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Journal of Clinical Microbiology logoLink to Journal of Clinical Microbiology
. 1995 Nov;33(11):2999–3003. doi: 10.1128/jcm.33.11.2999-3003.1995

Geographical clustering of human T-cell lymphotropic virus type 1 infection in Honduras.

I L de Rivera 1, L Amador 1, S Mourra 1, Z Li 1, S Rasheed 1
PMCID: PMC228622  PMID: 8576361

Abstract

Geographical clustering of human T-cell lymphotropic virus type 1 (HTLV-1) infection has been identified in the nonmestizo communities in several cities along the Atlantic coast of Honduras. Of the 2,651 serum samples tested, 122 samples were repeatedly reactive for HTLV-1 antibodies in two different enzyme immunoassays and 3 were indeterminate. These sera did not react in the HTLV-2-specific antibody tests. The presence of HTLV-1 antibodies was confirmed by HTLV-1 immunoblots or Western blots (immunoblots), and the infection was verified by the detection of HTLV-1-specific genetic sequences in the cellular DNA by PCR. Genomic DNA from the peripheral blood mononuclear cells was first tested with generic primers and probes that identified both HTLV-1 and HTLV-2. Next, all DNA samples that showed HTLV reactivity were tested by PCR with specific primers and probes that distinguished HTLV-1 sequences from those of HTLV-2. Our results indicate that only HTLV-1 infection was present in the blood of both mestizo and nonmestizo residents of 15 cities in the Republic of Honduras. The overall prevalence of HTLV-1 infection in the nonmestizo population was 8.1% (95% confidence limit, 6.6 to 9.7%). The mestizo population residing in the same geographical vicinities showed a HTLV-1 antibodies in 0.5% of serum samples tested (95% confidence limit, 0.6 to 1.7%), indicating a significantly greater prevalence of HTLV-1 infection in the nonmestizo population than in the mestizo ethnic groups living in Honduras (P = 0.0001). Since no HTLV-2 antibody reactivity or HTLV-2-specific genetic sequences were detected by PCR with different primers and probes, it was concluded that HTLV-2 infection was not present in the Honduran population groups we tested. Our study also suggested an endemic nature for this virus because there was no difference in the prevalence rate of HTLV-1 antibodies in the nonmestizo community living in the coastal towns of Honduras between 1989 and 1993. This is the first report of HTLV-1 cluster identification in Honduras, Central America.

