Cargando…
Serological Studies Confirm the Novel Astrovirus HMOAstV-C as a Highly Prevalent Human Infectious Agent
Molecular identification of a microbe is the first step in determining its prevalence of infection and pathogenic potential. Detection of specific adaptive immune responses can provide insights into whether a microbe is a human infectious agent and its epidemiology. Here we characterized human anti-...
Autores principales: | , , , , , , |
---|---|
Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2011
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3150362/ https://www.ncbi.nlm.nih.gov/pubmed/21829634 http://dx.doi.org/10.1371/journal.pone.0022576 |
_version_ | 1782209538470969344 |
---|---|
author | Burbelo, Peter D. Ching, Kathryn H. Esper, Frank Iadarola, Michael J. Delwart, Eric Lipkin, W. Ian Kapoor, Amit |
author_facet | Burbelo, Peter D. Ching, Kathryn H. Esper, Frank Iadarola, Michael J. Delwart, Eric Lipkin, W. Ian Kapoor, Amit |
author_sort | Burbelo, Peter D. |
collection | PubMed |
description | Molecular identification of a microbe is the first step in determining its prevalence of infection and pathogenic potential. Detection of specific adaptive immune responses can provide insights into whether a microbe is a human infectious agent and its epidemiology. Here we characterized human anti-IgG antibody responses by luciferase immunoprecipitation systems (LIPS) against two protein fragments derived from the capsid protein of the novel HMOAstV-C astrovirus. While antibodies to the N-terminal fragment were not informative, the C-terminal capsid fragment of HMOAstV-C showed a high frequency of immunoreactivity with serum from healthy blood donors. In contrast, a similar C-terminal capsid fragment from the related HMOAstV-A astrovirus failed to show immunoreactivity. Detailed analysis of adult serum from the United Sates using a standardized threshold demonstrated HMOAstV-C seropositivity in approximately 65% of the samples. Evaluation of serum samples from different pediatric age groups revealed that the prevalence of antibodies in 6–12 month, 1–2 year, 2–5 year and 5–10 year olds was 20%, 23%, 32% and 36%, respectively, indicating rising seroprevalence with age. Additionally, 50% (11/22) of the 0–6 month old children showed anti-HMOAstV-C antibody responses, likely reflecting maternal antibodies. Together these results document human humoral responses to HMOAstV-C and validate LIPS as a facile and effective approach for identifying humoral responses to novel infectious agents. |
format | Online Article Text |
id | pubmed-3150362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-31503622011-08-09 Serological Studies Confirm the Novel Astrovirus HMOAstV-C as a Highly Prevalent Human Infectious Agent Burbelo, Peter D. Ching, Kathryn H. Esper, Frank Iadarola, Michael J. Delwart, Eric Lipkin, W. Ian Kapoor, Amit PLoS One Research Article Molecular identification of a microbe is the first step in determining its prevalence of infection and pathogenic potential. Detection of specific adaptive immune responses can provide insights into whether a microbe is a human infectious agent and its epidemiology. Here we characterized human anti-IgG antibody responses by luciferase immunoprecipitation systems (LIPS) against two protein fragments derived from the capsid protein of the novel HMOAstV-C astrovirus. While antibodies to the N-terminal fragment were not informative, the C-terminal capsid fragment of HMOAstV-C showed a high frequency of immunoreactivity with serum from healthy blood donors. In contrast, a similar C-terminal capsid fragment from the related HMOAstV-A astrovirus failed to show immunoreactivity. Detailed analysis of adult serum from the United Sates using a standardized threshold demonstrated HMOAstV-C seropositivity in approximately 65% of the samples. Evaluation of serum samples from different pediatric age groups revealed that the prevalence of antibodies in 6–12 month, 1–2 year, 2–5 year and 5–10 year olds was 20%, 23%, 32% and 36%, respectively, indicating rising seroprevalence with age. Additionally, 50% (11/22) of the 0–6 month old children showed anti-HMOAstV-C antibody responses, likely reflecting maternal antibodies. Together these results document human humoral responses to HMOAstV-C and validate LIPS as a facile and effective approach for identifying humoral responses to novel infectious agents. Public Library of Science 2011-08-04 /pmc/articles/PMC3150362/ /pubmed/21829634 http://dx.doi.org/10.1371/journal.pone.0022576 Text en Burbelo et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Burbelo, Peter D. Ching, Kathryn H. Esper, Frank Iadarola, Michael J. Delwart, Eric Lipkin, W. Ian Kapoor, Amit Serological Studies Confirm the Novel Astrovirus HMOAstV-C as a Highly Prevalent Human Infectious Agent |
title | Serological Studies Confirm the Novel Astrovirus HMOAstV-C as a Highly Prevalent Human Infectious Agent |
title_full | Serological Studies Confirm the Novel Astrovirus HMOAstV-C as a Highly Prevalent Human Infectious Agent |
title_fullStr | Serological Studies Confirm the Novel Astrovirus HMOAstV-C as a Highly Prevalent Human Infectious Agent |
title_full_unstemmed | Serological Studies Confirm the Novel Astrovirus HMOAstV-C as a Highly Prevalent Human Infectious Agent |
title_short | Serological Studies Confirm the Novel Astrovirus HMOAstV-C as a Highly Prevalent Human Infectious Agent |
title_sort | serological studies confirm the novel astrovirus hmoastv-c as a highly prevalent human infectious agent |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3150362/ https://www.ncbi.nlm.nih.gov/pubmed/21829634 http://dx.doi.org/10.1371/journal.pone.0022576 |
work_keys_str_mv | AT burbelopeterd serologicalstudiesconfirmthenovelastrovirushmoastvcasahighlyprevalenthumaninfectiousagent AT chingkathrynh serologicalstudiesconfirmthenovelastrovirushmoastvcasahighlyprevalenthumaninfectiousagent AT esperfrank serologicalstudiesconfirmthenovelastrovirushmoastvcasahighlyprevalenthumaninfectiousagent AT iadarolamichaelj serologicalstudiesconfirmthenovelastrovirushmoastvcasahighlyprevalenthumaninfectiousagent AT delwarteric serologicalstudiesconfirmthenovelastrovirushmoastvcasahighlyprevalenthumaninfectiousagent AT lipkinwian serologicalstudiesconfirmthenovelastrovirushmoastvcasahighlyprevalenthumaninfectiousagent AT kapooramit serologicalstudiesconfirmthenovelastrovirushmoastvcasahighlyprevalenthumaninfectiousagent |