Journal of Clinical Virology 21 (2001) 75–79 CMV gB genotypes and outcome of vertical transmission: study on dried blood spots of congenitally infected babies Maria Barbi a, *, Sandro Binda a , Simona Caroppo a , Valeria Primache a , Patrizia Dido ` a , Paola Guidotti a , Carlo Corbetta b , Davide Melotti b a Institute of Virology, Uniersity of Milan, Via C. Pascal 38, 20133 Milano, Italy b Clinical Research Laboratory, ICP, Milan, Italy Received 25 September 2000; received in revised form 6 December 2000; accepted 10 December 2000 Abstract Background: The role of the virulence of the infecting cytomegalovirus (CMV) strain in the transmission of the virus from mother to fetus and the outcome of the fetal infection has not received much attention yet. Molecular analysis of the gene coding for the surface glycoprotein B (gB) has been used to investigate the relationship between genotype and virulence in groups of immunosuppressed patients. Objecties: (1) to assess the prevalence of different gB genotypes in babies with congenital CMV infection; (2) to investigate the possible relationship between genotype and severity of congenital CMV disease; (3) to evaluate the possibility of using dried blood on Guthrie cards (DBS) for genotyping. Study design: CMV DNA was extracted from DBS and from urine/saliva samples collected in the first two weeks of life of 98 congenitally infected babies, half of which were symptomatic at birth. Genotyping was performed through RFLP analysis of the region corresponding to the cleavage site of the gB protein. Results: The most prevalent genotype was gB1 (42%) followed by gB3 (26%), gB2 (19%) and gB4 (13%). Rates of disease and CNS damages were higher among children infected by gB1 (35%, 17%) and gB3 (31%, 28%) than in those infected by gB2 and gB4 (20%, 17% and 13%, 15%, respectively). These differences however did not reach the statistical significance. The parallel typing of DBS and urine/saliva strains gave a full concordance of results. Conclusions: All four major CMV gB genotypes (gB1–4) can cause a congenital infection but none seems to be associated to the development and the severity of disease. The possibility of using the neonatal DBS for genotyping opens a way to the examination of large numbers of cases of congenital CMV infection. © 2001 Elsevier Science B.V. All rights reserved. Keywords: Cytomegalovirus; Genotyping; Congenital infection; Guthrie card; Polymerase chain reaction www.elsevier.com/locate/jcv 1. Introduction CMV is the most widespread viral cause of congenital infection in humans with prevalence rates ranging from 0.3% to 2.2% depending on the population. The host factors that can influence Abbreiations: CMV – cytomegalovirus; DBS – dried blood spot; PCR – polymerase chain reaction; gB – glycoprotein B. * Corresponding author. Tel.: +39-2-2367494; fax: +39-2- 26680713. E-mail address: maria.barbi@unimi.it (M. Barbi). 1386-6532/01/$ - see front matter © 2001 Elsevier Science B.V. All rights reserved. PII:S1386-6532(00)00188-8