Volume 49, Issue 6 pp. 1146-1150

Serologic and molecular typing of human T-lymphotropic virus among blood donors in Maputo City, Mozambique

Eduardo Samo Gudo

Eduardo Samo Gudo

From the Departamento de Imunologia, Instituto Nacional de Saúde, Maputo, Mozambique; the Departamento de Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil; the Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil; and the Programa Nacional de Transfusão de Sangue, Ministério da Saúde, Maputo, Mozambique.

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Celina M. Abreu

Celina M. Abreu

From the Departamento de Imunologia, Instituto Nacional de Saúde, Maputo, Mozambique; the Departamento de Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil; the Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil; and the Programa Nacional de Transfusão de Sangue, Ministério da Saúde, Maputo, Mozambique.

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Tufária Mussá

Tufária Mussá

From the Departamento de Imunologia, Instituto Nacional de Saúde, Maputo, Mozambique; the Departamento de Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil; the Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil; and the Programa Nacional de Transfusão de Sangue, Ministério da Saúde, Maputo, Mozambique.

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Ângelo Do Rosário Augusto

Ângelo Do Rosário Augusto

From the Departamento de Imunologia, Instituto Nacional de Saúde, Maputo, Mozambique; the Departamento de Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil; the Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil; and the Programa Nacional de Transfusão de Sangue, Ministério da Saúde, Maputo, Mozambique.

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Koko Otsuki

Koko Otsuki

From the Departamento de Imunologia, Instituto Nacional de Saúde, Maputo, Mozambique; the Departamento de Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil; the Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil; and the Programa Nacional de Transfusão de Sangue, Ministério da Saúde, Maputo, Mozambique.

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Evelina Chambo

Evelina Chambo

From the Departamento de Imunologia, Instituto Nacional de Saúde, Maputo, Mozambique; the Departamento de Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil; the Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil; and the Programa Nacional de Transfusão de Sangue, Ministério da Saúde, Maputo, Mozambique.

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Nádia Amade

Nádia Amade

From the Departamento de Imunologia, Instituto Nacional de Saúde, Maputo, Mozambique; the Departamento de Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil; the Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil; and the Programa Nacional de Transfusão de Sangue, Ministério da Saúde, Maputo, Mozambique.

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Amílcar Tanuri

Amílcar Tanuri

From the Departamento de Imunologia, Instituto Nacional de Saúde, Maputo, Mozambique; the Departamento de Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil; the Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil; and the Programa Nacional de Transfusão de Sangue, Ministério da Saúde, Maputo, Mozambique.

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Orlando C. Ferreira Jr

Orlando C. Ferreira Jr

From the Departamento de Imunologia, Instituto Nacional de Saúde, Maputo, Mozambique; the Departamento de Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil; the Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil; and the Programa Nacional de Transfusão de Sangue, Ministério da Saúde, Maputo, Mozambique.

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Ilesh V. Jani

Ilesh V. Jani

From the Departamento de Imunologia, Instituto Nacional de Saúde, Maputo, Mozambique; the Departamento de Genética, Universidade Federal do Rio de Janeiro, Rio de Janeiro, Brazil; the Instituto Oswaldo Cruz, Fundação Oswaldo Cruz (FIOCRUZ), Rio de Janeiro, Brazil; and the Programa Nacional de Transfusão de Sangue, Ministério da Saúde, Maputo, Mozambique.

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First published: 01 June 2009
Citations: 22
Ilesh V. Jani, Departamento de Imunologia, Instituto Nacional de Saúde, PO Box 264, Maputo, Mozambique; e-mail: [email protected].

This study was funded by the Mozambican Ministry of Health and by the Brazilian National Council for Research and Development (CNPq) through the Pro-Africa program Grant 491.367/2005-8.

Abstract

BACKGROUND: Screening for human T-lymphotropic virus-1/2 (HTLV-1/2) infection is not performed in blood banks in Mozambique. The aim was to determine the prevalence of HTLV-1/2 among blood donors of the Maputo Central Hospital Blood Bank and measure the coinfection rate of HTLV-1/2 with human immunodeficiency virus (HIV), hepatitis B virus (HBV), and syphilis.

STUDY DESIGN AND METHODS: A total of 2019 consecutive blood donors were screened for HTLV-1/2 antibodies, HIV-1/2 antibodies, hepatitis B surface antigen (HBsAg), and rapid plasma reagin (RPR) for syphilis. Specimens reactive on a first HTLV-1/2 enzyme immunoassay (EIA) were retested using a second EIA. Specimens that were dually reactive on both EIAs were further tested using Western blot (WB) and real-time polymerase chain reaction (PCR).

RESULTS: All 18 dually reactive specimens (0.89%; 95% confidence interval, 0.48%-1.30%) were positive for the presence of HTLV-1 by WB and real-time PCR. HTLV-2 was not detected. The prevalences of anti-HIV, HBsAg, and reactivity in the RPR test were 5.72, 6.01, and 0.98 percent, respectively. There was no significant association between HTLV-1 infection and demographic variables (age and sex) or serologic markers (HIV, HBsAg, and RPR). For the 17 HTLV-1–positive donors for whom serologic data for HIV, HBsAg, and syphilis RPR were available, 2 showed coinfection with HIV and 1 with HBV.

CONCLUSION: Compared to other infectious agents, HTLV-1 is present at relatively low levels among blood donors in Mozambique. Cost and logistics will present as major challenges for introducing HTLV-1/2 screening in blood banks. In blood banks in Southern Africa where EIA testing is possible, a sequential algorithm of two EIAs may be a cost-efficient option for HTLV-1/2 screening.

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