Basic Science and Pathogenesis

The infectious hypothesis of Alzheimer's disease (AD) suggests that microbes may play a role in pathogenesis by triggering the pathologic cascade or contributing to disease progression. Herpesviruses, such as Epstein-Barr virus (EBV), have been of high interest in AD and related neurodegenerati...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Alzheimer's & dementia 2024-12, Vol.20 Suppl 1, p.e092787
Hauptverfasser: Piotrowski, Stacey L, Lee, Amanda, Tucker, Allison, Narver, Heather, Stein, Brianne, Oluoch, Julia, Zhang, Ting, Schaeffer, Lauren K Hayrynen, Silva, Afonso C, Carter, Gregory W, Jacobson, Steven, Rizzo, Stacey J Sukoff
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page
container_issue
container_start_page e092787
container_title Alzheimer's & dementia
container_volume 20 Suppl 1
creator Piotrowski, Stacey L
Lee, Amanda
Tucker, Allison
Narver, Heather
Stein, Brianne
Oluoch, Julia
Zhang, Ting
Schaeffer, Lauren K Hayrynen
Silva, Afonso C
Carter, Gregory W
Jacobson, Steven
Rizzo, Stacey J Sukoff
description The infectious hypothesis of Alzheimer's disease (AD) suggests that microbes may play a role in pathogenesis by triggering the pathologic cascade or contributing to disease progression. Herpesviruses, such as Epstein-Barr virus (EBV), have been of high interest in AD and related neurodegenerative diseases, in part due to their ability to establish lifelong latent infection and potentially reactivate. However, further research is needed to fully understand the role of herpesviruses in these diseases. The common marmoset (Callithrix jacchus) is not only a translationally relevant model of AD, but also herpesvirus infection. Callitrichine herpesvirus 3 (CalHV-3) is a naturally occurring gammaherpesvirus in the marmoset that is phylogenetically and biologically similar to EBV. This study aimed to understand the contribution of persistent gammaherpesvirus infection to AD-related pathology in the common marmoset. Whole blood from over 200 animals was collected from the NIH NINDS colony and the MARMO-AD colony at the University of Pittsburgh during routine health surveillance and experimental procedures. Plasma was evaluated using MesoScale Discovery (MSD) multi-plex ELISA Aβ peptide panel 4G8 and Neurology Panel 1 (GFAP, Neurofilament L, Total Tau). Peripheral blood mononuclear cells (PBMCs) were isolated using lymphocyte separation media. DNA was extracted from PBMCs and screened for CalHV-3 using a droplet digital PCR (ddPCR) assay that amplified the virus and a housekeeping gene to allow for the quantification of viral loads (copies of CalHV-3/10 cells). 20-30% of the tested colonies were positive for CalHV-3, with a range of viral loads and the highest prevalence in aged animals (≥8 years old). There was significantly higher plasma Neurofilament L (NfL) and total tau in virally infected aged animals compared to uninfected aged animals. The enhancement of plasma biomarkers, such as NfL and tau, in gammaherpesvirus infected aged marmosets suggests that viral infection may contribute to AD-related pathology and neurodegeneration. Investigation is ongoing in additional animals to further characterize the relationship of plasma biomarkers to viral infection and viral load. The common marmoset is a unique translational model that allows for the investigation of AD and the potential role that herpesviruses play in disease manifestation and progression.
