Rahman Md Habibur, Akther Sonia, Alam Md Shahin, Hassan Md Zakir, Sarker Md Samun, Ali Md Zulfekar, Giasuddin Md, Ahmed Sadek
Goat Production Research Division, Bangladesh Livestock Research Institute, Savar, Dhaka-1341, Bangladesh.
Sheep Production Research Division, Bangladesh Livestock Research Institute, Savar, Dhaka-1341, Bangladesh.
J Adv Vet Anim Res. 2023 Sep 30;10(3):538-544. doi: 10.5455/javar.2023.j707. eCollection 2023 Sep.
This research aimed to assess the prevalence of caprine pasteurellosis, isolate and identify pasteurellosis ( and ) in pneumonic goats, and discover the main bacterial cause of pneumonia.
One hundred and five samples (94 nasal swabs and 11 lung tissues) from goats suspected of having pneumonia were taken and transferred aseptically to the laboratory. Following the processing of the collected samples, spp. was isolated with the aid of plate culture methods. Biochemical characteristics were used to identify all bacterial isolates, which were then verified by polymerase chain reaction (PCR). Antimicrobial susceptibility testing was also carried out to evaluate the sensitivity profiles of various antibiotics. The serotype-specific antigen (PHSSA) gene was used to identify isolates of , and the KMT1 gene was used to identify isolates of .
From the 105 clinically suspicious samples, 51 (48.57%) were identified to be through bacteriological testing and also by PCR targeting the gene. Of these, 47.87% (45/94) were nasal swabs, and 54.55% (6/11) were lung tissues. Among confirmed samples, 70.59% (36/51) were identified as and 29.41% (15/51) were identified as . Resistance to tetracycline, streptomycin, oxytetracycline, gentamicin, and ceftriaxone was found in 50%-83% of the isolates. In addition, PCR identified the PHSSA and KMT1 genes from isolates of and , respectively.
The present study revealed that and primarily caused pasteurellosis in pneumonic goats in Bangladesh. However, when treating these animals, the proper choice of antimicrobials should be made to control this disease.
本研究旨在评估山羊巴氏杆菌病的患病率,分离并鉴定患肺炎山羊中的巴氏杆菌,并找出肺炎的主要细菌病因。
采集了105份疑似患有肺炎的山羊样本(94份鼻拭子和11份肺组织),并无菌转移至实验室。对采集的样本进行处理后,借助平板培养法分离出巴氏杆菌属细菌。利用生化特性鉴定所有细菌分离株,然后通过聚合酶链反应(PCR)进行验证。还进行了药敏试验以评估各种抗生素的敏感性。使用血清型特异性抗原(PHSSA)基因鉴定多杀性巴氏杆菌分离株,使用KMT1基因鉴定溶血曼氏杆菌分离株。
通过细菌学检测以及针对该基因的PCR,从105份临床可疑样本中鉴定出51份(48.57%)为阳性。其中,47.87%(45/94)为鼻拭子,54.55%(6/11)为肺组织。在确诊样本中,70.59%(36/51)被鉴定为多杀性巴氏杆菌,29.41%(15/51)被鉴定为溶血曼氏杆菌。50%-83%的分离株对四环素、链霉素、土霉素、庆大霉素和头孢曲松耐药。此外,PCR分别从多杀性巴氏杆菌和溶血曼氏杆菌分离株中鉴定出PHSSA和KMT1基因。
本研究表明,多杀性巴氏杆菌和溶血曼氏杆菌是孟加拉国患肺炎山羊巴氏杆菌病的主要病因。然而,在治疗这些动物时,应正确选择抗菌药物以控制这种疾病。