Genotypes of glycoprotein B gene among the Indian symptomatic neonates with congenital CMV infection

Abstract Background Cytomegalovirus [CMV] is a causative agent of congenital infection worldwide and often leads to neurological deficits and hearing loss in newborns. Infants born with symptomatic congenital Cytomegalovirus infection [cCMV] are at significant high risk for developing adverse long-t...

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Main Authors: Agniswar Sarkar, Dipanwita Das, Sabbir Ansari, Rajendra Prasad Chatterjee, Lopamudra Mishra, Biswanath Basu, Sanat Kumar Ghosh, Mala Bhattacharyay, Nilanjan Chakraborty
Format: Article
Language:English
Published: BMC 2019-08-01
Series:BMC Pediatrics
Subjects:
Online Access:http://link.springer.com/article/10.1186/s12887-019-1666-5
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spelling doaj-47f3c77f30094c2782d456ae604e204e2020-11-25T03:57:06ZengBMCBMC Pediatrics1471-24312019-08-0119111210.1186/s12887-019-1666-5Genotypes of glycoprotein B gene among the Indian symptomatic neonates with congenital CMV infectionAgniswar Sarkar0Dipanwita Das1Sabbir Ansari2Rajendra Prasad Chatterjee3Lopamudra Mishra4Biswanath Basu5Sanat Kumar Ghosh6Mala Bhattacharyay7Nilanjan Chakraborty8Virus Unit [NICED-ICMR], GB4-1st Floor, ID and BG HospitalVirus Unit [NICED-ICMR], GB4-1st Floor, ID and BG HospitalVirus Unit [NICED-ICMR], GB4-1st Floor, ID and BG HospitalVirus Unit [NICED-ICMR], GB4-1st Floor, ID and BG HospitalDr. B. C. Roy Post Graduate Institute of Pediatric SciencesDepartment of Pediatric Nephrology, Nil Ratan Sircar Medical College and HospitalDr. B. C. Roy Post Graduate Institute of Pediatric SciencesDr. B. C. Roy Post Graduate Institute of Pediatric SciencesVirus Unit [NICED-ICMR], GB4-1st Floor, ID and BG HospitalAbstract Background Cytomegalovirus [CMV] is a causative agent of congenital infection worldwide and often leads to neurological deficits and hearing loss in newborns. Infants born with symptomatic congenital Cytomegalovirus infection [cCMV] are at significant high risk for developing adverse long-term outcomes. In this study, we look into the sequence variability of surface glycoprotein B [gB] encoding region in newborns with symptomatic CMV infection for the first time in Eastern region of India. Methods 576 suspected newborns from seropositive mothers were subjected to the study and ELISA was used to confirm CMV infection. Different genotypes and their subtypes were determined using multiplex nested-PCR. Viral load of different glycoprotein B [gB] genotypes was measured using RT-PCR. Sequencing and phylogenetic analysis was then performed using Bayesian interference. Results The overall frequency of cCMV infection was 18.4%, where 16.0% neonates were symptomatic. Among the different gB genotypes, gB1 had the highest frequency [23.5%] and gB4 showed the lowest occurrence [5.8%]. 23.5% of symptomatic neonates had mixed genotypes of gB, probably indicating matrenal reinfection with CMV strains in Indian population. Significant genotypic clades [gB1-gB2-gB3-gB5] were grouped closely based on gene sequences, but the gB4 sequence was in the outlier region of the phylogenetic tree indicating the genetic polymorphism. Conclusion This is the first study on cCMV genotyping and its phylogenetic analysis from Eastern Indian neonatal population. The study holds importance in the assessment of cCMV seroprevalence in global perspective. gB protein can be used as a potential therapeutic target against CMV infection.http://link.springer.com/article/10.1186/s12887-019-1666-5CytomegalovirusMolecular epidemiologyGenotypingPolymerase chain reactionCongenital infectionGlycoprotein B
collection DOAJ
language English
format Article
sources DOAJ
author Agniswar Sarkar
Dipanwita Das
Sabbir Ansari
Rajendra Prasad Chatterjee
Lopamudra Mishra
Biswanath Basu
Sanat Kumar Ghosh
Mala Bhattacharyay
Nilanjan Chakraborty
spellingShingle Agniswar Sarkar
Dipanwita Das
Sabbir Ansari
Rajendra Prasad Chatterjee
Lopamudra Mishra
Biswanath Basu
Sanat Kumar Ghosh
Mala Bhattacharyay
Nilanjan Chakraborty
Genotypes of glycoprotein B gene among the Indian symptomatic neonates with congenital CMV infection
BMC Pediatrics
Cytomegalovirus
Molecular epidemiology
Genotyping
Polymerase chain reaction
Congenital infection
Glycoprotein B
author_facet Agniswar Sarkar
Dipanwita Das
Sabbir Ansari
Rajendra Prasad Chatterjee
Lopamudra Mishra
Biswanath Basu
Sanat Kumar Ghosh
Mala Bhattacharyay
Nilanjan Chakraborty
author_sort Agniswar Sarkar
title Genotypes of glycoprotein B gene among the Indian symptomatic neonates with congenital CMV infection
title_short Genotypes of glycoprotein B gene among the Indian symptomatic neonates with congenital CMV infection
title_full Genotypes of glycoprotein B gene among the Indian symptomatic neonates with congenital CMV infection
title_fullStr Genotypes of glycoprotein B gene among the Indian symptomatic neonates with congenital CMV infection
title_full_unstemmed Genotypes of glycoprotein B gene among the Indian symptomatic neonates with congenital CMV infection
title_sort genotypes of glycoprotein b gene among the indian symptomatic neonates with congenital cmv infection
publisher BMC
series BMC Pediatrics
issn 1471-2431
publishDate 2019-08-01
description Abstract Background Cytomegalovirus [CMV] is a causative agent of congenital infection worldwide and often leads to neurological deficits and hearing loss in newborns. Infants born with symptomatic congenital Cytomegalovirus infection [cCMV] are at significant high risk for developing adverse long-term outcomes. In this study, we look into the sequence variability of surface glycoprotein B [gB] encoding region in newborns with symptomatic CMV infection for the first time in Eastern region of India. Methods 576 suspected newborns from seropositive mothers were subjected to the study and ELISA was used to confirm CMV infection. Different genotypes and their subtypes were determined using multiplex nested-PCR. Viral load of different glycoprotein B [gB] genotypes was measured using RT-PCR. Sequencing and phylogenetic analysis was then performed using Bayesian interference. Results The overall frequency of cCMV infection was 18.4%, where 16.0% neonates were symptomatic. Among the different gB genotypes, gB1 had the highest frequency [23.5%] and gB4 showed the lowest occurrence [5.8%]. 23.5% of symptomatic neonates had mixed genotypes of gB, probably indicating matrenal reinfection with CMV strains in Indian population. Significant genotypic clades [gB1-gB2-gB3-gB5] were grouped closely based on gene sequences, but the gB4 sequence was in the outlier region of the phylogenetic tree indicating the genetic polymorphism. Conclusion This is the first study on cCMV genotyping and its phylogenetic analysis from Eastern Indian neonatal population. The study holds importance in the assessment of cCMV seroprevalence in global perspective. gB protein can be used as a potential therapeutic target against CMV infection.
topic Cytomegalovirus
Molecular epidemiology
Genotyping
Polymerase chain reaction
Congenital infection
Glycoprotein B
url http://link.springer.com/article/10.1186/s12887-019-1666-5
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