The emerging drug resistance and lack of safer and more potent antifungal agents make Candida infections another hot topic in the healthcare system. At the same time, the potential of plant products in developing novel antifungal drugs is also in the limelight. Considering these facts, we have investigated the different extracts of the flowers of Hibiscus rosa-sinensis of the Malvaceae family for their antifungal efficacy against five different pathogenic Candida strains. Among the various extracts, the chloroform extract showed the maximum zone of inhibition (26.6 ± 0.5 mm) against the Candida albicans strain.
Furthermore, the chloroform fraction was isolated, and a sterol compound was identified as β-sitosterol. Mechanistic studies were conducted to understand the mechanism of action, and the results showed that β-sitosterol has significant antifungal activity and is capable of interrupting biofilm formation and acts by inhibiting ergosterol biosynthesis in Candida albicans cells. Microscopic and molecular docking studies confirmed these findings. Overall, the study validates the antifungal efficacy of Candida albicans due to the presence of β-sitosterol which can act as an effective constituent for antifungal drug development individually or in combination.
Hepatitis B virus (HBV) infection highly increases the risk
for liver cirrhosis and hepatocellular carcinoma (HCC). The
clinical manifestation of HBV infection is determined by the
mutual interplay of the viral genotype, host genetic factors,
mode of transmission, adaptive mutations, and environmental
factors. Core promoter activation plays a critical role in the
pre-genomic RNA transcription of HBV for HBV replication.
The mutations of core promoter have been implicated in HCC
development. We had obtained HBV genes from Myanmar
HBV infectants and identified gene variations at the core promoter
region. For measuring the relative transactivation activity
on core promoter, we prepared the core-promoter reporter
construct. Both of A1762T and G1764A mutation were
consistently found in the HBV genes with hepatocellular carcinoma.
The A1762T/G1764A mutation was corresponding
to K130M/V131I of HBx protein. We prepared the core promoter-
luciferase reporter construct containing the double
A1762T/G1764A mutation and the K130M/V131I HBx protein
expression construct. The A1762T/G1764A mutation
highly was responsive to core promoter transactivation by
HBx, regardless of HBx mutation. The A1762T/G1764A mutation
newly created hepatocyte nuclear factor 1 (HNF1) responsive
element. Ectopic expression of HNF1 largely increased
the HBV core promoter containing A1762T/G1764A
mutation. In addition, hepatic rich fatty acid, palmitic acid
and oleic acid, increased K130M/V131I HBx level by core
promoter activation. These results provide biological properties
and clinical significance of specific HBV core promoter
mutants related with HCC development.
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The environment is under siege from a variety of pollution
sources. Fecal pollution is especially harmful as it disperses
pathogenic bacteria into waterways. Unraveling origins of
mixed sources of fecal bacteria is difficult and microbial
source tracking (MST) in complex environments is still a
daunting task. Despite the challenges, the need for answers
far outweighs the difficulties experienced. Advancements in
qPCR and next generation sequencing (NGS) technologies
have shifted the traditional culture-based MST approaches
towards culture independent technologies, where communitybased
MST is becoming a method of choice. Metagenomic
tools may be useful to overcome some of the limitations of
community-based MST methods as they can give deep insight
into identifying host specific fecal markers and their association
with different environments. Adoption of machine
learning (ML) algorithms, along with the metagenomic based
MST approaches, will also provide a statistically robust and
automated platform. To compliment that, ML-based approaches
provide accurate optimization of resources. With the
successful application of ML based models in disease prediction,
outbreak investigation and medicine prescription,
it would be possible that these methods would serve as a
better surrogate of traditional MST approaches in future.
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Due to accumulating protein structure information and advances
in computational methodologies, it has now become
possible to predict protein-compound interactions. In biology,
the classic strategy for drug discovery has been to manually
screen multiple compounds (small scale) to identify potential
drug compounds. Recent strategies have utilized computational
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