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 in | PloS one Vol. 8; no. 4; p. e61182 |
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Main Authors | , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
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Public Library of Science
25.04.2013
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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. |
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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 |
AuthorAffiliation_xml | – name: 7 Clinical Unit of Occupational Medicine, Department of Medical Sciences, University of Trieste, Trieste, Italy – name: 2 Section of Cell Biology and Molecular Genetics, University of Ferrara, Ferrara, Italy – name: 6 Institute for Maternal and Child Health – Istituto di Ricerca e Cura a Carattere Scientifico “Burlo Garofolo”– Trieste, University of Trieste, Trieste, Italy – name: 5 Section of Pediatrics, University of Ferrara, Ferrara, Italy – name: National Institutes of Health, United States of America – name: 10 Departement of Infectious Diseases, Istituto Superiore di Sanità, Rome, Italy – name: 1 Section of Microbiology, University of Ferrara, Ferrara, Italy – name: 9 Department of Obstetrics and Genecology, University of Ferrara, Ferrara, Italy – name: 4 Clinical Laboratory Analysis, County Hospital Delta, Lagosanto, Italy – name: 3 Clinical Laboratory Analysis, Ferrara City Hospital, Ferrara, Italy – name: 8 Clinical Laboratory Analysis, San Marino State Hospital, Borgo Maggiore, Republic of San Marino |
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BackLink | https://www.ncbi.nlm.nih.gov/pubmed/23634207$$D View this record in MEDLINE/PubMed |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 14 content type line 23 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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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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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 |
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