Show simple item record

dc.contributor.authorTang-Huau, T-L
dc.contributor.authorRosenke, K
dc.contributor.authorMeade-White, K
dc.contributor.authorCarmody, A
dc.contributor.authorSmith, BJ
dc.contributor.authorBosio, CM
dc.contributor.authorJarvis, Michael A
dc.contributor.authorFeldmann, H
dc.date.accessioned2021-08-09T12:35:37Z
dc.date.issued2021-04-22
dc.identifier.issn1999-4915
dc.identifier.issn1999-4915
dc.identifier.otherARTN 729
dc.identifier.urihttp://hdl.handle.net/10026.1/17494
dc.description.abstract

<jats:p>The multimammate mouse (Mastomys natalensis; M. natalensis) has been identified as a major reservoir for multiple human pathogens including Lassa virus (LASV), Leishmania spp., Yersinia spp., and Borrelia spp. Although M. natalensis are related to well-characterized mouse and rat species commonly used in laboratory models, there is an absence of established assays and reagents to study the host immune responses of M. natalensis. As a result, there are major limitations to our understanding of immunopathology and mechanisms of immunological pathogen control in this increasingly important rodent species. In the current study, a large panel of commercially available rodent reagents were screened to identify their cross-reactivity with M. natalensis. Using these reagents, ex vivo assays were established and optimized to evaluate lymphocyte proliferation and cytokine production by M. natalensis lymphocytes. In contrast to C57BL/6J mice, lymphocytes from M. natalensis were relatively non-responsive to common stimuli such as phytohaemagglutinin P and lipopolysaccharide. However, they readily responded to concanavalin A stimulation as indicated by proliferation and cytokine production. In summary, we describe lymphoproliferative and cytokine assays demonstrating that the cellular immune responses in M. natalensis to commonly used mitogens differ from a laboratory-bred mouse strain.</jats:p>

dc.format.extent729-729
dc.format.mediumElectronic
dc.languageen
dc.language.isoen
dc.publisherMDPI
dc.subjectMastomys natalensis
dc.subjectimmune response
dc.subjectT cell
dc.subjecteffector cytokines
dc.subjectconcanavalin A
dc.subjectphytohaemagglutinin P
dc.subjectlipopolysaccharide
dc.subjectLassa virus
dc.titleMastomys natalensis Has a Cellular Immune Response Profile Distinct from Laboratory Mice
dc.typejournal-article
dc.typeJournal Article
dc.typeResearch Support, N.I.H., Intramural
dc.typeResearch Support, Non-U.S. Gov't
plymouth.author-urlhttps://www.webofscience.com/api/gateway?GWVersion=2&SrcApp=PARTNER_APP&SrcAuth=LinksAMR&KeyUT=WOS:000654614600001&DestLinkType=FullRecord&DestApp=ALL_WOS&UsrCustomerID=11bb513d99f797142bcfeffcc58ea008
plymouth.issue5
plymouth.volume13
plymouth.publication-statusPublished online
plymouth.journalViruses
dc.identifier.doi10.3390/v13050729
plymouth.organisational-group/Plymouth
plymouth.organisational-group/Plymouth/Faculty of Health
plymouth.organisational-group/Plymouth/Faculty of Health/School of Biomedical Sciences
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA
plymouth.organisational-group/Plymouth/REF 2021 Researchers by UoA/UoA01 Clinical Medicine
plymouth.organisational-group/Plymouth/Research Groups
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)
plymouth.organisational-group/Plymouth/Research Groups/Institute of Translational and Stratified Medicine (ITSMED)/CBR
plymouth.organisational-group/Plymouth/Users by role
plymouth.organisational-group/Plymouth/Users by role/Academics
dc.publisher.placeSwitzerland
dcterms.dateAccepted2021-04-17
dc.rights.embargodate2021-12-3
dc.identifier.eissn1999-4915
dc.rights.embargoperiodNot known
rioxxterms.versionofrecord10.3390/v13050729
rioxxterms.licenseref.urihttp://www.rioxx.net/licenses/all-rights-reserved
rioxxterms.licenseref.startdate2021-04-22
rioxxterms.typeJournal Article/Review


Files in this item

Thumbnail
Thumbnail

This item appears in the following Collection(s)

Show simple item record


All items in PEARL are protected by copyright law.
Author manuscripts deposited to comply with open access mandates are made available in accordance with publisher policies. Please cite only the published version using the details provided on the item record or document. In the absence of an open licence (e.g. Creative Commons), permissions for further reuse of content should be sought from the publisher or author.
Theme by 
Atmire NV