Padukone Shashiraja, Mandal Jharna, Rajkumari Nonika, Bhat Ballambattu Vishnu, Swaminathan Rathinam Palamalai, Parija Subhash Chandra
Department of Microbiology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.
Department of Neonatology, Jawaharlal Institute of Postgraduate Medical Education and Research, Puducherry, India.
Trop Parasitol. 2018 Jan-Jun;8(1):33-40. doi: 10.4103/tp.TP_4_18. Epub 2018 May 28.
was identified almost a century ago, yet its biology and pathogenicity status in humans is obscure. Studies on in India are scanty and are mostly microscopy based. This study compared three detection modalities to determine their efficiency in the identification of in human feces.
A total of 279 stool samples were screened using microscopy, culture (Jones' medium), and polymerase chain reaction (PCR)-based methods. Among the three, PCR is considered the gold standard test for detection of , as it helps to authenticate the sensitivity, specificity, and kappa agreement obtained by the other two tests. The morphological features of were recorded at 24, 48, and 72 h. After positive morphological identification, ten samples were cultured on Löwenstein-Jensen (LJ) medium and Locke's egg slant medium.
The sensitivity and specificity determined on the basis of microscopy were 36.2% and 99.4%, respectively. On the other hand, Jones' medium showed 67.6% sensitivity and 100% specificity. Further, we documented various morphological and reproductive features of using various staining techniques on cultures positive in Jones' medium. In addition, we also found that LJ medium was not equally efficacious as Jones' medium in assisting the growth of .
Although molecular diagnosis is a necessary tool for understanding the true epidemiology of , in laboratories devoid of molecular detection facilities, stool microscopy in conjunction with stool culture on Jones' medium could serve as the best alternative tool for the detection of .
近一个世纪前就已被发现,但其在人类中的生物学特性和致病性状况仍不清楚。印度关于它的研究很少,且大多基于显微镜检查。本研究比较了三种检测方法,以确定它们在识别人类粪便中的它时的效率。
总共279份粪便样本通过显微镜检查、培养(琼斯培养基)和基于聚合酶链反应(PCR)的方法进行筛查。在这三种方法中,PCR被认为是检测它的金标准测试,因为它有助于验证其他两种测试获得的敏感性、特异性和kappa一致性。在24、48和72小时记录它的形态特征。在进行阳性形态学鉴定后,将十个样本接种在罗-琴(LJ)培养基和洛克鸡蛋斜面培养基上。
基于显微镜检查确定的敏感性和特异性分别为36.2%和99.4%。另一方面,琼斯培养基显示出67.6%的敏感性和100%的特异性。此外,我们使用各种染色技术记录了在琼斯培养基上呈阳性的培养物中它的各种形态和繁殖特征。此外,我们还发现LJ培养基在促进它生长方面不如琼斯培养基有效。
尽管分子诊断是了解它真实流行病学的必要工具,但在缺乏分子检测设施的实验室中,粪便显微镜检查结合在琼斯培养基上进行粪便培养可作为检测它的最佳替代工具。