Jiménez-Velásquez S, Pacheco-Montealegre M E, Torres-Higuera L, Uribe-Gutiérrez L, Burbano-David D, Dávila-Mora L L, Renjifo-Ibáñez C, Caro-Quintero A
Livestock Microbiology Laboratory, Tibaitatá Research Center, Corporación Colombiana de Investigación Agropecuaria (AGROSAVIA), Km 14 vía Bogotá a Mosquera, Cundinamarca, Colombia.
Departamento de Biología, Facultad de Ciencias, Max Planck Tandem Group in Holobionts, Universidad Nacional de Colombia, Bogotá, Colombia.
World J Microbiol Biotechnol. 2024 Oct 3;40(11):333. doi: 10.1007/s11274-024-04121-9.
The Staphylococcus genus comprises multiple pathogenic and opportunistic species that represent a risk to public health. Epidemiological studies require accurate taxonomic classification of isolates with enough resolution to distinguish clonal complexes. Unfortunately, 16 S rRNA molecular analysis and phenotypic characterization cannot distinguish all species and do not offer enough resolution to assess intraspecific diversity. Other approaches, such as Multilocus Sequence Tagging, provide higher resolution; however, they have been developed for Staphylococcus aureus and a few other species. Here, we developed a set of genus-targeted primers using five orthologous genes (pta, tuf, tpi, groEs, and sarA) to identify all Staphylococcus species within the genus. The primers were initially evaluated using 20 strains from the Collection of Microorganisms of Interest in Animal Health from AGROSAVIA (CMISA), and their amplified sequences were compared to a set of 33 Staphylococcus species. This allowed the taxonomic identification of the strains even on close species and the establishment of intraspecies diversity. To enhance the scope and cost-effectiveness of the proposed strategy, we customized the primer sets for an Illumina paired-end amplicon protocol, enabling gene multiplexing. We assessed five genes across 177 strains, generating 880 paired-end libraries from the CMISA. This approach significantly reduced sequencing costs, as all libraries can be efficiently sequenced in a single MiSeq run at a fraction (one-fourth or less) of the cost associated with Sanger sequencing. In summary, this method can be used for precise identification and diversity analysis of Staphylococcus species, offering an advancement over traditional techniques in both resolution and cost-effectiveness.
葡萄球菌属包含多种致病性和机会性物种,对公众健康构成风险。流行病学研究需要对分离株进行准确的分类,分辨率要足够高,以区分克隆复合体。不幸的是,16S rRNA分子分析和表型特征无法区分所有物种,也没有提供足够的分辨率来评估种内多样性。其他方法,如多位点序列标签法,提供了更高的分辨率;然而,它们是针对金黄色葡萄球菌和其他少数物种开发的。在这里,我们使用五个直系同源基因(pta、tuf、tpi、groEs和sarA)开发了一组针对属的引物,以鉴定葡萄球菌属内的所有葡萄球菌物种。这些引物最初使用来自AGROSAVIA动物健康感兴趣微生物收藏库(CMISA)的20个菌株进行评估,并将其扩增序列与一组33种葡萄球菌进行比较。这使得即使是亲缘关系较近的物种的菌株也能进行分类鉴定,并建立种内多样性。为了扩大所提出策略的范围和成本效益,我们为Illumina双端扩增子方案定制了引物集,实现了基因多重化。我们对177个菌株的五个基因进行了评估,从CMISA生成了880个双端文库。这种方法显著降低了测序成本,因为所有文库都可以在一次MiSeq运行中高效测序,成本仅为桑格测序的一小部分(四分之一或更低)。总之,这种方法可用于葡萄球菌物种的精确鉴定和多样性分析,在分辨率和成本效益方面都比传统技术有所进步。