» Articles » PMID: 27654468

Inability of 'Whole Genome Amplification' to Improve Success Rates for the Biomolecular Detection of Tuberculosis in Archaeological Samples

Overview
Journal PLoS One
Date 2016 Sep 23
PMID 27654468
Citations 3
Authors
Affiliations
Soon will be listed here.
Abstract

We assessed the ability of whole genome amplification (WGA) to improve the efficiency of downstream polymerase chain reactions (PCRs) directed at ancient DNA (aDNA) of members of the Mycobacterium tuberculosis complex (MTBC). Using extracts from a variety of bones and a tooth from human skeletons with or without lesions indicative of tuberculosis, from multiple time periods, we obtained inconsistent results. We conclude that WGA does not provide any advantage in studies of MTBC aDNA. The sporadic nature of our results are probably due to the fact that WGA is itself a PCR-based procedure which, although designed to deal with fragmented DNA, might be inefficient with the low concentration of templates in an aDNA extract. As such, WGA is subject to similar, if not the same, restrictions as PCR when applied to aDNA.

Citing Articles

Droplet based whole genome amplification for sequencing minute amounts of purified Mycobacterium tuberculosis DNA.

Dippenaar A, Ismail N, Heupink T, Grobbelaar M, Loubser J, Van Rie A Sci Rep. 2024; 14(1):9931.

PMID: 38689002 PMC: 11061190. DOI: 10.1038/s41598-024-60545-1.


The Evolution of Diagnostic Techniques in the Paleopathology of Tuberculosis: A Scoping Review.

Papa V, Galassi F, Varotto E, Gori A, Vaccarezza M Pathog Immun. 2023; 8(1):93-116.

PMID: 37900966 PMC: 10603826. DOI: 10.20411/pai.v8i1.597.


Tuberculosis in post-contact Native Americans of Brazil: Paleopathological and paleogenetic evidence from the Tenetehara-Guajajara.

Guedes L, Jaeger L, Liryo A, Rodrigues-Carvalho C, Mendonca de Souza S, Iniguez A PLoS One. 2018; 13(9):e0202394.

PMID: 30183732 PMC: 6124704. DOI: 10.1371/journal.pone.0202394.

References
1.
Barker D, Hansen M, Faruqi A, Giannola D, Irsula O, Lasken R . Two methods of whole-genome amplification enable accurate genotyping across a 2320-SNP linkage panel. Genome Res. 2004; 14(5):901-7. PMC: 479118. DOI: 10.1101/gr.1949704. View

2.
Frota C, Hunt D, Buxton R, Rickman L, Hinds J, Kremer K . Genome structure in the vole bacillus, Mycobacterium microti, a member of the Mycobacterium tuberculosis complex with a low virulence for humans. Microbiology (Reading). 2004; 150(Pt 5):1519-1527. PMC: 2964484. DOI: 10.1099/mic.0.26660-0. View

3.
Suzuki K, Takigawa W, Tanigawa K, Nakamura K, Ishido Y, Kawashima A . Detection of Mycobacterium leprae DNA from archaeological skeletal remains in Japan using whole genome amplification and polymerase chain reaction. PLoS One. 2010; 5(8):e12422. PMC: 2928730. DOI: 10.1371/journal.pone.0012422. View

4.
Telenius H, Carter N, Bebb C, Nordenskjold M, Ponder B, Tunnacliffe A . Degenerate oligonucleotide-primed PCR: general amplification of target DNA by a single degenerate primer. Genomics. 1992; 13(3):718-25. DOI: 10.1016/0888-7543(92)90147-k. View

5.
Kearse M, Moir R, Wilson A, Stones-Havas S, Cheung M, Sturrock S . Geneious Basic: an integrated and extendable desktop software platform for the organization and analysis of sequence data. Bioinformatics. 2012; 28(12):1647-9. PMC: 3371832. DOI: 10.1093/bioinformatics/bts199. View