Al-Maary Khalid S, Dawoud Turki M, Mubarak Ayman S, Hessain Ashgan M, Galal Hussein M, Kabli Saleh A, Mohamed Moussa I
Department of Botany and Microbiology, College of Science, King Saud University, Saudi Arabia.
Department of Health Science, College of Applied Studies and Community Service, King Saud University, P.O. Box 22459, Riyadh 11495, Saudi Arabia; Department of Microbiology, Faculty of Veterinary Medicine, Cairo University, P.O. 2446, Cairo, 14242 Giza, Egypt.
Saudi J Biol Sci. 2017 Feb;24(2):367-370. doi: 10.1016/j.sjbs.2016.06.006. Epub 2016 Jun 17.
The use of molecular techniques for detection and characterization of the is very important for rapid and specific detection and characterization of the organism. During the period from 15th February, 2014 to 15th April, 2015, 425 nasopharyngeal swabs and 175 lung and spleen samples were collected and examined by conventional methods, 80 strains (18.82%) of were isolated from the calves, sheep and goat with respiratory manifestation. Meanwhile, 77 strains (44%) were isolated from emergency slaughtered animals. All the recovered strains were positive for specific PCR for detection of strains previously identified as by standard microbiological techniques. Multiplex PCR for molecular typing of the capsular antigens of the recovered revealed positive amplification of 1044 bp fragments specific to the capsular antigen type A with 105 strains (66.88%), and amplification 511 bp fragments of the capsular antigen type E with 52 strain (33.12%) and absence of B, D and F antigens. Multiplex PCR for molecular typing of the capsular antigens of can be used as a simple, sensitive, rapid, reliable technique instead of the serological techniques for identification of the capsular antigens of .
使用分子技术检测和鉴定该病原体对于快速、特异性地检测和鉴定该生物体非常重要。在2014年2月15日至2015年4月15日期间,采集了425份鼻咽拭子以及175份肺和脾脏样本,并采用传统方法进行检测,从出现呼吸道症状的犊牛、绵羊和山羊中分离出80株该病原体(18.82%)。同时,从紧急屠宰的动物中分离出77株(44%)。所有回收菌株通过特异性PCR检测均呈阳性,该PCR用于检测先前经标准微生物技术鉴定为该病原体的菌株。对回收的该病原体荚膜抗原进行分子分型的多重PCR显示,105株(66.88%)出现了针对荚膜抗原A型的1044 bp片段的阳性扩增,52株(33.12%)出现了针对荚膜抗原E型的511 bp片段的扩增,且未检测到B、D和F抗原。用于该病原体荚膜抗原分子分型的多重PCR可作为一种简单、灵敏、快速、可靠的技术,替代血清学技术用于鉴定该病原体的荚膜抗原。