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Identification and comparative analysis of novel major histocompatibility complex-B haplotypes in Indonesian native chickens

  • Roshani Fernando (Department of Animal Science, Chungnam National University) ;
  • Trisha Nicole Agulto (Department of Animal Science, Chungnam National University) ;
  • Prabuddha Manjula (Department of Animal Science, Uva Wellassa University) ;
  • Minjun Kim (Department of Animal Science, Chungnam National University) ;
  • Eunjin Cho (Department of Bio-AI Convergence, Chungnam National University) ;
  • Jaewon Kim (Department of Animal Science, Chungnam National University) ;
  • Fatmawati Mustofa (Department of Animal Science, Universitas Diponegoro) ;
  • Dyah Maharani (Department of Animal Breeding and Reproduction, Universitas Gadjah Mada) ;
  • Jun Heon Lee (Department of Animal Science, Chungnam National University)
  • Received : 2025.11.03
  • Accepted : 2026.02.08
  • Published : 2026.06.01

Abstract

Objective: The major histocompatibility complex (MHC) is central to immunological protection. This study represents the assessment of MHC-B haplotype diversity in Indonesian native chickens. Methods: Six Indonesian native chicken populations were selected as study populations: Merawang (MRG), Pelung (PLG), Black Kedu (KJM), Sentul (STL), Nunukan (NNK), and Gaga (GAG), with 24, 17, 30, 16, 14, and 20 birds from each population, respectively. Samples were genotyped using the MHC-B single-nucleotide polymorphism (SNP) panel. To explore haplotype diversity, the results were analyzed using PHASE 2.1 software. Results: Genotyping of six Indonesian native chicken populations revealed high haplotype diversity, with a total of 126 distinct haplotypes: 38, 25, 19, 21, 11, and 12 from the MRG, PLG, KJM, STL, NNK, and GAG populations, respectively. Three haplotypes have been identified to be shared: BSNP-IND14 (KJM and STL populations), BSNP-IND26 (KJM, NNK, and MRG populations), and BSNP-IND31 (KJM and MRG populations). Accordingly, all haplotypes obtained from the GAG and PLG populations were unique. Phylogenetic analysis of the results did not reveal a distinct pattern for any population; nonetheless, three subclades were identified, with all six populations represented in each clade. A comparison of MHC-B haplotypes in Indonesian native chickens with MHC-B standard haplotypes shows no distinct clades; however, three possible subclades were also identified. Nevertheless, no Indonesian MHC-B haplotypes matched 100% with the known standard haplotypes, indicating that all Indonesian haplotypes identified in this study are novel. Furthermore, the comparison of Indonesian MHC-B haplotypes to those from other Asian regions reveals that the majority of Indonesian haplotypes cluster with those from Bangladesh, suggesting a shared evolutionary background among South and Southeast Asian chickens. Conclusion: This study identified unique MHC-B haplotypes in Indonesian native chickens, suggesting that the observed populations are diverse in the MHC-B region and may have variation in immune responses.

Keywords

Acknowledgement

This research was funded by a grant from the National Research Foundation, Republic of Korea (grant number RS-2025-16072125).

