Rapid diagnosis of human adenovirus B, C and E in the respiratory tract using multiplex quantitative polymerase chain reaction
Autor: | Caifeng Ma, Liu Qiong, Rui Chen, Ying Tan, Helu Liu, Li Yuxia, Jikun Du, Huijun Zhu, Dou Yuhong |
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Jazyk: | angličtina |
Rok vydání: | 2018 |
Předmět: |
0301 basic medicine
Cancer Research Genotype 030106 microbiology Biology Immunofluorescence Real-Time Polymerase Chain Reaction Serogroup Biochemistry Sensitivity and Specificity Adenovirus Infections Human 03 medical and health sciences Multiplex polymerase chain reaction Genetics medicine Humans Multiplex human adenovirus Molecular Biology Respiratory Tract Infections Human adenovirus B medicine.diagnostic_test Adenoviruses Human Outbreak virus diseases Articles respiratory tract Virology eye diseases throat swab samples Real-time polymerase chain reaction medicine.anatomical_structure Oncology DNA Viral Molecular Medicine multiplex qPCR Capsid Proteins Multiplex Polymerase Chain Reaction Respiratory tract |
Zdroj: | Molecular Medicine Reports |
ISSN: | 1791-3004 1791-2997 |
Popis: | Human adenovirus (HAdV) is increasingly recognized as a major cause of human respiratory tract viral infections. Its outbreaks and epidemics in various populations resulted in considerable morbidity and mortality. Therefore, a rapid and specific assay for HAdV in clinical samples is of crucial importance to diagnosing HAdV infections. The present study aimed to develop and evaluate a multiplex quantitative polymerase chain reaction (qPCR) assay for the rapid detection and accurate quantification of HAdV B, C and E. The lower limit of detection for this assay was two genomic copies per reaction, and quantitative linearity ranged from 2 to 2×106 copies per reaction of the input viral DNA. Furthermore, 3,160 throat swab samples that tested HAdV negative by the immunofluorescence assay were collected and retested using the multiplex qPCR assay. The results showed that 2,906 samples were HAdV negative and the other 254 samples were HAdV positive. The HAdV species identified included B (184 samples), C (51 samples), and E (39 samples). Among the three HAdV species, HAdV B and E were detected from 8 samples, and HAdV C and E were detected from other 12 samples. The overall results demonstrated that the sensitivity and specificity of the proposed assay were 100% (254/254) and 99.6% (2894/2906), respectively. From the perspective of routine clinical diagnosis, this assay represented a rapid (≤1.5 h) and economic strategy, and had the potential to be used for the rapid and accurate diagnosis of human respiratory infections caused by HAdV B, C and E. |
Databáze: | OpenAIRE |
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