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Comparison of serological assays to titrate Hantaan and Seoul hantavirus-specific antibodies.
Li, Weihong; Cao, Shouchun; Zhang, Quanfu; Li, Jiandong; Zhang, Shuo; Wu, Wei; Qu, Jing; Li, Chuan; Liang, Mifang; Li, Dexin.
Afiliação
  • Li W; Key Laboratory for Medical Virology, National Health and Family Planning Commission of the People's Republic of China; Laboratory for Viral Hemorrhagic Fever, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, 102206, People's Republic of China.
  • Cao S; Institute for Infectious Disease and Endemic Disease Control, Beijing CDC, Beijing, 100013, People's Republic of China.
  • Zhang Q; National Institutes for Food and Drug Control, Beijing, 100050, People's Republic of China.
  • Li J; Key Laboratory for Medical Virology, National Health and Family Planning Commission of the People's Republic of China; Laboratory for Viral Hemorrhagic Fever, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, 102206, People's Republic of China.
  • Zhang S; Key Laboratory for Medical Virology, National Health and Family Planning Commission of the People's Republic of China; Laboratory for Viral Hemorrhagic Fever, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, 102206, People's Republic of China.
  • Wu W; Key Laboratory for Medical Virology, National Health and Family Planning Commission of the People's Republic of China; Laboratory for Viral Hemorrhagic Fever, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, 102206, People's Republic of China.
  • Qu J; Key Laboratory for Medical Virology, National Health and Family Planning Commission of the People's Republic of China; Laboratory for Viral Hemorrhagic Fever, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, 102206, People's Republic of China.
  • Li C; Key Laboratory for Medical Virology, National Health and Family Planning Commission of the People's Republic of China; Laboratory for Viral Hemorrhagic Fever, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, 102206, People's Republic of China.
  • Liang M; Key Laboratory for Medical Virology, National Health and Family Planning Commission of the People's Republic of China; Laboratory for Viral Hemorrhagic Fever, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, 102206, People's Republic of China.
  • Li D; Key Laboratory for Medical Virology, National Health and Family Planning Commission of the People's Republic of China; Laboratory for Viral Hemorrhagic Fever, National Institute for Viral Disease Control and Prevention, China CDC, Beijing, 102206, People's Republic of China.
Virol J ; 14(1): 133, 2017 07 18.
Article em En | MEDLINE | ID: mdl-28720142
ABSTRACT

BACKGROUND:

Hantaan and Seoul viruses, in the Hantavirus genus, are known to cause hemorrhagic fever with renal syndrome (HFRS). The plaque reduction neutralization test (PRNT), as conventional neutralization test for hantaviruses, is laborious and time-consuming. Alternatives to PRNT for hantaviruses are required.

METHODS:

In this study, the methods for Hantaan and Seoul viruses serological typing including microneutralization test (MNT), pseudoparticle neutralization test (PPNT) and immunofluorescence assay based on viral glycoproteins (IFA-GP) were developed and compared with PRNT using a panel of 74 sera including 44 convalescent sera of laboratory confirmed HFRS patients and 30 patients sera of non-hantavirus infection. Antibody titres and serotyping obtained with different methods above were analyzed by paired-t, linear correlation, McNemar χ2 and Kappa agreement tests.

RESULTS:

Antibody titres obtained with MNT50, PPNT50 and IFA-GP were significantly correlated with that obtained with PRNT50 (p < 0.001). GMT determined by PPNT50 was statistically higher than that determined by PRNT50 (p < 0.001), while GMT determined by MNT50 and IFA-GP were equal with (p > 0.05) and less than (p < 0.001) that obtained with PRNT50 respectively. Serotyping obtained with MNT50 and PRNT50, PPNT50 and PRNT50 were highly consistent (p < 0.001), whereas that obtained with IFA-GP and PRNT50 were moderately consistent (p < 0.001). There were no significant differences for serotyping between PRNT50 and MNT50, as well as PRNT50 and PPNT50 (p > 0.05). IFA-GP was less sensitive than PRNT50 and MNT50 for serotyping of hantaviruses infection (p < 0.05). However, for 79.5% (35/44) samples, serotyping determined by IFA-GP and PRNT50 were consistent.

CONCLUSIONS:

MNT50 and PPNT50 both can be used as simple and rapid alternatives to PRNT50, and MNT50 is more specific while PPNT50 is more sensitive than other assays for neutralizing antibody determination. So far, this work has been the most comprehensive comparison of alternatives to PRNT.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sorotipagem / Vírus Hantaan / Vírus Seoul / Anticorpos Antivirais Tipo de estudo: Diagnostic_studies / Evaluation_studies Limite: Humans Idioma: En Revista: Virol J Assunto da revista: VIROLOGIA Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Sorotipagem / Vírus Hantaan / Vírus Seoul / Anticorpos Antivirais Tipo de estudo: Diagnostic_studies / Evaluation_studies Limite: Humans Idioma: En Revista: Virol J Assunto da revista: VIROLOGIA Ano de publicação: 2017 Tipo de documento: Article