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Detection of Clostridium perfringens in Sea Mud of Ariake Sea―I A New Method for Detection of Clostridium perfringens in Sea-Mud Specimens

机译:有明海海泥中产气荚膜梭菌的检测 - 一种检测海泥样品中产气荚膜梭菌的新方法

摘要

A new medium (KNP medium) was prepared to detect Clostridium perfringens in sea-mud specimens, and a new method for detection of the organisms was established using the new medium. KNP medium was prepared by modifying LAS medium as described below. i ) Kanamycin was added in addition to neomycin and polymyxin which were already in LAS medium. ii) The pH (7.0 to 7.1) was altered to 6.0, and iii) 0.2g of dried ground meat was added to 10ml of the medium in order to elongate the viable period of the cultures. The method for preparation of KNP medium is described in the footnote of Fig.2. The method for detection of C. perfringens in sea-mud specimens using KNP medium is shown in Fig.2. The average detection rate of C. perfringens in the KNP-positive cultures was 68%. Of the isolates which were positive in both KNP enrichment and egg yolk CW agar isolate cultures, 92% was C. perfringens. KNP medium was applicable to unheated specimens, but not to heated (100℃, 15min.) specimens.
机译:制备了一种新的培养基(KNP培养基)以检测海泥标本中的产气荚膜梭菌,并使用该新培养基建立了一种检测生物体的新方法。如下所述通过修饰LAS培养基来制备KNP培养基。 i)除了已经在LAS培养基中的新霉素和多粘菌素之外,还添加了卡那霉素。 ii)将pH(7.0至7.1)改变为6.0,并且iii)将0.2g干碎肉添加至10ml培养基中以延长培养的存活时间。 KNP培养基的制备方法在图2的脚注中进行了描述。使用KNP培养基检测海泥标本中产气荚膜梭菌的方法如图2所示。 KNP阳性培养物中产气荚膜梭菌的平均检出率为68%。在KNP富集和蛋黄CW琼脂分离培养物中均为阳性的分离株中,产气荚膜梭菌为92%。 KNP介质适用于未加热的样品,但不适用于加热(100℃,15分钟)的样品。

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  • 作者

    谷口 忠敬;

  • 作者单位
  • 年度 1976
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  • 原文格式 PDF
  • 正文语种 ja
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