Source:http://linkedlifedata.com/resource/pubmed/id/14625811
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Predicate | Object |
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rdf:type | |
lifeskim:mentions | |
pubmed:issue |
33-34
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pubmed:dateCreated |
2003-11-19
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pubmed:abstractText |
From a posteriori analyses of genetic variation, recombination can only be identified when the parental genomes are distinct. For viruses like HIV-1, this requires the producer cell to be infected by more than one virus. Using fluorescence in situ hybridisation, the provirus copy numbers in splenocytes from two HIV-1 patients were determined. More than 75% of infected splenocytes harboured two or more proviruses, range 1-8, with a mean of approximately 3-4 per cell. Sequencing of amplified DNA from single laser micro-dissected cells showed an extraordinary degree of diversity while numerous recombinants were evident. Given the dynamics of HIV-1 turnover in vivo and a recombination rate of approximately 3 cross-overs per cycle, some genomes from a fifteen year old infection may have undergone as many cross-overs as bases in the genome. Thus, recombination profoundly influences HIV evolution and gives it a non-clonal and transitory nature in vivo.
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pubmed:language |
eng
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pubmed:journal | |
pubmed:citationSubset |
IM
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pubmed:status |
MEDLINE
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pubmed:month |
Aug
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pubmed:issn |
1424-7860
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pubmed:author | |
pubmed:issnType |
Print
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pubmed:day |
23
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pubmed:volume |
133
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pubmed:owner |
NLM
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pubmed:authorsComplete |
Y
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pubmed:pagination |
451-4
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pubmed:dateRevised |
2011-2-15
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pubmed:meshHeading | |
pubmed:year |
2003
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pubmed:articleTitle |
The non-clonal and transitory nature of HIV in vivo.
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pubmed:affiliation |
Department of Virology, University of the Saarland, Homburg, Germany.
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pubmed:publicationType |
Journal Article,
Review,
Research Support, Non-U.S. Gov't
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