1997
DOI: 10.1016/s0166-0934(96)02167-2
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Use of inverse polymerase chain reaction to characterize a novel human herpesvirus 7 isolate

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Cited by 10 publications
(8 citation statements)
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“…After sequencing of the PCR products, 580-bp-long sequences were characterized. In order to obtain the entire sequences of the ␤-lactamase genes, the inverse PCR (IPCR) technique was used (20). This technique enabled us to amplify, by PCR, flanking regions of a DNA fragment.…”
Section: Methodsmentioning
confidence: 99%
“…After sequencing of the PCR products, 580-bp-long sequences were characterized. In order to obtain the entire sequences of the ␤-lactamase genes, the inverse PCR (IPCR) technique was used (20). This technique enabled us to amplify, by PCR, flanking regions of a DNA fragment.…”
Section: Methodsmentioning
confidence: 99%
“…Human herpesvirus 7 (HHV-7) was originally isolated from the stimulated CD4 ϩ T cells of a healthy individual (9) and was subsequently characterized as a ubiquitous virus, infecting most human beings (5,10,17,25,27). This virus was classified in the Betaherpesvirinae subfamily on the basis of its genetic organization (3,6,15,16).…”
mentioning
confidence: 99%
“…Only seven of these combinations (Co) were observed, and 75% of the samples corresponded to two of them, designated provisionally Co1 and Co2. The reference strain JI was defined as Co2, as were our reference isolate, IM (17), and the original HHV-7-positive sample which was the source of IM. The reference strain RK corresponded to an eighth combination (Co8) which was not observed in the group of human samples we investigated.…”
mentioning
confidence: 99%
“…HHV-6 variant A strain TAN and HHV-6 variant B strain MAR were obtained by coculture of peripheral blood mononuclear cells (PBMCs) from healthy blood donors (2). HHV-7 IM was obtained in our laboratory by culture of saliva from a healthy subject on PBMCs from healthy blood donors (19). Amplification of betaglobin gene sequences was performed with the primers previously described (21) to test for the presence of nucleated cells and to verify the absence of major Taq polymerase inhibitors.…”
mentioning
confidence: 99%