首页> 外文会议>2012 IEEE Symposium on Humanities, Science and Engineering Research >Random amplified polymorphism DNA profile of Listeria monocytogenes from raw and ready-to-eat foods in Malaysia
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Random amplified polymorphism DNA profile of Listeria monocytogenes from raw and ready-to-eat foods in Malaysia

机译:马来西亚生和即食食品中李斯特菌李斯特菌的随机扩增多态性DNA谱

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Listeria monocytogenes subtyping is important in food processing environment or in epidemiological studies in order to identify the contamination sources and spreading routes, and to investigate the food-borne outbreaks. This study employs the combination of serotyping and random amplified polymorphism DNA (RAPD) analysis methods to characterize the isolated L. monocytogenes strains in food samples from local markets. Listeria antisera kit was used in serotyping which grouped L. monocytogenes isolates based on the expression of somatic and flagellar antigens. The L. monocytogenes serovars were further classified into RAPD types based on polymorphic banding patterns generated by using 10 random RAPD primers. The 23 isolated strains were divided into four different serotypes consisting 4b (43.5%), 1/2b (34.8%), 4d (8.70%) and 4e (4.35%) with two untypable isolates (8.70%). 11 banding patterns were obtained from each selected primer, OPA10 and OPA14 with DNA fragments ranging from approximately 0.15 kb to 1.1 kb. The constructed dendograms showed similarity percentage of 4% to 100% for OPA10, 12% to 100% for OPA14 and 4% to 100% for combination of primers. At a comparative genetic similarity of more than 90%, 21 distinguish RAPD profiles were obtained. The discriminatory of RAPD analysis method was proven as it could distinguish the isolates from the same serovar. However, between the two primers used, OPA14 provide better discriminatory results than OPA10 although it failed to type one isolate. These findings suggest that the application of RAPD analysis could be a useful tool in characterization of L. monocytogenes isolated from foods as it may provide important information on cross-contamination potential sites. Thus, the microbial monitoring should be applied and continuously performed in order to control listeriosis infection. The data may be useful for the food producers or epidemiological and public health studies of Listeria spp.
机译:单核细胞增生李斯特菌亚型在食品加工环境或流行病学研究中很重要,以便识别污染源和传播途径,并调查食源性暴发。这项研究结合了血清分型和随机扩增多态性DNA(RAPD)分析方法来表征本地市场食品样本中分离出的单核细胞增生李斯特菌。使用李斯特菌抗血清试剂盒进行血清分型,根据体细胞和鞭毛抗原的表达将单核细胞增生李斯特氏菌分离株分组。根据使用10条随机RAPD引物产生的多态性条带模式,将单核细胞增生李斯特氏菌血清型进一步分为RAPD类型。将这23株分离出的菌株分为4种不同的血清型,分别是4b(43.5%),1 / 2b(34.8%),4d(8.70%)和4e(4.35%),其中有两个无法分离的菌株(8.70%)。从每个选择的引物OPA10和OPA14获得11种条带模式,DNA片段的范围约为0.15 kb至1.1 kb。构建的树状图显示,OPA10的相似百分比为4%至100%,OPA14的相似百分比为12%至100%,引物组合的相似百分比为4%至100%。在超过90%的比较遗传相似性下,获得了21种不同的RAPD图谱。证明了RAPD分析方法的差异性,因为它可以区分来自同一血清型的分离株。但是,在使用的两种引物之间,OPA14的鉴定结果优于OPA10,尽管它不能鉴定出一种分离株。这些发现表明,RAPD分析的应用可能是表征从食品中分离出的单核细胞增生李斯特菌的有用工具,因为它可能提供有关交叉污染潜在位点的重要信息。因此,为了控制李斯特菌病的感染,应进行微生物监测并连续进行。该数据可能对食品生产者或李斯特菌属的流行病学和公共卫生研究有用。

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