Human Cytomegalovirus Genome Diversity in Longitudinally Collected Breast Milk Samples
Reactivation and shedding of human cytomegalovirus (HCMV) in breast milk during lactation is highly frequent in HCMV-seropositive mothers. This represents a key transmission route for postnatal HCMV infection and can lead to severe disease in preterm neonates. Little is known about HCMV strain compo...
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Published in | Frontiers in cellular and infection microbiology Vol. 11; p. 664247 |
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Main Authors | , , , , , , , , , |
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Language | English |
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16.04.2021
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Abstract | Reactivation and shedding of human cytomegalovirus (HCMV) in breast milk during lactation is highly frequent in HCMV-seropositive mothers. This represents a key transmission route for postnatal HCMV infection and can lead to severe disease in preterm neonates. Little is known about HCMV strain composition or longitudinal intrahost viral population dynamics in breast milk from immunocompetent women. We performed HCMV-specific target enrichment and high-throughput sequencing of 38 breast milk samples obtained in Germany between days 10 and 60 postpartum from 15 mothers with HCMV DNA lactia, and assembled HCMV consensus sequences
. The genotype distribution and number of HCMV strains present in each sample were determined by quantifying genotype-specific sequence motifs in 12 hypervariable viral genes, revealing a wide range of genotypes (82/109) for these genes in the cohort and a unique, longitudinally stable strain composition in each mother. Reactivation of up to three distinct HCMV strains was detected in 8/15 of mothers, indicating that a representative subset of the woman's HCMV reservoir might be locally reactivated early during lactation. As described previously, nucleotide diversity of samples with multiple strains was much higher than that of samples with single strains. Breast milk as a main source of postnatal mother-to-infant transmission may serve as a repository for viral diversity and thus play an essential role in the natural epidemiology of HCMV. |
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AbstractList | Reactivation and shedding of human cytomegalovirus (HCMV) in breast milk during lactation is highly frequent in HCMV-seropositive mothers. This represents a key transmission route for postnatal HCMV infection and can lead to severe disease in preterm neonates. Little is known about HCMV strain composition or longitudinal intrahost viral population dynamics in breast milk from immunocompetent women. We performed HCMV-specific target enrichment and high-throughput sequencing of 38 breast milk samples obtained in Germany between days 10 and 60 postpartum from 15 mothers with HCMV DNA lactia, and assembled HCMV consensus sequences de novo. The genotype distribution and number of HCMV strains present in each sample were determined by quantifying genotype-specific sequence motifs in 12 hypervariable viral genes, revealing a wide range of genotypes (82/109) for these genes in the cohort and a unique, longitudinally stable strain composition in each mother. Reactivation of up to three distinct HCMV strains was detected in 8/15 of mothers, indicating that a representative subset of the woman’s HCMV reservoir might be locally reactivated early during lactation. As described previously, nucleotide diversity of samples with multiple strains was much higher than that of samples with single strains. Breast milk as a main source of postnatal mother-to-infant transmission may serve as a repository for viral diversity and thus play an essential role in the natural epidemiology of HCMV. Reactivation and shedding of human cytomegalovirus (HCMV) in breast milk during lactation is highly frequent in HCMV-seropositive mothers. This represents a key transmission route for postnatal HCMV infection and can lead to severe disease in preterm neonates. Little is known about HCMV strain composition or longitudinal intrahost viral population dynamics in breast milk from immunocompetent women. We performed HCMV-specific target enrichment and high-throughput sequencing of 38 breast milk samples obtained in Germany between days 10 and 60 postpartum from 15 mothers with HCMV DNA lactia, and assembled HCMV consensus sequences de novo . The genotype distribution and number of HCMV strains present in each sample were determined by quantifying genotype-specific sequence motifs in 12 hypervariable viral genes, revealing a wide range of genotypes (82/109) for these genes in the cohort and a unique, longitudinally stable strain composition in each mother. Reactivation of up to three distinct HCMV strains was detected in 8/15 of mothers, indicating that a representative subset of the woman’s HCMV reservoir might be locally reactivated early during lactation. As described previously, nucleotide diversity of samples with multiple strains was much higher than that of samples with single strains. Breast milk as a main source of postnatal mother-to-infant transmission may serve as a repository for viral diversity and thus play an essential role in the natural epidemiology of HCMV. Reactivation and shedding of human cytomegalovirus (HCMV) in breast milk during lactation is highly frequent in HCMV-seropositive mothers. This represents a key transmission route for postnatal HCMV infection and can lead