A complete genome for a commercial duck

Jim KAUFMAN

Front. Agr. Sci. Eng. ›› 2024, Vol. 11 ›› Issue (2) : 344 -346.

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Front. Agr. Sci. Eng. ›› 2024, Vol. 11 ›› Issue (2) : 344 -346. DOI: 10.15302/J-FASE-2024557
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A complete genome for a commercial duck

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Jim KAUFMAN. A complete genome for a commercial duck. Front. Agr. Sci. Eng., 2024, 11(2): 344-346 DOI:10.15302/J-FASE-2024557

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Biology has been revolutionized by the availability of whole genome sequences, along with all the associated approaches including genome-wide association studies, various -omics methodologies and now precise genome editing[16]. The study of domesticated animal food species has already benefitted from these basic technologies (for a few examples out of many[714]), and it is anticipated that there will be enormous advances arising from deep understanding and precise intervention. However, these improvements depend on the availability of a complete high-quality genomes.
Domestic ducks are an important staple food source in many Asian countries, and a source of fine food in other parts of the world. However, there has been concern about their role as reservoirs for influenza virus due to their apparent tolerance to many strains of avian influenza and thus their potential contribution to zoonotic infections[15,16]. While relatively resilient to avian influenza compared to poultry, such as chickens, there are also serious infections by the viruses responsible for duck hepatitis B, duck enteritis (duck plague) and duck egg drop syndrome (Tembusu), as well as by bacteria such as Salmonella, Campylobacter and Pasteurella[1521].
A significant milestone has been reached with the publication of a complete genome sequence of a domestic duck (Pekin duck, an indigenous breed in China) along with a careful analysis of the major histocompatibility complex (MHC) by Jiaxiang HU and colleagues from the team of Yinhua HUANG at the China Agricultural University in Beijing[22]. This genome sequence was generated and assembled by the latest technologies to the chromosome level, and appears to be the most complete duck genome sequence to date. Although there is much to be learned from the rest of the genome, the authors focused their analyses on the MHC, one of the key immune regions in the genomes of all jawed vertebrates, from sharks to humans.
Almost everything known about the MHC comes from research in humans and biomedical models like mice, but among non-mammalian vertebrates, the most detailed and wide-ranging work has been done with chickens[2325]. While the basic pathways are very similar, there are stark differences between the MHC of typical mammals and chickens. For example, the human MHC is at least 4 Mb long with hundreds of genes, including multigene families encoding the highly polymorphic class I and class II MHC molecules, which are central in disease resistance and vaccine responses. In contrast, the MHC of chickens is compact and simple (less than 0.1 Mb), with only a few genes devoted mostly to antigen presentation and immune responses, and only single dominantly-expressed class I and class II molecules, leading to strong genetic associations with resistance to infectious pathogens and responses to vaccines. Such compact simple MHC organizations have been found in ratite birds (ostriches and other flightless birds, thought to be the first lineage of extant birds), and are thought to be ancestral[26]
Unexpectedly, the MHC of the domestic duck is a relatively large genomic region (at least 1.35 Mb in those regions with genes comparable to the chicken MHC), mostly due to big expansions of key immune and regulatory genes, such as those encoding class II, DM2, butyrophilin, NK receptor and NK ligand molecules[22]. There are several other notable differences compared to chickens, and altogether these analyses of the duck MHC will provide the basis for understanding the immune response to and developing vaccines for influenza and various other pathogens that infect ducks. Also, the rest of the genome will provide a valuable information about immune responses, physiology, and behavior of domestic ducks, which will transform understanding of and the ability to improve domestic ducks as a livestock species.

