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Comparison of serological and molecular test for diagnosis of infectious mononucleosis

BACKGROUND: Epstein-Bar virus (EBV) is the main etiology of infectious mononucleosis (IM) syndrome that is characterized by fever, sore throat, and lymph adenopathy. Since, this virus could be associated with a number of malignancies, some hematologic disorders, and chronic fatigue syndrome, identif...

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Autores principales: Salehi, Hassan, Salehi, Marziyeh, Roghanian, Rasoul, Bozari, Majid, Taleifard, Shirin, Salehi, Mohamad Mahdi, Salehi, Maryam
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Medknow Publications & Media Pvt Ltd 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908787/
https://www.ncbi.nlm.nih.gov/pubmed/27308267
http://dx.doi.org/10.4103/2277-9175.183144
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author Salehi, Hassan
Salehi, Marziyeh
Roghanian, Rasoul
Bozari, Majid
Taleifard, Shirin
Salehi, Mohamad Mahdi
Salehi, Maryam
author_facet Salehi, Hassan
Salehi, Marziyeh
Roghanian, Rasoul
Bozari, Majid
Taleifard, Shirin
Salehi, Mohamad Mahdi
Salehi, Maryam
author_sort Salehi, Hassan
collection PubMed
description BACKGROUND: Epstein-Bar virus (EBV) is the main etiology of infectious mononucleosis (IM) syndrome that is characterized by fever, sore throat, and lymph adenopathy. Since, this virus could be associated with a number of malignancies, some hematologic disorders, and chronic fatigue syndrome, identification of IM is very important. The aim of study was to evaluate the specificity, as well as sensitivity of the two different methods that is, serology versus molecular diagnosis that are currently used for diagnosis of IM. MATERIALS AND METHODS: In this study, during a period of 3.5 years, 100 suspected patients as case group and 100 healthy individuals as a control group were studied. Fifty samples in each group were tested by polymerase chain reaction (PCR) and all the samples including case group and control group were carried out by enzyme-linked immunosorbent assay (ELISA). RESULTS: In 76% of patients and in 20% of the healthy individuals, samples were detected EBV DNA by PCR. On the other hand, 68.5% of the samples belong to the case group and 46% in the control group showed positivity by ELISA. CONCLUSION: By comparing the two methods, since PCR is very expensive and time consuming, and the percentages of difference ranges are narrow, ELISA could be applied as a first, easiest, and preliminary diagnostic test for IM. In addition, this test could be applied in various phases of the disease with a higher sensitivity comparing to PCR. Although PCR is routinely used for diagnosis of various infectious agents, it is considered as an expensive test and merely could be used after 1-2 weeks from the onset of the illness.
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spelling pubmed-49087872016-06-15 Comparison of serological and molecular test for diagnosis of infectious mononucleosis Salehi, Hassan Salehi, Marziyeh Roghanian, Rasoul Bozari, Majid Taleifard, Shirin Salehi, Mohamad Mahdi Salehi, Maryam Adv Biomed Res Brief Report BACKGROUND: Epstein-Bar virus (EBV) is the main etiology of infectious mononucleosis (IM) syndrome that is characterized by fever, sore throat, and lymph adenopathy. Since, this virus could be associated with a number of malignancies, some hematologic disorders, and chronic fatigue syndrome, identification of IM is very important. The aim of study was to evaluate the specificity, as well as sensitivity of the two different methods that is, serology versus molecular diagnosis that are currently used for diagnosis of IM. MATERIALS AND METHODS: In this study, during a period of 3.5 years, 100 suspected patients as case group and 100 healthy individuals as a control group were studied. Fifty samples in each group were tested by polymerase chain reaction (PCR) and all the samples including case group and control group were carried out by enzyme-linked immunosorbent assay (ELISA). RESULTS: In 76% of patients and in 20% of the healthy individuals, samples were detected EBV DNA by PCR. On the other hand, 68.5% of the samples belong to the case group and 46% in the control group showed positivity by ELISA. CONCLUSION: By comparing the two methods, since PCR is very expensive and time consuming, and the percentages of difference ranges are narrow, ELISA could be applied as a first, easiest, and preliminary diagnostic test for IM. In addition, this test could be applied in various phases of the disease with a higher sensitivity comparing to PCR. Although PCR is routinely used for diagnosis of various infectious agents, it is considered as an expensive test and merely could be used after 1-2 weeks from the onset of the illness. Medknow Publications & Media Pvt Ltd 2016-05-30 /pmc/articles/PMC4908787/ /pubmed/27308267 http://dx.doi.org/10.4103/2277-9175.183144 Text en Copyright: © 2016 Advanced Biomedical Research http://creativecommons.org/licenses/by-nc-sa/3.0 This is an open access article distributed under the terms of the Creative Commons Attribution-NonCommercial-ShareAlike 3.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
spellingShingle Brief Report
Salehi, Hassan
Salehi, Marziyeh
Roghanian, Rasoul
Bozari, Majid
Taleifard, Shirin
Salehi, Mohamad Mahdi
Salehi, Maryam
Comparison of serological and molecular test for diagnosis of infectious mononucleosis
title Comparison of serological and molecular test for diagnosis of infectious mononucleosis
title_full Comparison of serological and molecular test for diagnosis of infectious mononucleosis
title_fullStr Comparison of serological and molecular test for diagnosis of infectious mononucleosis
title_full_unstemmed Comparison of serological and molecular test for diagnosis of infectious mononucleosis
title_short Comparison of serological and molecular test for diagnosis of infectious mononucleosis
title_sort comparison of serological and molecular test for diagnosis of infectious mononucleosis
topic Brief Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4908787/
https://www.ncbi.nlm.nih.gov/pubmed/27308267
http://dx.doi.org/10.4103/2277-9175.183144
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