Literature DB >> 23806667

Distribution of cytomegalovirus gN variants and associated clinical sequelae in infants.

Edyta Paradowska1, Agnieszka Jabłońska, Mirosława Studzińska, Patrycja Suski, Beata Kasztelewicz, Barbara Zawilińska, Małgorzata Wiśniewska-Ligier, Katarzyna Dzierżanowska-Fangrat, Teresa Woźniakowska-Gęsicka, Justyna Czech-Kowalska, Bożena Lipka, Maria Kornacka, Dorota Pawlik, Tomasz Tomasik, Magdalena Kosz-Vnenchak, Zbigniew J Leśnikowski.   

Abstract

BACKGROUND: Human cytomegalovirus (HCMV) is the most widespread cause of congenital infection. The effects of various viral strains and viral loads on the infection outcome have been under debate.
OBJECTIVES: To determine the distribution of gN variants in HCMV strains isolated from children with congenital or postnatal infection and to establish the relationship between the viral genotype, the viral load, and the sequelae. STUDY
DESIGN: The study population included congenitally HCMV-infected newborns and children with postnatal or unproven congenital HCMV infection. The genotyping was performed by RFLP analysis of PCR-amplified fragments, and the viral load was measured by quantitative real-time PCR.
RESULTS: Our results demonstrated that the HCMV genotypes gN3b, gN4b, and gN4c were prevalent in the patients examined. There were no differences in the distributions of gN genotypes in the congenitally and postnatally infected children. Multiple HCMV strains were detected in both groups of children. A significant association between the HCMV gN4 genotype and the incidence of neurological disorders was observed (p=0.045). Our results suggest that the detection of the gN2 or the gN4 genotype may be indicative of serious manifestations in children. In contrast, the gN3b and the gN1 genotypes represent less pathogenic HCMV strains. The HCMV load in urine was significantly higher in children with congenital infection compared with children with postnatal infection. No correlation was found between the viral load and the genotype.
CONCLUSION: Our results suggest that the gN genotype may be a virological marker of symptomatic HCMV infection in newborns.
Copyright © 2013 Elsevier B.V. All rights reserved.

Entities:  

Keywords:  CI; CNS; CSF; Congenital infection; GE; Glycoprotein N; HCMV; Human cytomegalovirus; IUGR; OR; RFLP; SNHL; UPGMA; central nervous system; cerebrospinal fluid; confidence interval; gC; gN; genome equivalents; glycoprotein N; glycoprotein complex; human cytomegalovirus; intrauterine growth retardation; nPCR; nested polymerase chain reaction; odds ratio; restriction fragment length polymorphism; sensorineural hearing loss; unweighted pair group method

Mesh:

Substances:

Year:  2013        PMID: 23806667     DOI: 10.1016/j.jcv.2013.05.024

Source DB:  PubMed          Journal:  J Clin Virol        ISSN: 1386-6532            Impact factor:   3.168


  11 in total

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Authors:  Steven Sijmons; Kim Thys; Mirabeau Mbong Ngwese; Ellen Van Damme; Jan Dvorak; Marnix Van Loock; Guangdi Li; Ruth Tachezy; Laurent Busson; Jeroen Aerssens; Marc Van Ranst; Piet Maes
Journal:  J Virol       Date:  2015-05-13       Impact factor: 5.103

2.  Genotype distribution, viral load and clinical characteristics of infants with postnatal or congenital cytomegalovirus infection.

Authors:  Joppe Nijman; Femke S Mandemaker; Malgorzata A Verboon-Maciolek; Susan C Aitken; Anton M van Loon; Linda S de Vries; Rob Schuurman
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3.  Mixed infections with distinct cytomegalovirus glycoprotein B genotypes in Polish pregnant women, fetuses, and newborns.

Authors:  M Rycel; W Wujcicka; B Zawilińska; E Paradowska; P Suski; Z Gaj; J Wilczyński; Z Leśnikowski; D Nowakowska
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4.  Distribution of the CMV glycoprotein gH/gL/gO and gH/gL/pUL128/pUL130/pUL131A complex variants and associated clinical manifestations in infants infected congenitally or postnatally.

Authors:  Edyta Paradowska; Agnieszka Jabłońska; Mirosława Studzińska; Beata Kasztelewicz; Małgorzata Wiśniewska-Ligier; Katarzyna Dzierżanowska-Fangrat; Teresa Woźniakowska-Gęsicka; Justyna Czech-Kowalska
Journal:  Sci Rep       Date:  2019-11-08       Impact factor: 4.379

Review 5.  A Systematic Review on the Association of Acquired Human Cytomegalovirus Infection with Hearing Loss.

Authors:  Estrella Martinez-Gomez; Patricia Perez-Carpena; Marisa Flook; José A Lopez-Escamez
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6.  Cytomegalovirus Genotype Distribution Among Congenitally and Postnatally Infected Patients: Association of Particular Glycoprotein (g)B and gN Types With Symptomatic Disease.

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7.  Combined genetic variants of human cytomegalovirus envelope glycoproteins as congenital infection markers.

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8.  Distribution of Cytomegalovirus Genotypes among Neonates Born to Infected Mothers in Islamabad, Pakistan.

Authors:  Ghulam Mujtaba; Adnan Khurshid; Salmaan Sharif; Muhammad Masroor Alam; Uzma Bashir Aamir; Shahzad Shaukat; Mehar Angez; Muhammad Suleman Rana; Massab Umair; Aamer Ali Shah; Syed Sohail Zahoor Zaidi
Journal:  PLoS One       Date:  2016-07-01       Impact factor: 3.240

9.  Association of CMV genomic mutations with symptomatic infection and hearing loss in congenital CMV infection.

Authors:  G Clement Dobbins; Amit Patki; Dongquan Chen; Hemant K Tiwari; Curtis Hendrickson; William J Britt; Karen Fowler; Jake Y Chen; Suresh B Boppana; Shannon A Ross
Journal:  BMC Infect Dis       Date:  2019-12-10       Impact factor: 3.090

10.  Cytomegalovirus Genotype Distribution among Postnatally Infected Infants: Association of Glycoprotein B, Glycoprotein N and Glycoprotein H Types with CMV-Associated Thrombocytopenia.

Authors:  Hongbo Hu; Ying Cheng; Qiaoying Peng; Kun Chen
Journal:  Mediterr J Hematol Infect Dis       Date:  2020-09-01       Impact factor: 2.576

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