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Selected References

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  1. Bonis J., Baillou A., Barin F., Verdier M., Janvier B., Denis F. Discrimination between human T-cell lymphotropic virus type I and II (HTLV-I and HTLV-II) infections by using synthetic peptides representing an immunodominant region of the core protein (p19) of HTLV-I and HTLV-II. J Clin Microbiol. 1993 Jun;31(6):1481–1485. doi: 10.1128/jcm.31.6.1481-1485.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  2. Busch M. P., Laycock M., Kleinman S. H., Wages J. W., Jr, Calabro M., Kaplan J. E., Khabbaz R. F., Hollingsworth C. G. Accuracy of supplementary serologic testing for human T-lymphotropic virus types I and II in US blood donors. Retrovirus Epidemiology Donor Study. Blood. 1994 Feb 15;83(4):1143–1148. [PubMed] [Google Scholar]
  3. Chungue E., Boutin J. P., Le Marchand L., Philippon G., Le Guellec A., Chanteau S., Cartel J. L., Gras C., Martin P. M., Roux J. F. Seroepidemiological survey of HTLV-I infection in French Polynesia, Cook Islands and Fiji. Eur J Epidemiol. 1993 May;9(3):347–350. doi: 10.1007/BF00146276. [DOI] [PubMed] [Google Scholar]
  4. Duenas-Barajas E., Bernal J. E., Vaught D. R., Nerurkar V. R., Sarmiento P., Yanagihara R., Gajdusek D. C. Human retroviruses in Amerindians of Colombia: high prevalence of human T cell lymphotropic virus type II infection among the Tunebo Indians. Am J Trop Med Hyg. 1993 Dec;49(6):657–663. doi: 10.4269/ajtmh.1993.49.657. [DOI] [PubMed] [Google Scholar]
  5. Dueńas-Barajas E., Bernal J. E., Vaught D. R., Briceño I., Durán C., Yanagihara R., Gajdusek D. C. Coexistence of human T-lymphotropic virus types I and II among the Wayuu Indians from the Guajira Region of Colombia. AIDS Res Hum Retroviruses. 1992 Nov;8(11):1851–1855. doi: 10.1089/aid.1992.8.1851. [DOI] [PubMed] [Google Scholar]
  6. Ehrlich G. D., Glaser J. B., LaVigne K., Quan D., Mildvan D., Sninsky J. J., Kwok S., Papsidero L., Poiesz B. J. Prevalence of human T-cell leukemia/lymphoma virus (HTLV) type II infection among high-risk individuals: type-specific identification of HTLVs by polymerase chain reaction. Blood. 1989 Oct;74(5):1658–1664. [PubMed] [Google Scholar]
  7. Feigenbaum F., Fang C., Sandler S. G. Human T-lymphotropic virus type II in Panamanian Guaymi Indians. Transfusion. 1994 Feb;34(2):158–161. doi: 10.1046/j.1537-2995.1994.34294143946.x. [DOI] [PubMed] [Google Scholar]
  8. Gessain A., Barin F., Vernant J. C., Gout O., Maurs L., Calender A., de Thé G. Antibodies to human T-lymphotropic virus type-I in patients with tropical spastic paraparesis. Lancet. 1985 Aug 24;2(8452):407–410. doi: 10.1016/s0140-6736(85)92734-5. [DOI] [PubMed] [Google Scholar]
  9. Goubau P., Liu H. F., De Lange G. G., Vandamme A. M., Desmyter J. HTLV-II seroprevalence in pygmies across Africa since 1970. AIDS Res Hum Retroviruses. 1993 Aug;9(8):709–713. doi: 10.1089/aid.1993.9.709. [DOI] [PubMed] [Google Scholar]
  10. Guerena-Burgueno F., Benenson A. S., Sepulveda-Amor J., Ascher M. S., Vugia D. J., Gallo D. Prevalence of human T cell lymphotropic virus types 1 and 2 (HTLV-1/2) in selected Tijuana subpopulations. Am J Trop Med Hyg. 1992 Aug;47(2):127–132. doi: 10.4269/ajtmh.1992.47.127. [DOI] [PubMed] [Google Scholar]
  11. Hjelle B., Appenzeller O., Mills R., Alexander S., Torrez-Martinez N., Jahnke R., Ross G. Chronic neurodegenerative disease associated with HTLV-II infection. Lancet. 1992 Mar 14;339(8794):645–646. doi: 10.1016/0140-6736(92)90797-7. [DOI] [PubMed] [Google Scholar]
  12. Horal P., Hall W. W., Svennerholm B., Lycke J., Jeansson S., Rymo L., Kaplan M. H., Vahlne A. Identification of type-specific linear epitopes in the glycoproteins gp46 and gp21 of human T-cell leukemia viruses type I and type II using synthetic peptides. Proc Natl Acad Sci U S A. 1991 Jul 1;88(13):5754–5758. doi: 10.1073/pnas.88.13.5754. [DOI] [PMC free article] [PubMed] [Google Scholar]
  13. Jacobson S., Raine C. S., Mingioli E. S., McFarlin D. E. Isolation of an HTLV-1-like retrovirus from patients with tropical spastic paraparesis. Nature. 1988 Feb 11;331(6156):540–543. doi: 10.1038/331540a0. [DOI] [PubMed] [Google Scholar]
  14. Kalyanaraman V. S., Sarngadharan M. G., Robert-Guroff M., Miyoshi I., Golde D., Gallo R. C. A new subtype of human T-cell leukemia virus (HTLV-II) associated with a T-cell variant of hairy cell leukemia. Science. 1982 Nov 5;218(4572):571–573. doi: 10.1126/science.6981847. [DOI] [PubMed] [Google Scholar]
  15. Kwok S., Lipka J. J., McKinney N., Kellogg D. E., Poiesz B., Foung S. K., Sninsky J. J. Low incidence of HTLV infections in random blood donors with indeterminate western blot patterns. Transfusion. 1990 Jul-Aug;30(6):491–494. doi: 10.1046/j.1537-2995.1990.30690333477.x. [DOI] [PubMed] [Google Scholar]
