Farooq S, Wani S A, Hassan M N, Aalamgeer S, Kashoo Z A, Magray S N, Bhat M A
KVK-Kupwara, Sher-e-Kashmir University of Agricultural Sciences and Technology of Kashmir (SKUAST-K), Jammu and Kashmir, India.
Division of Veterinary Microbiology and Immunology, SKUAST-K, Shuhama (Alusteng), Srinagar, 190006, Jammu and Kashmir, India.
Anaerobe. 2018 Jun;51:36-41. doi: 10.1016/j.anaerobe.2018.03.010. Epub 2018 Mar 26.
The objective of this study was to determine the prevalence and identification of leukotoxin gene, lktA, variant strains of Fusobacterium necrophorum in the footrot lesions of sheep. The detection of F. necrophorum was carried out by PCR targeting the lktA gene fragment and identification of lktA variant strains was done by PCR-single stranded conformational polymorphism (PCR-SSCP) and gene sequencing. Of the 450 swabs collected from footrot lesions of sheep, 117 were lktA-positive for F. necrophorum. Of the 50 swabs collected from apparently asymptomatic sheep, only one was lktA-positive for F. necrophorum. The overall prevalence of F. necrophorum in footrot affected sheep in Kashmir valley was 26%, and ranged from 20 to 34.8%, respectively. PCR-SSCP of lktA gene fragment analysis revealed three lktA variants, designated as JKS-F1/F2/F3, while two samples (1.7%) showed multiple lktA variant strains of F. necrophorum in a single footrot-affected sheep hoof. This appears to be the first report on the presence of more than one lktA variant of F. necrophorum in a footrot lesion of sheep. The JKS-F3 lktA variant was the most frequent (75.4%), followed by JKS-F2 (14.4%) and JKS-F1 (8.4%), respectively. Among the three lktA variants identified, JKS-F3 was detected in 74 (86.0%) samples from severe footrot affected sheep with a lesion score of 4. The data suggest that JKS-F3 is the predominant lktA variant of F. necrophorum and is associated with severe footrot in sheep. Hence, JKS-F3 may be a significant variant contributing to the severity and duration of the disease in sheep.
本研究的目的是确定绵羊腐蹄病病变中坏死梭杆菌白细胞毒素基因lktA变异菌株的流行情况并进行鉴定。通过针对lktA基因片段的PCR检测坏死梭杆菌,并通过PCR-单链构象多态性(PCR-SSCP)和基因测序鉴定lktA变异菌株。从绵羊腐蹄病病变采集的450份拭子中,117份坏死梭杆菌lktA呈阳性。从明显无症状的绵羊采集的50份拭子中,只有1份坏死梭杆菌lktA呈阳性。克什米尔山谷患腐蹄病绵羊中坏死梭杆菌的总体流行率为26%,分别在20%至34.8%之间。lktA基因片段分析的PCR-SSCP显示有三种lktA变异体,命名为JKS-F1/F2/F3,而在一只患腐蹄病的绵羊蹄中,有两个样本(1.7%)显示出坏死梭杆菌的多种lktA变异菌株。这似乎是关于绵羊腐蹄病病变中存在不止一种坏死梭杆菌lktA变异体的首次报道。JKS-F3 lktA变异体最为常见(75.4%),其次分别是JKS-F2(14.4%)和JKS-F1(8.4%)。在鉴定出的三种lktA变异体中,JKS-F3在74份(86.0%)病变评分为4的严重腐蹄病绵羊样本中被检测到。数据表明,JKS-F3是坏死梭杆菌的主要lktA变异体,与绵羊严重腐蹄病有关。因此,JKS-F3可能是导致绵羊疾病严重程度和病程的一个重要变异体。