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Evaluation of the Polymerase Chain Reaction for Diagnosis of Lassa Virus Infection
Sam G. Trappier
Sam G. Trappier
Special Pathogens Branch, Division of Viral and Rickettsial Diseases, National Center of Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia
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Ann L. Conaty
Ann L. Conaty
Special Pathogens Branch, Division of Viral and Rickettsial Diseases, National Center of Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia
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Bertha B. Farrar
Bertha B. Farrar
Special Pathogens Branch, Division of Viral and Rickettsial Diseases, National Center of Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia
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Dave D. Auperin
Dave D. Auperin
Special Pathogens Branch, Division of Viral and Rickettsial Diseases, National Center of Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia
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Joseph B. McCormick
Joseph B. McCormick
Special Pathogens Branch, Division of Viral and Rickettsial Diseases, National Center of Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia
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Susan P. Fisher-Hoch
Susan P. Fisher-Hoch
Special Pathogens Branch, Division of Viral and Rickettsial Diseases, National Center of Infectious Diseases, Centers for Disease Control and Prevention, Atlanta, Georgia
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We evaluated the polymerase chain reaction (PCR) and hybridization procedures for diagnosis of Lassa fever. Primers were derived from a region of the small RNA segment of Lassa virus coding for the glycoprotein. Serum samples stored for a 14-year period from patients in Sierra Leone, West Africa were examined retrospectively. Blinded samples were then tested prospectively. Eighty-eight virus isolation-negative control sera were negative by PCR and hybridization. In the retrospective study, virus was isolated from 51 of 98 specimens from patients with Lassa fever, and 33 of these were positive for Lassa virus RNA by PCR, and 42 by PCR and hybridization. Fifteen were positive by PCR and hybridization but isolation-negative, and nine were positive by isolation but PCR/hybridization-negative. Thirty-two were negative by all methods (sensitivity by PCR/hybridization compared with virus isolation 0.82, specificity 0.68). In a prospective blinded study of 195 patient sera, 51 were positive by PCR and virus isolation, and 24 were PCR positive but virus isolation-negative (sensitivity 0.66, specificity 0.71). After hybridization, 66 virus isolation-positive sera were positive. The sensitivity was 0.86 and the specificity was 0.59, and the probability of false-positive results compared with virus isolation was 32%, (x2 = 21.9, by McNemar's test). Since some specimens may not have contained viable virus, we re-analyzed the data of individual patients using laboratory-confirmed case definitions for Lassa fever. All specimens from patients in whom Lassa fever was excluded by serologic tests were negative by PCR/hybridization. The PCR/hybridization was positive longer in the disease course and false positives may reflect its greater sensitivity when compared with virus isolation. The PCR/hybridization did not detect Lassa virus RNA of some Lassa virus isolates from other countries in West Africa, or in every plaque of all isolates. Although some strains may not be detected until broader-reacting primers are available, the PCR is a reliable, safe, and sensitive tool for the rapid diagnosis of Lassa fever.
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| Past two years | Past Year | Past 30 Days | |
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| Abstract Views | 907 | 559 | 16 |
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