Unveiling genetic variants: Tetra-primer ARMS-PCR diagnosis and structural insights into BLAD, BC, and DUMPS in Pakistani cattle herds

Iram Ilyas, Fakhar Un Nisa, Muhammad Basil Ali, Fazeela Arshad, Najida Irfan, Muhammad Asif, Imran Amin

Research output: Contribution to journalArticlepeer-review

Abstract / Description of output

BACKGROUND: Bovine leukocyte adhesion deficiency (BLAD), bovine citrullinemia (BC), and deficiency of Uridine monophosphate synthetase (DUMPS) are the common autosomal recessive disorders affecting the global dairy industry. BLAD leads to poor wound healing and recurrent infections. In BC, ammonia builds up leading to neurological disorders and death. DUMPS results in developmental abnormalities.

METHODOLOGY: In this study, tetra-primer amplification refractory mutation system polymerase chain reaction (ARMS PCR) based diagnostic tests were optimized for BLAD, BC, and DUMPS. A total of 250 animals (58 indigenous and 192 Holstein Friesian (HF)) were screened from all across Pakistan. In addition to validation of ARMS-PCR results through Sanger sequencing, the protein modeling provided structural insights of the disease-associated reported SNPs. Pathway analysis illustrated gene functions under normal and mutated conditions. Furthermore, haplotype and phylogenetic analysis of ASS1 (Argininosuccinate synthetase) gene were performed on study samples and NCBI retrieved sequences.

RESULTS: The study's focus was to screen the herds for prevalence of carriers of genetic disorders, as they are the main source of disease dissemination. One animal was found carrier for BC, whereas no carriers were found for BLAD and DUMPS. The protein models corroborated the reported amino acid change in BLAD, and protein truncation in both BC and DUMPS proteins. SNPs found in NCBI retrieved sequences were either silent or missense and had no effect on protein structure. DNA network presented graphical illustration of haplotype interactions and phylogenetic analysis conferred evolutionary landscape of ASS1 gene. The combination of these approaches produced an in-depth genetic picture of BC in Pakistani cattle.

CONCLUSION: The development of diagnostic tests and identification of the heterozygous BC sample underscores the significance of constant monitoring to avoid the unwanted dissemination of mutant alleles among Pakistani cattle, thereby promoting the general well-being and sustainability of the dairy sector.

Original languageEnglish
Article number963
Pages (from-to)1-17
Number of pages17
JournalMolecular biology reports
Volume51
Issue number1
Early online date5 Sept 2024
DOIs
Publication statusPublished - Dec 2024

Keywords / Materials (for Non-textual outputs)

  • Animals
  • Cattle
  • Pakistan
  • Cattle Diseases/genetics
  • Polymorphism, Single Nucleotide/genetics
  • Leukocyte-Adhesion Deficiency Syndrome/genetics
  • Phylogeny
  • Polymerase Chain Reaction/methods
  • Haplotypes/genetics
  • Argininosuccinate Synthase/genetics
  • Genetic Variation/genetics
  • Mutation/genetics

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