The development of a strategic protocol is fundamental to the control of Rhipicephalus microplus. The efficacy of different strategic tick control protocols (Day 1 to Day 119) using commercial acaricides according to R. microplus burden on bovines was evaluated. Female ticks (4.5-8 mm in length) were initially counted on cattle to form four groups of bovines with low and high tick burdens (treated and control), with 10 animals each. The animals were then (Day 0) kept in different paddocks, and the bovines from the two treated groups received their first treatment. The main difference in the protocols was the use of a spray formulation on animals with high tick burden. Additionally, the criterion for animal re-treatment (treatment interval) during the proposed strategic protocol was evaluated according to tick length by visual inspection - if 30% of the bovines of a group presented ticks < 4 mm between their legs and dewlap, the treatment was applied, which could change the originally proposed intervals. The number of days for which animals from the treated groups remained without acaricide administration (palliative control, ≥30 tick females < 4 mm) after the end of the strategic tick control protocol was recorded. Tick counts and visual inspection were done weekly until days 203 and 119, respectively. The results showed that the adopted protocol was successful based on calculated efficacy. Mean efficacies from Day 7 to Day 119 were 86.1% and 96.1% for treated groups with low and high tick burdens, respectively, and mean tick count did not differ between them (P > 0.05) but did differ from their respectively controls (P = <0.0001). The use of spray formulation at the beginning of the protocol for animals with a high tick burden helped to avoid harmful tick infestations. Visual analysis of tick length anticipated the proposed treatment intervals. Treated groups remained without palliative treatment for 70 days, while control groups needed treatment every 28 days. It was concluded that strategic control protocols must be developed according to tick burden, and tick length can be used to indicate when treatment needs to be applied.
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http://dx.doi.org/10.1016/j.ttbdis.2021.101737 | DOI Listing |
Methods Mol Biol
January 2025
Institute of Science and Technology Austria (ISTA), Klosterneuburg, Austria.
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Zhejiang University-University of Edinburgh Institute, School of Medicine, Zhejiang University, Jiaxing, 314400, China.
Therapeutic resistance in cancer is responsible for numerous cancer deaths in clinical practice. While target mutations are well recognized as the basis of genetic resistance to targeted therapy, nontarget mutation resistance (or nongenetic resistance) remains poorly characterized. Despite its complex and unintegrated mechanisms in the literature, nongenetic resistance is considered from our perspective to be a collective response of innate or acquired resistant subpopulations in heterogeneous tumors to therapy.
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View Article and Find Full Text PDFCell Mol Neurobiol
January 2025
Neuroscience Department, International School for Advanced Studies (SISSA), Via Bonomea 265, Trieste, TS, Italy.
In clinics, physical injuries to the spinal cord cause a temporary motor areflexia below lesion, known as spinal shock. This topic is still underexplored due to the lack of preclinical spinal cord injury (SCI) models that do not use anesthesia, which would affect spinal excitability. Our innovative design considered a custom-made micro impactor that provides localized and calibrated strikes to the ventral surface of the thoracic spinal cord of the entire CNS isolated from neonatal rats.
View Article and Find Full Text PDFJ Clin Microbiol
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Chrono-environnement UMR6249, CNRS, University of Franche-Comté, Besançon, Bourgogne-Franche-Comté, France.
Unlabelled: The aim of this study was to identify parameters influencing DNA extraction and PCR amplification efficiencies in an attempt to standardize Mucorales qPCR. The Fungal PCR Initiative Mucorales Laboratory Working Group distributed two panels of simulated samples to 26 laboratories: Panel A (six sera spiked with Mucorales DNA and one negative control serum) and Panel B (six Mucorales DNA extracts). Panel A underwent DNA extraction in each laboratory according to the local procedure and were sent to a central laboratory for testing using three different qPCR techniques: one in-house qPCR assay and two commercial assays (MucorGenius and Fungiplex).
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