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Sökning: id:"swepub:oai:DiVA.org:umu-35733" > Human adenoviruses :

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00004144nam a2200409 4500
001oai:DiVA.org:umu-35733
003SwePub
008100901s2010 | |||||||||||000 ||eng|
020 a 9789174590562q print
024a https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-357332 URI
040 a (SwePub)umu
041 a engb eng
042 9 SwePub
072 7a vet2 swepub-contenttype
072 7a dok2 swepub-publicationtype
100a Andersson, Emma,d 1978-u Umeå universitet,Virologi4 aut0 (Swepub:umu)anoema01
2451 0a Human adenoviruses :b new bioassays for antiviral screening and CD46 interaction
264 1a Umeå :b Umeå university,c 2010
300 a 81 s.
338 a electronic2 rdacarrier
490a Umeå University medical dissertations,x 0346-6612 ;v 1366
520 a Adenoviruses are common pathogens all over the world. The majority of the population has at some point been infected with an adenovirus. Although severe disease can occur in otherwise healthy individuals an adenovirus infection is most commonly self limited in these cases. For immunocompromised individuals however, adenoviruses can be life-threatening pathogens capable of causing disseminated disease and multiple organ failure. Still there is no approved drug specific for treatment of adenovirus infections. We have addressed this using a unique whole cell viral replication reporter gene assay to screen small organic molecules for anti-adenoviral effect. This RCAd11pGFP-vector based assay allowed screening without any preconceived idea of the mechanism for adenovirus inhibition. As a result of the screening campaign 2-[[2-(benzoylamino)benzoyl]amino]-benzoic acid turned out to be a potent inhibitor of adenoviral replication. To establish a structure-activity relationship a number of analogs were synthesized and evaluated for their anti-adenoviral effect. The carboxylic acid moiety of the molecule was important for efficient inhibition of adenovirus replication.There are 54 adenovirus types characterized today and these are divided into seven species, A-G. The receptors used by species B and other adenoviruses are not fully characterized. CD46 is a complement regulatory molecule suggested to be used by all species B types and some species D types but this is not established. We have designed a new bioassay for assessment of the interaction between adenoviruses and CD46 and investigated the CD46-binding capacity of adenovirus types indicated to interact with CD46. We concluded that Ad11p, Ad34, Ad35, and Ad50 clearly bind CD46 specifically, whereas Ad3p, Ad7p, Ad14, and Ad37 do not.CD46 is expressed on all human nucleated cells and serves as a receptor for a number of different bacteria and viruses. Downregulation of CD46 on the cell surface occurs upon binding by some of these pathogens. We show that early in infection Ad11p virions downregulate CD46 upon binding to a much higher extent than the complement regulatory molecules CD55 and CD59.These findings may lead to a better understanding of the pathogenesis of adenoviruses in general and species B adenoviruses in particular and hopefully we have discovered a molecule that can be the basis for development of new anti-adenoviral drugs.
650 7a MEDICIN OCH HÄLSOVETENSKAPx Medicinska och farmaceutiska grundvetenskaperx Mikrobiologi inom det medicinska området0 (SwePub)301092 hsv//swe
650 7a MEDICAL AND HEALTH SCIENCESx Basic Medicinex Microbiology in the medical area0 (SwePub)301092 hsv//eng
653 a Adenovirus
653 a CD46
653 a hemagglutination
653 a antiviral
653 a small molecule
653 a screening
653 a Virology
653 a Virologi
700a Wadell, Göran,c Professor emeritusu Umeå universitet,Virologi4 ths
700a Olofsson, Sigvard,c Professoru Institutionen för Biomedicin, Göteborgs universitet4 opn
710a Umeå universitetb Virologi4 org
856u https://umu.diva-portal.org/smash/get/diva2:346552/FULLTEXT01.pdfx primaryx Raw objecty fulltext
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:umu:diva-35733

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