47 research outputs found
Coreceptor usage of primary human immunodeficiency virus type 1 isolates varies according to biological phenotype.
Heterogeneity in oligosaccharides from theO-polysaccharide chain of the lipopolysaccharide fromSalmonella typhi 253Ty determined by fast atom bombardment mass spectrometry
Synthesis of polysaccharides 10. Synthesis of a regular glucan with alternating ?-(1? 4) and ?-(1?6) linkages
Standard conditions of virus isolation reveal biological variability of HIV type 1 in different regions of the world. WHO Network for HIV Isolation and Characterization
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Previous issue date: 1994-11Georg-Speyer-Haus Chemotherapeutisches Forschunginstitut. Frankfurt, GermanyGeorg-Speyer-Haus Chemotherapeutisches Forschunginstitut. Frankfurt, GermanyNational Institute of Biological Standards and Control. London, UKLos Alamos National Laboratory. HIV Sequence Database. Los Alamos, New MexicoGeorg-Speyer-Haus Chemotherapeutisches Forschunginstitut. Frankfurt, GermanyNational Institute of Biological Standards and Control. London, UKNational Institute of Biological Standards and Control. London, UKFundação Oswaldo Cruz. Centro de Pesquisas Gonçalo Moniz. Salvador, BA, BrasilInstitute of Tropical Medicine. Department of Microbiology. Antwerp, BelgiumUganda Virus Research Institute. Entebbe, UgandaMahidol University. Faculty of Medicine Siriraj Hospital. Department of Microbiology, Division of Virology. Bangkok, ThailandWorld Health Organization. Global Programme on AIDS. Geneva, SwitzerlandLos Alamos National Laboratory. HIV Sequence Database. Los Alamos, New MexicoWHO Network for HIV Isolation and CharacterizationHIV-1 isolates were obtained from four countries within the framework of the WHO Network for HIV
Isolation and Characterization. The use of standard HIV isolation procedures allowed us to compare the biological
properties of 126 HIV-1 isolates spanning five genetic subtypes. In primary isolation cultures, viruses
from Uganda and Brazil appeared early and replicated without delay, whereas the replication of Thai viruses
was delayed by several weeks. Regardless of genetic subtype or country of origin, blood samples collected more
than 2 years after seroconversion yielded virus that replicated efficiently in the primary isolation cultures.
None of the isolates obtained from Thailand or Rwanda replicated in cell lines, whereas 5 of the 13 Brazilian
isolates and 7 of the 11 Ugandan isolates replicated and induced syncytia in Ml -2 cells. As expected for virus
isolates obtained early in HIV-1 infection (within 2 years of seroconversion), all viruses from Brazil, Rwanda,
and Thailand showed a slow/low replicative pattern. For the Ugandan samples, the time from seroconversion
was known precisely for a few of the samples and only in one case was less than 2 years. This may explain why
the five viruses that were able to replicate in all cell lines, and thus classified as rapid/high, were of Ugandan
origin. Viruses able to induce syncytia in MT-2 cells, also induced syncytia in PBMC. However, 8 slow/low
viruses (out of 27) gave discordant results, inducing syncytia in PBMC but not in MT-2 cells. Furthermore, using
syncytium induction as a marker, changes in virus populations during early in vitro passage in PBMC
could be observed. The results indicate that biological variation is a general property of HIV-1 in different regions
of the world. Moreover, the time from HIV-1 infection, rather than genetic subtype, seems to be linked to
viral phenotype