Alemu Solomon Addisu, Belachew Yosef Deneke, Tefera Takele Abayneh
Bonga University, Department of Veterinary Medicine, Bonga, Ethiopia.
Jimma University, School of Veterinary Medicine, Jimma, Ethiopia.
Vet Med (Auckl). 2023 Dec 27;14:233-244. doi: 10.2147/VMRR.S435932. eCollection 2023.
Pneumonic pasteurellosis is a respiratory system disease of sheep caused by , and responsible for the low productivity and economic loss resulting from death and treatment costs. This study was conducted to isolate and molecularly detect causative agents and antibiotic susceptibility tests from a nasal swab sample of the Bonga sheep breed that was suspected to have pneumonic pasteurellosis in selected areas of Southwest Ethiopian Peoples Regional State.
A cross-sectional study design was used along with purposive sampling of nasal swab samples from sheep that were brought to veterinary clinics during the study period. Bacterial isolation and phenotypic characterization were carried out using microbiological and biochemical tests that followed standard microbiological techniques. To molecularly confirm the isolates, and , species-specific PCR primer genes were used. Using the disc diffusion method, molecularly confirmed isolates were subjected to an in vitro antibiotic susceptibility test.
The 85 samples that were scrutinized had an overall isolation rate of 31.76%, whereas the isolates of and had species compositions of 40.7% and 59.25%, respectively. Overall, 12.5% of the and 18.18% of the species were verified from phenotypical isolates using the species-specific PCR primer genes and , respectively. An in vitro antibiotic susceptibility test was carried out on all four PCR-confirmed isolates for seven commonly used antibiotics used to treat ovine pasteurellosis in the study area. It was found that both bacterial species were resistant to chloramphenicol and penicillin G.
Using phenotypic and molecular diagnostic techniques, the results of our current inquiry revealed that and are the causative agents of ovine pneumonic pasteurellosis in the study area.
肺炎巴氏杆菌病是绵羊的一种呼吸系统疾病,由[具体病原体]引起,会导致生产力低下以及因死亡和治疗成本造成经济损失。本研究旨在从埃塞俄比亚西南部人民区域州选定地区疑似患有肺炎巴氏杆菌病的邦加绵羊品种的鼻拭子样本中分离并分子检测病原体,并进行药敏试验。
采用横断面研究设计,并在研究期间对送至兽医诊所的绵羊鼻拭子样本进行目的抽样。使用遵循标准微生物技术的微生物学和生化试验进行细菌分离和表型特征分析。为了从分子水平确认分离株,使用了[具体引物基因1]和[具体引物基因2]这两种物种特异性PCR引物基因。采用纸片扩散法对经分子确认的分离株进行体外药敏试验。
85份样本的总体分离率为31.76%,而[具体细菌1]和[具体细菌2]的分离株的物种组成分别为40.7%和59.25%。总体而言,分别使用物种特异性PCR引物基因[具体引物基因1]和[具体引物基因2]从表型分离株中验证出12.5%的[具体细菌1]和18.18%的[具体细菌2]。对所有4株经PCR确认的分离株进行了针对研究区域用于治疗绵羊巴氏杆菌病的7种常用抗生素的体外药敏试验。发现这两种细菌对氯霉素和青霉素G均耐药。
通过表型和分子诊断技术,我们当前调查的结果显示,[具体细菌1]和[具体细菌2]是研究区域绵羊肺炎巴氏杆菌病的病原体。