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Diverse Geno- and Phenotypes of Persistent Listeria monocytogenes Isolates from Fermented Meat Sausage Production Facilities in Portugal

机译:葡萄牙发酵肉香肠生产设施中持久性单核细胞增生李斯特菌基因组和表型的多样性

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The persistence of Listeria monocytogenes in food-associated environments represents a key factor in transmission of this pathogen. To identify persistent and transient strains associated with production of fermented meat sausages in northern Portugal, 1,723 L. monocytogenes isolates from raw material and finished products from 11 processors were initially characterized by random amplification of polymorphic DNA (RAPD), PCR-based molecular serotyping, and epidemic clone characterization, as well as cadmium, arsenic, and tetracycline resistance typing. Pulsed-field gel electrophoresis (PFGE) typing of 240 representative isolates provided evidence for persistence of L. monocytogenes for periods of time ranging from 10 to 32 months for all seven processors for which isolates from different production dates were available. Among 50 L. monocytogenes isolates that included one representative for each PFGE pattern obtained from a given sample, 12 isolates showed reduced invasion efficiency in Caco-2 cells, including 8 isolates with premature stop codons in inlA . Among 41 isolates representing sporadic and persistent PFGE types, 22 isolates represented lysogens. Neither strains with reduced invasion nor lysogens were overrepresented among persistent isolates. While the susceptibility of isolates to lysogenic phages also did not correlate with persistence, it appeared to be associated with molecular serotype. Our data show the following. (i) RAPD may not be suitable for analysis of large sets of L. monocytogenes isolates. (ii) While a large diversity of L. monocytogenes subtypes is found in Portuguese fermented meat sausages, persistence of L. monocytogenes in this food chain is common. (iii) Persistent L. monocytogenes strains are diverse and do not appear to be characterized by unique genetic or phenotypic characteristics.
机译:与食物相关的环境中单核细胞增生李斯特菌的持续存在是该病原体传播的关键因素。为了确定葡萄牙北部地区与发酵肉香肠生产相关的持久性和暂时性菌株,最初对11个加工者的原料和成品中的1,723株单核细胞增生李斯特菌进行了分离,首先通过随机扩增多态性DNA(RAPD),基于PCR的分子血清分型法进行了表征,和流行性克隆特征以及镉,砷和四环素抗性分型。脉冲场凝胶电泳(PFGE)类型的240个代表性分离株为单核细胞增生李斯特氏菌持续存在的证据提供了对所有7个加工者的10到32个月不等的分离时间,这些分离株可用于不同生产日期的分离株。在50种单核细胞增生李斯特氏菌分离株中,包括从给定样品中获得的每种PFGE模式的一个代表,其中12种分离株在Caco-2细胞中的侵袭效率降低,其中包括8种在inlA中具有终止密码子的分离株。在代表散发性和持久性PFGE类型的41个分离株中,有22个分离株代表溶原菌。在持久性分离株中,侵袭性降低的菌株和溶原原均未过量表达。尽管分离株对溶原性噬菌体的敏感性也与持久性无关,但似乎与分子血清型有关。我们的数据显示以下内容。 (i)RAPD可能不适用于分析大量单核细胞增生李斯特菌分离株。 (ii)虽然在葡萄牙发酵的肉香肠中发现了单核细胞增生李斯特菌亚型的多样性,但在此食物链中持续存在单核细胞增生李斯特菌是很普遍的。 (iii)持久性单核细胞增生李斯特氏菌菌株多种多样,似乎没有独特的遗传或表型特征。

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