Serological Evidence of an Early Seroconversion to Simian Virus 40 in Healthy Children and Adolescents

At present Simian virus 40 (SV40) infection in humans appears to be transmitted independently from early contaminated vaccines. In order to test the spread of SV40 infection in children, an immunologic assay employing specific SV40 synthetic peptides corresponding to its viral protein (VP) antigens...

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Published inPloS one Vol. 8; no. 4; p. e61182
Main Authors Taronna, Angelo, Mazzoni, Elisa, Corallini, Alfredo, Bononi, Ilaria, Pietrobon, Silvia, Guerra, Giovanni, Palmonari, Caterina, Borgna-Pignatti, Caterina, Comar, Manola, Bovenzi, Massimo, Casali, Ferruccio, Marci, Roberto, Rezza, Giovanni, Barbanti-Brodano, Giuseppe, Tognon, Mauro, Martini, Fernanda
Format Journal Article
LanguageEnglish
Published United States Public Library of Science 25.04.2013
Public Library of Science (PLoS)
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Abstract At present Simian virus 40 (SV40) infection in humans appears to be transmitted independently from early contaminated vaccines. In order to test the spread of SV40 infection in children, an immunologic assay employing specific SV40 synthetic peptides corresponding to its viral protein (VP) antigens was employed to estimate the seroprevalence of this polyomavirus in Italian infants and adolescents. Serum samples from 328 children and adolescents, up to 17 years, were investigated. Serum antibodies against SV40 VPs were detected by indirect enzyme-linked immunosorbent assays. The seroprevalence of this polyomavirus was calculated after stratifying the subjects by age. Anti-viral capsid protein 1-2-3 SV40 IgG antibodies were detected in 16% of the study participants. The prevalence of antibodies against SV40 VPs tended to increase with age in children, up to 10 year old (21%). Then, in the cohort of individuals aged 11-17 years, the prevalence decreased (16%). A higher prevalence rate (23%) of SV40 VP antibodies was detected in the cohorts of 1-3 year and 7-10 year old children, than in children and adolescents of the other age groups. This age corresponds to children starting nursery and primary school, respectively, in Italy. IgM antibodies against SV40 VP mimotopes were detected in 6-8 month old children suggesting that SV40 seroconversion can occur early in life. SV40 VP antibodies are present at low prevalence in Italian children (16%), suggesting that SV40 infection, although acquired early in life, probably through different routes, is not widespread. The low SV40 seroprevalence suggests that SV40 is less transmissible than other common polyomaviruses, such as BKV and JCV. Alternatively, our immunologic data could be due to another, as yet undiscovered, human polyomavirus closely related to SV40.
AbstractList At present Simian virus 40 (SV40) infection in humans appears to be transmitted independently from early contaminated vaccines. In order to test the spread of SV40 infection in children, an immunologic assay employing specific SV40 synthetic peptides corresponding to its viral protein (VP) antigens was employed to estimate the seroprevalence of this polyomavirus in Italian infants and adolescents. Serum samples from 328 children and adolescents, up to 17 years, were investigated. Serum antibodies against SV40 VPs were detected by indirect enzyme-linked immunosorbent assays. The seroprevalence of this polyomavirus was calculated after stratifying the subjects by age. Anti-viral capsid protein 1-2-3 SV40 IgG antibodies were detected in 16% of the study participants. The prevalence of antibodies against SV40 VPs tended to increase with age in children, up to 10 year old (21%). Then, in the cohort of individuals aged 11-17 years, the prevalence decreased (16%). A higher prevalence rate (23%) of SV40 VP antibodies was detected in the cohorts of 1-3 year and 7-10 year old children, than in children and adolescents of the other age groups. This age corresponds to children starting nursery and primary school, respectively, in Italy. IgM antibodies against SV40 VP mimotopes were detected in 6-8 month old children suggesting that SV40 seroconversion can occur early in life. SV40 VP antibodies are present at low prevalence in Italian children (16%), suggesting that SV40 infection, although acquired early in life, probably through different routes, is not widespread. The low SV40 seroprevalence suggests that SV40 is less transmissible than other common polyomaviruses, such as BKV and JCV. Alternatively, our immunologic data could be due to another, as yet undiscovered, human polyomavirus closely related to SV40.
