2,594 research outputs found

    Fish and amphibians as bat predators

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    Although bats (Chiroptera) belong to the most diverse mammalian orders, study of diversity of their natural predators has been seriously neglected for a long time. While some recent reviews contain comprehensive overviews of our recent knowledge on these phenomena for some animal groups, such work is still lacking for anamniotes - fishes and amphibians. Here, I am summarising bat predation incidences by anamniotes that were published in scientific journals and public web domains. I found out that at least 14 species of fishes and 14 species of frogs were observed as feeding on bats. Moreover, 7 and 16 species of bats were recorded as victims of hunting activity of fishes and frogs, respectively. Majority of localised incidences came from the New World; frog (between latitude 49°N to 28°S) attacks were distributed mainly in tropical or subtropical areas < 30° from equator (70% of all records), fish (44°N to 20°S) incidences reach same proportion in colder areas (> 30° from equator) and warmer areas. In some cases, these predators can regularly feed on bats, especially when hunting near roosting places of bats; however, with respect to number of recorded cases (21 for fishes and 37 for amphibians), bat predation by anamniotes seems to be very rare and opportunistic with only very limited influence on bat populations or their behaviour

    Heaven Poured Right

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    Novel mutations in the toll like receptor genes cause hyporesponsiveness to Mycobacterium avium subsp. paratuberculosis infection

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    Toll like receptors play a central role in the recognition of pathogen associated molecular patterns (PAMPs). Mutations in TLR1, TLR2 and TLR4 genes may change the PAMP reorganization ability which causes altered responsiveness to the bacterial pathogens. A case control study, performed to assess the association between TLR gene mutations and susceptibility to Mycobacterium avium subsp. paratuberculosis (MAP), revealed novel mutations (TLR1 - Ser150Gly and Val220Met; TLR2 - Phe670Leu) that hindered either PAMP recognition or further downstream TLR pathway activation. A cytokine expression experiments (IL-4, IL-8, IL-10, IL-12 and IFN-γ) in the challenged mutant and wild type moDCs (mocyte derived dendritic cells) confirmed the negative impact of these mutations and altered TLR downstream activation. Further In silico analysis of the TLR1 and TLR4 ectodomains (ECD) revealed the polymorphic nature of the central ECD and irregularities in the central LRR motifs. The most critical positions that may alter the pathogen recognition ability of TLR were: the 9th amino acid position in LRR motif (TLR1, LRR10) and 4th residue downstream to LRR domain (exta LRR region of TLR4). The study describes novel mutations in the TLRs and presents their association with the MAP infection
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