  16. Lairmore M. D., Jacobson S., Gracia F., De B. K., Castillo L., Larreategui M., Roberts B. D., Levine P. H., Blattner W. A., Kaplan J. E. Isolation of human T-cell lymphotropic virus type 2 from Guaymi Indians in Panama. Proc Natl Acad Sci U S A. 1990 Nov;87(22):8840–8844. doi: 10.1073/pnas.87.22.8840. [DOI] [PMC free article] [PubMed] [Google Scholar]
  17. Lal R. B., Heneine W., Rudolph D. L., Present W. B., Hofhienz D., Hartley T. M., Khabbaz R. F., Kaplan J. E. Synthetic peptide-based immunoassays for distinguishing between human T-cell lymphotropic virus type I and type II infections in seropositive individuals. J Clin Microbiol. 1991 Oct;29(10):2253–2258. doi: 10.1128/jcm.29.10.2253-2258.1991. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Lee H., Swanson P., Shorty V. S., Zack J. A., Rosenblatt J. D., Chen I. S. High rate of HTLV-II infection in seropositive i.v. drug abusers in New Orleans. Science. 1989 Apr 28;244(4903):471–475. doi: 10.1126/science.2655084. [DOI] [PubMed] [Google Scholar]
  19. Maloney E. M., Biggar R. J., Neel J. V., Taylor M. E., Hahn B. H., Shaw G. M., Blattner W. A. Endemic human T cell lymphotropic virus type II infection among isolated Brazilian Amerindians. J Infect Dis. 1992 Jul;166(1):100–107. doi: 10.1093/infdis/166.1.100. [DOI] [PubMed] [Google Scholar]
  20. Moreira E. D., Jr, Ribeiro T. T., Swanson P., Sampaio Filho C., Melo A., Brites C., Badaró R., Toedter G., Lee H., Harrington W., Jr Seroepidemiology of human T-cell lymphotropic virus type I/II in northeastern Brazil. J Acquir Immune Defic Syndr. 1993 Aug;6(8):959–963. [PubMed] [Google Scholar]
  21. Nerurkar V. R., Babu P. G., Song K. J., Melland R. R., Gnanamuthu C., Saraswathi N. K., Chandy M., Godec M. S., John T. J., Yanagihara R. Sequence analysis of human T cell lymphotropic virus type I strains from southern India: gene amplification and direct sequencing from whole blood blotted onto filter paper. J Gen Virol. 1993 Dec;74(Pt 12):2799–2805. doi: 10.1099/0022-1317-74-12-2799. [DOI] [PubMed] [Google Scholar]
  22. Olaleye D. O., Bernstein L., Sheng Z., Ekweozor C. C., Li X. Y., Sullivan-Halley J., Rasheed S. Type-specific immune response to human T cell lymphotropic virus (HTLV) type I and type II infections in Nigeria. Am J Trop Med Hyg. 1994 Apr;50(4):479–486. doi: 10.4269/ajtmh.1994.50.479. [DOI] [PubMed] [Google Scholar]
  23. Olaleye D. O., Ekweozor C. C., Sheng Z., Rasheed S. Evidence of serological cross-reactivities with human immunodeficiency virus types 1 and 2 and human T-lymphotropic virus types I and II in sera of pregnant women in Ibadan, Nigeria. Int J Epidemiol. 1995 Feb;24(1):198–203. doi: 10.1093/ije/24.1.198. [DOI] [PubMed] [Google Scholar]
  24. Pardi D., Switzer W. M., Hadlock K. G., Kaplan J. E., Lal R. B., Folks T. M. Complete nucleotide sequence of an Amerindian human T-cell lymphotropic virus type II (HTLV-II) isolate: identification of a variant HTLV-II subtype b from a Guaymi Indian. J Virol. 1993 Aug;67(8):4659–4664. doi: 10.1128/jvi.67.8.4659-4664.1993. [DOI] [PMC free article] [PubMed] [Google Scholar]
  25. Poiesz B. J., Ruscetti F. W., Gazdar A. F., Bunn P. A., Minna J. D., Gallo R. C. Detection and isolation of type C retrovirus particles from fresh and cultured lymphocytes of a patient with cutaneous T-cell lymphoma. Proc Natl Acad Sci U S A. 1980 Dec;77(12):7415–7419. doi: 10.1073/pnas.77.12.7415. [DOI] [PMC free article] [PubMed] [Google Scholar]
  26. Roberts C. R., Mitra R., Hyams K., Brodine S. K., Lal R. B. Serologic differentiation of human T lymphotropic virus type I from type II infection by synthetic peptide immunoassays. J Med Virol. 1992 Apr;36(4):298–302. doi: 10.1002/jmv.1890360412. [DOI] [PubMed] [Google Scholar]
  27. Rosenblatt J. D., Golde D. W., Wachsman W., Giorgi J. V., Jacobs A., Schmidt G. M., Quan S., Gasson J. C., Chen I. S. A second isolate of HTLV-II associated with atypical hairy-cell leukemia. N Engl J Med. 1986 Aug 7;315(6):372–377. doi: 10.1056/NEJM198608073150606. [DOI] [PubMed] [Google Scholar]
  28. Sanders R. C., Wai'in P. M., Alexander S. S., Levin A. G., Blattner W. A., Alpers M. P. The prevalence of antibodies to human T-lymphotropic virus type I in different population groups in Papua New Guinea. Arch Virol. 1993;130(3-4):327–334. doi: 10.1007/BF01309664. [DOI] [PubMed] [Google Scholar]
  29. Yoshida M., Seiki M., Yamaguchi K., Takatsuki K. Monoclonal integration of human T-cell leukemia provirus in all primary tumors of adult T-cell leukemia suggests causative role of human T-cell leukemia virus in the disease. Proc Natl Acad Sci U S A. 1984 Apr;81(8):2534–2537. doi: 10.1073/pnas.81.8.2534. [DOI] [PMC free article] [PubMed] [Google Scholar]

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