At present Simian virus 40 (SV40) infection in humans appears to be transmitted independently from early contaminated vaccines. In order to test the spread of SV40 infection in children, an immunologic assay employing specific SV40 synthetic peptides corresponding to its viral protein (VP) antigens was employed to estimate the seroprevalence of this polyomavirus in Italian infants and adolescents. Serum samples from 328 children and adolescents, up to 17 years, were investigated. Serum antibodies against SV40 VPs were detected by indirect enzyme-linked immunosorbent assays. The seroprevalence of this polyomavirus was calculated after stratifying the subjects by age. Anti-viral capsid protein 1-2-3 SV40 IgG antibodies were detected in 16% of the study participants. The prevalence of antibodies against SV40 VPs tended to increase with age in children, up to 10 year old (21%). Then, in the cohort of individuals aged 11-17 years, the prevalence decreased (16%). A higher prevalence rate (23%) of SV40 VP antibodies was detected in the cohorts of 1-3 year and 7-10 year old children, than in children and adolescents of the other age groups. This age corresponds to children starting nursery and primary school, respectively, in Italy. IgM antibodies against SV40 VP mimotopes were detected in 6-8 month old children suggesting that SV40 seroconversion can occur early in life. SV40 VP antibodies are present at low prevalence in Italian children (16%), suggesting that SV40 infection, although acquired early in life, probably through different routes, is not widespread. The low SV40 seroprevalence suggests that SV40 is less transmissible than other common polyomaviruses, such as BKV and JCV. Alternatively, our immunologic data could be due to another, as yet undiscovered, human polyomavirus closely related to SV40.At present Simian virus 40 (SV40) infection in humans appears to be transmitted independently from early contaminated vaccines. In order to test the spread of SV40 infection in children, an immunologic assay employing specific SV40 synthetic peptides corresponding to its viral protein (VP) antigens was employed to estimate the seroprevalence of this polyomavirus in Italian infants and adolescents. Serum samples from 328 children and adolescents, up to 17 years, were investigated. Serum antibodies against SV40 VPs were detected by indirect enzyme-linked immunosorbent assays. The seroprevalence of this polyomavirus was calculated after stratifying the subjects by age. Anti-viral capsid protein 1-2-3 SV40 IgG antibodies were detected in 16% of the study participants. The prevalence of antibodies against SV40 VPs tended to increase with age in children, up to 10 year old (21%). Then, in the cohort of individuals aged 11-17 years, the prevalence decreased (16%). A higher prevalence rate (23%) of SV40 VP antibodies was detected in the cohorts of 1-3 year and 7-10 year old children, than in children and adolescents of the other age groups. This age corresponds to children starting nursery and primary school, respectively, in Italy. IgM antibodies against SV40 VP mimotopes were detected in 6-8 month old children suggesting that SV40 seroconversion can occur early in life. SV40 VP antibodies are present at low prevalence in Italian children (16%), suggesting that SV40 infection, although acquired early in life, probably through different routes, is not widespread. The low SV40 seroprevalence suggests that SV40 is less transmissible than other common polyomaviruses, such as BKV and JCV. Alternatively, our immunologic data could be due to another, as yet undiscovered, human polyomavirus closely related to SV40.