doi_str_mv 10.1002/alz.092787
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_proquest_miscellaneous_3151211065</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>3151211065</sourcerecordid><originalsourceid>FETCH-LOGICAL-p561-125b4aaba10dc74bce8141e2816b299779147503afbcf79ea8df309c94c1cf4a3</originalsourceid><addsrcrecordid>eNpNj0tLw0AURgdRbK1u_AElSzep984jk1lqqQ8oKNh9uDO50UheZpqF_noFK7g63-LwwRHiEmGFAPKamq8VOGlzeyTmaIxMjbTu-N-eibMY3wE05GhOxUw5a1AhzsXylmIdkpdQcxc4oa5Mnmn_1r9yx7GO5-KkoibyxYELsbvb7NYP6fbp_nF9s00Hk2GK0nhN5AmhDFb7wDlqZJlj5qVz1jrU1oCiyofKOqa8rBS44HTAUGlSC3H1ezuM_cfEcV-0dQzcNNRxP8VCoUGJCJn5UZcHdfItl8Uw1i2Nn8VfkvoGyjVK0A</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3151211065</pqid></control><display><type>article</type><title>Basic Science and Pathogenesis</title><source>MEDLINE</source><source>Wiley Online Library Open Access</source><source>Wiley Online Library Journals Frontfile Complete</source><source>PubMed Central</source><source>PubMed Central Open Access</source><creator>Piotrowski, Stacey L ; Lee, Amanda ; Tucker, Allison ; Narver, Heather ; Stein, Brianne ; Oluoch, Julia ; Zhang, Ting ; Schaeffer, Lauren K Hayrynen ; Silva, Afonso C ; Carter, Gregory W ; Jacobson, Steven ; Rizzo, Stacey J Sukoff</creator><creatorcontrib>Piotrowski, Stacey L ; Lee, Amanda ; Tucker, Allison ; Narver, Heather ; Stein, Brianne ; Oluoch, Julia ; Zhang, Ting ; Schaeffer, Lauren K Hayrynen ; Silva, Afonso C ; Carter, Gregory W ; Jacobson, Steven ; Rizzo, Stacey J Sukoff</creatorcontrib><description>The infectious hypothesis of Alzheimer's disease (AD) suggests that microbes may play a role in pathogenesis by triggering the pathologic cascade or contributing to disease progression. Herpesviruses, such as Epstein-Barr virus (EBV), have been of high interest in AD and related neurodegenerative diseases, in part due to their ability to establish lifelong latent infection and potentially reactivate. However, further research is needed to fully understand the role of herpesviruses in these diseases. The common marmoset (Callithrix jacchus) is not only a translationally relevant model of AD, but also herpesvirus infection. Callitrichine herpesvirus 3 (CalHV-3) is a naturally occurring gammaherpesvirus in the marmoset that is phylogenetically and biologically similar to EBV. This study aimed to understand the contribution of persistent gammaherpesvirus infection to AD-related pathology in the common marmoset. Whole blood from over 200 animals was collected from the NIH NINDS colony and the MARMO-AD colony at the University of Pittsburgh during routine health surveillance and experimental procedures. Plasma was evaluated using MesoScale Discovery (MSD) multi-plex ELISA Aβ peptide panel 4G8 and Neurology Panel 1 (GFAP, Neurofilament L, Total Tau). Peripheral blood mononuclear cells (PBMCs) were isolated using lymphocyte separation media. DNA was extracted from PBMCs and screened for CalHV-3 using a droplet digital PCR (ddPCR) assay that amplified the virus and a housekeeping gene to allow for the quantification of viral loads (copies of CalHV-3/10 cells). 20-30% of the tested colonies were positive for CalHV-3, with a range of viral loads and the highest prevalence in aged animals (≥8 years old). There was significantly higher plasma Neurofilament L (NfL) and total tau in virally infected aged animals compared to uninfected aged animals. The enhancement of plasma biomarkers, such as NfL and tau, in gammaherpesvirus infected aged marmosets suggests that viral infection may contribute to AD-related pathology and neurodegeneration. Investigation is ongoing in additional animals to further characterize the relationship of plasma biomarkers to viral infection and viral load. The common marmoset is a unique translational model that allows for the investigation of AD and the potential role that herpesviruses play in disease manifestation and progression.