to severe disease in preterm neonates. Little is known about HCMV strain composition or longitudinal intrahost viral population dynamics in breast milk from immunocompetent women. We performed HCMV-specific target enrichment and high-throughput sequencing of 38 breast milk samples obtained in Germany between days 10 and 60 postpartum from 15 mothers with HCMV DNA lactia, and assembled HCMV consensus sequences . The genotype distribution and number of HCMV strains present in each sample were determined by quantifying genotype-specific sequence motifs in 12 hypervariable viral genes, revealing a wide range of genotypes (82/109) for these genes in the cohort and a unique, longitudinally stable strain composition in each mother. Reactivation of up to three distinct HCMV strains was detected in 8/15 of mothers, indicating that a representative subset of the woman's HCMV reservoir might be locally reactivated early during lactation. As described previously, nucleotide diversity of samples with multiple strains was much higher than that of samples with single strains. Breast milk as a main source of postnatal mother-to-infant transmission may serve as a repository for viral diversity and thus play an essential role in the natural epidemiology of HCMV. |
Author | Götting, Jasper Rabe, Tabea Hamprecht, Klaus Davison, Andrew J Ganzenmueller, Tina Steinbrück, Lars Schulz, Thomas F Lazar, Katrin Goelz, Rangmar Suárez, Nicolás M |
AuthorAffiliation | 1 Institute of Virology, Hannover Medical School , Hannover , Germany 2 Institute for Medical Virology and Epidemiology of Viral Diseases, University Hospital Tuebingen , Tuebingen , Germany 4 Department of Neonatology, University Children’s Hospital , Tuebingen , Germany 3 MRC-University of Glasgow Centre for Virus Research , Glasgow , United Kingdom |
AuthorAffiliation_xml | – name: 3 MRC-University of Glasgow Centre for Virus Research , Glasgow , United Kingdom – name: 1 Institute of Virology, Hannover Medical School , Hannover , Germany – name: 4 Department of Neonatology, University Children’s Hospital , Tuebingen , Germany – name: 2 Institute for Medical Virology and Epidemiology of Viral Diseases, University Hospital Tuebingen , Tuebingen , Germany |
Author_xml | – sequence: 1 givenname: Jasper surname: Götting fullname: Götting, Jasper organization: Institute of Virology, Hannover Medical School, Hannover, Germany – sequence: 2 givenname: Katrin surname: Lazar fullname: Lazar, Katrin organization: Institute for Medical Virology and Epidemiology of Viral Diseases, University Hospital Tuebingen, Tuebingen, Germany – sequence: 3 givenname: Nicolás M surname: Suárez fullname: Suárez, Nicolás M organization: MRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom – sequence: 4 givenname: Lars surname: Steinbrück fullname: Steinbrück, Lars organization: Institute of Virology, Hannover Medical School, Hannover, Germany – sequence: 5 givenname: Tabea surname: Rabe fullname: Rabe, Tabea organization: Institute for Medical Virology and Epidemiology of Viral Diseases, University Hospital Tuebingen, Tuebingen, Germany – sequence: 6 givenname: Rangmar surname: Goelz fullname: Goelz, Rangmar organization: Department of Neonatology, University Children's Hospital, Tuebingen, Germany – sequence: 7 givenname: Thomas F surname: Schulz fullname: Schulz, Thomas F organization: Institute of Virology, Hannover Medical School, Hannover, Germany – sequence: 8 givenname: Andrew J surname: Davison fullname: Davison, Andrew J organization: MRC-University of Glasgow Centre for Virus Research, Glasgow, United Kingdom – sequence: 9 givenname: Klaus surname: Hamprecht fullname: Hamprecht, Klaus organization: Institute for Medical Virology and Epidemiology of Viral Diseases, University Hospital Tuebingen, Tuebingen, Germany – sequence: 10 givenname: Tina surname: Ganzenmueller fullname: Ganzenmueller, Tina organization: Institute for Medical Virology and Epidemiology of Viral Diseases, University Hospital Tuebingen, Tuebingen, Germany |
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Copyright | Copyright © 2021 Götting, Lazar, Suárez, Steinbrück, Rabe, Goelz, Schulz, Davison, Hamprecht and Ganzenmueller. Copyright © 2021 Götting, Lazar, Suárez, Steinbrück, Rabe, Goelz, Schulz, Davison, Hamprecht and Ganzenmueller 2021 Götting, Lazar, Suárez, Steinbrück, Rabe, Goelz, Schulz, Davison, Hamprecht and Ganzenmueller |
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Keywords | genomes diversity cytomegalovirus lactation genotyping breast milk immunocompetent strains |
Language | English |
License | Copyright © 2021 Götting, Lazar, Suárez, Steinbrück, Rabe, Goelz, Schulz, Davison, Hamprecht and Ganzenmueller. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms. |
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Notes | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 Edited by: Qiliang Cai, Fudan University, China Reviewed by: Neelam Sharma-Walia, Rosalind Franklin University of Medicine and Science, United States; Juliet Spencer, Texas Woman’s University, United States This article was submitted to Virus and Host, a section of the journal Frontiers in Cellular and Infection Microbiology |
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SubjectTerms | breast milk Cellular and Infection Microbiology cytomegalovirus diversity genomes genotyping strains |
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Title | Human Cytomegalovirus Genome Diversity in Longitudinally Collected Breast Milk Samples |
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