Cargando…

Genetic Variants and Increased Expression of Parascaris equorum P-glycoprotein-11 in Populations with Decreased Ivermectin Susceptibility

Macrocyclic lactones (MLs) represent the major drug class for control of parasitic infections in humans and animals. However, recently reports of treatment failures became more frequent. In addition to human and ruminant parasitic nematodes this also is the case for the horse-nematode Parascaris equ...

Descripción completa

Detalles Bibliográficos
Autores principales: Janssen, I. Jana I., Krücken, Jürgen, Demeler, Janina, Basiaga, Marta, Kornaś, Sławomir, von Samson-Himmelstjerna, Georg
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634834/
https://www.ncbi.nlm.nih.gov/pubmed/23637871
http://dx.doi.org/10.1371/journal.pone.0061635
_version_ 1782267161498091520
author Janssen, I. Jana I.
Krücken, Jürgen
Demeler, Janina
Basiaga, Marta
Kornaś, Sławomir
von Samson-Himmelstjerna, Georg
author_facet Janssen, I. Jana I.
Krücken, Jürgen
Demeler, Janina
Basiaga, Marta
Kornaś, Sławomir
von Samson-Himmelstjerna, Georg
author_sort Janssen, I. Jana I.
collection PubMed
description Macrocyclic lactones (MLs) represent the major drug class for control of parasitic infections in humans and animals. However, recently reports of treatment failures became more frequent. In addition to human and ruminant parasitic nematodes this also is the case for the horse-nematode Parascaris equorum. Nevertheless, to date the molecular basis of ML resistance is still not understood. Unspecific resistance mechanisms involving transporters such as P-glycoproteins (Pgps) are expected to contribute to ML resistance in nematodes. Here, complete sequences of two P. equorum Pgps were cloned and identified as orthologs of Caenorhabditis elegans Ppg-11 and an unnamed Caenorhabditis briggsae Pgp designated as Pgp-16 using phylogenetic analysis. Quantitative real-time PCR was used to compare expression between tissues. Significantly higher PeqPgp-11 expression was found in the gut for both genders, whereas for PeqPgp-16 the body wall was identified as predominant expression site. Furthermore, Pgps were analyzed regarding their participation in resistance development. Using SeqDoC analyses, Pgp-sequences of P. equorum populations with different ML susceptibility were compared. This approach revealed three single nucleotide polymorphisms (SNPs) causing missense mutations in the PeqPgp-11 sequence which correlated with decreased ML susceptibility. However, no resistance associated differences in mRNA expression levels were detected between embryonated eggs of these populations. In contrast, comparison of two pre-adult groups with different ivermectin (IVM) susceptibility revealed the presence of the three SNPs and in addition statistically significant PeqPgp-11 overexpression in the group of worms with reduced susceptibility. These results indicate that Pgp-11 might be involved in IVM resistance in P. equorum as it shows increased expression in an IVM exposed life-cycle stage of an IVM resistant population as well as occurrence of putatively resistance associated SNPs in populations with reduced IVM susceptibility. These SNPs are promising diagnostic candidates for detection of ML resistance with potential also for other parasitic nematode species.
format Online
Article
Text
id pubmed-3634834
institution National Center for Biotechnology Information
language English
publishDate 2013
publisher Public Library of Science
record_format MEDLINE/PubMed
spelling pubmed-36348342013-05-01 Genetic Variants and Increased Expression of Parascaris equorum P-glycoprotein-11 in Populations with Decreased Ivermectin Susceptibility Janssen, I. Jana I. Krücken, Jürgen Demeler, Janina Basiaga, Marta Kornaś, Sławomir von Samson-Himmelstjerna, Georg PLoS One Research Article Macrocyclic lactones (MLs) represent the major drug class for control of parasitic infections in humans and animals. However, recently reports of treatment failures became more frequent. In addition to human and ruminant parasitic nematodes this also is the case for the horse-nematode Parascaris equorum. Nevertheless, to date the molecular basis of ML resistance