</description><identifier>ISSN: 1552-5279</identifier><identifier>EISSN: 1552-5279</identifier><identifier>DOI: 10.1002/alz.092787</identifier><identifier>PMID: 39751311</identifier><language>eng</language><publisher>United States</publisher><subject>Alzheimer Disease - virology ; Amyloid beta-Peptides - metabolism ; Animals ; Callithrix ; Disease Models, Animal ; Female ; Gammaherpesvirinae - genetics ; Gammaherpesvirinae - pathogenicity ; Herpesviridae Infections ; Male ; Neurofilament Proteins - blood ; tau Proteins</subject><ispartof>Alzheimer's &amp; dementia, 2024-12, Vol.20 Suppl 1, p.e092787</ispartof><rights>2024 The Alzheimer's Association. Alzheimer's &amp; Dementia published by Wiley Periodicals LLC on behalf of Alzheimer's Association.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/39751311$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Piotrowski, Stacey L</creatorcontrib><creatorcontrib>Lee, Amanda</creatorcontrib><creatorcontrib>Tucker, Allison</creatorcontrib><creatorcontrib>Narver, Heather</creatorcontrib><creatorcontrib>Stein, Brianne</creatorcontrib><creatorcontrib>Oluoch, Julia</creatorcontrib><creatorcontrib>Zhang, Ting</creatorcontrib><creatorcontrib>Schaeffer, Lauren K Hayrynen</creatorcontrib><creatorcontrib>Silva, Afonso C</creatorcontrib><creatorcontrib>Carter, Gregory W</creatorcontrib><creatorcontrib>Jacobson, Steven</creatorcontrib><creatorcontrib>Rizzo, Stacey J Sukoff</creatorcontrib><title>Basic Science and Pathogenesis</title><title>Alzheimer's &amp; dementia</title><addtitle>Alzheimers Dement</addtitle><description>The infectious hypothesis of Alzheimer's disease (AD) suggests that microbes may play a role in pathogenesis by triggering the pathologic cascade or contributing to disease progression. Herpesviruses, such as Epstein-Barr virus (EBV), have been of high interest in AD and related neurodegenerative diseases, in part due to their ability to establish lifelong latent infection and potentially reactivate. However, further research is needed to fully understand the role of herpesviruses in these diseases. The common marmoset (Callithrix jacchus) is not only a translationally relevant model of AD, but also herpesvirus infection. Callitrichine herpesvirus 3 (CalHV-3) is a naturally occurring gammaherpesvirus in the marmoset that is phylogenetically and biologically similar to EBV. This study aimed to understand the contribution of persistent gammaherpesvirus infection to AD-related pathology in the common marmoset. Whole blood from over 200 animals was collected from the NIH NINDS colony and the MARMO-AD colony at the University of Pittsburgh during routine health surveillance and experimental procedures. Plasma was evaluated using MesoScale Discovery (MSD) multi-plex ELISA Aβ peptide panel 4G8 and Neurology Panel 1 (GFAP, Neurofilament L, Total Tau). Peripheral blood mononuclear cells (PBMCs) were isolated using lymphocyte separation media. DNA was extracted from PBMCs and screened for CalHV-3 using a droplet digital PCR (ddPCR) assay that amplified the virus and a housekeeping gene to allow for the quantification of viral loads (copies of CalHV-3/10 cells). 20-30% of the tested colonies were positive for CalHV-3, with a range of viral loads and the highest prevalence in aged animals (≥8 years old). There was significantly higher plasma Neurofilament L (NfL) and total tau in virally infected aged animals compared to uninfected aged animals. The enhancement of plasma biomarkers, such as NfL and tau, in gammaherpesvirus infected aged marmosets suggests that viral infection may contribute to AD-related pathology and neurodegeneration. Investigation is ongoing in additional animals to further characterize the relationship of plasma biomarkers to viral infection and viral load. The common marmoset is a unique translational model that allows for the investigation of AD and the potential role that herpesviruses play in disease manifestation and progression.