Please use this identifier to cite or link to this item: http://hdl.handle.net/10553/118296
Title: Dirofilaria immitis: Genotyping Randomly Selected European Clinical Samples and USA Laboratory Isolates with Molecular Markers Associated with Macrocyclic Lactone Susceptibility and Resistance
Authors: Curry, Emily
Traversa, Donato
Carretón Gómez, Elena 
Kramer, Laura
Sager, Heinz
Young, Lisa
Prichard, Roger
UNESCO Clasification: 310904 Medicina interna
Keywords: Dirofilaria Immitis
Dirofilariosis
Macrocyclic Lactones
Molecular Markers
Resistance, et al
Issue Date: 2022
Journal: Pathogens 
Abstract: Dirofilaria immitis is a parasitic nematode and causes dirofilariosis, a potentially fatal pulmonary infection which primarily infects canids. Dirofilariosis infections are controlled via prophylactic macrocyclic lactone (ML) regimens. Recent evidence has confirmed the development of ML-resistant isolates in the USA, which are genetically distinct from wildtype populations. Single nucleotide polymorphisms (SNP) associated with ML-resistant phenotypes were clinically validated in USA populations. In this study, 3 USA laboratory-maintained isolates (Berkeley, Georgia II, and WildCat) and 11 randomly selected European clinical samples from 7 hosts were analyzed. The samples tested were fresh microfilaria (mf) in blood or adult worms preserved in ethanol. The samples underwent MiSeq sequencing of the top 9 SNP associated with ML resistance. The results provide the first genotypic analysis of the three USA laboratory-maintained isolates and any European samples. The European clinical samples show no genomic evidence of ML resistance based on the 9 SNP. The early adoption of genotyping of clinical D. immitis samples could provide an early indication of the potential development of ML resistance and aid to distinguish clinical cases of heartworm infection due to ML resistance from those due to a lack compliance with the recommended treatments, as has been seen in North America.
URI: http://hdl.handle.net/10553/118296
ISSN: 2076-0817
DOI: 10.3390/pathogens11080934
Source: Pathogens [EISSN 2076-0817], v. 11 (8), (Agosto 2022)
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