In silico identification of Single Nucleotide Polymorphisms in the Varroa destructor Cytochrome c Oxidase Subunit 1 (cox1) and Cytochrome b (cytb) genes, haplotype analysis, and assessment of population structure

IF 2.1 3区 农林科学 Q2 AGRICULTURE, MULTIDISCIPLINARY
Seyma Gunyakti Kilinc, Figen Celik, Harun Kaya Kesik, Sami Simsek
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引用次数: 0

Abstract

Varroa destructor is an ectoparasite that has been identified as the primary pathogen of the western honey bee, Apis mellifera, globally. Investigating the genetic variations of this mite in different geographical regions is crucial for understanding its population dynamics and evolutionary potential. Genetic diversity data are essential for tracking its spread, identifying emerging lineages, and developing effective control strategies. The objective of this study was to investigate haplotype diversity, genetic variation and population structure by in silico phylogenetic analysis of mitochondrial cox1 and cytb gene sequences of V. destructor isolates submitted to GenBank from different regions of the world. For this purpose, 509 sequences covering 399 bp of the cox1 gene region and 215 sequences covering 628 bp of the cytb gene region were used for the analyses. A total of 37 polymorphic sites and 24 haplotypes were identified in the cox1 sequences, while 31 polymorphic sites and 23 haplotypes were observed in the cytb region. Both gene regions exhibited high negative values for diversity and neutrality indices, indicating possible recent population expansion or selective pressures. This study also evaluated single nucleotide polymorphisms (SNPs) within GenBank-derived sequences and analysed their impact on haplotype differentiation and population structure. The results revealed considerable haplotype diversity, including several region-specific variants and potential signs of recent population expansion. The findings highlight ongoing microevolution within V. destructor populations, likely driven by host movement, acaricide use and ecological pressures. These insights are vital for apiculture, as the spread of genetically diverse and potentially more virulent mite lineages could undermine mite control efficacy and honey bee health. Future surveillance efforts should integrate genetic monitoring into management practices to support sustainable beekeeping worldwide.

Abstract Image

细胞色素c氧化酶亚基1 (cox1)和细胞色素b (cytb)基因的单核苷酸多态性鉴定、单倍型分析和种群结构评估
破坏瓦螨是一种体外寄生虫,已被确定为西方蜜蜂的主要病原体。研究该螨在不同地理区域的遗传变异对了解其种群动态和进化潜力具有重要意义。遗传多样性数据对于追踪其传播、识别新出现的谱系和制定有效的控制策略至关重要。本研究的目的是通过对来自世界不同地区的V. destructor分离株线粒体cox1和cytb基因序列的计算机系统发育分析,探讨其单倍型多样性、遗传变异和种群结构。为此,我们使用了覆盖399 bp的cox1基因区域的509个序列和覆盖628 bp的cytb基因区域的215个序列进行分析。在cox1序列中共鉴定出37个多态性位点和24个单倍型,在cytb区域共鉴定出31个多态性位点和23个单倍型。两个基因区域的多样性和中性指数均呈高负值,表明可能存在近期种群扩张或选择压力。本研究还评估了genbank衍生序列中的单核苷酸多态性(SNPs),并分析了它们对单倍型分化和种群结构的影响。结果显示了相当大的单倍型多样性,包括一些区域特异性变异和近期种群扩张的潜在迹象。这一发现突出表明,在宿主移动、杀螨剂的使用和生态压力的驱动下,灭螨螨种群正在进行微进化。这些见解对养蜂业至关重要,因为遗传多样性和潜在毒性更强的螨虫谱系的传播可能会破坏螨虫控制效果和蜜蜂健康。未来的监测工作应将遗传监测纳入管理实践,以支持全球范围内的可持续养蜂业。
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来源期刊
Annals of Applied Biology
Annals of Applied Biology 生物-农业综合
CiteScore
5.50
自引率
0.00%
发文量
71
审稿时长
18-36 weeks
期刊介绍: Annals of Applied Biology is an international journal sponsored by the Association of Applied Biologists. The journal publishes original research papers on all aspects of applied research on crop production, crop protection and the cropping ecosystem. The journal is published both online and in six printed issues per year. Annals papers must contribute substantially to the advancement of knowledge and may, among others, encompass the scientific disciplines of: Agronomy Agrometeorology Agrienvironmental sciences Applied genomics Applied metabolomics Applied proteomics Biodiversity Biological control Climate change Crop ecology Entomology Genetic manipulation Molecular biology Mycology Nematology Pests Plant pathology Plant breeding & genetics Plant physiology Post harvest biology Soil science Statistics Virology Weed biology Annals also welcomes reviews of interest in these subject areas. Reviews should be critical surveys of the field and offer new insights. All papers are subject to peer review. Papers must usually contribute substantially to the advancement of knowledge in applied biology but short papers discussing techniques or substantiated results, and reviews of current knowledge of interest to applied biologists will be considered for publication. Papers or reviews must not be offered to any other journal for prior or simultaneous publication and normally average seven printed pages.
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