key: cord-323749-lvtfv7ny authors: Sai Suresh Chalichem, Nehru; Bethapudi, Bharathi; Mundkinajeddu, Deepak title: Aminoglycosides can be a better choice over Macrolides in COVID-19 regimen: Plausible Mechanism for repurposing strategy date: 2020-06-10 journal: Med Hypotheses DOI: 10.1016/j.mehy.2020.109984 sha: doc_id: 323749 cord_uid: lvtfv7ny In the current COVID-19 pandemic, prioritizing the immunity enhancers is equally important to anti-virals. Defensins are the forgotten molecules that enhance the innate immunity against various microbes. Although macrolides like azithromycin and clarithromycin etc., have been reported to act against respiratory infections but they lack the ability of immunity enhancement through defensins. The aminoglycosides were proved to have defensin mediated antiviral activity, that could enhance the immunity. So, Consideration of aminoglycosides can be a double edge sword viz., against respiratory infection as well as Immunity enhancer (along with anti-virals) for COVID-19 regimen. Although various nations throughout the globe making several strategies viz, different drug combinations, proposing lock downs and herd immunity etc., to control the wide spread of COVID-19 and to tolerate its severity, the radical behaviour of virus is evident. Understanding the virus behaviour, its complete genome, identifying suitable therapeutic targets, cost and ethical issues are the bars to come with new molecule, in the current (pandemic) situation. So, Ddrug repurposing strategy i.e., application of widely and existing approved drugs for different focus, could be an ideal approach in the current pandemic situation. The current situation enlightened many people about importance of immune health which boosted up the usage of various traditional things like Aashwagandha, Eechinacea, Llicorice and aAndrographis etc., as immune supplements, out of which Aandrographolides of Aandrographis were proved as immune builders through defensins and inhibitor of virus Immunity in the respiratory organs is one of the important aspects to consider as they are under continuous challenges with different particulates through inhalation and other contacts with nasal or oral surfaces. In the instances like current pandemic of COVID-19, where infection control becomes a great challenge, immune mediators could be a vital link. So, strengthening respiratory epithelium is also an important aspect to control lung infection 4, 5 . Defensins are part of innate immunity and it is the only group of antimicrobial peptides present in both animals (vertebrates and invertebrates) and plants 6, 7 . They present in cytoplasmic granules of immune cells like neutrophils and macrophages along with other antimicrobial factors and if from epithelial cells, released into extracellular environment 8 . Defensins (mammalian) are classified as, the alpha, beta and theta defensins, which differ in their distribution and disulphide links (bonds) between conserved cysteine residues. Based on their disulfide bonding pattern, divided into alpha, beta and theta defensins. The theta defensins exist as pseudo genes (cannot express) due to the presence of premature termination codon 9 . However, aminoglycosides (AGs) were proved to produce functional peptides from theta defensins (called as retrocyclins) that are active against HIV 10 . So, herewith we hypothesize addition of AGs into the therapeutic regimen of COVID-19, could be a beneficial one. Macrolides like clarithromycin and azithromycin etc., are well known for H. Influenza as well as upper and lower respiratory infections. And moreover, certain clinical studies supported the usage of macrolides during panbronchiolitis and cystic fibrosis 11 and also due to their possible anti-inflammatory nature 12 . These might be the reasons for the inclusion Aazithromycin in combination with hHydroxy cChloroquine. But we come with novel idea of inclusion of Aaminoglycosides rather than Mmacrolides with other combinations. As mentioned below, defensins, the natural immune enhancers, could play a role in enhancing the immunity. Although widespread proved research is lacking to claim the ability of Aminoglycosides (AGs) in enhancing the defensins, it has been proved against HIV, which is also a deadly virus. As AGs were proved against deadly immune suppressing virus 10 and moreover AGs are currently in use, they can be used for current situation without any regulatory or ethical restrictions. Direct Iinstillation of retrocyclins into mouse lung was proved to reduce the mortality from SARS corona virus infection. And moreover, various studies claimed the protective role of defensins against influenza viruses 13-16 .  They promote the viral aggregation which could reduce infectious titers and finally will be cleared from airway 17 .  Defensins can block viral infection by directly acting on the virion or by affecting the target cell and thereby indirectly interfering with viral infection. So, that fusion of virion to target membrane is blocked results in the impairment of replication process 18, 19 . Drug repurposing strategy is an ideal and rationale strategy to bring the therapeutic product in to market in quick times. Although AGs were proved only for their enhancing/modulating capability towards Ttheta defensins (against HIV), their role in enhancing other defensins cannot be eliminated. Since the safety profile of AGs is already established, selection of these drugs for COVID-19 therapeutic regimen could be an ideal choice. None to declare Andrographolide prevents EV-D68 replication by inhibiting the acidification of virus-containing endocytic vesicles Dehydroandrographolide enhances innate immunity of intestinal tract through up-regulation the expression of hBD-2 Defensins and cathelicidins in lung immunity Airway epithelial versus immune cell Stat1 function for innate defense against respiratory viral infection Plant defensins Human defensins Defensins: natural component of human innate immunity The chemistry and biology of theta defensins Humanized θ-defensins (retrocyclins) enhance Hapivirins and diprovirins: novel θ-defensin analogs with potent activity against influenza A virus βdefensin inhibits influenza virus replication by cell-mediated mechanism (s) Human neutrophil defensins increase neutrophil uptake of influenza A virus and bacteria and modify virus-induced respiratory burst responses Selsted ME. θ-Defensins: cyclic peptides with endless potential Defensins in innate antiviral immunity