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Vol. 15. Issue 6.
Pages 547-552 (November - December 2011)
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Vol. 15. Issue 6.
Pages 547-552 (November - December 2011)
Original article
Open Access
Magnetic bead technology for viral RNA extraction from serum in blood bank screening
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Guilherme Ambrozio Albertoni1,
Corresponding author
albertonig@nefro.epm.br

Correspondence to: Av. Jandira, 1260 Indianópolis 04080-006 São Paulo, SP Brazil Phone: +55 11 5055-6588 R-39 Fax: +55 11 5055-6588.
, Carine Prisco Arnoni1, Patricia Regina Barboza Araujo1, Sheila Siqueira Andrade1, Fabrício Oliveira Carvalho2, Manoel João Batista Castello Girão3, Nestor Schor4, José Augusto Barreto5
1 Colsan – Associação Beneficente de Coleta de Sangue, São Paulo, SP, Brazil
2 Colsan – Associação Beneficente de Coleta de Sangue, São Paulo, SP, Brazil
3 Colsan – Associação Beneficente de Coleta de Sangue, São Paulo, SP, Brazil
4 Universidade Federal de São Paulo (UNIFESP), SP, Brazil
5 Head, Colsan – Associação Beneficente de Coleta de Sangue, São Paulo, SP, Brazil
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Abstract

Nucleic acid amplification testing (NAT) was recently recommended by Brazilian legislation and has been implemented at some blood banks in the city of São Paulo, Brazil, in an attempt to reduce blood-born transmission of human immunodeficiency virus (HIV) and hepatitis C virus.

Objective

Manual magnetic particle-based extraction methods for HIV and HCV viral nucleic acids were evaluated in combination with detection by reverse transcriptase -polymerase chain reaction (RT-PCR) one-step.

Methods

Blood donor samples were collected from January 2010 to September 2010, and minipools of them were submitted to testing. ELISA was used for the analysis of anti-HCV/HIV antibodies. Detection and amplification of viral RNA was performed using real-time PCR.

Results

Out of 20.808 samples screened, 53 samples (29 for HCV and 24 for HIV) were confirmed as positive by serological and NAT methods.

Conclusion

The manual magnetic bead-based extraction in combination with real-time PCR detection can be used to routinely screen blood donation for viremic donors to further increase the safety of blood products.

Keywords:
HCV
HIV
infection
reverse transcriptase polymerase chain reaction
blood banks
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