %) samples tested positive for NTS. We found 12/392 (3.06 %) of tissue samples, 7/460 (1.52 %) of poultry products, and 2/363 (0.55 %) of environmental samples tested positive for NTS. All the Salmonella isolates were resistant to oxytetracycline, which is routinely used as poultry feed additive. The multiplex PCR results allowed 16/21 isolates to be classified as S. Typhimurium, and five isolates as S. Enteritidis. Of the five S. Enteritidis isolates, four were identified as group D Salmonella by allele-specific PCR. All of the isolates produced different banding patterns in ERIC PCR. Of the thirteen macro restriction profiles (MRPs) obtained by PFGE, MRP 6 was predominant which included 6 (21 %) isolates. In conclusion, the findings of the study revealed higher incidence of contamination of NTS Salmonella in poultry tissue and animal protein sources used for poultry. The results of the study warrants further investigation on different type of animal feed sources, food market chains, processing plants, live bird markets etc., to evaluate the risk factors, transmission and effective control measures of human Salmonella infection from poultry products.
引用
收藏
页码:319 / 326
页数:8
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