Yaya Aboubakar, Manso-Silván Lucía, Blanchard Alain, Thiaucourt François
CIRAD UPR15 Control of animal diseases, OIE & FAO reference laboratory for CBPP, Montpellier, France - LANAVET, Laboratoire national vétérinaire, Garoua, Cameroon.
Vet Res. 2008 Mar-Apr;39(2):14. doi: 10.1051/vetres:2007052. Epub 2008 Jan 29.
Mycoplasma mycoides subsp. mycoides SC (MmmSC) is the etiological agent of contagious bovine pleuropneumonia (CBPP). Although eradicated in most developed countries, the disease reappeared in Europe in the 1990s. This reappearance may have been caused either by importation from sub-Saharan Africa, where CBPP is still endemic, or by the reemergence of virulent strains in Europe, as suggested by earlier studies. A multilocus sequence analysis scheme has been developed to address this issue and, most importantly, to be able to monitor new epidemics. The alignment of the full genome sequence of the reference strain PG1 and the partial genome sequence of a pathogenic strain allowed the identification of polymorphic sites. Nineteen initial loci were selected within housekeeping genes, genes of unknown function and non coding sequences. The suitability of these loci for genotyping MmmSC strains was first tested on six strains of diverse geographic origin. The analyses showed that the published PG1 sequence contained a number of specific polymorphisms that were therefore of no use for molecular typing. Among the eight informative polymorphic loci finally selected, only one (ftsY) was positioned within a housekeeping gene. Three main groups and 31 different allelic profiles were identified among 51 strains and strain variants examined. Cluster analysis confirmed that European strains from the 1990s did not originate from Africa. It also showed a genetic link between a European strain isolated in 1967 and those found in southern Africa and Australia. This was in agreement with historical data showing that CBPP was introduced in these regions during colonisation in the 19th century.
丝状支原体丝状亚种小菌落型(MmmSC)是牛传染性胸膜肺炎(CBPP)的病原体。尽管在大多数发达国家已被根除,但该疾病在20世纪90年代在欧洲再度出现。这种再度出现可能是由于从撒哈拉以南非洲进口所致,在那里CBPP仍然流行,或者如早期研究所表明的,是由于欧洲有毒力菌株的重新出现。已开发出一种多位点序列分析方案来解决这个问题,最重要的是能够监测新的疫情。参考菌株PG1的全基因组序列与一株致病菌株的部分基因组序列的比对使得能够鉴定多态性位点。在管家基因、功能未知的基因和非编码序列中选择了19个初始位点。首先在6株地理来源不同的菌株上测试了这些位点对MmmSC菌株基因分型的适用性。分析表明,已发表的PG1序列包含许多特定的多态性,因此对分子分型没有用处。在最终选择的8个信息性多态性位点中,只有一个(ftsY)位于管家基因内。在检查的51株菌株和菌株变体中鉴定出3个主要组和31种不同的等位基因谱。聚类分析证实,20世纪90年代的欧洲菌株并非源自非洲。它还显示出1967年分离的一株欧洲菌株与在南部非洲和澳大利亚发现的菌株之间存在遗传联系。这与历史数据一致,历史数据表明CBPP在19世纪殖民期间被引入这些地区。