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Dominance of variant A in Human Herpesvirus 6 viraemia after renal transplantation

BACKGROUND: Human herpesvirus 6 (HHV-6), mostly variant B reactivation in renal transplant patients has been published by other authors, but the pathogenetic role of HHV-6 variant A has not been clarified. Our aims were to examine the prevalence of HHV-6, to determine the variants, and to investigat...

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Autores principales: Csoma, Eszter, Mészáros, Beáta, Gáll, Tamás, Asztalos, László, Kónya, József, Gergely , Lajos
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2011
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166939/
https://www.ncbi.nlm.nih.gov/pubmed/21843348
http://dx.doi.org/10.1186/1743-422X-8-403
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author Csoma, Eszter
Mészáros, Beáta
Gáll, Tamás
Asztalos, László
Kónya, József
Gergely , Lajos
author_facet Csoma, Eszter
Mészáros, Beáta
Gáll, Tamás
Asztalos, László
Kónya, József
Gergely , Lajos
author_sort Csoma, Eszter
collection PubMed
description BACKGROUND: Human herpesvirus 6 (HHV-6), mostly variant B reactivation in renal transplant patients has been published by other authors, but the pathogenetic role of HHV-6 variant A has not been clarified. Our aims were to examine the prevalence of HHV-6, to determine the variants, and to investigate the interaction between HHV-6 viraemia, human cytomegalovirus (HCMV) infection and clinical symptoms. METHODS: Variant-specific HHV-6 nested PCR and quantitative real-time PCR were used to examine blood samples from renal transplant patients and healthy blood donors for the presence and load of HHV-6 DNA and to determine the variants. Active HHV-6 infection was proved by RT-PCR, and active HCMV infection was diagnosed by pp65 antigenaemia test. RESULTS: HHV-6 viraemia was significantly more frequent in renal transplant patients compared to healthy blood donors (9/200 vs. 0/200; p = 0.004), while prevalence of HHV-6 latency was not significantly different (13/200 vs. 19/200; p > 0.05). Dominance of variant A was revealed in viraemias (8/9), and the frequency of HHV-6A was significantly higher in active infections compared with latency in renal transplant patients (8/9 vs. 2/13; p = 0.0015). Latency was established predominantly by HHV-6B both in renal transplant patients and in healthy blood donors (11/13 and 18/19). There was no statistical significant difference in occurrence of HCMV and HHV-6 viraemia in renal transplant patients (7/200 vs. 9/200). Statistical analysis did not reveal interaction between HHV-6 viraemia and clinical symptoms in our study. CONCLUSIONS: Contrary to previous publications HHV-6A viraemia was found to be predominant in renal transplant patients. Frequency of variant A was significantly higher in cases of active infection then in latency.
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spelling pubmed-31669392011-09-06 Dominance of variant A in Human Herpesvirus 6 viraemia after renal transplantation Csoma, Eszter Mészáros, Beáta Gáll, Tamás Asztalos, László Kónya, József Gergely , Lajos Virol J Research BACKGROUND: Human herpesvirus 6 (HHV-6), mostly variant B reactivation in renal transplant patients has been published by other authors, but the pathogenetic role of HHV-6 variant A has not been clarified. Our aims were to examine the prevalence of HHV-6, to determine the variants, and to investigate the interaction between HHV-6 viraemia, human cytomegalovirus (HCMV) infection and clinical symptoms. METHODS: Variant-specific HHV-6 nested PCR and quantitative real-time PCR were used to examine blood samples from renal transplant patients and healthy blood donors for the presence and load of HHV-6 DNA and to determine the variants. Active HHV-6 infection was proved by RT-PCR, and active HCMV infection was diagnosed by pp65 antigenaemia test. RESULTS: HHV-6 viraemia was significantly more frequent in renal transplant patients compared to healthy blood donors (9/200 vs. 0/200; p = 0.004), while prevalence of HHV-6 latency was not significantly different (13/200 vs. 19/200; p > 0.05). Dominance of variant A was revealed in viraemias (8/9), and the frequency of HHV-6A was significantly higher in active infections compared with latency in renal transplant patients (8/9 vs. 2/13; p = 0.0015). Latency was established predominantly by HHV-6B both in renal transplant patients and in healthy blood donors (11/13 and 18/19). There was no statistical significant difference in occurrence of HCMV and HHV-6 viraemia in renal transplant patients (7/200 vs. 9/200). Statistical analysis did not reveal interaction between HHV-6 viraemia and clinical symptoms in our study. CONCLUSIONS: Contrary to previous publications HHV-6A viraemia was found to be predominant in renal transplant patients. Frequency of variant A was significantly higher in cases of active infection then in latency. BioMed Central 2011-08-15 /pmc/articles/PMC3166939/ /pubmed/21843348 http://dx.doi.org/10.1186/1743-422X-8-403 Text en Copyright ©2011 Csoma et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research
Csoma, Eszter
Mészáros, Beáta
Gáll, Tamás
Asztalos, László
Kónya, József
Gergely , Lajos
Dominance of variant A in Human Herpesvirus 6 viraemia after renal transplantation
title Dominance of variant A in Human Herpesvirus 6 viraemia after renal transplantation
title_full Dominance of variant A in Human Herpesvirus 6 viraemia after renal transplantation
title_fullStr Dominance of variant A in Human Herpesvirus 6 viraemia after renal transplantation
title_full_unstemmed Dominance of variant A in Human Herpesvirus 6 viraemia after renal transplantation
title_short Dominance of variant A in Human Herpesvirus 6 viraemia after renal transplantation
title_sort dominance of variant a in human herpesvirus 6 viraemia after renal transplantation
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3166939/
https://www.ncbi.nlm.nih.gov/pubmed/21843348
http://dx.doi.org/10.1186/1743-422X-8-403
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