</description><subject>Alzheimer Disease - virology</subject><subject>Amyloid beta-Peptides - metabolism</subject><subject>Animals</subject><subject>Callithrix</subject><subject>Disease Models, Animal</subject><subject>Female</subject><subject>Gammaherpesvirinae - genetics</subject><subject>Gammaherpesvirinae - pathogenicity</subject><subject>Herpesviridae Infections</subject><subject>Male</subject><subject>Neurofilament Proteins - blood</subject><subject>tau Proteins</subject><issn>1552-5279</issn><issn>1552-5279</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpNj0tLw0AURgdRbK1u_AElSzep984jk1lqqQ8oKNh9uDO50UheZpqF_noFK7g63-LwwRHiEmGFAPKamq8VOGlzeyTmaIxMjbTu-N-eibMY3wE05GhOxUw5a1AhzsXylmIdkpdQcxc4oa5Mnmn_1r9yx7GO5-KkoibyxYELsbvb7NYP6fbp_nF9s00Hk2GK0nhN5AmhDFb7wDlqZJlj5qVz1jrU1oCiyofKOqa8rBS44HTAUGlSC3H1ezuM_cfEcV-0dQzcNNRxP8VCoUGJCJn5UZcHdfItl8Uw1i2Nn8VfkvoGyjVK0A</recordid><startdate>202412</startdate><enddate>202412</enddate><creator>Piotrowski, Stacey L</creator><creator>Lee, Amanda</creator><creator>Tucker, Allison</creator><creator>Narver, Heather</creator><creator>Stein, Brianne</creator><creator>Oluoch, Julia</creator><creator>Zhang, Ting</creator><creator>Schaeffer, Lauren K Hayrynen</creator><creator>Silva, Afonso C</creator><creator>Carter, Gregory W</creator><creator>Jacobson, Steven</creator><creator>Rizzo, Stacey J Sukoff</creator><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>7X8</scope></search><sort><creationdate>202412</creationdate><title>Basic Science and Pathogenesis</title><author>Piotrowski, Stacey L ; Lee, Amanda ; Tucker, Allison ; Narver, Heather ; Stein, Brianne ; Oluoch, Julia ; Zhang, Ting ; Schaeffer, Lauren K Hayrynen ; Silva, Afonso C ; Carter, Gregory W ; Jacobson, Steven ; Rizzo, Stacey J Sukoff</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-p561-125b4aaba10dc74bce8141e2816b299779147503afbcf79ea8df309c94c1cf4a3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Alzheimer Disease - virology</topic><topic>Amyloid beta-Peptides - metabolism</topic><topic>Animals</topic><topic>Callithrix</topic><topic>Disease Models, Animal</topic><topic>Female</topic><topic>Gammaherpesvirinae - genetics</topic><topic>Gammaherpesvirinae - pathogenicity</topic><topic>Herpesviridae Infections</topic><topic>Male</topic><topic>Neurofilament Proteins - blood</topic><topic>tau Proteins</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Piotrowski, Stacey L</creatorcontrib><creatorcontrib>Lee, Amanda</creatorcontrib><creatorcontrib>Tucker, Allison</creatorcontrib><creatorcontrib>Narver, Heather</creatorcontrib><creatorcontrib>Stein, Brianne</creatorcontrib><creatorcontrib>Oluoch, Julia</creatorcontrib><creatorcontrib>Zhang, Ting</creatorcontrib><creatorcontrib>Schaeffer, Lauren K Hayrynen</creatorcontrib><creatorcontrib>Silva, Afonso C</creatorcontrib><creatorcontrib>Carter, Gregory W</creatorcontrib><creatorcontrib>Jacobson, Steven</creatorcontrib><creatorcontrib>Rizzo, Stacey J Sukoff</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>MEDLINE - Academic</collection><jtitle>Alzheimer's &amp; dementia</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Piotrowski, Stacey L</au><au>Lee, Amanda</au><au>Tucker, Allison</au><au>Narver, Heather</au><au>Stein, Brianne</au><au>Oluoch, Julia</au><au>Zhang, Ting</au><au>Schaeffer, Lauren K Hayrynen</au><au>Silva, Afonso C</au><au>Carter, Gregory W</au><au>Jacobson, Steven</au><au>Rizzo, Stacey J Sukoff</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Basic Science and Pathogenesis</atitle><jtitle>Alzheimer's &amp; dementia</jtitle><addtitle>Alzheimers