Applications of polymerase chain reaction for identification of dengue viruses isolated from patient sera

A simple and sensitive procedure of reverse transcriptase polymerase chain reaction (RT-PCR) was developed previously such that all 4 serotypes of dengue viruses could be detected and their serotypes identified simultaneously in a single-step procedure. In this study we compared the RT-PCR with a co...

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Main Authors: Maneekarn N., Morita K., Tanaka M., Igarashi A., Usawattanakul W., Sirisanthana V., Innis BL., Sittisombut N., Nisalak A., Nimmanitya S.
Format: Comparative Study
Language:English
Published: 2014
Online Access:http://www.ncbi.nlm.nih.gov/pubmed/3502482
http://cmuir.cmu.ac.th/handle/6653943832/3534
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Institution: Chiang Mai University
Language: English
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spelling th-cmuir.6653943832-35342014-08-30T02:35:00Z Applications of polymerase chain reaction for identification of dengue viruses isolated from patient sera Maneekarn N. Morita K. Tanaka M. Igarashi A. Usawattanakul W. Sirisanthana V. Innis BL. Sittisombut N. Nisalak A. Nimmanitya S. A simple and sensitive procedure of reverse transcriptase polymerase chain reaction (RT-PCR) was developed previously such that all 4 serotypes of dengue viruses could be detected and their serotypes identified simultaneously in a single-step procedure. In this study we compared the RT-PCR with a conventional immunoperoxidase (PAP) staining method for the identification of dengue viruses currently isolated from patient sera. Sixty-six sera taken from dengue hemorrhagic fever (DHF) patients were subjected to virus isolation by inoculating onto C6/36 cell cultures. Screening for the presence of dengue viruses in culture fluids was done after 7 days of incubation by PAP staining using hyperimmune rabbit anti-dengue virus antibody as the primary reagent. Dengue viruses in positive cultures were further identified for their serotypes by PAP using type-specific monoclonal antibodies (MAb) and by RT-PCR. Thirty-two out of the 66 serum specimens tested (48.5%) were positive for dengue viruses. Of these, 5 were type 1 (DEN-1), 25 were type 2 (DEN-2) and 2 contained both DEN-1 and DEN-2. All cultures that were positive by PAP method were also positive by RT-PCR and vice versa. Thus, the results obtained by RT-PCR were in good agreement with those by PAP. It is important to point out that while all 5 DEN-1 isolates reacted readily with the MAb 1F1, only 2 of them could be identified by the MAb 15F3. Our data suggest that antigenic variation among DEN-1 isolates occur frequently and this should be taken into consideration in the selection of appropriate type-specific MAb for serotyping of dengue viruses.(ABSTRACT TRUNCATED AT 250 WORDS) 2014-08-30T02:35:00Z 2014-08-30T02:35:00Z 1993 Comparative Study 0385-5600 8474356 http://www.ncbi.nlm.nih.gov/pubmed/3502482 http://cmuir.cmu.ac.th/handle/6653943832/3534 eng
institution Chiang Mai University
building Chiang Mai University Library
country Thailand
collection CMU Intellectual Repository
language English
description A simple and sensitive procedure of reverse transcriptase polymerase chain reaction (RT-PCR) was developed previously such that all 4 serotypes of dengue viruses could be detected and their serotypes identified simultaneously in a single-step procedure. In this study we compared the RT-PCR with a conventional immunoperoxidase (PAP) staining method for the identification of dengue viruses currently isolated from patient sera. Sixty-six sera taken from dengue hemorrhagic fever (DHF) patients were subjected to virus isolation by inoculating onto C6/36 cell cultures. Screening for the presence of dengue viruses in culture fluids was done after 7 days of incubation by PAP staining using hyperimmune rabbit anti-dengue virus antibody as the primary reagent. Dengue viruses in positive cultures were further identified for their serotypes by PAP using type-specific monoclonal antibodies (MAb) and by RT-PCR. Thirty-two out of the 66 serum specimens tested (48.5%) were positive for dengue viruses. Of these, 5 were type 1 (DEN-1), 25 were type 2 (DEN-2) and 2 contained both DEN-1 and DEN-2. All cultures that were positive by PAP method were also positive by RT-PCR and vice versa. Thus, the results obtained by RT-PCR were in good agreement with those by PAP. It is important to point out that while all 5 DEN-1 isolates reacted readily with the MAb 1F1, only 2 of them could be identified by the MAb 15F3. Our data suggest that antigenic variation among DEN-1 isolates occur frequently and this should be taken into consideration in the selection of appropriate type-specific MAb for serotyping of dengue viruses.(ABSTRACT TRUNCATED AT 250 WORDS)
format Comparative Study
author Maneekarn N.
Morita K.
Tanaka M.
Igarashi A.
Usawattanakul W.
Sirisanthana V.
Innis BL.
Sittisombut N.
Nisalak A.
Nimmanitya S.
spellingShingle Maneekarn N.
Morita K.
Tanaka M.
Igarashi A.
Usawattanakul W.
Sirisanthana V.
Innis BL.
Sittisombut N.
Nisalak A.
Nimmanitya S.
Applications of polymerase chain reaction for identification of dengue viruses isolated from patient sera
author_facet Maneekarn N.
Morita K.
Tanaka M.
Igarashi A.
Usawattanakul W.
Sirisanthana V.
Innis BL.
Sittisombut N.
Nisalak A.
Nimmanitya S.
author_sort Maneekarn N.
title Applications of polymerase chain reaction for identification of dengue viruses isolated from patient sera
title_short Applications of polymerase chain reaction for identification of dengue viruses isolated from patient sera
title_full Applications of polymerase chain reaction for identification of dengue viruses isolated from patient sera
title_fullStr Applications of polymerase chain reaction for identification of dengue viruses isolated from patient sera
title_full_unstemmed Applications of polymerase chain reaction for identification of dengue viruses isolated from patient sera
title_sort applications of polymerase chain reaction for identification of dengue viruses isolated from patient sera
publishDate 2014
url http://www.ncbi.nlm.nih.gov/pubmed/3502482
http://cmuir.cmu.ac.th/handle/6653943832/3534
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