References

  1. Sumiati, Fadilah R, Darmawan A, Nadia R. Challenges and constraints to the sustainability of poultry farming in Indonesia. Anim Biosci 2025;38:802-17. https://doi.org/10.5713/ab.24.0678
  2. Hidayat C, Asmarasari SA. Native chicken production in Indonesia: a review. J Peternak Indones 2015;17:1-11. https://doi.org/10.25077/jpi.17.1.1-11.2015
  3. Riztyan, Kawabe K, Shimogiri T, et al. Genetic diversity and ancestral relationships of red junglefowls and domestic chickens in Southeast Asia. J Poult Sci 2014;51:369-74. https://doi.org/10.2141/jpsa.0130206
  4. Ulfah M, Kawahara-Miki R, Farajalllah A, et al. Genetic features of red and green junglefowls and relationship with Indonesian native chickens Sumatera and Kedu Hitam. BMC Genom 2016;17:320. https://doi.org/10.1186/s12864-016-2652-z
  5. Maw AA, Shimogiri T, Riztyan, Kawabe K, Kawamoto Y, Okamoto S. Genetic diversity of Myanmar and Indonesia native chickens together with two jungle fowl species by using 102 indels polymorphisms. Asian-Australas J Anim Sci 2012;25:927-34. https://doi.org/10.5713/ajas.2011.11511
  6. Mwacharo JM, Jianlin H, Amano T. Native African chicken: valuable genetic resources for future breeding improvement. J Anim Genet 2006;34:63-9. https://doi.org/10.5924/abgri2000.34.2_63
  7. Kaufman J, Jacob J, Shaw J, et al. Gene organisation determines evolution of function in the chicken MHC. Immunol Rev 1999;167:101-17. https://doi.org/10.1111/j.1600-065X.1999.tb01385.x
  8. Miller MM, Taylor RL Jr. Brief review of the chicken major histocompatibility complex: the genes, their distribution on chromosome 16, and their contributions to disease resistance. Poult Sci 2016;95:375-92. https://doi.org/10.3382/ps/pev379
  9. Minias P, Pikus E, Whittingham LA, Dunn PO. A global analysis of selection at the avian MHC. Evolution 2018;72: 1278-93. https://doi.org/10.1111/evo.13490
  10. Shiina T, Briles WE, Goto RM, et al. Extended gene map reveals tripartite motif, C-type lectin, and Ig superfamily type genes within a subregion of the chicken MHC-B affecting infectious disease. J Immunol 2007;178:7162-72. https://doi.org/10.4049/jimmunol.178.11.7162
  11. Jin YC, Wei P, Wei XX, Zhao ZY, Li Y. Marek's disease resistant/susceptible MHC haplotypes in Xiayan chickens identified on the basis of BLB2 PCR-RFLP and BLB2/BF2 sequence analyses. Br Poult Sci 2010;51:530-9. https://doi.org/10.1080/00071668.2010.508489
  12. Owen JP, Delany ME, Mullens BA. MHC haplotype involvement in avian resistance to an ectoparasite. Immunogenetics 2008;60:621-31. https://doi.org/10.1007/s00251-008-0314-2
  13. Schou TW, Labouriau R, Permin A, et al. MHC haplotype and susceptibility to experimental infections (Salmonella enteritidis, Pasteurella multocida or Ascaridia galli) in a commercial and an indigenous chicken breed. Vet Immunol Immunopathol 2010;135:52-63. https://doi.org/10.1016/j.vetimm.2009.10.030
  14. Kim M, Ediriweera TK, Cho E, et al. Major histocompatibility complex genes exhibit a potential immunological role in mixed Eimeria-infected broiler cecum analyzed using RNA sequencing. Anim Biosci 2024;37:993-1000. https://doi.org/10.5713/ab.23.0412
  15. Chazara O, Fulton J, Juul-Madsen H, Chang CS, Bed'Hom B. High-resolution chicken MHC genotyping using a SNP panel. 32nd Conference of the International Society of Animal Genetics (ISAG); 2010 Jul 26-30; Edinburgh, UK.
  16. Fulton JE, McCarron AM, Lund AR, et al. A high-density SNP panel reveals extensive diversity, frequent recombination and multiple recombination hotspots within the chicken major histocompatibility complex B region between BG2 and CD1A1. Genet Sel Evol 2016;48:1. https://doi.org/10.1186/s12711-015-0181-x
  17. Manjula P, Fulton JE, Seo D, Lee JH. Major histocompatibility complex B variability in Korean native chicken breeds. Poult Sci 2020;99:4704-13. https://doi.org/10.1016/j.psj.2020.05.049
  18. Manjula P, Fulton JE, Seo D, Lee JH. Comparison of major histocompatibility complex-B variability in Sri Lankan indigenous chickens with five global chicken populations using MHC-B SNP panel. Anim Genet 2021;52:824-33. https://doi.org/10.1111/age.13137
  19. Fulton JE, Lund AR, McCarron AM, et al. MHC variability in heritage breeds of chickens. Poult Sci 2016;95:393-9. https://doi.org/10.3382/ps/pev363
