Animal Biosciences and Biotechnology Laboratory, USDA-ARS, 10300 Baltimore Avenue, Beltsville, MD 20705.
Department of Animal Science and Technology, Konkuk University, 120 Neungdong-ro, Gwangjin-gu, Seoul 05029, South Korea.
Avian Dis. 2020 Dec 1;64(4):490-495. doi: 10.1637/0005-2086-64.4.490.
Necrotic enteritis (NE) is a devastating enteric disease caused by Clostridium perfringens type A/G, which affects global poultry industry by compromising the performance, health, and welfare of chickens. The causative main virulent factor responsible for NE pathogenesis has been shifted from a phospholipase C portion of an α-toxin, to an NE B-like (NetB) toxin, a plasmid-encoded pore-forming heptameric protein, in NE development. Therefore, the ability to detect NetB toxin will enable early diagnosis of field NE. Because the NetB protein can only be detected by western blot analysis with polyclonal anti-NetB antiserum, we developed a NetB-specific monoclonal antibody (mAb)-based capture enzyme-linked immunosorbent assay (ELISA). Twenty mAbs reacting with Escherichia coli-expressed NetB protein were selected, isotyped, and conjugated with horseradish peroxidase for antibody pair tests. Multiple mAb pairs were found to detect E. coli NetB protein and native NetB protein secreted by netB-positive C. perfringens isolates. The developed capture (sandwich) ELISA could be useful to identify in vitro production of native NetB protein secreted from netB-positive field C. perfringens isolates and to conduct a large field test of commercial chickens undergoing NE infection. Here, we first report that native NetB toxin can be detected in C. perfringens NetB-specific mAb-based capture ELISA.
坏死性肠炎(NE)是一种由 A/G 型产气荚膜梭菌引起的毁灭性肠道疾病,它通过损害鸡的性能、健康和福利来影响全球家禽业。导致 NE 发病机制的主要毒力因子已从α-毒素的磷脂酶 C 部分转移到 NE B 样(NetB)毒素,即一种质粒编码的、形成孔的七聚体蛋白,这在 NE 的发展中起着重要作用。因此,能够检测 NetB 毒素将能够实现对现场 NE 的早期诊断。由于 NetB 蛋白只能通过用多克隆抗 NetB 抗血清进行 Western blot 分析来检测,因此我们开发了一种基于 NetB 特异性单克隆抗体(mAb)的捕获酶联免疫吸附试验(ELISA)。我们选择了 20 种与表达 NetB 蛋白的大肠杆菌反应的 mAb 进行鉴定,并与辣根过氧化物酶偶联用于抗体对测试。发现多个 mAb 对可检测大肠杆菌 NetB 蛋白和 netB 阳性产气荚膜梭菌分离株分泌的天然 NetB 蛋白。开发的捕获(夹心)ELISA 可用于鉴定从 netB 阳性产气荚膜梭菌分离株体外产生的天然 NetB 蛋白,并对发生 NE 感染的商业鸡进行大规模现场测试。在这里,我们首次报告天然 NetB 毒素可以在产气荚膜梭菌 NetB 特异性 mAb 捕获 ELISA 中检测到。