ArticleParasites & vectors2012
Development of a cDNA microarray for the measurement of gene expression in the sheep scab mite Psoroptes ovis.
Article in Parasites & vectors, 2012. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 10 papers.
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Who cites it
10 citing papers in PubMed, 18 citations in OpenAlex.
- Over-expression and increased copy numbers of a cytochrome P450 and two UDP-glucuronosyltransferase genes in macrocyclic lactone resistant Psoroptes ovis of cattle.PLoS pathogens · 2025Article
- Sheep scab spatial distribution: the roles of transmission pathways.Parasites & vectors · 2021Article
- Sheep scab transmission: a spatially explicit dynamic metapopulation model.Veterinary research · 2021Article
- A genomic analysis and transcriptomic atlas of gene expression in Psoroptes ovis reveals feeding- and stage-specific patterns of allergen expression.BMC genomics · 2019Article
- Gene silencing by RNA interference in the ectoparasitic mite, Psoroptes ovis.Veterinary research · 2018Article
- Treatment strategies for sheep scab: An economic model of farmer behaviour.Preventive veterinary medicine · 2017Article
- A recombinant subunit vaccine for the control of ovine psoroptic mange (sheep scab).Veterinary research · 2016Article
- Population identification and divergence threshold in Psoroptidae based on ribosomal ITS2 and mitochondrial COI genes.Parasitology research · 2015Article
- DNA microarray-based gene expression profiling of estrogenic chemicals.Cellular and molecular life sciences : CMLS · 2014Review
- Hormonal and behavioral changes induced by acute and chronic experimental infestation with Psoroptes cuniculi in the domestic rabbit Oryctolagus cuniculus.Parasites & vectors · 2013Article
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Authors and funding
8 authors at 3 institutions in 1 country.
Funding
Abstract
backgroundSheep scab is caused by the ectoparasitic mite Psoroptes ovis which initiates a profound cutaneous inflammatory response, leading to the development of the skin lesions which are characteristic of the disease. Existing control strategies rely upon injectable endectocides and acaricidal dips but concerns over residues, eco-toxicity and the development of acaricide resistance limit the sustainability of this approach. In order to identify alternative means of disease control, a deeper understanding of both the parasite and its interaction with the host are required.
methodsHerein we describe the development and utilisation of an annotated P. ovis cDNA microarray containing 3,456 elements for the measurement of gene expression in this economically important ectoparasite. The array consists of 981 P. ovis EST sequences printed in triplicate along with 513 control elements. Array performance was validated through the analysis of gene expression differences between fed and starved P. ovis mites.
resultsSequences represented on the array include homologues of major house dust mite allergens and tick salivary proteins, along with factors potentially involved in mite reproduction and xenobiotic metabolism. In order to validate the performance of this unique resource under biological conditions we used the array to analyse gene expression differences between fed and starved P. ovis mites. These analyses identified a number of house dust mite allergen homologues up-regulated in fed mites and P. ovis transcripts involved in stress responses, autophagy and chemosensory perception up-regulated in starved mites.
conclusionThe P. ovis cDNA microarray described here has been shown to be both robust and reproducible and will enable future studies to analyse gene expression in this important ectoparasite.
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