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1.
Exp Parasitol ; 205: 107734, 2019 Oct.
Article in English | MEDLINE | ID: mdl-31394093

ABSTRACT

Parasitism by Haemonchus contortus is one of the main limiting factors in small ruminant production around the globe. Although several studies suggest the use of integrated management practices, these parasites have been controlled essentially with synthetic anthelmintic drugs. The resistance mechanism against the imidazothiazole derivative levamisole in Haemonchus contortus has not been fully described. Recently, resistance was associated with a 63bp deletion in the Hco-acr-8b gene that encodes a subunit for a nicotinic acetylcholine receptor. This study aimed to standardize a real time PCR (qPCR) protocol for levamisole resistance diagnosis in H. contortus populations based on this polymorphism and use it to characterize 23 field H. contortus populations obtained from different localities of Ceará State, Northeast Brazil. In addition, two populations of H. contortus were used as a standard of susceptibility and resistance, Inbred Strain Edinburgh (ISE) and Kokstad, respectively. Larval development tests (LDT) were performed on five field isolates and both EC50 and EC95 were estimated. LDT EC95 values provided a wider interval between susceptible and resistant populations than EC50 values (EC95 = 1.96-57.93 µM; EC50 = 0.05-0.39 µM), and were found to be more appropriate for differentiating them. Real time PCR results showed resistance allele frequencies ranged from 20.9 to 76.7%. Our results suggest that levamisole resistance may be present in field populations but it is not as widespread as benzimidazole resistance. This methodology may be useful to monitor levamisole resistance in field populations of H. contortus.


Subject(s)
Antinematodal Agents/pharmacology , Drug Resistance/genetics , Haemonchus/drug effects , Levamisole/pharmacology , Animals , Benzimidazoles/pharmacology , DNA, Helminth/isolation & purification , Feces/parasitology , Gene Frequency/genetics , Haemonchiasis/drug therapy , Haemonchiasis/parasitology , Haemonchiasis/veterinary , Haemonchus/genetics , Haemonchus/growth & development , Larva/drug effects , Larva/growth & development , Neuromuscular Junction/drug effects , Neuromuscular Junction/metabolism , Real-Time Polymerase Chain Reaction/veterinary , Receptors, Cholinergic/drug effects , Receptors, Nicotinic/drug effects , Sequence Alignment/veterinary , Sheep , Sheep Diseases/drug therapy , Sheep Diseases/parasitology , Tetramisole/pharmacology
2.
Vet Parasitol ; 248: 90-95, 2017 Dec 15.
Article in English | MEDLINE | ID: mdl-29173548

ABSTRACT

Parasitism by Haemonchus contortus is one of the main limiting factors in small ruminant production in tropical areas. Benzimidazoles (BZ) and macrocyclic lactones (ML) are the most used anthelmintic classes in gastrointestinal nematodes control. There is considerable scientific evidence of a possible relation between the anthelmintic resistance to BZ and ML. This study aimed to characterize the dynamics of anthelmintic resistance in an H. contortus susceptible isolate under selection pressure for BZ and ML alone or in combination and the role of isotype 1 ß-tubulin gene SNPs in these situations. A total of 12 Somali sheep were infected with 5000 third stage larvae of H. contortus Inbred-Susceptible Edinburgh (ISE) isolate. Once infection was established, animals were distributed in three groups (n=4), each treated with crescent doses of oxfendazole (OXF), ivermectin (IVM) and oxfendazole plus ivermectin (IVMOXF). An additional control group with untreated animals was maintained during the entire experiment. After each treatment, eggs were collected and real-time PCR was performed to identify single nucleotide polymorphisms (SNPs) F167Y, F200Y and E198A, in addition to egg hatch test (EHT) for BZ and larval development test (LDT) for ivermectin resistance. All treatments led to increased resistance allelic frequencies at SNPs F200Y and F167Y (p <0.05). In vitro results showed increased phenotypic resistance against both anthelmintic classes in groups IVM and IVMOXF while group OXF only developed resistance against BZ. Finally, we provide evidence that while isotype 1 ß-tubulin gene SNPs may have some involvement with ML resistance, the presence of these ß-tubulin SNPs alone are not sufficient to develop ML resistance.


Subject(s)
Antinematodal Agents/pharmacology , Drug Resistance , Haemonchus/drug effects , Polymorphism, Single Nucleotide/drug effects , Selection, Genetic , Tubulin/genetics , Animals , Benzimidazoles/pharmacology , Haemonchiasis/drug therapy , Haemonchiasis/parasitology , Haemonchiasis/veterinary , Haemonchus/genetics , Ivermectin/pharmacology , Male , Sheep , Sheep Diseases/drug therapy , Sheep Diseases/parasitology
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