Trichoderma atroviride is a common fungus found in various
ecosystems that shows mycoparasitic ability on other fungi.
A novel dsRNA virus was isolated from T. atroviride NFCF377
strain and its molecular features were analyzed. The viral
genome consists of a single segmented double-stranded RNA
and is 9,584 bp in length, with two discontinuous open reading
frames (ORF1 and ORF2). A mycoviral structural protein
and an RNA-dependent RNA polymerase (RdRp) are encoded
by ORF1 and ORF2, respectively, between which is found a
canonical shifty heptameric signal motif (AAAAAAC) followed
by an RNA pseudoknot. Analysis of sequence similarity
and phylogeny showed that it is closely related to members
of the proposed family “Fusagraviridae”, with a highest similarity
to the Trichoderma atroviride mycovirus 1 (TaMV1).
Although the sequence similarity of deduced amino acid to
TaMV1 was evident, sequence deviations were distinctive at
untranslated regions (UTRs) due to the extended size. Thus,
we inferred this dsRNA to be a different strain of Trichoderma
atroviride mycovirus 1 (TaMV1-NFCF377). Electron
microscopy image exhibited an icosahedral viral particle of
40 nm diameter. Virus-cured isogenic isolates were generated
and no differences in growth rate, colony morphology, or
conidia production were observed between virus-infected and
virus-cured strains. However, culture filtrates of TaMV1-
NFCF377-infected strain showed enhanced antifungal activity
against the plant pathogen Rhizoctonia solani but not to
edible mushroom Pleurotus ostreatus. These results suggested
that TaMV1-NFCF377 affected the metabolism of the fungal
host to potentiate antifungal compounds against a plant pathogen,
but this enhanced antifungal activity appeared to be
species-specific.
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bacteria. Considering the progressive antibiotic resistance,
cathelicidin is a candidate for use as an alternative approach
to treat and overcome the challenge of antimicrobial resistance.
Cathelicidin-BF (Cath-BF) is a short antimicrobial peptide,
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related derivatives exert strong antimicrobial and weak hemolytic
properties. This study investigates the bactericidal
and cytotoxic effects of Cath-BF and its analogs (Cath-A and
Cath-B). Cath-A and Cath-B were designed to increase their
net positive charge, to have more activity against methicillin
resistant S. aureus (MRSA). The results of this study show
that Cath-A, with a +17-net charge, has the most noteworthy
antimicrobial activity against MRSA strains, with minimum
inhibitory concentration (MIC) ranging between 32–128
μg/ml. The bacterial kinetic analysis by 1 × MIC concentration
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against human erythrocytes at concentrations up to 250 μg/ml.
Altogether, these results suggest that Cath-A and Cath-B are
competent candidates as novel antimicrobial compounds
against MRSA and possibly other multidrug resistant bacteria.
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