Anaerobians Laboratory, Department of Preventive Veterinary Medicine, Veterinary School of Federal University of Minas Gerais, Antônio Carlos Avenue, 6627, Belo Horizonte, Brazil.
Arch Microbiol. 2009 Nov;191(11):847-51. doi: 10.1007/s00203-009-0510-y. Epub 2009 Sep 25.
Clostridium perfringens type D produces enterotoxemia, an enteric disease in ruminants, also known as pulpy kidney disease. Caused by epsilon toxin, enterotoxemia is a major exotoxin produced by this microorganism. Epsilon toxin is also the main component of vaccines against this enteric disorder. In this study, a standardized dot-blot was used to choose strains of C. perfringens type D that are producers of epsilon toxin. Clones producing epsilon toxin were chosen by limiting dilution; after three passages, lethal minimum dose titers were determined by soroneutralization test in mice. These clones produced epsilon toxin 240 times more concentrated than the original strain. The presence of the epsilon toxin gene (etx) was verified by polymerase chain reaction. All clones were positive, including those determined to be negative by dot-blot tests, suggesting that mechanisms in addition to the presence of the etx gene can influence toxin production. The dot-blot test was efficient for the selection of toxigenic colonies of C. perfringens type D and demonstrated that homogeneous populations selected from toxigenic cultures produce higher titers of epsilon toxin.
D 型产气荚膜梭菌可引起肠毒血症,这是反刍动物的一种肠道疾病,也称为软肾病。肠毒血症由ε 毒素引起,是该微生物产生的主要外毒素。ε 毒素也是针对这种肠道紊乱的疫苗的主要成分。在这项研究中,采用标准化点印迹法选择产生ε 毒素的 D 型产气荚膜梭菌菌株。通过有限稀释选择产生 ε 毒素的克隆,经过 3 次传代,通过小鼠中和试验确定致死最小剂量滴度。这些克隆产生的 ε 毒素比原始菌株浓缩了 240 倍。通过聚合酶链反应验证了 ε 毒素基因(etx)的存在。所有克隆均为阳性,包括点印迹试验确定为阴性的克隆,这表明除了存在 etx 基因外,其他机制也会影响毒素的产生。点印迹试验是选择 D 型产气荚膜梭菌产毒克隆的有效方法,证明从产毒培养物中选择的同质群体可产生更高滴度的 ε 毒素。