Audience Academic
Author Bononi, Ilaria
Palmonari, Caterina
Martini, Fernanda
Mazzoni, Elisa
Borgna-Pignatti, Caterina
Casali, Ferruccio
Guerra, Giovanni
Taronna, Angelo
Pietrobon, Silvia
Tognon, Mauro
Bovenzi, Massimo
Marci, Roberto
Comar, Manola
Rezza, Giovanni
Barbanti-Brodano, Giuseppe
Corallini, Alfredo
AuthorAffiliation 1 Section of Microbiology, University of Ferrara, Ferrara, Italy
2 Section of Cell Biology and Molecular Genetics, University of Ferrara, Ferrara, Italy
3 Clinical Laboratory Analysis, Ferrara City Hospital, Ferrara, Italy
5 Section of Pediatrics, University of Ferrara, Ferrara, Italy
4 Clinical Laboratory Analysis, County Hospital Delta, Lagosanto, Italy
6 Institute for Maternal and Child Health – Istituto di Ricerca e Cura a Carattere Scientifico “Burlo Garofolo”– Trieste, University of Trieste, Trieste, Italy
7 Clinical Unit of Occupational Medicine, Department of Medical Sciences, University of Trieste, Trieste, Italy
9 Department of Obstetrics and Genecology, University of Ferrara, Ferrara, Italy
8 Clinical Laboratory Analysis, San Marino State Hospital, Borgo Maggiore, Republic of San Marino
10 Departement of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy
National Institutes of Health, United States of America
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BackLink https://www.ncbi.nlm.nih.gov/pubmed/23634207$$D View this record in MEDLINE/PubMed
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2013 Taronna et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
2013 Taronna et al 2013 Taronna et al
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– notice: 2013 Taronna et al. This is an open-access article distributed under the terms of the Creative Commons Attribution License: https://creativecommons.org/licenses/by/4.0/ (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.
– notice: 2013 Taronna et al 2013 Taronna et al
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Conceived and designed the experiments: AC GBB GR MT FM. Performed the experiments: AT EM AC IB SP FM. Analyzed the data: AT EM AC GG CP CB MC MB FC RM GR GBB MT FM. Contributed reagents/materials/analysis tools: GG CP MC CB MB FC RM GR. Wrote the paper: EM AC GR GBB FM MT.
Competing Interests: The authors have declared that no competing interests exist.
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15015494 - Virology. 2004 Jan 5;318(1):1-9
9833757 - Int J Cancer. 1998 Dec 9;78(6):669-74
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Snippet At present Simian virus 40 (SV40) infection in humans appears to be transmitted independently from early contaminated vaccines. In order to test the spread of...
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StartPage e61182
SubjectTerms Adolescent
Adolescents
Age
Analysis
Antibodies
Antibodies, Viral - blood
Antibodies, Viral - immunology
Antigens
Antiviral agents
Biology
Capsid protein
Capsid Proteins - chemistry
Child
Child, Preschool
Children
Contamination
Early Diagnosis
Enzyme-Linked Immunosorbent Assay
Enzymes
Epitopes - immunology
Female
Health
Humans
Immunization
Immunoassays
Immunoglobulin G
Immunoglobulin M
Immunoglobulin M - blood
Immunoglobulin M - immunology
Infant
Infant, Newborn
Infants
Infection
Infections
Laboratories
Male
Medicine
Monkeys
Peptide Fragments - immunology
Peptides
Polyomavirus Infections - blood
Polyomavirus Infections - diagnosis
Seroconversion
Serologic Tests
Simian virus 40 - immunology
Simian virus 40 - physiology
Studies
Synthetic peptides
Teenagers
Tumor Virus Infections - blood
Tumor Virus Infections - diagnosis
Vaccines
Vice presidents (Organizations)
Viral proteins
Viruses
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Title Serological Evidence of an Early Seroconversion to Simian Virus 40 in Healthy Children and Adolescents
URI https://www.ncbi.nlm.nih.gov/pubmed/23634207
https://www.proquest.com/docview/1346593078
https://www.proquest.com/docview/1347788559
https://pubmed.ncbi.nlm.nih.gov/PMC3636242
https://doaj.org/article/d25d19d286904898baa349ef5124f952
http://dx.doi.org/10.1371/journal.pone.0061182
Volume 8
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