Parodi Pablo, Armúa-Fernández María T, Schanzembach Marcos, Mir Daiana, Benítez-Galeano María José, Rodríguez-Osorio Nélida, Rivero Rodolfo, Venzal José M
Instituto Nacional de Investigación Agropecuaria (INIA), Plataforma de Salud Animal, Estación experimental INIA Tacuarembó, Tacuarembó, Uruguay.
Laboratorio Regional Noroeste "Miguel C. Rubino", División de Laboratorios Veterinarios "Miguel C. Rubino", Paysandú, Uruguay.
Front Vet Sci. 2022 Sep 20;9:990228. doi: 10.3389/fvets.2022.990228. eCollection 2022.
The major surface protein 1a gene has been used to characterize genetic diversity. This pathogen causes significant productivity and economic losses to the cattle industry. The objective of the present study was to report the first characterization of genetic diversity in Uruguay based on MSP1a genotypes and their putative relationship with . This cross-sectional study was conducted between 2016 and 2020. The study included whole blood samples from clinical cases of bovine anaplasmosis obtained from 30 outbreaks located in six Uruguay territorial departments. Diagnosis was performed using Giemsa-stained smears and confirmed by nested Polymerase Chance Reaction (nPCR) targeting the major surface protein gene. The genetic diversity of strains was characterized by analyzing the microsatellite and tandem repeats of MSP1a. Based on the microsatellite structure, four genotypes were identified. Genotype E was the most prevalent. Analysis of MSP1a tandem repeats showed 28 different strains from the combination of 31 repeats, with τ-10-15 and α-β-β-β-Γ being the most common. Repeats Γ, β, α, and γ were associated with the absence of with statistical significance ( < 0.05). Molecular observations showed that 46.7% of the strains identified in our samples lacked the ability to bind to tick cells; therefore, they were probably transmitted by other vectors. Strain genetic diversity provides valuable information for understanding the epidemiological behavior of A. and could contribute to the development of effective vaccines for the control of this disease.
主要表面蛋白1a基因已被用于表征遗传多样性。这种病原体给养牛业带来了巨大的生产力损失和经济损失。本研究的目的是报告基于MSP1a基因型及其与……的假定关系在乌拉圭进行的首次遗传多样性表征。这项横断面研究于2016年至2020年期间开展。该研究纳入了从乌拉圭六个地区部门的30起疫情中获得的牛无浆体病临床病例的全血样本。诊断采用吉姆萨染色涂片,并通过针对主要表面蛋白基因的巢式聚合酶链反应(nPCR)进行确认。通过分析MSP1a的微卫星和串联重复序列来表征菌株的遗传多样性。基于微卫星结构,鉴定出四种基因型。基因型E最为普遍。对MSP1a串联重复序列的分析显示,31个重复序列组合产生了28种不同的菌株,其中τ-10-15和α-β-β-β-Γ最为常见。重复序列Γ、β、α和γ与……的缺失具有统计学意义相关(<0.05)。分子观察表明,我们样本中鉴定出的46.7%的菌株缺乏与蜱细胞结合的能力;因此,它们可能是由其他媒介传播的。菌株遗传多样性为了解无浆体病的流行病学行为提供了有价值的信息,并可能有助于开发控制这种疾病的有效疫苗。