Bottari Benedetta, Felis Giovanna E, Salvetti Elisa, Castioni Anna, Campedelli Ilenia, Torriani Sandra, Bernini Valentina, Gatti Monica
Department of Food and Drug Science, University of Parma, Viale delle Scienze 49/A, 43124 Parma, Italy.
Multidisciplinary Interdepartmental Dairy Center - MILC, University of Parma, Parma, Italy.
Microbiology (Reading). 2017 Jul;163(7):950-960. doi: 10.1099/mic.0.000497. Epub 2017 Jul 21.
Lactobacillus casei,Lactobacillus paracasei and Lactobacillusrhamnosus form a closely related taxonomic group (the L. casei group) within the facultatively heterofermentative lactobacilli. Strains of these species have been used for a long time as probiotics in a wide range of products, and they represent the dominant species of nonstarter lactic acid bacteria in ripened cheeses, where they contribute to flavour development. The close genetic relationship among those species, as well as the similarity of biochemical properties of the strains, hinders the development of an adequate selective method to identify these bacteria. Despite this being a hot topic, as demonstrated by the large amount of literature about it, the results of different proposed identification methods are often ambiguous and unsatisfactory. The aim of this study was to develop a more robust species-specific identification assay for differentiating the species of the L. casei group. A taxonomy-driven comparative genomic analysis was carried out to select the potential target genes whose similarity could better reflect genome-wide diversity. The gene mutL appeared to be the most promising one and, therefore, a novel species-specific multiplex PCR assay was developed to rapidly and effectively distinguish L. casei, L. paracasei and L. rhamnosus strains. The analysis of a collection of 76 wild dairy isolates, previously identified as members of the L. casei group combining the results of multiple approaches, revealed that the novel designed primers, especially in combination with already existing ones, were able to improve the discrimination power at the species level and reveal previously undiscovered intraspecific biodiversity.
干酪乳杆菌、副干酪乳杆菌和鼠李糖乳杆菌在兼性异源发酵乳杆菌中形成了一个密切相关的分类群(干酪乳杆菌群)。这些菌种的菌株长期以来一直作为益生菌用于多种产品中,并且它们是成熟奶酪中非发酵剂乳酸菌的优势菌种,对风味的形成有贡献。这些菌种之间密切的遗传关系以及菌株生化特性的相似性,阻碍了开发一种合适的选择性方法来鉴定这些细菌。尽管这是一个热门话题,大量相关文献也证明了这一点,但不同的鉴定方法所得结果往往不明确且不尽人意。本研究的目的是开发一种更可靠的种特异性鉴定方法,以区分干酪乳杆菌群的各个菌种。进行了一项基于分类学的比较基因组分析,以选择其相似性能够更好地反映全基因组多样性的潜在靶基因。mutL基因似乎是最有前景的一个,因此,开发了一种新的种特异性多重PCR方法,以快速有效地区分干酪乳杆菌、副干酪乳杆菌和鼠李糖乳杆菌菌株。对76株野生乳制品分离株进行分析,这些分离株先前结合多种方法的结果被鉴定为干酪乳杆菌群的成员,结果表明,新设计的引物,特别是与现有引物结合使用时,能够提高在种水平上的鉴别能力,并揭示以前未发现的种内生物多样性。