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  • 1
    Electronic Resource
    Electronic Resource
    s.l. : American Chemical Society
    Journal of chemical information and modeling 20 (1980), S. 158-162 
    ISSN: 1520-5142
    Source: ACS Legacy Archives
    Topics: Chemistry and Pharmacology
    Type of Medium: Electronic Resource
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  • 2
    ISSN: 1570-7458
    Keywords: Diptera ; Calliphoridae ; Muscidae ; Oestridae ; blowfly ; odour ; dimethyl trisulphide ; attraction ; phylogeny
    Source: Springer Online Journal Archives 1860-2000
    Topics: Biology
    Notes: Abstract A field test with synthetic dimethyl trisulphide as attractant in flight traps was carried out in Finnmark, northern Norway, in July 1992 and 1994. The reindeer oestrids Hypoderma (=Oedemagena) tarandi (L.) and Cephenemyia trompe (Modeer) (Diptera: Oestridae), previously shown to react positively to dimethyl trisulphide on the olfactory receptor level, were only caught in small numbers, with no significant differences between baited and unbaited traps. In both years, however, the baited traps caught significantly more individuals of Calliphoridae and Hydrotaea anxia (Zetterstedt) (Diptera: Muscidae) than unbaited control traps. In 1992, Protophormia terraenovae (Robineau-Desvoidy) (Diptera: Calliphoridae) and H. anxia were the predominant species (78.5% and 20.5%, respectively). In 1994, H. anxia was the most prevalent species (73.6%). Seven species of Calliphoridae were caught, with P. terraenovae, Calliphora vomitoria (L.), C. uralensis (Villeneuve) and C. loewi (Enderlain) as the most numerous ones. Dimethyl trisulphide is probably a decomposition product from bacterial activity and may be one of the major cues for calliphorid host finding. The significance of the reaction for oestrids on the receptor level, but evidently not on a behavioural level, remains unclear.
    Type of Medium: Electronic Resource
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  • 3
    Publication Date: 2013-09-04
    Description: Background: Small ruminant lentiviruses (SRLV) are members of the Retroviridae family and infect goats and sheep worldwide. Detection of specific antibodies using AGID and ELISA is the most commonly used means of diagnosing SRLV infection. The most frequent molecular method for detecting the provirus genome is PCR, using peripheral blood leucocytes as target cells. Real time PCR has also recently been used. The aim of this study was to develop a real time PCR for detection of SRLV in order to improve molecular diagnostics of SRLV infections in sheep and goats. Results: Two new real time PCR assays using TaqMan probes for the specific detection of genotype A (MVV assay) and genoptype B (CAEV assay) SRLV strains and differentiation between them were developed and validated at both analytical and diagnostic levels following MIQE guidelines. The validation results showed that the new real time PCR is 100% specific, with a reliable limit of detection of 26 (CAEV assay) and 72 (MVV assay) plasmid DNA copies, while compared to ELISA the diagnostic sensitivity of both assays was 79% when tested with Slovenian SRLV field samples. Intra-assay and inter-assay coefficients of variation showed overall good repeatability and reproducibility of the new real time PCR assays, except for the highest dilutions. Conclusions: Two new TaqMan probe based real time PCR assays for the specific detection of genotype A and B SRLV strains and differentiation between them were developed and validated. They can serve as an additional tool for confirming infection with SRLV and may also be useful for early detection of infected animals prior to seroconversion.
    Electronic ISSN: 1746-6148
    Topics: Medicine
    Published by BioMed Central
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