Skip to main content
Log in

HIV colonizing peripheral blood monocytes follows lymphocytic isolates in shifting from NSI to SI genotype

  • Original Papers
  • Published:
Archives of Virology Aims and scope Submit manuscript

Summary

Non-syncytium inducing (NSI) and syncytium inducing (SI) variants of human immunodeficiency virus (HIV) isolated from peripheral blood mononuclear cells (PBMC) could be definitely typed by sequence analysis of the env-gene V3 region. It was thus possible to compare the genotypes of viral variants isolated from PBMC and accompanying monocyte cultures and those derived directly from the patients' blood cells prior to cultivation. Within the investigated group of patients it was shown that HIV variants colonizing monocytes displayed a similar shift from NSI to SI as observed previously for PBMC, i.e. lymphocyte derived isolates. Lymphocytic SI variants could be isolated from the blood of patients, while simultaneously the predominant provirus in both blood and monocytic isolate was NSI. Consequently, we observed a delayed switch in the predominant provirus genotype found in blood which was associated with a synchronous change in the genotype of the corresponding monocytic isolate. The results show that monocytes/macrophages can be colonized by heterogeneous HIV variants in vivo and can therefore also function as carriers for the spread of highly virulent SI variants into the tissues.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

References

  1. Arendrup M, Olofson S, Nielsen JO, Hansen JES (1994) HIV-1 infection of in vitro cultured human monocytes: early events and influence of HIV-1 antibodies. Arch Virol 136: 35–52

    Google Scholar 

  2. Cabot EL, Beckenbach AT (1989) Simultaneous editing multiple nucleic acid and protein sequences with ESEE. Comp Appl Biosci 5: 233–234

    Google Scholar 

  3. Cheng-Mayer C, Quiroga M, Tung JW, Dina D, Levy JA (1990) Viral determinants of human immunodeficiency virus type 1 T-cell or macrophage tropism, cytopathogenicity, and CD4 antigen modulation. J Virol 64: 4390–4398

    Google Scholar 

  4. Cheng-Mayer C, Shioda T, Levy JA (1991) Host range, replicative, and cytopathic properties of human immunodeficiency virus type 1 are determined by very few amino acid changes intat andgp 120. J Virol 65: 6931–6941

    Google Scholar 

  5. De Jong J-J, Goudsmit J, Keulen W, Klaver B, Krone W, Tersmette M, De Ronde A (1992) Human immunodeficiency virus type 1 clones chimeric for the envelope V3 domain differ in syncytium formation and replication capacity. J Virol 66: 757–765

    Google Scholar 

  6. DeWolf F, Hogervorst E, Goudsmit J, Fenyö EM, Rübsamen-Waigmann H, Holmes H, Galvao-Castro B, Karita E, Wasi C, Sempala SDK, Baan E, Zorgdrager F, Lukashov V, Osmanov S, Kuiken C, Cornelissen M, WHO Network for HIV Isolation and Characterization (1994) Syncytium-inducing and nonsyncytium-inducing capacity of human immunodeficiency virus type 1 subtypes other than B: phenotypic and genotypic characteristics. AIDS Res Hum Retroviruses 10: 1387–1400

    Google Scholar 

  7. Donaldson YK, Bell JE, Holmes EC, Hughes ES, Brown HK, Simmonds P (1994) In vivo distribution and cytopathology of variants of human immunodeficiency virus type I showing restricted sequence variability in the V3 loop. J Virol 68: 5991–6005

    Google Scholar 

  8. Fenyö EM, Morfeldt-Manson L, Chiodi F, Lind A, von Gegerfelt A, Albert J, Olausson E, Asjö B (1988) Distinct replicative cytopathic characteristics of human immunodeficiency virus isolates. J Virol 62: 4414–4419

    Google Scholar 

  9. Fouchier RAM, Groenink M, Kootstra NA, Tersmette M, Huisman HG, Miedema F, Schuitemaker H (1992) Phenotype-associated sequence variation in the third variable domain of human immunodeficiency virus type 1 gp 120 molecule. J Virol 66: 3183–3187

    Google Scholar 

  10. Hultman T, Bergh S, Moks T, Uhlén M (1991) Bidirectional solid-phase sequencing of in vitro-amplified plasmid DNA. Biotechniques 10: 84–93

    Google Scholar 

  11. Innocenti P, Ottman M, Morand O, Leclercq P, Seigneurin J (1992) HIV-1 in blood monocytes: frequency of detection of proviral DNA using PCR and comparison with total CD4 count. AIDS Res Hum Retroviruses 8: 261–268

    Google Scholar 

  12. Innocenti-Francillard P, Brengel K, Guillon C, Mallet F, Morand P, Gruters R, Seigneurin J-M (1994) Blood monocytes infected in vivo by HIV-1 variants with a syncytium-inducing phenotype. AIDS Res Hum Retroviruses 10: 683–690

    Google Scholar 

  13. Kasper P, Kaiser R, Oldenburg J, Brackmann H-H, Matz B, Schneweis KE (1993) Parallel evolution in the V3 region of HIV type 1 after infection of hemophiliacs from a homogeneous source. AIDS Res Hum Retroviruses 10: 1669–1678

