Abstract:As the human cost of the pandemic caused by the severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is still being witnessed worldwide, the development of broad-spectrum antiviral agents against emerging and re-emerging viruses is seen as a necessity to hamper the spread of infections.
Various targets during the viral life-cycle can be considered to inhibit viral infection, from viral attachment to viral fusion or replication. Macromolecules represent a particularly attractive class of therapeutics du… Show more
“…So, polymers func-tionalized with the guanidine moiety show a broad spectrum of antiviral activity against Equine herpes virus type 1, Rhinotracheitis infectious bovine and Equine infectious anemia virus. 171 Such polymers showed antiviral properties only when administered prior to infection, thus suggesting that the mode of action of these polymers was again inhibition of viral attachment to the host cells by itself binding to the phospholipids of the host cell membrane. 171…”
Section: Biomaterials Science Reviewmentioning
confidence: 99%
“…171 Such polymers showed antiviral properties only when administered prior to infection, thus suggesting that the mode of action of these polymers was again inhibition of viral attachment to the host cells by itself binding to the phospholipids of the host cell membrane. 171…”
Section: Antimicrobial Mechanisms Of Macroscale Biomaterialsmentioning
Overcoming the global concern of antibiotic resistance is one of the biggest challenge faced by scientists today and the key to tackle this issue of emerging infectious diseases is the...
“…So, polymers func-tionalized with the guanidine moiety show a broad spectrum of antiviral activity against Equine herpes virus type 1, Rhinotracheitis infectious bovine and Equine infectious anemia virus. 171 Such polymers showed antiviral properties only when administered prior to infection, thus suggesting that the mode of action of these polymers was again inhibition of viral attachment to the host cells by itself binding to the phospholipids of the host cell membrane. 171…”
Section: Biomaterials Science Reviewmentioning
confidence: 99%
“…171 Such polymers showed antiviral properties only when administered prior to infection, thus suggesting that the mode of action of these polymers was again inhibition of viral attachment to the host cells by itself binding to the phospholipids of the host cell membrane. 171…”
Section: Antimicrobial Mechanisms Of Macroscale Biomaterialsmentioning
Overcoming the global concern of antibiotic resistance is one of the biggest challenge faced by scientists today and the key to tackle this issue of emerging infectious diseases is the...
“…While here the focus is exclusively on sGAG mimetic polymeric compounds, there are also other classes of polymers with antiviral activity, and we direct the readers to recent reviews on the topic. 156 , 157 …”
Section: Hs Mimetics As Viral Inhibitorsmentioning
Heparin (HP) and heparan sulfate (HS) are linear, anionically
charged
polysaccharides well-known for their diverse biological activities.
While HP is generally localized in mast cells and in connective tissues,
HS is part of the glycocalyx and involved in the attachment of viruses
to host cells, constituting the first step of an infection. HP and
HS also exhibit antiviral activity by blocking viral receptors, thereby
inhibiting viruses from engaging with host cells. Inspired by their
structural features, such as their high molecular weight and polyanionic
character, various synthetic polymers mimicking HP/HS have been developed
and used as model systems to study bioactivity, as well as for therapeutic
applications. This Perspective provides an overview of the roles of
HP/HS in viral engagement, and examines historical and recent approaches
toward oligo-/polysaccharide, glycopolymer, and anionic polymer HP/HS
mimetics. An overview of current applications and future prospects
of these molecules is provided, demonstrating their potential in addressing
current and future epidemics and pandemics.
“…Because of its broad-spectrum mechanism and huge potential sequence diversity, peptides that inhibit viral entry may potentially meet the demand for new antiviral therapy; however, to optimize or evolve sequence design to combat a wide range of viral diseases, their mechanisms need to be better understood ( 28 ). Notably, the low yields and difficulties in the extraction and purification of AMPs have hindered their industry and scientific research applications.…”
The rapid evolution of highly infectious pathogens is a major threat to global public health. In the front line of defense against bacteria, fungi, and viruses, antimicrobial peptides (AMPs) are naturally produced by all living organisms and offer new possibilities for next-generation antibiotic development. However, the low yields and difficulties in the extraction and purification of AMPs have hindered their industry and scientific research applications. To overcome these barriers, we enabled high expression of bomidin, a commercial recombinant AMP based upon bovine myeloid antimicrobial peptide-27. This novel AMP, which can be expressed in Escherichia coli by adding methionine to the bomidin sequence, can be produced in bulk and is more biologically active than chemically synthesized AMPs. We verified the function of bomidin against a variety of bacteria and enveloped viruses, including severe acute respiratory syndrome coronavirus-2 (SARS-CoV-2), herpes simplex virus (HSV), dengue virus (DENV), and chikungunya virus (CHIKV). Furthermore, based on the molecular modeling of bomidin and membrane lipids, we elucidated the possible mechanism by which bomidin disrupts bacterial and viral membranes. Thus, we obtained a novel AMP with an optimized, efficient heterologous expression system for potential therapeutic application against a wide range of life-threatening pathogens.
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