References

[1]

Wolf S M, Green R C. Return of results in genomic research using large-scale or whole genome sequencing: toward a new normal. Annual Review of Genomics and Human Genetics, 2023, 24(1): 393–414

[2]

Damas J, Corbo M, Lewin H A. Vertebrate chromosome evolution. Annual Review of Animal Biosciences, 2021, 9(1): 1–27

[3]

Deng Y, Finck A, Fan R. Single-cell omics analyses enabled by microchip technologies. Annual Review of Biomedical Engineering, 2019, 21(1): 365–393

[4]

Fischer H P. Towards quantitative biology: integration of biological information to elucidate disease pathways and to guide drug discovery. Biotechnology Annual Review, 2005, 11: 1–68

[5]

Nelson C E, Gersbach C A. Engineering delivery vehicles for genome editing. Annual Review of Chemical and Biomolecular Engineering, 2016, 7(1): 637–662

[6]

Holtzman L, Gersbach C A. Editing the epigenome: reshaping the genomic landscape. Annual Review of Genomics and Human Genetics, 2018, 19(1): 43–71

[7]

Berry D P, Spangler M L. Animal board invited review: practical applications of genomic information in livestock. Animal, 2023, 17(11): 100996

[8]

Goddard M E, Hayes B J. Mapping genes for complex traits in domestic animals and their use in breeding programmes. Nature Reviews. Genetics, 2009, 10(6): 381–391

[9]

Bekele R, Taye M, Abebe G, Meseret S. Genomic regions and candidate genes associated with milk production traits in holstein and its crossbred cattle: a review. International Journal of Genomics, 2023, 2023: 8497453

[10]

Narayana S G, de Jong E, Schenkel F S, Fonseca P A S, Chud T C S, Powell D, Wachoski-Dark G, Ronksley P E, Miglior F, Orsel K, Barkema H W. Underlying genetic architecture of resistance to mastitis in dairy cattle: a systematic review and gene prioritization analysis of genome-wide association studies. Journal of Dairy Science, 2023, 106(1): 323–351

[11]

Smith J, Alfieri J M, Anthony N, Arensburger P, Athrey G N, Balacco J, Balic A, Bardou P, Barela P, Bigot Y, Blackmon H, Borodin P M, Carroll R, Casono M C, Charles M, Cheng H, Chiodi M, Cigan L, Coghill L M, Crooijmans R, Das N, Davey S, Davidian A, Degalez F, Dekkers J M, Derks M, Diack A B, Djikeng A, Drechsler Y, Dyomin A, Fedrigo O, Fiddaman S R, Formenti G, Frantz L A F, Fulton J E, Gaginskaya E, Galkina S, Gallardo R A, Geibel J, Gheyas A A, Godinez C J P, Goodell A, Graves J A M, Griffin D K, Haase B, Han J L, Hanotte O, Henderson L J, Hou Z C, Howe K, Huynh L, Ilatsia E, Jarvis E D, Johnson S M, Kaufman J, Kelly T, Kemp S, Kern C, Keroack J H, Klopp C, Lagarrigue S, Lamont S J, Lange M, Lanke A, Larkin D M, Larson G, Layos J K N, Lebrasseur O, Malinovskaya L P, Martin R J, Martin Cerezo M L, Mason A S, McCarthy F M, McGrew M J, Mountcastle J, Muhonja C K, Muir W, Muret K, Murphy T D, Ng’ang’a I, Nishibori M, O’Connor R E, Ogugo M, Okimoto R, Ouko O, Patel H R, Perini F, Pigozzi M I, Potter K C, Price P D, Reimer C, Rice E S, Rocos N, Rogers T F, Saelao P, Schauer J, Schnabel R D, Schneider V A, Simianer H, Smith A, Stevens M P, Stiers K, Tiambo C K, Tixier-Boichard M, Torgasheva A A, Tracey A, Tregaskes C A, Vervelde L, Wang Y, Warren W C, Waters P D, Webb D, Weigend S, Wolc A, Wright A E, Wright D, Wu Z, Yamagata M, Yang C, Yin Z T, Young M C, Zhang G, Zhao B, Zhou H. Fourth report on chicken genes and chromosomes. Cytogenetic and Genome Research, 2022, 162(8–9): 405–528

[12]

Suminda G G D, Ghosh M, Son Y O. The innovative informatics approaches of high-throughput technologies in livestock: spearheading the sustainability and resiliency of agrigenomics research. Life, 2022, 12(11): 1893

