Giebel Katharina, Green Laura E, Purdy Kevin J
School of Life Sciences, University of Warwick, Coventry, United Kingdom.
School of Agriculture, Food and the Environment, Royal Agricultural University, Gloucestershire, United Kingdom.
Front Vet Sci. 2020 Dec 2;7:581342. doi: 10.3389/fvets.2020.581342. eCollection 2020.
is the essential pathogen in ovine footrot, an important cause of lameness in sheep that reduces productivity and welfare. The aim of this study was to investigate the feasibility of using multiple locus variable number tandem repeat analysis (MLVA) developed to investigate isolates to understand the molecular epidemiology of in ovine footrot by investigation of communities of strains. MLVA sensitivity was improved by optimizing PCR conditions to 100% specificity for . The improved MLVA scheme was used to investigate non-cultured DNA purified from swabs (swab DNA) and cultured DNA from isolates (isolate DNA) from 152 foot and 38 gingival swab samples from 10 sheep sampled on four occasions in a longitudinal study. Isolate DNA was obtained from 6/152 (3.9%) feet and 5/6 yielded complete MLVA profiles, three strains were detected. Two of the three isolate strains were also detected in isolate DNA from 2 gingival crevice cultures. Complete MLVA profiles were obtained from swab DNA from 39 (25.7%) feet. There were 22 community types that were comprised of 7 single strain and 15 multi-strain communities. Six community types were detected more than once and three of these were detected on the same four sheep and the same two feet over time. There were a minimum of 17 and a maximum of 25 strain types of in the study. The three isolate strain types were also the most frequently detected strain types in swab DNA. We conclude that the MLVA from swab DNA detects the same strains as culture, is much more sensitive and can be used to describe and differentiate communities and strains on sheep, feet and over time. It is therefore a sensitive molecular tool to study strains directly from DNA without culture.
是绵羊蹄腐病的主要病原体,绵羊蹄腐病是导致绵羊跛足的一个重要原因,会降低生产力并影响羊的健康状况。本研究的目的是调查使用多基因座可变数目串联重复序列分析(MLVA)来研究分离株的可行性,通过对菌株群落的调查来了解绵羊蹄腐病中该病原体的分子流行病学。通过优化PCR条件提高了MLVA的灵敏度,使其对该病原体的特异性达到100%。在一项纵向研究中,对10只绵羊在四个时间点采集的152份足部拭子和38份牙龈拭子样本进行了检测,使用改进后的MLVA方案研究了从拭子中纯化的未培养DNA(拭子DNA)和分离株的培养DNA(分离株DNA)。从6/152(3.9%)只足部获得了分离株DNA,其中5/6产生了完整的MLVA图谱,检测到了三个菌株。在来自2份牙龈沟培养物的分离株DNA中也检测到了这三个分离株中的两个。从39(25.7%)只足部的拭子DNA中获得了完整的MLVA图谱。有22种该病原体群落类型,包括7个单菌株群落和15个多菌株群落。检测到6种群落类型不止一次,其中三种在同一四只绵羊和同一两只足部随时间被检测到。研究中该病原体的菌株类型最少有17种,最多有25种。这三种分离株菌株类型也是拭子DNA中最常检测到的菌株类型。我们得出结论,从拭子DNA进行的MLVA检测到的菌株与培养法相同,灵敏度更高,可用于描述和区分绵羊、足部以及不同时间的群落和菌株。因此,它是一种无需培养即可直接从DNA研究该病原体菌株的灵敏分子工具。