Dement</addtitle><date>2024-12</date><risdate>2024</risdate><volume>20 Suppl 1</volume><spage>e092787</spage><pages>e092787-</pages><issn>1552-5279</issn><eissn>1552-5279</eissn><abstract>The infectious hypothesis of Alzheimer's disease (AD) suggests that microbes may play a role in pathogenesis by triggering the pathologic cascade or contributing to disease progression. Herpesviruses, such as Epstein-Barr virus (EBV), have been of high interest in AD and related neurodegenerative diseases, in part due to their ability to establish lifelong latent infection and potentially reactivate. However, further research is needed to fully understand the role of herpesviruses in these diseases. The common marmoset (Callithrix jacchus) is not only a translationally relevant model of AD, but also herpesvirus infection. Callitrichine herpesvirus 3 (CalHV-3) is a naturally occurring gammaherpesvirus in the marmoset that is phylogenetically and biologically similar to EBV. This study aimed to understand the contribution of persistent gammaherpesvirus infection to AD-related pathology in the common marmoset. Whole blood from over 200 animals was collected from the NIH NINDS colony and the MARMO-AD colony at the University of Pittsburgh during routine health surveillance and experimental procedures. Plasma was evaluated using MesoScale Discovery (MSD) multi-plex ELISA Aβ peptide panel 4G8 and Neurology Panel 1 (GFAP, Neurofilament L, Total Tau). Peripheral blood mononuclear cells (PBMCs) were isolated using lymphocyte separation media. DNA was extracted from PBMCs and screened for CalHV-3 using a droplet digital PCR (ddPCR) assay that amplified the virus and a housekeeping gene to allow for the quantification of viral loads (copies of CalHV-3/10 cells). 20-30% of the tested colonies were positive for CalHV-3, with a range of viral loads and the highest prevalence in aged animals (≥8 years old). There was significantly higher plasma Neurofilament L (NfL) and total tau in virally infected aged animals compared to uninfected aged animals. The enhancement of plasma biomarkers, such as NfL and tau, in gammaherpesvirus infected aged marmosets suggests that viral infection may contribute to AD-related pathology and neurodegeneration. Investigation is ongoing in additional animals to further characterize the relationship of plasma biomarkers to viral infection and viral load. The common marmoset is a unique translational model that allows for the investigation of AD and the potential role that herpesviruses play in disease manifestation and progression.</abstract><cop>United States</cop><pmid>39751311</pmid><doi>10.1002/alz.092787</doi></addata></record>
fulltext fulltext
identifier ISSN: 1552-5279
ispartof Alzheimer's & dementia, 2024-12, Vol.20 Suppl 1, p.e092787
issn 1552-5279
1552-5279
language eng
recordid cdi_proquest_miscellaneous_3151211065
source MEDLINE; Wiley Online Library Open Access; Wiley Online Library Journals Frontfile Complete; PubMed Central; PubMed Central Open Access
subjects Alzheimer Disease - virology
Amyloid beta-Peptides - metabolism
Animals
Callithrix
Disease Models, Animal
Female
Gammaherpesvirinae - genetics
Gammaherpesvirinae - pathogenicity
Herpesviridae Infections
Male
Neurofilament Proteins - blood
tau Proteins
title Basic Science and Pathogenesis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-02-09T15%3A37%3A04IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Basic%20Science%20and%20Pathogenesis&rft.jtitle=Alzheimer's%20&%20dementia&rft.au=Piotrowski,%20Stacey%20L&rft.date=2024-12&rft.volume=20%20Suppl%201&rft.spage=e092787&rft.pages=e092787-&rft.issn=1552-5279&rft.eissn=1552-5279&rft_id=info:doi/10.1002/alz.092787&rft_dat=%3Cproquest_pubme%3E3151211065%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=3151211065&rft_id=info:pmid/39751311&rfr_iscdi=true