Register Karen B, Nicholson Tracy L, Brunelle Brian W
Ruminant Diseases and Immunology Research Unit, USDA/Agricultural Research Service/National Animal Disease Center, 1920 Dayton Avenue, Ames, IA 50010, United States.
Virus and Prion Research Unit, USDA/Agricultural Research Service/National Animal Disease Center, 1920 Dayton Avenue, Ames, IA 50010, United States.
J Microbiol Methods. 2016 Oct;129:117-126. doi: 10.1016/j.mimet.2016.08.008. Epub 2016 Aug 16.
PvuII ribotyping and MLST are each highly discriminatory methods for genotyping Bordetella bronchiseptica, but a direct comparison between these approaches has not been undertaken. The goal of this study was to directly compare the discriminatory power of PvuII ribotyping and MLST, using a single set of geographically and genetically diverse strains, and to determine whether subtyping based on repeat region sequences of the pertactin gene (prn) provides additional resolution. One hundred twenty-two isolates were analyzed, representing 11 mammalian or avian hosts, sourced from the United States, Europe, Israel and Australia. Thirty-two ribotype patterns were identified; one isolate could not be typed. In comparison, all isolates were typeable by MLST and a total of 30 sequence types was identified. An analysis based on Simpson's Index of Diversity (SID) revealed that ribotyping and MLST are nearly equally discriminatory, with SIDs of 0.920 for ribotyping and 0.919 for MLST. Nonetheless, for ten ribotypes and eight MLST sequence types, the alternative method discriminates among isolates that otherwise type identically. Pairing prn repeat region typing with ribotyping yielded 54 genotypes and increased the SID to 0.954. Repeat region typing combined with MLST resulted in 47 genotypes and an SID of 0.944. Given the technical and practical advantages of MLST over ribotyping, and the nominal difference in their SIDs, we conclude MLST is the preferred primary typing tool. We recommend the combination of MLST and prn repeat region typing as a high-resolution, objective and standardized approach valuable for investigating the population structure and epidemiology of B. bronchiseptica.
PvuII核糖体分型和多位点序列分型(MLST)都是对支气管败血波氏杆菌进行基因分型的高分辨率方法,但尚未对这两种方法进行直接比较。本研究的目的是使用一组地理和基因上具有多样性的菌株,直接比较PvuII核糖体分型和MLST的分辨能力,并确定基于百日咳杆菌粘附素基因(prn)重复区域序列的亚型分型是否能提供额外的分辨率。分析了122株分离株,它们代表11种哺乳动物或禽类宿主,来源地包括美国、欧洲、以色列和澳大利亚。共鉴定出32种核糖体分型模式;有1株分离株无法分型。相比之下,所有分离株都能用MLST分型,共鉴定出30种序列类型。基于辛普森多样性指数(SID)的分析表明,核糖体分型和MLST的分辨能力几乎相同,核糖体分型的SID为0.920,MLST的SID为0.919。尽管如此,对于10种核糖体分型和8种MLST序列类型,另一种方法能区分原本分型相同的分离株。将prn重复区域分型与核糖体分型相结合产生了54种基因型,SID提高到0.954。重复区域分型与MLST相结合产生了47种基因型,SID为0.944。鉴于MLST相对于核糖体分型在技术和实际应用方面的优势,以及它们的SID的名义差异,我们得出结论,MLST是首选的主要分型工具。我们建议将MLST和prn重复区域分型相结合,作为一种高分辨率、客观且标准化的方法,对研究支气管败血波氏杆菌的种群结构和流行病学具有重要价值。