Tanida Konstantin, Hahn Andreas, Eberhardt Kirsten Alexandra, Tannich Egbert, Landt Olfert, Kann Simone, Feldt Torsten, Sarfo Fred Stephen, Di Cristanziano Veronica, Frickmann Hagen, Loderstädt Ulrike
Department of Microbiology and Hospital Hygiene, Bundeswehr Hospital Hamburg, 20359 Hamburg, Germany.
Department of Medical Microbiology, Virology and Hygiene, University Medicine Rostock, 18057 Rostock, Germany.
Pathogens. 2021 May 26;10(6):656. doi: 10.3390/pathogens10060656.
Microsporidiosis is an infection predominantly occurring in immunosuppressed patients and infrequently also in travelers. This study was performed to comparatively evaluate the diagnostic accuracy of real-time PCR assays targeting microsporidia with etiological relevance in the stool of human patients in a latent class analysis-based test comparison without a reference standard with perfect accuracy. Thereby, two one-tube real-time PCR assays and two two-tube real-time PCR assays targeting and spp. were included in the assessment with reference stool material (20), stool samples from Ghanaian HIV-positive patients (903), and from travelers, migrants and Colombian indigenous people (416). Sensitivity of the assays ranged from 60.4% to 97.4% and specificity from 99.1% to 100% with substantial agreement according to Cohen's kappa of 79.6%. Microsporidia DNA was detected in the reference material and the stool of the HIV patients but not in the stool of the travelers, migrants, and the Colombian indigenous people. Accuracy-adjusted prevalence was 5.8% ( = 78) for the study population as a whole. In conclusion, reliable detection of enteric disease-associated microsporidia in stool samples by real-time PCR could be demonstrated, but sensitivity between the compared microsporidia-specific real-time PCR assays varied.
微孢子虫病是一种主要发生在免疫抑制患者中的感染,在旅行者中也很少见。本研究旨在通过基于潜在类别分析的测试比较,在没有完美准确性参考标准的情况下,比较评估针对微孢子虫的实时PCR检测在人类患者粪便中的诊断准确性,这些微孢子虫与病因相关。因此,评估中纳入了两种单管实时PCR检测和两种双管实时PCR检测,它们分别针对 和 属。评估使用了参考粪便样本(20份)、来自加纳HIV阳性患者的粪便样本(903份)以及来自旅行者、移民和哥伦比亚原住民的粪便样本(416份)。检测的灵敏度范围为60.4%至97.4%,特异性范围为99.1%至100%,根据科恩kappa系数,一致性较高,为79.6%。在参考样本和HIV患者的粪便中检测到了微孢子虫DNA,但在旅行者、移民和哥伦比亚原住民的粪便中未检测到。整个研究人群经准确性调整后的患病率为5.8%( = 78)。总之,通过实时PCR可以可靠地检测粪便样本中与肠道疾病相关的微孢子虫,但所比较的微孢子虫特异性实时PCR检测之间的灵敏度有所不同。