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Sökning: onr:"swepub:oai:DiVA.org:uu-326221" > Simultaneous Single...

LIBRIS Formathandbok  (Information om MARC21)
FältnamnIndikatorerMetadata
00005029naa a2200433 4500
001oai:DiVA.org:uu-326221
003SwePub
008170809s2017 | |||||||||||000 ||eng|
009oai:DiVA.org:su-144695
024a https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-3262212 URI
024a https://doi.org/10.1128/JVI.00166-172 DOI
024a https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-1446952 URI
040 a (SwePub)uud (SwePub)su
041 a engb eng
042 9 SwePub
072 7a ref2 swepub-contenttype
072 7a art2 swepub-publicationtype
100a Krzywkowski, Tomaszu Stockholms universitet,Institutionen för biokemi och biofysik,Science for Life Laboratory (SciLifeLab),Stockholm Univ, Dept Biochem & Biophys, Sci Life Lab, Stockholm, Sweden.4 aut0 (Swepub:su)maku5421
2451 0a Simultaneous Single-Cell In Situ Analysis of Human Adenovirus Type 5 DNA and mRNA Expression Patterns in Lytic and Persistent Infection
264 1b AMER SOC MICROBIOLOGY,c 2017
338 a print2 rdacarrier
520 a An efficient adenovirus infection results in high-level accumulation of viral DNA and mRNAs in the infected cell population. However, the average viral DNA and mRNA content in a heterogeneous cell population does not necessarily reflect the same abundance in individual cells. Here, we describe a novel padlock probe-based rolling-circle amplification technique that enables simultaneous detection and analysis of human adenovirus type 5 (HAdV-5) genomic DNA and virus-encoded mRNAs in individual infected cells. We demonstrate that the method is applicable for detection and quantification of HAdV-5 DNA and mRNAs in short-term infections in human epithelial cells and in long-term infections in human B lymphocytes. Single-cell evaluation of these infections revealed high heterogeneity and unique cell subpopulations defined by differential viral DNA content and mRNA expression. Further, our single-cell analysis shows that the specific expression pattern of viral E1A 13S and 12S mRNA splice variants is linked to HAdV-5 DNA content in the individual cells. Furthermore, we show that expression of a mature form of the HAdV-5 histone-like protein VII affects virus genome detection in HAdV-5-infected cells. Collectively, padlock probes combined with rolling-circle amplification should be a welcome addition to the method repertoire for the characterization of the molecular details of the HAdV life cycle in individual infected cells. IMPORTANCE Human adenoviruses (HAdVs) have been extensively used as model systems to study various aspects of eukaryotic gene expression and genome organization. The vast majority of the HAdV studies are based on standard experimental procedures carried out using heterogeneous cell populations, where data averaging often masks biological differences. As every cell is unique, characteristics and efficiency of an HAdV infection can vary from cell to cell. Therefore, the analysis of HAdV gene expression and genome organization would benefit from a method that permits analysis of individual infected cells in the heterogeneous cell population. Here, we show that the padlock probe-based rolling-circle amplification method can be used to study concurrent viral DNA accumulation and mRNA expression patterns in individual HAdV-5-infected cells. Hence, this versatile method can be applied to detect the extent of infection and virus gene expression changes in different HAdV-5 infections.
650 7a NATURVETENSKAPx Biologi0 (SwePub)1062 hsv//swe
650 7a NATURAL SCIENCESx Biological Sciences0 (SwePub)1062 hsv//eng
653 a adenovirus
653 a persistent infection
653 a lytic infection
653 a rolling-circle amplification
653 a single-cell analysis
653 a Biochemistry
700a Ciftci, Sibelu Stockholms universitet,Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi,Stockholm Univ, Dept Biochem & Biophys, Sci Life Lab, Stockholm, Sweden,Institutionen för biokemi och biofysik,Science for Life Laboratory (SciLifeLab),Uppsala University, Sweden4 aut0 (Swepub:su)sici8691
700a Assadian, Farzanehu Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi4 aut0 (Swepub:uu)faras942
700a Nilsson, Matsu Stockholms universitet,Institutionen för biokemi och biofysik,Science for Life Laboratory (SciLifeLab),Stockholm Univ, Dept Biochem & Biophys, Sci Life Lab, Stockholm, Sweden.4 aut0 (Swepub:su)matsn
700a Punga, Tanelu Uppsala universitet,Institutionen för medicinsk biokemi och mikrobiologi4 aut0 (Swepub:uu)tpu01907
710a Stockholms universitetb Institutionen för biokemi och biofysik4 org
773t Journal of Virologyd : AMER SOC MICROBIOLOGYg 91:11q 91:11x 0022-538Xx 1098-5514
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:uu:diva-326221
8564 8u https://doi.org/10.1128/JVI.00166-17
8564 8u https://urn.kb.se/resolve?urn=urn:nbn:se:su:diva-144695

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