TY - JOUR
T1 - Identification of Ancylostoma caninum in Domestic Dogs from Ecuador via Various Techniques
AU - Peralta, Roberto Darwin Coello
AU - Andrada, Aldo Rubén
AU - Vinueza, Rommel Lenin
AU - Gómez, Betty Judith Pazmiño
AU - Gonzaga, Eduardo David Valencia
AU - Burnham, Enrique X.Rodríguez
AU - de Lourdes Salazar Mazamba, María
AU - Ramallo, Geraldine
N1 - Publisher Copyright:
© 2025 International Scientific Information, Inc.. All rights reserved.
PY - 2025
Y1 - 2025
N2 - 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/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.
AB - 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/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.
KW - Ancylostomiasis
KW - Culture
KW - Diagnostic Techniques and Procedures
KW - Methods
KW - Parasites
UR - http://www.scopus.com/inward/record.url?scp=85214590768&partnerID=8YFLogxK
U2 - 10.12659/MSM.947069
DO - 10.12659/MSM.947069
M3 - Artículo
C2 - 39754349
AN - SCOPUS:85214590768
SN - 1234-1010
VL - 31
JO - Medical Science Monitor
JF - Medical Science Monitor
M1 - e947069
ER -