[13]

Dehau T, Ducatelle R, van Immerseel F, Goossens E. Omics technologies in poultry health and productivity—Part 1: current use in poultry research. Avian Pathology, 2022, 51(5): 407–417

[14]

Rieblinger B, Sid H, Duda D, Bozoglu T, Klinger R, Schlickenrieder A, Lengyel K, Flisikowski K, Flisikowska T, Simm N, Grodziecki A, Perleberg C, Bähr A, Carrier L, Kurome M, Zakhartchenko V, Kessler B, Wolf E, Kettler L, Luksch H, Hagag I T, Wise D, Kaufman J, Kaufer B B, Kupatt C, Schnieke A, Schusser B. Cas9-expressing chickens and pigs as resources for genome editing in livestock. Proceedings of the National Academy of Sciences of the United States of America, 2021, 118(10): e2022562118

[15]

Kim J K, Negovetich N J, Forrest H L, Webster R G. Ducks: the “Trojan horses” of H5N1 influenza. Influenza and Other Respiratory Viruses, 2009, 3(4): 121–128

[16]

Chmielewski R, Swayne D E. Avian influenza: public health and food safety concerns. Annual Review of Food Science and Technology, 2011, 2(1): 37–57

[17]

Funk A, Mhamdi M, Will H, Sirma H. Avian hepatitis B viruses: molecular and cellular biology, phylogenesis, and host tropism. World Journal of Gastroenterology, 2007, 13(1): 91–103

[18]

Dhama K, Kumar N, Saminathan M, Tiwari R, Karthik K, Kumar M A, Palanivelu M, Shabbir M Z, Malik Y S, Singh R K. Duck virus enteritis (duck plague)—A comprehensive update. Veterinary Quarterly, 2017, 37(1): 57–80

[19]

Cui Y, Pan Y, Guo J, Wang D, Tong X, Wang Y, Li J, Zhao J, Ji Y, Wu Z, Zeng P, Zhou J, Feng X, Hou L, Liu J. The evolution, genomic epidemiology, and transmission dynamics of Tembusu virus. Viruses, 2022, 14(6): 1236

[20]

Jafari S, Ebrahimi M, Luangtongkum T. The worldwide trend of Campylobacter spp., infection from duck-related isolates and associated phenotypic and genotypic antibiotic resistance, since 1985: identifying opportunities and challenges for prevention and control. Poultry Science, 2021, 100(8): 101213

[21]

Cai Q, Li Y, Chang Y F, Tang Z, Zhang H, Xie Q. Pasteurella multocida causes liver injury in ducks by mediating inflammatory, apoptotic and autophagic pathways. Microbial Pathogenesis, 2023, 184: 106336

[22]

Hu J, Song L, Ning M, Niu X, Han M, Gao C, Feng X, Cai H, Li T, Li F, Li H, Gong D, Song W, Liu L, Pu J, Liu J, Smith J, Sun H, Huang Y. A new chromosome-scale duck genome shows a major histocompatibility complex with several expanded multigene families. BMC Biology, 2024, 22(1): 31

[23]

Trowsdale J, Knight J C. Major histocompatibility complex genomics and human disease. Annual Review of Genomics and Human Genetics, 2013, 14(1): 301–323

[24]

Kaufman J. Unfinished business: evolution of the MHC and the adaptive immune system of jawed vertebrates. Annual Review of Immunology, 2018, 36(1): 383–409

[25]

Kaufman J. Generalists and specialists: a new view of how MHC class I molecules fight infectious pathogens. Trends in Immunology, 2018, 39(5): 367–379

[26]

He K, Liang C H, Zhu Y, Dunn P, Zhao A, Minias P. Reconstructing macroevolutionary patterns in avian MHC architecture with genomic data. Frontiers in Genetics, 2022, 13: 823686

RIGHTS & PERMISSIONS

The Author(s) 2024. Published by Higher Education Press. This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0)

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