Statements in which the resource exists as a subject.
PredicateObject
rdf:type
lifeskim:mentions
pubmed:issue
12
pubmed:dateCreated
2001-5-17
pubmed:databankReference
pubmed:abstractText
Vertically transmitted endogenous retroviruses pose an infectious risk in the course of pig-to-human transplantation of cells, tissues, and organs. Two classes of polytropic type C porcine endogenous retroviruses (PERV) which are infectious for human cells in vitro are known. Recently, we described the cloning and characterization of replication-competent PERV-B sequences from productively infected human cells (F. Czauderna, N. Fischer, K. Boller, R. Kurth, and R. R. Tönjes, J. Virol. 74:4028-4038, 2000). Here, we report the isolation of infectious molecular PERV-A and PERV-B clones from pig cells and compare these proviruses with clones derived from infected human 293 cells. In addition to clone PERV-A(42) derived from 293 cells, four "native" full-length proviral PERV sequences derived from a genomic library of the porcine cell line PK15 were isolated. Three identical class A clones, designated PK15-PERV-A(42), PK15-PERV-A(45), and PK15-PERV-A(58), and one class B clone, PK15-PERV-B(213), were characterized. PK15-PERV-B(213) is highly homologous but distinct from the previously described clone PERV-B(43). PK15-PERV-A(58) demonstrates close homology to PERV-A(42) in env and to PERV-C in long terminal repeat, gag, and pro/pol sequences. All three PERV clones described here were replication competent upon infection of susceptible cell lines. The findings suggest that the pig genome harbors a limited number of infectious PERV-A and -B sequences.
pubmed:commentsCorrections
http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-10211967, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-10438850, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-10455044, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-10516026, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-10590090, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-10756014, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-10779159, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-10936400, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-10993079, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-11021668, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-11222700, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-1698615, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-2786206, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-2926863, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-6169994, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-6274085, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-7489406, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-7584963, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-7585204, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-8291094, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-8564824, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-8692967, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-9055854, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-9121275, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-9338777, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-9343206, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-9525633, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-9557749, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-9728985, http://linkedlifedata.com/resource/pubmed/commentcorrection/11356953-9811736
pubmed:language
eng
pubmed:journal
pubmed:citationSubset
IM
pubmed:status
MEDLINE
pubmed:month
Jun
pubmed:issn
0022-538X
pubmed:author
pubmed:issnType
Print
pubmed:volume
75
pubmed:owner
NLM
pubmed:authorsComplete
Y
pubmed:pagination
5465-72
pubmed:dateRevised
2009-11-18
pubmed:meshHeading
pubmed:year
2001
pubmed:articleTitle
Comparison of replication-competent molecular clones of porcine endogenous retrovirus class A and class B derived from pig and human cells.
pubmed:affiliation
Paul-Ehrlich-Institut, D-63225 Langen, Germany.
pubmed:publicationType
Journal Article, Comparative Study, Research Support, Non-U.S. Gov't