孟加拉国部分地区产气荚膜梭菌在蛋鸡群中的发生:分子分型、抗菌药物敏感性

M. Arif, Nigar Sultana, S. S. Islam, Arunima Oarin Tresha, S. Abdullah-Al-Mamun, Md Ashiquen Nobi, Mohammad Jahidur Rahman Khan, S. Kabir
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引用次数: 0

摘要

坏死性肠炎(NE)是由产气荚膜梭菌引起的重要家禽肠道疾病之一,给家禽养殖者造成了巨大的经济损失。本研究旨在估计孟加拉国Mymensingh和Gazipur地区蛋鸡中产气荚膜梭菌的患病率、危险因素并确认其分子模式和抗菌药物敏感性状况,共收集了287份样本,其中包括水(30份)、工人洗手(30份)和饲料(30份)作为环境汇总样本;作为单独的样本,通过基础(培养、生化试验)和多重PCR毒素分型进行评估。通过与农场主的半结构化访谈收集潜在危险因素的群体水平数据,并通过单变量和多变量逻辑回归分析进行评估,其中p值<0.05被认为具有统计学意义。产气荚膜梭菌的总体种群水平患病率为6.3%(95%可信区间[CI]: 3.8-9.7%)。产气荚膜梭菌在肠道样本中的发生率最高(12.8%,95% CI: 4.8 ~ 25.7%),其次是饲料(6.7%,95% CI: 0.8 ~ 22.1%)、肛肠棉签(6.0%,95% CI: 2.8 ~ 11.1%)和工人洗手(3.3%,95% CI: 0.1 ~ 12.2%)。在蛋鸡中发现免疫抑制病史(如新城病/落蛋综合征/感染性法氏囊病)[比值比(OR) = 22.16, 95% CI: 1.40 ~ 349.36, P = 0.027]和鸡群规模(OR = 11.16, 95% CI: 1.26 ~ 98.25, P = 0.029)与产气荚膜原菌感染状况相关。在本研究中,产气荚膜荚膜原毒素A型在蛋鸡中流行,其中72.2%的分离株显示出3至6种抗菌药物的耐药性,被确定为多重耐药。需要采取循证控制措施,即使用益生菌、益生元、有机酸和植物提取物作为天然替代品,包括控制免疫抑制疾病,以尽量减少低生物安全蛋鸡群的NE感染和抗菌素耐药性。亚洲Australas。j . Biosci。生物工程学报,2014,7 (2),36-49
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Occurrence of Clostridium perfringens in layer flocks of selected districts in Bangladesh: molecular typing, antimicrobial susceptibility
Necrotic enteritis (NE) is one of the important enteric diseases in poultry caused by Clostridium perfringens which leads to considerable economic losses for poultry raisers. The present research was carried out to estimate prevalence, risk factors and to confirm molecular pattern, antimicrobial susceptibility status of Clostridium perfringens in layer flocks in Mymensingh and Gazipur districts of Bangladesh, where a total of 287 samples were collected that comprised of water (30), workers’ hand washing (30), and feed (30) as environmental pooled samples; cloacal swab (150) and post mortem sample (intestine) (47) as individual samples, and evaluated by basic (culture, biochemical test), and finally toxinotyping multiplex PCR assays. The flock-level data on potential risk factors were collected through semi-structured interviews with the farm owners and evaluated via univariable and multivariable logistic regression analyses where a p-value of <0.05 was considered as statistically significant. Overall flock-level prevalence of Clostridium perfringens was confirmed to be 6.3% (95% confidence interval [CI]: 3.8-9.7%). The occurrence of C. perfringens was found to be higher in the intestine samples (12.8%, 95% CI: 4.8- 25.7%) followed by feed (6.7%, 95% CI: 0.8-22.1%), cloacal swabs (6.0%, 95% CI: 2.8-11.1%) and workers’ hand washing (3.3%, 95% CI: 0.1- 12.2%). History of immune-suppressive disease (like New castle disease/egg drop syndrome/infectious bursal disease) [Odds Ratio (OR) = 22.16, 95% CI: 1.40-349.36, P = 0.027] and flock size more than 3000 birds (OR = 11.16, 95% CI: 1.26-98.25, P = 0.029) were found to be associated with C. perfringens infection status in the layer flocks. In this study, C. perfringens toxinotype A is circulating in layer flocks with 72.2% of isolates were established as multidrug-resistant as they demonstrated resistance between 3 to 6 antimicrobial agents. Evidence-based control measures to be taken namely use of probiotics, prebiotic, organic acids, and plant extracts as natural alternatives including control of immune-suppressive diseases are needed to minimize the NE infection and antimicrobial resistance in low biosecurity layer flocks. Asian Australas. J. Biosci. Biotechnol. 2022, 7(2), 36-49
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