Musa Jasini A, O O Bale James, Kazeem Haruna M, Nwankpa Nicholas D, Di Provvido Andrea, Sacchini Flavio, Zilli Katiusia, Abass Anna, Scacchia Massimo, Pini Attilio
Istituto Zooprofilattico Sperimentale dell' Abruzzo e Molise (IZSAM) 'G. Caporale', Via Campo Boario, 64100 Teramo, Italy.
Department of Veterinary Microbiology, Ahmadu Bello University, Zaria, Nigeria.
Int J Vet Sci Med. 2016 Dec 10;4(2):46-53. doi: 10.1016/j.ijvsm.2016.10.007. eCollection 2016 Dec.
Contagious bovine pleuropneumonia (CBPP) is a highly contagious respiratory disease affecting cattle and is widely distributed in the sub-Saharan Africa. The objective of this study was to detect subspecies () the causative agent of CBPP from 90 cattle at slaughter using polymerase chain reaction-Restriction fragment length polymorphism. In this study, 450 samples suggestive of CBPP in Maiduguri, Yola and Gombe township abattoirs were processed according to standard protocols. The isolation rate was found to be 3.33% and percentage of identification with PCR-RFLP yielded 1.56%. Subsequently, QIAxcel revealed molecular size of 574 bp for subcluster. Further analysis of PCR amplicons with restriction digestion, confirmed the presence of 16 S rRNA of CAP 21 genomic region with molecular sizes of 180 bp and 380 bp. Thus, the 380 bp fragments delineated from subsp. . Three isolates (BL5, BL6 and AL1) were from lungs and four from pleural fluids (APF2, APF8A, APF8B and APF9) were isolated and identified, while a vaccine strain T1/44 was re-detected along with the field isolates. No sample from Gombe had . In conclusion, the findings of this study have detected the presence of as causative agent of CBPP. Measures such as surveillance, quarantine and vaccination are hereby recommended for the control of CBPP in Nigeria.
牛传染性胸膜肺炎(CBPP)是一种影响牛的高度传染性呼吸道疾病,广泛分布于撒哈拉以南非洲地区。本研究的目的是使用聚合酶链反应-限制性片段长度多态性技术,从90头屠宰牛中检测牛传染性胸膜肺炎的病原体亚种()。在本研究中,对迈杜古里、约拉和贡贝镇屠宰场的450份疑似CBPP的样本按照标准方案进行处理。分离率为3.33%,PCR-RFLP鉴定百分比为1.56%。随后,QIAxcel显示亚群的分子大小为574 bp。对PCR扩增产物进行限制性消化的进一步分析,证实存在分子大小为180 bp和380 bp的CAP 21基因组区域的16S rRNA。因此,380 bp的片段是从亚种中划分出来的。分离并鉴定出3株来自肺脏的菌株(BL5、BL6和AL1)和4株来自胸水的菌株(APF-2、APF-8A、APF-8B和APF-9),同时与现场分离株一起重新检测到一株疫苗株T1/44。贡贝没有样本检测到。总之,本研究结果检测到了作为CBPP病原体的存在。特此建议采取监测、检疫和疫苗接种等措施来控制尼日利亚的CBPP。