  20. Fulton JE, Berres ME, Kantanen J, Honkatukia M. MHC-B variability within the Finnish Landrace chicken conservation program. Poult Sci 2017;96:3026-30. https://doi.org/10.3382/ps/pex102
  21. Sartika T, Saputra F, Takahashi H. Genetic diversity of eight native Indonesian chicken breeds on microsatellite markers. HAYATI J Biosci 2022;30:122-30. https://doi.org/10.4308/hjb.30.1.122-130
  22. Ediriweera TK, Manjula P, Kim J, et al. Identification of new major histocompatibility complex-B haplotypes in Bangladesh native chickens. Anim Biosci 2024;37:826-31. https://doi.org/10.5713/ab.23.0295
  23. Nam S, Manjula P, Kim J, et al. Diversity of MHC-B SNP haplotypes in the Vietnamese Ri chicken. J Anim Sci Technol 2025;30:982-8. https://doi.org/10.5187/jast.2024.e54
  24. Mustofa F, Sari APZN, Fathoni A, et al. Microsatellite marker LEI0258 variability in six Indonesian local chicken populations. Adv Biol Sci Res 2022;19:355-62. https://doi.org/10.2991/absr.k.220305.055
  25. Tribudi YA, Nurgiartiningsih VMA, Ulfah M, et al. Phenotypic characterization of six Indonesian local chicken populations. Cogent Food Agric 2025;11:2523576. https://doi.org/10.1080/23311932.2025.2523576
  26. Ramezani A, Brujeni GN, Sheikhi N, Asadollahi KP. MHClinked microsatellite LEI0258 variability and population structure of chicken ecotypes in Iran. Iran J Vet Res 2024;25: 312-8. https://doi.org/10.22099/ijvr.2024.50968.7544
  27. Sulandari S, Zein MSA, Sartika T. Analysis of genetic relationship among Indonesian native chicken breeds based on 335 D-loop sequences. J Ilmu Ternak Vet 2008;13:295-307. https://doi.org/10.14334/jitv.v13i4.574
  28. Nguyen-Phuc H, Fulton JE, Berres ME. Genetic variation of major histocompatibility complex (MHC) in wild red junglefowl (Gallus gallus). Poult Sci 2016;95:400-11. https://doi.org/10.3382/ps/pev364
  29. da Silva AP, Gallardo RA. The chicken MHC: insights into genetic resistance, immunity, and inflammation following infectious bronchitis virus infections. Vaccines 2020;8:637. https://doi.org/10.3390/vaccines8040637
  30. Bacon LD. Influence of the major histocompatibility complex on disease resistance and productivity. Poult Sci 1987;66:802-11. https://doi.org/10.3382/ps.0660802
  31. Lillehoj HS, Ruff MD, Bacon LD, Lamont SJ, Jeffers TK. Genetic control of immunity to Eimeria tenella. Interaction of MHC genes and non-MHC linked genes influences levels of disease susceptibility in chickens. Vet Immunol Immunopathol 1989;20:135-48. https://doi.org/10.1016/0165-2427(89)90094-9
  32. Dunnington EA, Briles WE, Briles RW, Siegel PB. Immunoresponsiveness in chickens: association of antibody production and the B system of the major histocompatibility complex. Poult Sci 1996;75:1156-60. https://doi.org/10.3382/ps.0751156
  33. Fulton JE, Arango J, Wolc A. Effect of MHC haplotype on mortality due to Marek's disease in commercial laying hens. Animals 2025;15:1647. https://doi.org/10.3390/ani15111647
  34. Leroy G, Kayang BB, Youssao IAK, et al. Gene diversity, agroecological structure and introgression patterns among village chicken populations across North, West and Central Africa. BMC Genet 2012;13:34. https://doi.org/10.1186/1471-2156-13-34
  35. Islam MA, Nishibori M. Phylogenetic analysis of native chicken from Bangladesh and neighboring Asian countries based on complete sequence of mitochondrial DNA D-loop region. J Poult Sci 2012;49:237-44. https://doi.org/10.2141/jpsa.0120007
  36. Oka T, Ino Y, Nomura K, et al. Analysis of mtDNA sequences shows Japanese native chickens have multiple origins. Anim Genet 2007;38:287-93. https://doi.org/10.1111/j.1365-2052.2007.01604.x
  37. Wang MS, Thakur M, Peng MS, et al. 863 Genomes reveal the origin and domestication of chicken. Cell Res 2020;30: 693-701. https://doi.org/10.1038/s41422-020-0349-y
  38. Osman SAM, Nishibori M. Phylogenetic analysis of South East Asian countries chickens based on mitochondrial DNA variations. J Poult Sci 2014;51:248-61. https://doi.org/10.2141/jpsa.0130190
  39. Lestari D, Murtini S, Ulupi N, Gunawan A, Sumantri C. Novel MHC BLB2 gene polymorphism and its association with IgY concentration and Newcastle disease antibody titer in IPB-D2 chickens. Arch Anim Breed 2023;66:275-83. https://doi.org/10.5194/aab-66-275-2023