is still not understood. Unspecific resistance mechanisms involving transporters such as P-glycoproteins (Pgps) are expected to contribute to ML resistance in nematodes. Here, complete sequences of two P. equorum Pgps were cloned and identified as orthologs of Caenorhabditis elegans Ppg-11 and an unnamed Caenorhabditis briggsae Pgp designated as Pgp-16 using phylogenetic analysis. Quantitative real-time PCR was used to compare expression between tissues. Significantly higher PeqPgp-11 expression was found in the gut for both genders, whereas for PeqPgp-16 the body wall was identified as predominant expression site. Furthermore, Pgps were analyzed regarding their participation in resistance development. Using SeqDoC analyses, Pgp-sequences of P. equorum populations with different ML susceptibility were compared. This approach revealed three single nucleotide polymorphisms (SNPs) causing missense mutations in the PeqPgp-11 sequence which correlated with decreased ML susceptibility. However, no resistance associated differences in mRNA expression levels were detected between embryonated eggs of these populations. In contrast, comparison of two pre-adult groups with different ivermectin (IVM) susceptibility revealed the presence of the three SNPs and in addition statistically significant PeqPgp-11 overexpression in the group of worms with reduced susceptibility. These results indicate that Pgp-11 might be involved in IVM resistance in P. equorum as it shows increased expression in an IVM exposed life-cycle stage of an IVM resistant population as well as occurrence of putatively resistance associated SNPs in populations with reduced IVM susceptibility. These SNPs are promising diagnostic candidates for detection of ML resistance with potential also for other parasitic nematode species. Public Library of Science 2013-04-24 /pmc/articles/PMC3634834/ /pubmed/23637871 http://dx.doi.org/10.1371/journal.pone.0061635 Text en © 2013 Janssen et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Janssen, I. Jana I.
Krücken, Jürgen
Demeler, Janina
Basiaga, Marta
Kornaś, Sławomir
von Samson-Himmelstjerna, Georg
Genetic Variants and Increased Expression of Parascaris equorum P-glycoprotein-11 in Populations with Decreased Ivermectin Susceptibility
title Genetic Variants and Increased Expression of Parascaris equorum P-glycoprotein-11 in Populations with Decreased Ivermectin Susceptibility
title_full Genetic Variants and Increased Expression of Parascaris equorum P-glycoprotein-11 in Populations with Decreased Ivermectin Susceptibility
title_fullStr Genetic Variants and Increased Expression of Parascaris equorum P-glycoprotein-11 in Populations with Decreased Ivermectin Susceptibility
title_full_unstemmed Genetic Variants and Increased Expression of Parascaris equorum P-glycoprotein-11 in Populations with Decreased Ivermectin Susceptibility
title_short Genetic Variants and Increased Expression of Parascaris equorum P-glycoprotein-11 in Populations with Decreased Ivermectin Susceptibility
title_sort genetic variants and increased expression of parascaris equorum p-glycoprotein-11 in populations with decreased ivermectin susceptibility
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3634834/
https://www.ncbi.nlm.nih.gov/pubmed/23637871
http://dx.doi.org/10.1371/journal.pone.0061635
work_keys_str_mv AT janssenijanai geneticvariantsandincreasedexpressionofparascarisequorumpglycoprotein11inpopulationswithdecreasedivermectinsusceptibility
AT kruckenjurgen geneticvariantsandincreasedexpressionofparascarisequorumpglycoprotein11inpopulationswithdecreasedivermectinsusceptibility
AT demelerjanina geneticvariantsandincreasedexpressionofparascarisequorumpglycoprotein11inpopulationswithdecreasedivermectinsusceptibility
AT basiagamarta geneticvariantsandincreasedexpressionofparascarisequorumpglycoprotein11inpopulationswithdecreasedivermectinsusceptibility
AT kornassławomir geneticvariantsandincreasedexpressionofparascarisequorumpglycoprotein11inpopulationswithdecreasedivermectinsusceptibility
AT vonsamsonhimmelstjernageorg geneticvariantsandincreasedexpressionofparascarisequorumpglycoprotein11inpopulationswithdecreasedivermectinsusceptibility