Molecular Detection of Anaplasma marginale in the Central Region of Venezuela: A PCR-based Assessment of the msp2 and msp5 Genes

IF 1.5 3区 农林科学 Q4 PARASITOLOGY
Mariana Carolina Eleizalde, Marta Mendoza, Armando Reyna-Bello, Lucinda Tavares-Marques, Miguel Martínez-Fresneda, Ely Gómez-Piñeres, José Rubén Ramírez-Iglesias
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引用次数: 0

Abstract

Background

Bovine anaplasmosis reduces livestock productivity in cattle, making timely and accurate diagnosis essential for epidemiological surveillance.

Purpose

To explore alternative primers for pathogen detection beyond the reference 19A/19B set targeting the single-copy msp5 gene and to update epidemiologic data we evaluated analytical and field performance of primers designed for the multicopy msp2 gene, using conserved terminal regions (msp2A/B). We also described the prevalence of A. marginale in specific sampled herds from several regions of Venezuela.

Methods

PCR conditions were standardized, and the analytical sensitivity of msp2A/B and 19A/B was evaluated. Field evaluations involved 208 cattle from small farms in four distinct geographical regions of Venezuela (Aragua, Cojedes, Guárico, and Miranda), divided into two groups with different clinical characteristics.

Results

Both primer sets detected the pathogen at concentrations as low as 0.01 ng. In a herd of 24 cattle experiencing an anaplasmosis outbreak, positivity rates were 12.5% and 66.67% using primers msp2A/B and 19A/B, respectively. One of the positive field-sample amplicons was cloned and sequenced to confirm bacterial identity, yielding a 97% BLAST identity with complete coverage to the reference strain Florida. Additionally, 10 and 5 nucleotide substitutions were detected at the 5′ and 3′ ends, respectively, compared to the reference isolate. This suggests terminal heterogeneity in the gene that may contribute to the reduced diagnostic performance of msp2A/B. Additionally, 184 clinically healthy cattle analyzed solely with 19A/B revealed a subclinical prevalence of 41.85%.

Conclusion

In a country with limited recent molecular reports, these findings underscore the epidemiological relevance of persistent infections. This study also constitutes the first report of an msp2 sequence from a Venezuelan A. marginale isolate, providing preliminary insights of the genetic diversity of A. marginale and support using msp5-based PCR for routine field detection and surveillance in Venezuela.

委内瑞拉中部地区边缘无原体的分子检测:基于pcr的msp2和msp5基因评估
背景:牛无形体病降低了牛的牲畜生产力,使及时准确的诊断对流行病学监测至关重要。目的:为了探索针对msp5单拷贝基因的参考引物19A/19B之外的其他病原体检测引物,并更新流行病学数据,我们利用保守末端区(msp2A/B)评估了针对msp2多拷贝基因设计的引物的分析和现场性能。我们还描述了在委内瑞拉几个地区的特定采样群中边缘蠓的流行情况。方法:标准化PCR条件,评价msp2A/B和19A/B的分析敏感性。实地评估涉及来自委内瑞拉四个不同地理区域(阿拉瓜、科耶德斯、Guárico和米兰达)的小农场的208头牛,它们被分为两组,具有不同的临床特征。结果:两组引物均可检出低至0.01 ng的病原菌。在发生无形体病暴发的24头牛群中,使用引物msp2A/B和19A/B的阳性率分别为12.5%和66.67%。积极的野外样品的扩增子是克隆和测序证实细菌身份,收益率97%爆炸身份与参考应变佛罗里达完全覆盖。此外,与参考分离物相比,在5‘和3’端分别检测到10和5个核苷酸取代。这表明该基因的终末异质性可能导致msp2A/B的诊断性能降低。此外,184头临床健康牛单独分析19A/B显示亚临床患病率为41.85%。结论:在一个最近分子报告有限的国家,这些发现强调了持续感染的流行病学相关性。该研究还首次报道了委内瑞拉边角a分离物的msp2序列,为边角a的遗传多样性提供了初步见解,并为在委内瑞拉使用基于msp5的PCR进行常规野外检测和监测提供了支持。
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来源期刊
Acta Parasitologica
Acta Parasitologica 医学-寄生虫学
CiteScore
3.10
自引率
6.70%
发文量
149
审稿时长
6-12 weeks
期刊介绍: Acta Parasitologica is an international journal covering the latest advances in the subject. Acta Parasitologica publishes original papers on all aspects of parasitology and host-parasite relationships, including the latest discoveries in biochemical and molecular biology of parasites, their physiology, morphology, taxonomy and ecology, as well as original research papers on immunology, pathology, and epidemiology of parasitic diseases in the context of medical, veterinary and biological sciences. The journal also publishes short research notes, invited review articles, book reviews. The journal was founded in 1953 as "Acta Parasitologica Polonica" by the Polish Parasitological Society and since 1954 has been published by W. Stefanski Institute of Parasitology of the Polish Academy of Sciences in Warsaw. Since 1992 in has appeared as Acta Parasitologica in four issues per year.
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