Optimization and Evaluation of a Multiplex Quantitative PCR Assay for Detection of Nucleic Acids in Human Blood Samples from Patients with Spotted Fever Rickettsiosis, Typhus Rickettsiosis, Scrub Typhus, Monocytic Ehrlichiosis, and Granulocytic Anaplasmosis

被引:18
作者
Reller, Megan E. [1 ,2 ]
Dumler, J. Stephen [1 ,3 ]
机构
[1] Johns Hopkins Univ, Sch Med, Dept Pathol, Div Med Microbiol, Baltimore, MD 21205 USA
[2] Duke Univ, Duke Hubert Yeargan Ctr Global Hlth, Duke Global Hlth Inst, Dept Med,Sch Med,Div Infect Dis, Durham, NC 27706 USA
[3] Uniformed Serv Univ Hlth Sci, F Edward Hebert Sch Med, Joint Dept Pathol, Bethesda, MD 20814 USA
基金
美国国家卫生研究院;
关键词
spotted fever and typhus group rickettsioses; scrub typhus; ehrlichioses; anaplasmosis; Orientia spp; Rickettsia spp; Ehrlichia chaffeensis; Anaplasma phagocytophilum; Rickettsiales; ticks; diagnostics; etiology of fever studies; REAL-TIME PCR; SOUTH-CENTRAL REGIONS; FEBRILE ILLNESS; DIAGNOSIS; CHAFFEENSIS; INFECTIONS; NORTHERN; BORNE; PHAGOCYTOPHILUM; DIFFERENTIATION;
D O I
10.1128/JCM.01802-19
中图分类号
Q93 [微生物学];
学科分类号
071005 ; 100705 ;
摘要
Spotted fever group rickettsioses (SFGR), typhus group rickettsioses (TGR), scrub typhus (caused by Orientia tsutsugamushi), ehrlichiosis, and anaplasmosis often present as undifferentiated fever but are not treated by agents (penicillins and cephalosporins) typically used for acute febrile illness. Inability to diagnose these infections when the patient is acutely ill leads to excess morbidity and mortality. Failure to confirm these infections retrospectively if a convalescent blood sample is not obtained also impairs epidemiologic and clinical research. We designed a multiplex real-time quantitative PCR (qPCR) assay to detect SFGR, TGR, O. tsutsugamushi, and infections caused by Anaplasma phagocytophilum and Ehrlichia chaffeensis with the ompA, 17-kDa surface antigen gene, tsa56, msp2 (p44), and vlpt gene targets, respectively. Analytical sensitivity was >= 2 copies/mu l (linear range, 2 to 2 x 10(5)) and specificity was 100%. Clinical sensitivities for SFGR, TGR, and O. tsutsugamushi were 25%, 20%, and 27%, respectively, and specificities were 98%, 99%, and 100%, respectively. Clinical sensitivities for A. phagocytophilum and E. chaffeensis were 93% and 84%, respectively, and specificities were 99% and 98%, respectively. This multiplex qPCR assay could support early clinical diagnosis and treatment, confirm acute infections in the absence of a convalescent-phase serum sample, and provide the high-throughput testing required to support large clinical and epidemiologic studies. Because replication of SFGR and TGR in endothelial cells results in very low bacteremia, optimal sensitivity of qPCR for these rickettsioses will require use of larger volumes of input DNA, which could be achieved by improved extraction of DNA from blood and/or extraction of DNA from a larger initial volume of blood.
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页数:9
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