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Hemoglobin
international journal for hemoglobin research
Volume 42, 2018 - Issue 3
279
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Original Article

A Simple Whole-Blood Polymerase Chain Reaction without DNA Extraction for Thalassemia Diagnosis

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Pages 178-183 | Received 30 Mar 2018, Accepted 05 Jun 2018, Published online: 04 Oct 2018
 

Abstract

Polymerase chain reaction (PCR) diagnosis of thalassemia usually relies on using genomic DNA. Preparing the genomic DNA can lead to sample-to-sample contamination. This report was aimed to establish the PCR protocol using whole-blood for detecting mutations of α- and β-globin genes causing the thalassemia syndrome. First, the PCR facilitators, betaine and bovine serum albumin (BSA), were tested, simultaneously with an adjustment of PCR thermal cycler and of whole-blood volume. Thereafter, the established whole-blood PCR was applied for detecting, in both known and unknown samples, the HBA1 Southeast Asian (– –SEA) (NG_000006.1: g.26264_45564del19301) deletion, Hb Constant Spring (Hb CS, HBA2: c.427T>C, αCSα), codon 17 (A>T) (HBB: c.52A>T), codons 41/42 (–TTCT) (HBB: c.126_129delCTTT) deletion, –28 (A>G) (HBB: c.-78A>G) and codon 26 (G>A) (Hb E or HBB: c.79G>A). It was shown that the whole-blood PCR worked successfully in 9.0% (w/v) betaine, with 1 μL of EDTA whole blood and with addition of 10 heat-cool steps (3 min. at 94 °C, followed by 3 min. at 55 °C) prior to the typical thermal cycles for the mutations. The capability of the new whole-blood PCR was similar to that of the typical DNA-based PCR. Therefore, the newly established whole-blood PCR could be performed for PCR diagnosis of thalassemia. Using this platform, sample-to-sample contamination should be eliminated.

Acknowledgements

We thank the Research Administrative Center, Chiang Mai University, Chiang Mai, Thailand, for providing the English proofreading of this manuscript. We also thank Dr. Denis R. Sweatman, an Australian native English speaker, of the Department of Physics and Material Science, Faculty of Science, Chiang Mai University, Chiang Mai, Thailand, for proofreading the English language in this manuscript.

Disclosure statement

The authors report no conflicts of interest. The authors alone are responsible for the content and writing of this article.

Additional information

Funding

This study was supported by the National Sciences and Technology Development Agency (NSTDA) Research Chair Grant, Thailand and the National Research University Project under the Thailand Office of the Higher Education Commission.

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