Failure to detect enterovirus in the spinal cord of ALS patients using a sensitive RT-PCR method

被引:36
作者
Nix, WA
Berger, MM
Oberste, MS
Brooks, BR
Mckenna-Yasek, DM
Brown, RH
Roos, RP
Pallansch, MA
机构
[1] Ctr Dis Control & Prevent, Resp & Enter Viruses Branch, Div Viral & Rickettsial Dis, Natl Ctr Infect Dis, Atlanta, GA 30333 USA
[2] Univ Calif Irvine, Dept Med, Orange, CA 92668 USA
[3] Univ Wisconsin, Sch Med, Dept Neurol, Madison, WI USA
[4] William S Middleton Mem Vet Adm Med Ctr, Serv Neurol, Madison, WI 53705 USA
[5] Massachusetts Gen Hosp, Cecil B Day Lab Neuromuscular Res, Charlestown, MA USA
[6] Univ Chicago, Dept Neurol, Chicago, IL 60637 USA
关键词
D O I
10.1212/01.WNL.0000123258.86752.51
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Objective: To assess the association of enteroviruses (EV) with ALS by applying a sensitive seminested reverse transcription (RT) PCR protocol to the detection of enteroviral RNA in a blinded set of archived tissues from ALS and control cases. Methods: The specimen set consisted of 24 frozen spinal cord samples from ALS cases, 17 frozen spinal cord samples from negative control (non-ALS) cases, and 5 frozen spinal cord positive control samples. The positive controls were two human spinal cord samples spiked with poliovirus (PV) and three spinal cords from PV-infected transgenic mice. A sensitive, EV-specific, seminested RT-PCR assay was used to detect EV genome in RNA extracted from the specimens and controls. Results: The assay detected EV RNA in a 10(-5) dilution of infected mouse tissue. EV RNA was not detected in the ALS specimens or in specimens from control cases, despite the presence of amplifiable RNA as assessed by amplification with control primers, whereas all of the positive control specimens yielded the expected PV amplification product. Conclusion: The reported association between EV infection and ALS was not confirmed by testing this set of specimens with these sensitive methods.
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页码:1372 / 1377
页数:6
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