Edgar Maiss

Prof. Edgar Maiss


Research Focus & Metrics

Academic Career Length

44Years (1983-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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1 January 2002 in Journal of Virological Methods
Verified
Journal Article
Closed access
WMW. Menzel
W. Menzel
WJW. Jelkmann
W. Jelkmann
EMEdgar Maiss
Edgar Maiss

1 August 2014 in Virus Research
Verified
Journal Article
Closed access
MNMax Nibert
Max Nibert
SGSaid A. Ghabrial
Said A. Ghabrial
EMEdgar Maiss
Edgar Maiss
TLTill Lesker
Till Lesker
Eeva VainioEeva Vainio
Eeva Vainio
NSNobuhiro Suzuki
Nobuhiro Suzuki

1 January 2018 in Journal of General Virology
Verified
Journal Article
Open access
Eeva VainioEeva Vainio
Eeva Vainio
SCSotaro Chiba
Sotaro Chiba
SGSaid A. Ghabrial
Said A. Ghabrial
EMEdgar Maiss
Edgar Maiss
MRMarilyn Roossinck
Marilyn Roossinck
ICICTV Report Consortium
ICTV Report Consortium
The Partitiviridae is a family of small, isometric, non-enveloped viruses with bisegmented double-stranded (ds) RNA genomes of 3–4.8 kbp. The two genome segments are individually encapsidated. The family has five genera, with characteristic hosts for members of each genus: either plants or fungi for genera Alphapartitivirus and Betapartitivirus, fungi for genus Gammapartitivirus, plants for genus Deltapartitivirus and protozoa for genus Cryspovirus. Partitiviruses are transmitted intracellularly via seeds (plants), oocysts (protozoa) or hyphal anastomosis, cell division and sporogenesis (fungi); there are no known natural vectors. This is a summary of the International Committee on Taxonomy of Viruses (ICTV) Report on the taxonomy of the Partitiviridae, which is available at www.ictv.global/report/partitiviridae.

1 October 2003 in Journal of General Virology
Verified
Journal Article
Closed access
CDChristof Dietrich
Christof Dietrich
EMEdgar Maiss
Edgar Maiss
The distribution of potyviruses in mixed infected Nicotiana benthamiana plants was investigated by using green and red fluorescent proteins (GFP, DsRed). Full-length cDNA clones of Plum pox virus (PPV-NAT-AgfpS; PPV-NAT-red), Tobacco vein mottling virus (TVMV-gfp; TVMV-red) and Clover yellow vein virus (ClYVV-GFP) expressing fluorescent proteins, referred to here as labelled viruses, were used to characterize the distribution of different potyviral populations (e.g. TVMV-gfp/PPV-NAT-red), as well as populations of identical, but differently labelled potyviruses (e.g. PPV-NAT-AgfpS/PPV-NAT-red) or in mixed infections of potyviruses with labelled Potato virus X (PVX). Plants infected by any of the PVX/potyvirus combinations exhibited synergistic symptoms and large numbers of cells were doubly infected. In contrast, co-infections of differently labelled potyvirus populations appeared non-synergistic and remained predominantly separate in the infected plants, independent of whether different viruses or identical but differently labelled viruses were co-infecting. Contact of differently labelled virus populations that exhibited spatial separation was restricted to a small number of cells at the border of different fluorescent cell clusters.

1 March 1989 in Journal of General Virology
Verified
Journal Article
Closed access
EMEdgar Maiss
Edgar Maiss
UTU. Timpe
U. Timpe
ABA. Brisske
A. Brisske
WJW. Jelkmann
W. Jelkmann
RCR. Casper
R. Casper
HKH. W. D. Katinger
H. W. D. Katinger
Summary The complete nucleotide sequence of the RNA of an aphid non-transmissible plum pox virus (PPV-NAT) isolate has been determined from five overlapping cDNA clones. cDNA prepared by primer extension was used to determine the 5′ terminus. The assembled RNA is 9741 nucleotides in length, excluding a 3′ terminal poly(A) sequence. One large open reading frame starts at nucleotide positions 36 to 38 and is terminated with an UAG codon at positions 9522 to 9524. The putative start codon is located at positions 147 to 149. The encoded polyprotein has a predicted M r of 353.8K. Comparison of cistrons from tobacco vein mottling virus and tobacco etch virus with those predicted for PPV-NAT indicated a similar genome organization. A highly conserved sequence of 12 nucleotides was found in the 5′ non-coding region of these three potyviruses. The potential polyadenylation signal from yeast (UAUGU) was found in the 3′ non-coding region of PPV-NAT and several other members of the potyvirus group.

1 January 1994 in Virology
Verified
Journal Article
Closed access
AAA.A. Agranovsky
A.A. Agranovsky
EKE.V. Koonin
E.V. Koonin
VBV.P. Boyko
V.P. Boyko
EMEdgar Maiss
Edgar Maiss
RFR. Frötschl
R. Frötschl
JAJ.G. Atabekov
J.G. Atabekov