Experimental infection of rhesus macaques with West Nile virus: Level and duration of viremia and kinetics of the antibody response after infection

被引:57
作者
Ratterree, MS
Gutierrez, RA
da Rosa, APAT
Dille, BJ
Beasley, DWC
Bohm, RP
Desai, SM
Didier, PJ
Bikenmeyer, LG
Dawson, GJ
Leary, TP
Schochetman, G
Phillippi-Falkenstein, K
Arroyo, J
Barrett, ADT
Tesh, RB
机构
[1] Univ Texas, Med Branch, Dept Pathol, Galveston, TX 77555 USA
[2] Tulane Univ, Tulane Natl Primate Res Ctr, Div Vet Med, Covington, LA USA
[3] Abbott Labs, Abbott Diagnost Div, Hepatitis Retrovirus & Infect Dis Core Res & Dev, Abbott Pk, IL 60064 USA
[4] Univ Texas, Med Branch, Ctr Biodef & Emerging Infect Dis, Galveston, TX 77555 USA
[5] Acambis, Cambridge, MA USA
关键词
D O I
10.1086/381461
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Reports of transfusion-associated cases of West Nile virus (WNV) infection indicate the need for sensitive screening methods to identify WNV-infected blood products. We experimentally infected 5 rhesus macaques with WNV, to determine the level and duration of viremia, the kinetics of the humoral immune response, and the sensitivity of various assay systems for detecting WNV in blood. All macaques developed subclinical infections with low levels of viremia; nested reverse-transcription polymerase chain reaction was the most sensitive method for detecting virus or viral RNA in blood. Specific WNV antibodies appeared during the second week of infection; the results of an IgM enzyme-linked immunosorbent assay became positive on the ninth or tenth day after infection, followed in 1-2 days by hemagglutination-inhibiting and neutralizing antibodies. Our results suggest that both nucleic acid and serological testing may be needed to determine exposure to WNV and to identify potentially infected blood donors.
引用
收藏
页码:669 / 676
页数:8
相关论文
共 31 条
  • [1] The West Nile Virus outbreak of 1999 in New York: The flushing hospital experience
    Asnis, DS
    Conetta, R
    Teixeira, AA
    Waldman, G
    Sampson, BA
    [J]. CLINICAL INFECTIOUS DISEASES, 2000, 30 (03) : 413 - 418
  • [2] Limited evolution of West Nile virus has occurred during its southwesterly spread in the United States
    Beasley, DWC
    Davis, CT
    Guzman, H
    Vanlandingham, DL
    da Rosa, APAT
    Parsons, RE
    Higgs, S
    Tesh, RB
    Barrett, ADT
    [J]. VIROLOGY, 2003, 309 (02) : 190 - 195
  • [3] Mouse neuroinvasive phenotype of West Nile virus strains varies depending upon virus genotype
    Beasley, DWC
    Li, L
    Suderman, MT
    Barrett, ADT
    [J]. VIROLOGY, 2002, 296 (01) : 17 - 23
  • [4] Beaty BJ., 1989, Diagnostic procedures for viral, rickettsial and chlamydial infections, P797
  • [5] Centers for Disease Control and Prevention (CDC), 2002, MMWR Morb Mortal Wkly Rep, V51, P1133
  • [6] Centers for Disease Control and Prevention (CDC), 2002, MMWR Morb Mortal Wkly Rep, V51, P1129
  • [7] Centers for Disease Control and Prevention (CDC), 2002, MMWR Morb Mortal Wkly Rep, V51, P879
  • [8] Centers for Disease Control and Prevention (CDC), 2002, MMWR Morb Mortal Wkly Rep, V51, P833
  • [9] DETERMINATION OF HUMAN-IGG AND IGM CLASS ANTIBODIES TO WEST NILE VIRUS BY ENZYME LINKED IMMUNOSORBENT-ASSAY (ELISA)
    FEINSTEIN, S
    AKOV, Y
    ELLACHMI, B
    LEHRER, S
    RANNON, L
    KATZ, D
    [J]. JOURNAL OF MEDICAL VIROLOGY, 1985, 17 (01) : 63 - 72
  • [10] WEST NILE FEVER - THE CLINICAL FEATURES OF THE DISEASE AND THE ISOLATION OF WEST NILE VIRUS FROM THE BLOOD OF 9 HUMAN CASES
    GOLDBLUM, N
    STERK, VV
    PADERSKI, B
    [J]. AMERICAN JOURNAL OF HYGIENE, 1954, 59 (01): : 89 - 103