Extracellular vesicles (EVs), of diverse origin and content, are membranous structures secreted by a broad range of cell types. Recent advances in molecular biology have highlighted the pivotal role of EVs in mediating intercellular communication, facilitated by their ability to transport a diverse range of biomolecules, including proteins, lipids, DNA, RNA and metabolites. A striking feature of EVs is their ability to exert dual effects during viral infections, involving both proviral and antiviral effects. This review explores the dual roles of EVs, particularly in the context of pandemic viruses such as HIV-1 and SARS-CoV-2. On the one hand, EVs can enhance viral replication and exacerbate pathogenesis by transferring viral components to susceptible cells. On the other hand, they have intrinsic antiviral properties, including activation of immune responses and direct inhibition of viral infection. By exploring these contrasting functions, our review emphasizes the complexity of EV-mediated interactions in viral pathogenesis and highlights their potential as targets for therapeutic intervention. The insights obtained from investigating EVs in the context of HIV-1 and SARS-CoV-2 provide a deeper understanding of viral mechanisms and pathologies, and offer a new perspective on managing and mitigating the impact of these global health challenges.
Citations
Citations to this article as recorded by
Differential Impact of Spike Protein Mutations on SARS-CoV-2 Infectivity and Immune Evasion: Insights from Delta and Kappa Variants Tae-Hun Kim, Sojung Bae, Jinjong Myoung Journal of Microbiology and Biotechnology.2024; 34(12): 2506. CrossRef
Meiosis is a process through which diploid cells divide into haploid cells, thus promoting genetic diversity. This diversity
arises from the formation of genetic crossovers (COs) that repair DNA double-strand breaks (DSBs), through homologous
recombination (HR). Deficiencies in HR can lead to chromosomal abnormality resulting from chromosomal nondisjunction,
and genetic disorders. Therefore, investigating the mechanisms underlying effective HR is crucial for reducing genome
instability. Budding yeast serves as an ideal model for studying HR mechanisms due to its amenability to gene modifications
and the ease of inducing synchronized meiosis to yield four spores. During meiosis, at the DNA level, programmed DSBs
are repaired as COs or non-crossovers (NCOs) through structural alterations in the nascent D-loop, involving single-end
invasions (SEIs) and double-Holliday junctions (dHJs). This repair occurs using homologous templates rather than sister
templates. This protocol, using Southern blotting, allows for the analysis and monitoring of changes in DNA structures in the
recombination process. One-dimensional (1D) gel electrophoresis is employed to detect DSBs, COs, and NCOs, while twodimensional
(2D) gel electrophoresis is utilized to identify joint molecules (JMs). Therefore, physical analysis is considered
the most effective method for investigating the HR mechanism. Our protocol provides more comprehensive information than
previous reports by introducing conditions for obtaining a greater number of cells from synchronized yeast and a method
that can analyze not only meiotic/mitotic recombination but also mitotic replication.
Although bacteria have diverse membrane proteins, the function
of many of them remains unknown or uncertain even
in Escherichia coli. In this study, to investigate the function
of hypothetical membrane proteins, genome-wide analysis
of phenotypes of hypothetical membrane proteins was performed
under various envelope stresses. Several genes responsible
for adaptation to envelope stresses were identified.
Among them, deletion of YhcB, a conserved inner membrane
protein of unknown function, caused high sensitivities to various
envelope stresses and increased membrane permeability,
and caused growth defect under normal growth conditions.
Furthermore, yhcB deletion resulted in morphological
aberration, such as branched shape, and cell division defects,
such as filamentous growth and the generation of chromosome-
less cells. The analysis of antibiotic susceptibility
showed that the yhcB mutant was highly susceptible to various
anti-folate antibiotics. Notably, all phenotypes of the yhcB
mutant were completely or significantly restored by YhcB
without the transmembrane domain, indicating that the localization
of YhcB on the inner membrane is dispensable for its
function. Taken together, our results demonstrate that YhcB
is involved in cell morphology and cell division in a membrane
localization-independent manner.
Citations
Citations to this article as recorded by
Co-ordinated assembly of the multilayered cell envelope of Gram-negative bacteria Elayne M Fivenson, Laurent Dubois, Thomas G Bernhardt Current Opinion in Microbiology.2024; 79: 102479. CrossRef
Loss of YhcB results in overactive fatty acid biosynthesis Hannah M. Stanley, M. Stephen Trent, K. Heran Darwin mBio.2024;[Epub] CrossRef
A New Factor LapD Is Required for the Regulation of LpxC Amounts and Lipopolysaccharide Trafficking Alicja Wieczorek, Anna Sendobra, Akshey Maniyeri, Magdalena Sugalska, Gracjana Klein, Satish Raina International Journal of Molecular Sciences.2022; 23(17): 9706. CrossRef
Loss of YhcB results in dysregulation of coordinated peptidoglycan, LPS and phospholipid synthesis during Escherichia coli cell growth Emily C. A. Goodall, Georgia L. Isom, Jessica L. Rooke, Karthik Pullela, Christopher Icke, Zihao Yang, Gabriela Boelter, Alun Jones, Isabel Warner, Rochelle Da Costa, Bing Zhang, James Rae, Wee Boon Tan, Matthias Winkle, Antoine Delhaye, Eva Heinz, Jean-F PLOS Genetics.2021; 17(12): e1009586. CrossRef
The inner membrane protein LapB is required for adaptation to cold stress in an LpxC-independent manner Han Byeol Lee, Si Hyoung Park, Chang-Ro Lee Journal of Microbiology.2021; 59(7): 666. CrossRef
Skin Microbiome and Acne: Microbial Imbalances and Impact – Interview with Three Key Opinion Leaders Brigitte Scott EMJ Dermatology.2024; : 83. CrossRef