Identification of SNPs Related to Salmonella Resistance in Chickens Using RNA-Seq and Integrated Bioinformatics Approach
Author:
Dar Mashooq Ahmad12, Bhat Basharat1, Nazir Junaid13ORCID, Saleem Afnan1, Manzoor Tasaduq1, Khan Mahak1, Haq Zulfqarul4, Bhat Sahar Saleem1ORCID, Ahmad Syed Mudasir5ORCID
Affiliation:
1. Division of Animal Biotechnology, Faculty of Veterinary Sciences and Animal Husbandry, Shuhama, SKUAST-Kashmir, Srinagar 190006, India 2. Laboratory of Preclinical Testing of Higher Standard, Nencki Institute of Experimental Biology of Polish Academy of Sciences 3, 02-093 Warsaw, Poland 3. Department of Clinical Biochemistry, Lovely Professional University, Phagwara 144402, India 4. Indian Council of Medical Research Project, Division of Livestock Production and Management, F.V.Sc & AH, Shuhama, Sher-e-Kashmir University of Agricultural Sciences and Technology of Kashmir, Srinagar 190006, India 5. Genomics Lab, ABT, FVSC & AH, SKUAST-Kashmir, Srinagar 190006, India
Abstract
Potential single nucleotide polymorphisms (SNPs) were detected between two chicken breeds (Kashmir favorella and broiler) using deep RNA sequencing. This was carried out to comprehend the coding area alterations, which cause variances in the immunological response to Salmonella infection. In the present study, we identified high impact SNPs from both chicken breeds in order to delineate different pathways that mediate disease resistant/susceptibility traits. Samples (liver and spleen) were collected from Salmonella resistant (K. favorella) and susceptible (broiler) chicken breeds. Salmonella resistance and susceptibility were checked by different pathological parameters post infection. To explore possible polymorphisms in genes linked with disease resistance, SNP identification analysis was performed utilizing RNA seq data from nine K. favorella and ten broiler chickens. A total of 1778 (1070 SNPs and 708 INDELs) and 1459 (859 SNPs and 600 INDELs) were found to be specific to K. favorella and broiler, respectively. Based on our results, we conclude that in broiler chickens the enriched pathways mostly included metabolic pathways like fatty acid metabolism, carbon metabolism and amino acid metabolism (Arginine and proline metabolism), while as in K. favorella genes with high impact SNPs were enriched in most of the immune-related pathways like MAPK signaling pathway, Wnt signaling pathway, NOD-like receptor signaling pathway, etc., which could be a possible resistance mechanism against salmonella infection. In K. favorella, protein–protein interaction analysis also shows some important hub nodes, which are important in providing defense against different infectious diseases. Phylogenomic analysis revealed that indigenous poultry breeds (resistant) are clearly separated from commercial breeds (susceptible). These findings will offer fresh perspectives on the genetic diversity in chicken breeds and will aid in the genomic selection of poultry birds.
Funder
Science and Engineering Research Board (SERB), Department of Science and Technology, Government of India
Subject
Genetics (clinical),Genetics
Reference56 articles.
1. Comparative RNA-Seq analysis reveals insights in Salmonella disease resistance of chicken; and database development as resource for gene expression in poultry;Dar;Genomics,2022 2. Dar, M.A., Ahmed, R., Urwat, U., Ahmad, S.M., Dar, P.A., Kushoo, Z.A., Dar, T.A., Mumtaz, P.T., Bhat, S.A., and Amin, U. (2018). Expression kinetics of natural resistance associated macrophage protein (NRAMP) genes in Salmonella typhimurium-infected chicken. BMC Vet. Res., 14. 3. Dar, M.A., Mumtaz, P.T., Bhat, S.A., Taban, Q., Khan, S.A., Banday, T., and Ahmad, S.M. (2019). New Insight into Brucella Infection and Foodborne Diseases, IntechOpen. 4. Characterization of non-typhoidal Salmonella isolates from children with acute gastroenteritis, Kolkata, India, during 2000–2016;Jain;Braz. J. Microbiol.,2020 5. Food Attribution and Economic Cost Estimates for Meat- and Poultry-Related Illnesses;Scharff;J. Food Prot.,2020
|
|