Extreme-QTL mapping of monepantel resistance in Haemonchus contortus

Haemonchus contortus, a gastrointestinal nematode parasite of sheep, is mainly controlled by anthelmintics; the occurrence of anthelmintic resistance leads to treatment failures and increases economic burden. Because molecular mechanisms involved in drug resistance can be elucidated by genomic studi...

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Veröffentlicht in:Parasites & vectors 2019-08, Vol.12 (1), p.403-403, Article 403
Hauptverfasser: Niciura, Simone Cristina Méo, Tizioto, Polyana Cristine, Moraes, Caroline Valério, Cruvinel, Giovanna Gabrielle, de Albuquerque, Ana Cláudia Alexandre, Santana, Raul Costa Mascarenhas, Chagas, Ana Carolina de Souza, Esteves, Sergio Novita, Benavides, Magda Vieira, do Amarante, Alessandro Francisco Talamini
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Sprache:eng
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Zusammenfassung:Haemonchus contortus, a gastrointestinal nematode parasite of sheep, is mainly controlled by anthelmintics; the occurrence of anthelmintic resistance leads to treatment failures and increases economic burden. Because molecular mechanisms involved in drug resistance can be elucidated by genomic studies, an extreme quantitative trait locus (X-QTL) mapping approach was used to identify co-segregation of the resistance phenotype with genetic markers to detect the genome-wide variants associated with monepantel resistance in H. contortus. A cross between H. contortus isolates using parental susceptible (Par-S) males and monepantel resistant (Par-R) females resulted in SR progeny, while reciprocal cross resulted in RS progeny. Pools (n = 30,000) of infective larvae (L3) recovered from Par-R, and from SR and RS populations in the F3 generation, collected both before (unselected group) and 7 days after (selected group) selection with monepantel treatment in sheep hosts, were subjected to genome sequencing (Pool-Seq). Pairwise comparisons of allele frequencies between unselected and selected groups were performed for each population by Fisher's exact test (FET) and for both populations combined by a Cochran-Mantel-Haenszel (CMH) test. Mapping rates varied from 80.29 to 81.77% at a 90.4X mean coverage of aligned reads. After correction for multiple testing, significant (P 
ISSN:1756-3305
1756-3305
DOI:10.1186/s13071-019-3663-9