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Genome-Wide Surveillance of Genital Herpes Simplex Virus Type 1 From Multiple Anatomic Sites Over Time

Here we present genomic and in vitro analyses of temporally separated episodes of herpes simplex virus type 1 (HSV-1) shedding by an HSV-1–seropositive and human immunodeficiency virus (HIV)/HSV-2–seronegative individual who has frequent recurrences of genital HSV-1. Using oligonucleotide enrichment...

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Autores principales: Shipley, Mackenzie M, Renner, Daniel W, Ott, Mariliis, Bloom, David C, Koelle, David M, Johnston, Christine, Szpara, Moriah L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047417/
https://www.ncbi.nlm.nih.gov/pubmed/29920588
http://dx.doi.org/10.1093/infdis/jiy216
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author Shipley, Mackenzie M
Renner, Daniel W
Ott, Mariliis
Bloom, David C
Koelle, David M
Johnston, Christine
Szpara, Moriah L
author_facet Shipley, Mackenzie M
Renner, Daniel W
Ott, Mariliis
Bloom, David C
Koelle, David M
Johnston, Christine
Szpara, Moriah L
author_sort Shipley, Mackenzie M
collection PubMed
description Here we present genomic and in vitro analyses of temporally separated episodes of herpes simplex virus type 1 (HSV-1) shedding by an HSV-1–seropositive and human immunodeficiency virus (HIV)/HSV-2–seronegative individual who has frequent recurrences of genital HSV-1. Using oligonucleotide enrichment, we compared viral genomes from uncultured swab specimens collected on different days and from distinct genital sites. We found that viral genomes from 7 swab specimens and 3 cultured specimens collected over a 4-month period from the same individual were 98.5% identical. We observed a >2-fold difference in the number of minority variants between swab specimens from lesions, swab specimens from nonlesion sites, and cultured specimens. This virus appeared distinct in its phylogenetic relationship to other strains, and it contained novel coding variations in 21 viral proteins. This included a truncation in the UL11 tegument protein, which is involved in viral egress and spread. Normal immune responses were identified, suggesting that unique viral genomic features may contribute to the recurrent genital infection that this participant experiences.
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spelling pubmed-60474172018-07-19 Genome-Wide Surveillance of Genital Herpes Simplex Virus Type 1 From Multiple Anatomic Sites Over Time Shipley, Mackenzie M Renner, Daniel W Ott, Mariliis Bloom, David C Koelle, David M Johnston, Christine Szpara, Moriah L J Infect Dis Major Articles and Brief Reports Here we present genomic and in vitro analyses of temporally separated episodes of herpes simplex virus type 1 (HSV-1) shedding by an HSV-1–seropositive and human immunodeficiency virus (HIV)/HSV-2–seronegative individual who has frequent recurrences of genital HSV-1. Using oligonucleotide enrichment, we compared viral genomes from uncultured swab specimens collected on different days and from distinct genital sites. We found that viral genomes from 7 swab specimens and 3 cultured specimens collected over a 4-month period from the same individual were 98.5% identical. We observed a >2-fold difference in the number of minority variants between swab specimens from lesions, swab specimens from nonlesion sites, and cultured specimens. This virus appeared distinct in its phylogenetic relationship to other strains, and it contained novel coding variations in 21 viral proteins. This included a truncation in the UL11 tegument protein, which is involved in viral egress and spread. Normal immune responses were identified, suggesting that unique viral genomic features may contribute to the recurrent genital infection that this participant experiences. Oxford University Press 2018-08-15 2018-06-18 /pmc/articles/PMC6047417/ /pubmed/29920588 http://dx.doi.org/10.1093/infdis/jiy216 Text en © The Author(s) 2018. Published by Oxford University Press for the Infectious Diseases Society of America http://creativecommons.org/licenses/by-nc-nd/4.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Major Articles and Brief Reports
Shipley, Mackenzie M
Renner, Daniel W
Ott, Mariliis
Bloom, David C
Koelle, David M
Johnston, Christine
Szpara, Moriah L
Genome-Wide Surveillance of Genital Herpes Simplex Virus Type 1 From Multiple Anatomic Sites Over Time
title Genome-Wide Surveillance of Genital Herpes Simplex Virus Type 1 From Multiple Anatomic Sites Over Time
title_full Genome-Wide Surveillance of Genital Herpes Simplex Virus Type 1 From Multiple Anatomic Sites Over Time
title_fullStr Genome-Wide Surveillance of Genital Herpes Simplex Virus Type 1 From Multiple Anatomic Sites Over Time
title_full_unstemmed Genome-Wide Surveillance of Genital Herpes Simplex Virus Type 1 From Multiple Anatomic Sites Over Time
title_short Genome-Wide Surveillance of Genital Herpes Simplex Virus Type 1 From Multiple Anatomic Sites Over Time
title_sort genome-wide surveillance of genital herpes simplex virus type 1 from multiple anatomic sites over time
topic Major Articles and Brief Reports
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6047417/
https://www.ncbi.nlm.nih.gov/pubmed/29920588
http://dx.doi.org/10.1093/infdis/jiy216
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