Deveau Hélène, Labrie Simon J, Chopin Marie-Christine, Moineau Sylvain
Groupe de Recherche en Ecologie Buccale (GREB), Faculté de Médecine Dentaire, Université Laval, Quebec City, Quebec, Canada G1K 7P4.
Appl Environ Microbiol. 2006 Jun;72(6):4338-46. doi: 10.1128/AEM.02517-05.
For this study, an in-depth review of the classification of Lactococcus lactis phages was performed. Reference phages as well as unclassified phages from international collections were analyzed by stringent DNA-DNA hybridization studies, electron microscopy observations, and sequence analyses. A new classification scheme for lactococcal phages is proposed that reduces the current 12 groups to 8. However, two new phages (Q54 and 1706), which are unrelated to known lactococcal phages, may belong to new emerging groups. The multiplex PCR method currently used for the rapid identification of phages from the three main lactococcal groups (936, c2, and P335) was improved and tested against the other groups, none of which gave a PCR product, confirming the specificity of this detection tool. However, this method does not detect all members of the highly diverse P335 group. The lactococcal phages characterized here were deposited in the Félix d'Hérelle Reference Center for Bacterial Viruses and represent a highly diverse viral community from the dairy environment.
在本研究中,对乳酸乳球菌噬菌体的分类进行了深入综述。通过严格的DNA-DNA杂交研究、电子显微镜观察和序列分析,对来自国际菌种保藏中心的参考噬菌体以及未分类的噬菌体进行了分析。提出了一种新的乳酸乳球菌噬菌体分类方案,该方案将目前的12个组减少到8个。然而,两种与已知乳酸乳球菌噬菌体无关的新噬菌体(Q54和1706)可能属于新出现的组。目前用于快速鉴定来自三个主要乳酸乳球菌组(936、c2和P335)噬菌体的多重PCR方法得到了改进,并针对其他组进行了测试,这些组均未产生PCR产物,证实了该检测工具的特异性。然而,该方法不能检测高度多样化的P335组的所有成员。这里鉴定的乳酸乳球菌噬菌体保藏于费利克斯·德赫雷尔细菌病毒参考中心,代表了来自乳制品环境的高度多样化的病毒群落。