Recent enterovirus infection in type 1 diabetes: Evidence with a novel IgM method
Autor: | Hong Yin, Amal Elfaitouri, Anna-Karin Berg, Torsten Tuvemo, Gun Frisk, Jonas Blomberg |
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Rok vydání: | 2007 |
Předmět: |
Adolescent
viruses Enzyme-Linked Immunosorbent Assay medicine.disease_cause Virus law.invention law Virology Enterovirus Infections medicine Humans Child Antigens Viral Polymerase chain reaction Enterovirus biology medicine.diagnostic_test Aseptic meningitis medicine.disease Diabetes Mellitus Type 1 Infectious Diseases Immunoglobulin M Immunoassay Immunology Leukocytes Mononuclear biology.protein Antibody Clinical virology |
Zdroj: | Journal of Medical Virology. 79:1861-1867 |
ISSN: | 1096-9071 0146-6615 |
DOI: | 10.1002/jmv.21008 |
Popis: | Quantitative real-time PCR (QPCR) technology has been very useful for diagnosis of viral diseases. QPCR has recently reached a level of sensitivity, simplicity, and reproducibility which allows a large number of samples to be screened rapidly, make it a suitable tool for the clinical virology diagnostics. In this thesis, broadly targeted and degenerated quantitative QPCR assays were used. A somewhat novel single-tube real-time reverse transcription-polymerase chain reaction (QRT-PCR), with takes advantage of ability of rTth DNA polymerase to reverse transcribe RNA in the presence of Mn2+ at elevated temperatures and includes protection against amplimer contamination by using thermolabile UNG, was developed. A new technique for diagnostic of recent viral infection by detection of viral immunoglobulin M (IgM) was also developed. In the first paper, a sensitive single-tube QRT-PCR for detection of enteroviral RNA in patients with aseptic meningitis was presented. In the second paper, a single-serum-dilution real-time PCR-based PIA (PCR-enhanced immunoassay), called quantitative PIA (QPIA), to detect enterovirus IgM for diagnosis of EV infection in patients with aseptic meningitis, was also developed. In the third paper, a broadly targeted, simple, single tube degenerated quantitative QPCR technique for detection of JCV, BKV and SV40 DNA was developed. A conserved region of the VP2 gene of JCV, BKV and SV40 was targeted. A false positive result due to contamination with commonly used SV40 T-antigen plasmids was therefore avoided. In manuscript four, the QPIA assay provide a rational strategy for detection of EV IgM, allows the use of viral antigens isolate from newly diagnosed Type 1 diabetes patients (T1D-EV-QPIA) to measured IgM against diabetogenic viruses in serum from newly diagnosed T1D children, siblings, and healthy children. To conclude, novel broadly targeted real-time PCR methods for diagnosis of entero- and polyoma viral infections were developed. |
Databáze: | OpenAIRE |
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