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An appropriate management strategy of bluetongue vectors should include larvicidal treatments in their larval development sites utilizing active substances with low environmental impact. A selection of biorational insecticides with potential against dipteran larvae was assayed in the laboratory against field collected Culicoides larvae including C. cataneii, C. circumscriptus, and C. imicola, determining their median lethal concentrations in water and mud/water substrate. The efficacy of formulations containing the insect growth regulators pyriproxyfen and cyromazine, the botanical insecticide azadirachtin, and the entomopathogenic bacteria Bacillus thuringiensis israelensis and Brevibacillus laterosporus, was also assessed in field conditions in a comparative study conducted in sheep farm larval development sites, including treatments with the organophosphate temephos. Significant larvicidal properties were associated with the various insecticides evaluated in the laboratory assays and in field trials, although with different levels of effectiveness. While temephos was confirmed to be an effective broad spectrum larvicidal substance, B. laterosporus appeared to be the most effective among entomopathogens, while insect growth regulators combined a good efficacy to a long-lasting residual effect in the field. Everything considered, the use of these biorational insecticides alone or in combination with larval habitat manipulation techniques appears to be a promising method to complement integrated biting midge management programs., (Copyright © 2019 Elsevier B.V. All rights reserved.)

Sardinia is a hotspot for studying tick-borne diseases in the Mediterranean region, where cases of notifiable tick-borne diseases are increasing. The aim of this study was to determine the presence of tick-borne bacteria of medical and veterinary importance in ixodid ticks collected from domestic and wild animals, humans, and vegetation from different collection sites in Sardinia. Using standard PCR and sequencing techniques, the presence of Rickettsia, Anaplasma, Ehrlichia, and Bartonella species, as well as Coxiella burnetii was evaluated. A total of 1619 ticks were morphologically identified as Rhipicephalus sanguineus sensu lato, R. bursa, R. annulatus, Dermacentor marginatus, Haemaphysalis punctata, Ha. sulcata, Hyalomma lusitanicum, H. marginatum, Ixodes festai (sometimes referred to erroneously as I. ventalloi), and Argas reflexus. Results indicated the presence of several circulating pathogens in Sardinian ticks. DNA of Rickettsia species was detected in 58 out of 1619 (4%) belonging to R. sanguineus s.l., D. marginatus, Ha. punctata, H. marginatum, and I. festai species. Ehrlichia canis DNA was detected in 33 out of 1619 ticks (2%) belonging to R. sanguineus s.l., R. bursa, and Ha. punctata species. A total of 61 out of 1619 (4%) ticks (R. sanguineus s. l., R. bursa, Ha. punctata, and I. festai) tested positive for Anaplasma spp. Coxiella burnetii was detected in 21 out of 1619 (1%) ticks belonging to R. sanguineus s.l., R. bursa, R. annulatus, and H. marginatum species. Five R. sanguineus s.l. and one R. bursa ticks were positive for the presence of Bartonella sp. 16S rRNA gene. Our findings expand the knowledge on tick-borne microorganism repertoires and tick distribution in Sardinia. Tick distribution should be monitored for effective control of these arthropods and the infections they transmit., (Copyright © 2018 Elsevier GmbH. All rights reserved.)