Kabuki D Y, Kuaye A Y, Wiedmann M, Boor K J
Department of Food Science, Cornell University, Ithaca, NY 14853, USA.
J Dairy Sci. 2004 Sep;87(9):2803-12. doi: 10.3168/jds.S0022-0302(04)73408-6.
Latin-style fresh cheeses, which have been linked to at least 2 human listeriosis outbreaks in the United States, are considered to be high-risk foods for Listeria monocytogenes contamination. We evaluated L. monocytogenes contamination patterns in 3 Latin-style fresh-cheese processing plants to gain a better understanding of L. monocytogenes contamination sources in the manufacture of these cheeses. Over a 6-mo period, 246 environmental samples were collected and analyzed for L. monocytogenes using both the Food and Drug Administration (FDA) method and the Biosynth L. monocytogenes detection system (LMDS). Finished cheese samples from the same plants (n = 111) were also analyzed by the FDA method, which was modified to include L. monocytogenes plating medium (LMPM) and the L. monocytogenes confirmatory plating medium (LMCM) used in the LMDS method. Listeria monocytogenes was detected in 6.3% of cheese and 11.0% of environmental samples. Crates, drains, and floor samples showed the highest contamination rates, with 55.6, 30.0, and 20.6% L. monocytogenes positive samples, respectively. Finished products and food contact surfaces were positive in only one plant. The FDA method showed a higher sensitivity than the LMDS method for detection of L. monocytogenes from environmental samples. The addition of LMPM and LMCM media did not further enhance the performance of the FDA method for L. monocytogenes detection from finished products. Molecular subtyping (PCR-based allelic analysis of the virulence genes actA and hly and automated ribotyping) was used to track contamination patterns. Ribotype DUP-1044A, which had previously been linked to a 1998 multistate human listeriosis outbreak in the United States, was the most commonly identified subtype (20/36 isolates) and was isolated from 2 plants. This ribotype was persistent and widespread in one factory, where it was also responsible for the contamination of finished products. We hypothesize that this ribotype may represent a clonal group with a specific ability to persist in food processing environments. While previous listeriosis outbreaks were linked to Latin-style fresh cheeses made from unpasteurized milk, the presence of this organism in pasteurized cheese products illustrates that persistent environmental contamination also represents an important source of finished product contamination.
拉丁风味的新鲜奶酪在美国已与至少两起人类李斯特菌病疫情相关联,被认为是易受单核细胞增生李斯特菌污染的高风险食品。我们评估了3家拉丁风味新鲜奶酪加工厂中单核细胞增生李斯特菌的污染模式,以便更好地了解这些奶酪生产过程中单核细胞增生李斯特菌的污染源。在6个月的时间里,共采集了246份环境样本,并使用美国食品药品监督管理局(FDA)的方法和Biosynth单核细胞增生李斯特菌检测系统(LMDS)对样本中的单核细胞增生李斯特菌进行分析。同时,还采用FDA方法对来自相同工厂的111份成品奶酪样本进行分析,该方法进行了改进,加入了LMDS方法中使用的单核细胞增生李斯特菌平板计数培养基(LMPM)和单核细胞增生李斯特菌确证平板计数培养基(LMCM)。在奶酪样本中,单核细胞增生李斯特菌的检出率为6.3%,环境样本中的检出率为11.0%。板条箱、排水口和地面样本的污染率最高,单核细胞增生李斯特菌阳性样本分别占55.6%、30.0%和20.6%。仅在一家工厂的成品和食品接触表面检测到阳性结果。对于环境样本中单核细胞增生李斯特菌的检测,FDA方法显示出比LMDS方法更高的灵敏度。在检测成品中的单核细胞增生李斯特菌时,加入LMPM和LMCM培养基并未进一步提高FDA方法的性能。采用分子分型方法(基于毒力基因actA和hly的PCR等位基因分析以及自动核糖体分型)来追踪污染模式。核糖体分型DUP-1044A是最常见的亚型(36株分离株中有20株),此前曾与1998年美国多州的人类李斯特菌病疫情相关联,并且在2家工厂中均有分离。这种核糖体分型在一家工厂中持续存在且分布广泛,也是造成成品污染的原因。我们推测,这种核糖体分型可能代表了一个在食品加工环境中具有特定生存能力的克隆群体。虽然之前的李斯特菌病疫情与用未杀菌牛奶制成的拉丁风味新鲜奶酪有关,但这种病菌在杀菌奶酪产品中的存在表明,持续的环境污染也是成品污染的一个重要来源。