Occurrence and molecular characterization of Salmonella Typhimurium and Salmonella Enteritidis isolates from contaminated food samples from Palestine

被引:0
|
作者
Adwan, G. [1 ,5 ]
Abuseir, S. [2 ,6 ]
Khreishi, O. [3 ]
Hussein, A. [4 ]
Khraim, N. [2 ]
Al-Daym, M. Abed [2 ]
机构
[1] An Najah Natl Univ, Dept Biol & Biotechnol, Mol Microbiol Virol, Nablus, Palestine
[2] An Najah Natl Univ, Fac Agr & Vet Med, Dept Vet Med, Nablus, Palestine
[3] Minist Agr, Qalqilya Vet Serv & Anim Hlth Directorate, Nablus St, Qalqilya, Palestine
[4] An Najah Natl Univ, Fac Med & Hlth Sci, Med Lab Sci Dept, Nablus, Palestine
[5] An Najah Natl Univ, Dept Biol & Biotechnol, Mol Microbiol Virol, POB 7, Nablus, West Bank, Palestine
[6] An Najah Natl Univ, Fac Agr & Vet Med, Dept Vet Med, POB 7, Nablus, West Bank, Palestine
来源
关键词
foodborne pathogens; Salmonella Typhimurium; Salmonella Enteritidis; molecular characterization; Pal-estine; VIRULENCE-ASSOCIATED GENES; ANTIMICROBIAL RESISTANCE; PREVALENCE; ENTERICA; SEROVARS; CHICKEN; PCR; EPIDEMIOLOGY; DIVERSITY; SOUTH;
D O I
10.12681/jhvms.31088
中图分类号
S85 [动物医学(兽医学)];
学科分类号
0906 ;
摘要
Salmonella is one of the most frequently isolated foodborne pathogens. It is of major public health concern worldwide. Poultry meat and eggs represent important sources of Salmonellae organisms with an impact on consumers' health. This study aims to evaluate the occurrence of Salmonella Typhimurium and Salmonella Enteritidis using multiplex PCR (mPCR) among isolates collected from samples of the local food market and to assess genetic relationships between isolates of S. Typhimurium, which was the only serotype isolated from the tested food samples. This was achieved using virulence factors profiling and fingerprint profiling, which were assessed by random amplified polymorphic DNA (RAPD-PCR) and repetitive sequence PCR (REP-PCR). Both enterobacterial repetitive intergenic consensus (ERIC-PCR) and interspersed repetitive DNA sequence BOXAIR-PCR were used for this purpose.The overall occurrence percentage of S. Typhimurium and S. Enteritidis out of 51 isolates was 54.9% and 0.0%, respec-tively. Only 13 out of 17 virulence genes were detected in these isolates. The occurrence of the detected virulence genes among these isolates was 100%, 50.0%,46.4%, 39.3%, 35.7%, 35.7%, 32.1%, 25.0%, 25.0%, 17.6%, 14.3%, 14.3%, 3.6% for invA, sopB, prgH, sitC, pefA, tolC, cdtB, msgA, sifA, iroN, spiA, ipfC and pagC, respectively. The remaining virulence genes were absent in all of the isolates. Based on the combination of the presence and absence of virulence genes, eight profiles were detected among these isolates, the most common genetic profile was V5 (each 32.1%). Based on this genetic profile at cut-off point 96.0%, both ERIC and BOX primers allowed for discrimination into 4 and 6 clus-ters or clones of 16 S. Typhimurium isolates, respectively. Results of PCR typing methods showed that, three strains clustered together using both ERIC-PCR and BOX-PCR typing methods and they had the same virulotype (V1), while other four strains also clustered together by both typing methods and had the same virulotype (V4).Contamination of food with Salmonellae, especially with S. Typhimurium, was high and affected the microbiological quality of food. This emphasizes the need for rigorous public health and food safety control methods to lower the hu-man health hazard and risk associated with Salmonellae infection.
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收藏
页码:6201 / 6212
页数:13
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