Coello Peralta Roberto Darwin, Andrada Aldo Rubén, Vinueza Rommel Lenin, Pazmiño Gómez Betty Judith, Valencia Gonzaga Eduardo David, Rodríguez Burnham Enrique X, Salazar Mazamba María de Lourdes, Ramallo Geraldine
Department of Microbiology, Universidad de Guayaquil, Guayaquil, Ecuador.
Institute of Genetics and Microbiology, Fundación Miguel Lillo, San Miguel de Tucumán, Argentina.
Med Sci Monit. 2025 Jan 4;31:e947069. doi: 10.12659/MSM.947069.
BACKGROUND Ancylostoma caninum is a soil-borne, soil-transmitted helminth with infective larvae and produces cutaneous larva migrans in humans. The objective of this study was to confirm the presence of A. caninum in domestic dogs from the urban-marginal and rural sectors of the Ecuadorian coast through morphometry, culture, and molecular techniques. MATERIAL AND METHODS A total of 498 domestic dogs were analyzed via 5 coproparasitic screening methods: direct, modified flotation, sedimentation with centrifugation using saline solution (identification of eggs), and modified Baermann and Harada-Mori methods (identification of larvae). For confirmation, culture (agar in plates, Müller-Hinton agar plates, MacConkey agar plates, and artisanal media with sand and/or ravine soil, both sterile, and all prepared in Petri dishes), polymerase chain reaction (PCR), and DNA sequencing analyses were subsequently conducted via morphometric methods. RESULTS A total of 250 domestic dogs were diagnosed with A. caninum (50.20%) via coproparasitic methods. The parasite was subsequently confirmed via morphometry, cultured in 5 culture media, and detected by PCR, and phylogenetic characterization was performed. CONCLUSIONS The coproparasitic methods used for screening increased the sensitivity of the results. Morphometry is an easily accessible and low-cost confirmatory method. The culture method was used to test the good adaptability of and infection by the parasite. The presence of A. caninum was detected for the first time via PCR, and its phylogenetic profile was analyzed using the molecular marker cox1.
背景 犬钩口线虫是一种土源性、土壤传播的蠕虫,其幼虫具有感染性,可在人类中引起皮肤幼虫移行症。本研究的目的是通过形态测量、培养和分子技术,确认厄瓜多尔海岸城市边缘和农村地区家犬体内犬钩口线虫的存在。
材料与方法 通过5种粪便寄生虫筛查方法对498只家犬进行分析:直接涂片法、改良漂浮法、使用盐溶液离心沉淀法(虫卵鉴定)以及改良贝曼法和原田-森氏法(幼虫鉴定)。为进行确认,随后通过形态测量方法进行培养(平板琼脂、Müller-Hinton琼脂平板、麦康凯琼脂平板以及含有沙子和/或沟壑土壤的手工培养基,均为无菌,且全部在培养皿中制备)、聚合酶链反应(PCR)和DNA测序分析。
结果 通过粪便寄生虫方法共诊断出250只家犬感染犬钩口线虫(50.20%)。随后通过形态测量对该寄生虫进行了确认,在5种培养基中进行了培养,并通过PCR进行了检测,同时进行了系统发育特征分析。
结论 用于筛查的粪便寄生虫方法提高了结果的敏感性。形态测量是一种易于获取且成本低廉的确认方法。培养方法用于测试寄生虫的良好适应性和感染情况。首次通过PCR检测到犬钩口线虫的存在,并使用分子标记cox1分析了其系统发育图谱。