Enhancing the sensitivity of Dengue virus serotype detection by RT-PCR among infected children in India
Autor: | Rosario Vivek, Anmol Chandele, Kaustuv Nayak, Anita Shet, Murali Krishna Kaja, Syed Fazil Ahamed, Shalini Kotabagi |
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Rok vydání: | 2017 |
Předmět: |
0301 basic medicine
Serotype viruses 030106 microbiology 030231 tropical medicine Population India Biology Dengue virus medicine.disease_cause Polymerase Chain Reaction Sensitivity and Specificity law.invention Dengue fever Serology Dengue 03 medical and health sciences 0302 clinical medicine law Virology medicine Humans Serotyping Child education Polymerase chain reaction DNA Primers Viral Structural Proteins education.field_of_study Reverse Transcriptase Polymerase Chain Reaction virus diseases Sequence Analysis DNA Dengue Virus medicine.disease Real-time polymerase chain reaction Molecular Diagnostic Techniques Primer (molecular biology) |
Zdroj: | Journal of Virological Methods. 244:46-54 |
ISSN: | 0166-0934 |
DOI: | 10.1016/j.jviromet.2017.02.014 |
Popis: | Dengue surveillance relies on reverse transcription-polymerase chain reaction (RT-PCR), for confirmation of dengue virus (DENV) serotypes. We compared efficacies of published and modified primer sets targeting envelope (Env) and capsid-premembrane (C-prM) genes for detection of circulating DENV serotypes in southern India. Acute samples from children with clinically-diagnosed dengue were used for RT-PCR testing. All samples were also subjected to dengue serology (NS1 antigen and anti-dengue-IgM/IgG rapid immunochromatographic assay). Nested RT-PCR was performed on viral RNA using three methods targeting 654bp C-prM, 511bp C-prM and 641bp Env regions, respectively. RT-PCR-positive samples were validated by population sequencing. Among 171 children with suspected dengue, 121 were dengue serology-positive and 50 were dengue serology-negative. Among 121 serology-positives, RT-PCR detected 91 (75.2%) by CprM654, 72 (59.5%) by CprM511, and 74 (61.1%) by Env641. Among 50 serology-negatives, 10 (20.0%) were detected by CprM654, 12 (24.0%) by CprM511, and 11 (22.0%) by Env641. Overall detection rate using three methods sequentially was 82.6% (100/121) among serology-positive and 40.0% (20/50) among serology-negative samples; 6.6% (8/120) had co-infection with multiple DENV serotypes. We conclude that detection of acute dengue was enhanced by a modified RT-PCR method targeting the 654bp C-prM region, and further improved by using all three methods sequentially. |
Databáze: | OpenAIRE |
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