Development and validation of a universal primer pair for the taxonomic and phylogenetic studies of vertebrates

Mol Biol Rep. 2024 Feb 23;51(1):332. doi: 10.1007/s11033-023-09175-w.

Abstract

Background: Recent studies in the field of molecular identification have described 16S rRNA gene as a highly informative fragment of mitochondrial DNA for species discrimination. This study presents a newly developed universal primer pair yielding an approximately 350 bp fragment of mitochondrial 16S rRNA, variable enough to encompass and identify all vertebrate classes.

Methods and results: The primers were designed by aligning and analyzing over 1500 16S rRNA sequences downloaded from the NCBI nucleotide database. A total of 93 vertebrate species, spanning 27 orders and 55 families, were PCR-amplified to validate the primers. All the target species were successfully amplified and identified when aligned with reference sequences from the NCBI nucleotide database. Using the Kimura 2-parameter model, low intra-species genetic divergence of the target region was observed - from 0 to 4.63%, whereas relatively higher inter-species genetic divergence was observed, ranging from 4.88% to 69.81%. Moreover, the newly developed primers were successfully applied to a direct PCR protocol, making the workflow very cost-effective, time-saving and less laborious in comparison to conventional PCR.

Conclusions: The short length, high variability and conserved priming sites of the target fragment across all vertebrate species make it a highly desirable marker for species identification and discrimination.

Keywords: 16S rRNA; Direct PCR; Mitochondrial DNA; Species identification; Vertebrates.

MeSH terms

  • Animals
  • DNA, Mitochondrial* / genetics
  • Humans
  • Nucleotides
  • Phylogeny
  • RNA, Ribosomal, 16S / analysis
  • RNA, Ribosomal, 16S / genetics
  • Sequence Analysis, DNA
  • Vertebrates* / genetics

Substances

  • RNA, Ribosomal, 16S
  • DNA, Mitochondrial
  • Nucleotides