Genetic resistance to vector-borne hemoprotozoa in livestock: molecular markers, host-parasite interactions, and implications for breeding and control.

IF 1.5 3区 农林科学 Q2 VETERINARY SCIENCES
Journal of Veterinary Science Pub Date : 2025-09-01 Epub Date: 2025-08-26 DOI:10.4142/jvs.25125
Bashir Salim, Saeed Alasmari, Mohammed A Bakheit
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引用次数: 0

Abstract

Importance: Vector-borne hemoparasitic diseases, such as Theileria, Babesia, Trypanosoma, Leishmania, and Anaplasma, pose significant constraints to livestock production, particularly in Africa and other tropical regions. These infections cause considerable economic losses from mortality, decreased productivity, and the high costs of treatment and control efforts.

Observations: Resistance to hemoparasitic infections in livestock is strongly influenced by the genetic factors of the host. The key host genes involved in immune responses (e.g., BoLA-DRB3 and TLR4), oxidative stress defense (SOD2 and GPX1), drug metabolism (ABCB1 and CYP3A4), and ectoparasite resistance (MC1R and MHC) have been identified as contributors to resistance phenotypes. On the parasite side, the genes responsible for immune evasion (VSG and AP2), drug resistance (MDR1 and CYTB), and host cell invasion (AMA1 and HSP90) play pivotal roles in infection persistence and treatment failure. The advances in genomic and transcriptomic tools, including genome-wide association studies, CRISPR, and multi-omics profiling, have enhanced the understanding of these host-parasite interactions and enabled identification of the molecular markers for resistance traits.

Conclusions and relevance: Advanced genetic resistance offers a sustainable, long-term solution to managing vector-borne parasitic infections in livestock. The integration of resistance-associated markers into selective breeding programs, coupled with genome editing and real-time surveillance, can improve livestock resilience. Aligning these efforts with One Health strategies and collaborative genomic initiatives will be essential for achieving effective, regionally adapted disease control.

家畜对媒介传播的血原虫的遗传抗性:分子标记、宿主-寄生虫相互作用以及对育种和控制的影响。
重要性:病媒传播的血液寄生虫病,如希勒氏菌、巴贝斯虫、锥虫、利什曼原虫和无形体,对牲畜生产构成重大制约,特别是在非洲和其他热带地区。这些感染造成了巨大的经济损失,包括死亡、生产力下降以及治疗和控制工作的高昂费用。观察:家畜对血寄生虫感染的抵抗力受到宿主遗传因素的强烈影响。参与免疫应答的关键宿主基因(如BoLA-DRB3和TLR4)、氧化应激防御(SOD2和GPX1)、药物代谢(ABCB1和CYP3A4)和外寄生虫抗性(MC1R和MHC)已被确定为抗性表型的因素。在寄生虫方面,负责免疫逃避(VSG和AP2)、耐药(MDR1和CYTB)和宿主细胞入侵(AMA1和HSP90)的基因在感染持续和治疗失败中发挥关键作用。基因组学和转录组学工具的进步,包括全基因组关联研究、CRISPR和多组学分析,增强了对这些宿主-寄生虫相互作用的理解,并使鉴定耐药性状的分子标记成为可能。结论和相关性:先进的遗传抗性为管理牲畜媒介传播的寄生虫感染提供了可持续的长期解决方案。将抗性相关标记整合到选择性育种计划中,再加上基因组编辑和实时监测,可以提高牲畜的抵御能力。将这些努力与“同一个健康”战略和基因组合作倡议结合起来,对于实现有效的、适应区域的疾病控制至关重要。
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来源期刊
Journal of Veterinary Science
Journal of Veterinary Science 农林科学-兽医学
CiteScore
3.10
自引率
5.60%
发文量
86
审稿时长
1.3 months
期刊介绍: The Journal of Veterinary Science (J Vet Sci) is devoted to the advancement and dissemination of scientific knowledge concerning veterinary sciences and related academic disciplines. It is an international journal indexed in the Thomson Scientific Web of Science, SCI-EXPANDED, Sci Search, BIOSIS Previews, Biological Abstracts, Focus on: Veterinary Science & Medicine, Zoological Record, PubMed /MEDLINE, Index Medicus, Pubmed Central, CAB Abstracts / Index Veterinarius, EBSCO, AGRIS and AGRICOLA. This journal published in English by the Korean Society of Veterinary Science (KSVS) being distributed worldwide.
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