Chao Chien-Chung, Belinskaya Tatyana, Zhang Zhiwen, Ching Wei-Mei
Viral and Rickettsial Diseases Department, Infectious Diseases Directorate, Naval Medical Research Center, Silver Spring, Maryland, United States of America; Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
Uniformed Services University of the Health Sciences, Bethesda, Maryland, United States of America.
PLoS Negl Trop Dis. 2015 Jul 10;9(7):e0003884. doi: 10.1371/journal.pntd.0003884. eCollection 2015.
Sensitive, specific and rapid diagnostic tests for the detection of Orientia tsutsugamushi (O. tsutsugamushi) and Rickettsia typhi (R. typhi), the causative agents of scrub typhus and murine typhus, respectively, are necessary to accurately and promptly diagnose patients and ensure that they receive proper treatment. Recombinase polymerase amplification (RPA) assays using a lateral flow test (RPA-nfo) and real-time fluorescent detection (RPA-exo) were developed targeting the 47-kDa gene of O. tsutsugamushi or 17 kDa gene of R. typhi. The RPA assay was capable of detecting O. tsutsugamushi or R. typhi at levels comparable to that of the quantitative PCR method. Both the RPA-nfo and RPA-exo methods performed similarly with regards to sensitivity when detecting the 17 kDa gene of R. typhi. On the contrary, RPA-exo performed better than RPA-nfo in detecting the 47 kDa gene of O. tsutsugamushi. The clinical performance of the O. tsutsugamushi RPA assay was evaluated using either human patient samples or infected mouse samples. Eight out of ten PCR confirmed positives were determined positive by RPA, and all PCR confirmed negative samples were negative by RPA. Similar results were obtained for R. typhi spiked patient sera. The assays were able to differentiate O. tsutsugamushi and R. typhi from other phylogenetically related bacteria as well as mouse and human DNA. Furthermore, the RPA-nfo reaction was completed in 20 minutes at 37°C followed by a 10 minute incubation at room temperature for development of an immunochromatographic strip. The RPA-exo reaction was completed in 20 minutes at 39°C. The implementation of a cross contamination proof cassette to detect the RPA-nfo fluorescent amplicons provided an alternative to regular lateral flow detection strips, which are more prone to cross contamination. The RPA assays provide a highly time-efficient, sensitive and specific alternative to other methods for diagnosing scrub typhus or murine typhus.
分别用于检测恙虫病东方体(O. tsutsugamushi)和伤寒立克次体(R. typhi)(恙虫病和鼠型斑疹伤寒的病原体)的灵敏、特异且快速的诊断检测方法,对于准确及时地诊断患者并确保他们获得恰当治疗是必要的。利用侧流检测(RPA-nfo)和实时荧光检测(RPA-exo)的重组酶聚合酶扩增(RPA)检测方法,针对恙虫病东方体的47 kDa基因或伤寒立克次体的17 kDa基因进行了开发。RPA检测能够以与定量PCR方法相当水平检测恙虫病东方体或伤寒立克次体。在检测伤寒立克次体的17 kDa基因时,RPA-nfo和RPA-exo方法在灵敏度方面表现相似。相反,在检测恙虫病东方体的47 kDa基因时,RPA-exo比RPA-nfo表现更好。利用人类患者样本或感染小鼠样本评估了恙虫病东方体RPA检测的临床性能。10份经PCR确认的阳性样本中有8份经RPA判定为阳性,所有经PCR确认的阴性样本经RPA检测也为阴性。对于添加了伤寒立克次体的患者血清也获得了类似结果。这些检测方法能够将恙虫病东方体和伤寒立克次体与其他系统发育相关细菌以及小鼠和人类DNA区分开来。此外,RPA-nfo反应在37°C下20分钟内完成,随后在室温下孵育10分钟以显影免疫层析条带。RPA-exo反应在39°C下20分钟内完成。用于检测RPA-nfo荧光扩增子的防交叉污染盒的应用,为更易发生交叉污染的常规侧流检测条提供了一种替代方法。RPA检测为诊断恙虫病或鼠型斑疹伤寒的其他方法提供了一种高效、灵敏且特异的替代方案。