CESAM-Centro de Estudos do Ambiente e do Mar, Departamento de Biologia Animal, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749-016 Lisboa, Portugal.
CESAM-Centro de Estudos do Ambiente e do Mar, Departamento de Biologia Animal, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749-016 Lisboa, Portugal; Departamento de Biologia da Universidade de Aveiro, Campus Universitário de Santiago, 3810-193 Aveiro, Portugal.
Sci Total Environ. 2023 Nov 20;900:166290. doi: 10.1016/j.scitotenv.2023.166290. Epub 2023 Aug 14.
Growing evidence of widespread resistance to anticoagulant rodenticides (ARs) in house mice pose significant challenges to pest control efforts. First-generation ARs were introduced in the early 1950s but resistance to these emerged later that decade. Second-generation rodenticides were then developed, with resistance being reported in the late 1970s. Research has linked resistance to ARs with mutations in the Vkorc1 gene, leading to the use of more toxic and environmentally harmful compounds. In this study, 243 tail tips of house mice from mainland Portugal and Southern Spain, the Azores and Madeira archipelagos were analysed for all 3 exons of the Vkorc1 gene. Mutations L128S, Y139C, along with the so-called spretus genotype Vkorc1 are considered responsible for reduced susceptibility of house mice to ARs. All these sequence variants were broadly detected throughout the sampling regions. Vkorc1 was the most often recorded among mainland populations, whereas Y139C was nearly ubiquitous among the insular populations. In contrast, L128S was only detected in mainland Portugal and four islands of the Azores archipelago. All first generation ARs such as warfarin and coumatetralyl are deemed ineffective against all Vkorc1 variants identified in this study. Second-generation bromadiolone and difenacoum should also be discarded to control populations carrying Vkorc1, Y139C or L128S mutations. Inadequate use of ARs in regions where resistant animals have been found in large proportions will result in the spreading of rodenticide resistance among rodent populations through the positive selection of non-susceptible individuals. Consequently, ineffectiveness of rodent control will increase and potentiate environmental contamination, hazarding non-target wildlife through secondary poisoning. We highlight the need for Vkorc1 screening as a crucial tool in rodent management, aiding in the selection of the most appropriate control/eradication method in order to prevent misuse of these toxic biocides and the spread of rodenticide resistance among house mouse populations.
越来越多的证据表明,家鼠对抗凝血灭鼠剂(ARs)的广泛耐药性对害虫防治工作构成了重大挑战。第一代 ARs 于 20 世纪 50 年代初引入,但在十年后就出现了耐药性。随后开发了第二代灭鼠剂,在 20 世纪 70 年代末就报告了耐药性。研究表明,ARs 的耐药性与 Vkorc1 基因的突变有关,这导致了更有毒和对环境更有害的化合物的使用。在这项研究中,分析了来自葡萄牙大陆、西班牙南部、亚速尔群岛和马德拉群岛的 243 只家鼠的尾尖,以研究 Vkorc1 基因的所有 3 个外显子。L128S、Y139C 突变以及所谓的 spretus 基因型 Vkorc1 被认为是导致家鼠对 ARs 敏感性降低的原因。所有这些序列变体在整个采样区域都广泛检测到。Vkorc1 在大陆种群中最为常见,而 Y139C 在岛屿种群中几乎普遍存在。相比之下,L128S 仅在葡萄牙大陆和亚速尔群岛的四个岛屿上被检测到。所有第一代 ARs,如华法林和氯鼠酮,都被认为对本研究中发现的所有 Vkorc1 变体无效。第二代溴敌隆和敌鼠酮也应该被丢弃,以控制携带 Vkorc1、Y139C 或 L128S 突变的种群。在发现耐药动物比例较高的地区,如果不适当使用 ARs,将会导致抗药性在鼠群中通过对非敏感个体的正选择而传播。因此,鼠类控制的效果将会降低,并加剧环境的污染,通过二次中毒危害非目标野生动物。我们强调了 Vkorc1 筛查作为鼠类管理的重要工具的必要性,这有助于选择最合适的控制/根除方法,以防止这些有毒杀生物剂的滥用和家鼠种群中抗药性的传播。