    Google Scholar 

  14. Korber BTM, Kunstman KJ, Patterson BK, Furtado M, McEvilly MM, Levy R, Wolinsky SM (1994) Genetic differences between blood-and brain-derived viral sequences from human immunodeficiency virus type 1-infected patients: evidence of conserved elements in the V3 region of the envelope protein of brain-derived sequences. J Virol 68: 7467–7481

    Google Scholar 

  15. LaRosa GJ, Davide JP, Weinhold JA, Waterbury JA, Profy AT, Lewis JA, Langlois AJ, Dreesman GR, Boswell RN, Shadduck P (1990) Conserved sequence and structural elements in the HIV-1 principle neutralizing determinant. Science 249: 932–935

    Google Scholar 

  16. Leitner T, Halapi E, Scarlatti G, Roosi P, Albert J, Fenyö E-M, Uhlén M (1993) Analysis of heterogeneous viral populations by direct DNA sequencing. Biotechniques 15: 120–127

    Google Scholar 

  17. Levy JA (1993) Pathogenesis of human immunodeficiency virus infection. Microbiol Rev 57: 183–289

    Google Scholar 

  18. McElrath MJ, Steinmann RM, Cohn ZA (1991) Latent HIV-1 infection in enriched populations of blood monocytes and T cells from seropositive patients. J Clin Invest 87: 27–30

    Google Scholar 

  19. Miller SA, Dykes DD, Polesky HF (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16: 1215

    Google Scholar 

  20. Saag MS, Hahn BH, Gibbons J, Li Y, Parks ES, Parks WP, Shaw GM (1988) Extensive variation of human immunodeficiency virus type 1 in vivo. Nature 334: 440–444

    Google Scholar 

  21. Sakai K, Dewhurst S, Xiaoyue Ma, Volsky DJ (1988) Differences in cytopathogenicity and host cell range among infectious molecular clones of human immunodeficiency virus type 1 simultaneously isolated from an individual. J Virol 62: 4078–4085

    Google Scholar 

  22. Sambrook J, Fritsch EF, Maniatis T (1989) Molecular cloining: a laboratory manual, 2nd ed. Cold Spring Harbor Laboratory Press, New York

    Google Scholar 

  23. Schmidtmayerova H, Bolmont C, Baghdiguian S, Hirsch I, Cherman J-C (1992) Distinctive pattern of infection and replication of HIV-1 strains in blood-derived macrophages. Virology 190: 124–133

    Google Scholar 

  24. Schneweis KE, Kleim J-P, Bailly E, Niese D, Wagner N, Brackmann HH (1990) Graded cytopathogenicity of the human immunodeficiency virus (HIV) in the course of HIV infection. Med Microbiol Immunol 179: 193–203

    Google Scholar 

  25. Schuitemaker H, Koot M, Kootstra NA, Dercksen MW, De Goede REY, Van Steenwijk RP, Lange JMA, Schattenkerk EJKM, Miedema F, Tersmette M (1992) Biological phenotype of human immunodeficiency virus type 1 clones at different stages of infection: progression of disease is associated with a shift from monocytotropic to T-cell-tropic virus populations. J Virol 66: 1354–1360

    Google Scholar 

  26. Schuitemaker H, Kootstra NA, De Goede REY, DeWolf F, Miedema F, Tersmette M (1991) Monocytotropic human immunodeficiency virus type 1 (HIV-1) variants detectable in all stages of HIV-1 infection lack T-cell line tropism and syncytium-inducing ability in primary T-cell culture. J Virol 65: 356–363

    Google Scholar 

  27. Shioda T, Levy JA, Cheng-Mayer C (1991) Macrophage and T cell-line tropisms of HIV-1 are determined by specific regions of the envelope gp 120 gene. Nature 349: 167–169

    Google Scholar 

  28. Simmonds P, Balfe P, Ludlam CA, Zhang LQ, Bishop JO, Brown AJL (1990) Analysis of sequence diversity in hypervariable regions of the external glycoprotein of human immunodeficiency virus type 1. J Virol 64: 5840–5850

    Google Scholar 

  29. Sodroski J, Goh WC, Rosen C, Campbell K, Haseltine WA (1986) Role of the HTLV-III/LAV envelope in syncytium formation and cytopathicity. Nature 322: 470–473

    Google Scholar 

  30. Tersmette M, De Goede REY, Al BJM, Winkel IN, Gruters RA, Cuypers HT, Huisman HG, Miedema F (1988) Differential syncytium-inducing capacity of human immunodeficiency virus isolates: frequent detection of syncytium-inducing isolates in patients with acquired immunodeficiency syndrome (AIDS) and AIDS-related complex. J Virol 62: 2026–2032

    Google Scholar 

  31. Valentin A, Albert J, Fenyö EM, Asjö B (1994) Dual tropism for macrophages and lymphocytes is a common feature of primary human immunodeficiency virus type 1 and 2 isolates. J Virol 68: 6684–6689

    Google Scholar 

  32. Wain-Hobson S (1989) HIV genome variability in vivo. AIDS 3: 13–18

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Rights and permissions

Reprints and permissions

About this article

Cite this article

Witt, A., Kaiser, R., Mayer, A. et al. HIV colonizing peripheral blood monocytes follows lymphocytic isolates in shifting from NSI to SI genotype. Archives of Virology 141, 1833–1846 (1996). https://doi.org/10.1007/BF01718198

Download citation

  • Received:

  • Accepted:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF01718198

Keywords

Navigation