Please use this identifier to cite or link to this item: http://223.31.159.10:8080/jspui/handle/123456789/1220
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dc.contributor.authorCosta, José Hélio-
dc.contributor.authorMohanapriya, Gunasekaran-
dc.contributor.authorBharadwaj, Revuru-
dc.contributor.authorNoceda, Carlos-
dc.contributor.authorThiers, Karine Leitão Lima-
dc.contributor.authorAziz, Shahid-
dc.contributor.authorSrivastava, Shivani-
dc.contributor.authorOliveira, Manuela-
dc.contributor.authorGupta, Kapuganti Jagadis-
dc.contributor.authorKumari, Aprajita-
dc.contributor.authorSircar, Debabrata-
dc.contributor.authorKumar, Sarma Rajeev-
dc.contributor.authorAchra, Arvind-
dc.contributor.authorSathishkumar, Ramalingam-
dc.contributor.authorAdholeya, Alok-
dc.contributor.authorArnholdt-Schmitt, Birgit-
dc.date.accessioned2021-07-28T09:01:22Z-
dc.date.available2021-07-28T09:01:22Z-
dc.date.issued2021-
dc.identifier.citationFrontiers in Immunology, 12: 673692en_US
dc.identifier.issn1664-3224-
dc.identifier.otherhttps://doi.org/10.3389/fimmu.2021.673692-
dc.identifier.urihttps://www.frontiersin.org/articles/10.3389/fimmu.2021.673692/full-
dc.identifier.urihttp://223.31.159.10:8080/jspui/handle/123456789/1220-
dc.descriptionAccepted date: 17 June 2021en_US
dc.description.abstractIn a perspective entitled 'From plant survival under severe stress to anti-viral human defense' we raised and justified the hypothesis that transcript level profiles of justified target genes established from in vitro somatic embryogenesis (SE) induction in plants as a reference compared to virus-induced profiles can identify differential virus signatures that link to harmful reprogramming. A standard profile of selected genes named 'ReprogVirus' was proposed for in vitro-scanning of early virus-induced reprogramming in critical primary infected cells/tissues as target trait. For data collection, the 'ReprogVirus platform' was initiated. This initiative aims to identify in a common effort across scientific boundaries critical virus footprints from diverse virus origins and variants as a basis for anti-viral strategy design. This approach is open for validation and extension. In the present study, we initiated validation by experimental transcriptome data available in public domain combined with advancing plant wet lab research. We compared plant-adapted transcriptomes according to 'RegroVirus' complemented by alternative oxidase (AOX) genes during de novo programming under SE-inducing conditions with in vitro corona virus-induced transcriptome profiles. This approach enabled identifying a major complex trait for early de novo programming during SARS-CoV-2 infection, called 'CoV-MAC-TED'. It consists of unbalanced ROS/RNS levels, which are connected to increased aerobic fermentation that links to alpha-tubulin-based cell restructuration and progression of cell cycle. We conclude that anti-viral/anti-SARS-CoV-2 strategies need to rigorously target 'CoV-MAC-TED' in primary infected nose and mouth cells through prophylactic and very early therapeutic strategies. We also discuss potential strategies in the view of the beneficial role of AOX for resilient behavior in plants. Furthermore, following the general observation that ROS/RNS equilibration/redox homeostasis is of utmost importance at the very beginning of viral infection, we highlight that 'de-stressing' disease and social handling should be seen as essential part of anti-viral/anti-SARS-CoV-2 strategies.en_US
dc.description.sponsorshipJC is grateful to CNPq for the Researcher fellowship (CNPq grant 309795/2017-6). GM is grateful to UGC, India, for doctoral grant from BSR fellowship. GM, RS, and BA-S acknowledge support for academic cooperation and researcher’s mobility by the IndiaPortugal Bilateral Cooperation Program (2013-2015), funded by “Fundação para a Ciência e Tecnologia” (FCT), Portugal, and the Department of Science and Technology (DST), India. BR and SS acknowledge the infrastructure and stay support provided by DBT-TDNBC-DEAKIN – Research Network Across continents for learning and innovation (DTD-RNA) for AMF related work at The Energy and Resources Institute, TERI, India. CN acknowledges the international scientific network BIOALICYTED, which contributed to establish FunCROP contacts. KT is grateful to CNPq for the Doctoral fellowship. SA is grateful to CAPES for the Doctoral fellowship. KG, MO, and BA-S acknowledge support by the India-Portugal Bilateral Cooperation Program ‘DST/INT/Portugal/P-03/2017’. MO Research is partially supported by National Funds through. FCT. Fundação para a Ciencia e a Tecnologia, projects UIDB/04674/2020 (CIMA). BA-S ̂ wants to thank Dr. Natascha Sommer for helpful discussions and comments on the manuscript during its development on the background of her experience as medical doctor in the group of Prof. Dr. Norbert Weissmann, Chair for ‘Molecular Mechanisms of Emphysema, Hypoxia and Lung Aging’ at the Universities of Giessen and Marburg Lung Center (UGMLC), Germany, and as investigator involved in mitochondrial redox biology also by help of transgenic AOX-mice. BAS acknowledges the strong engagement and clear view of Dr. Kim Berit Lewerenz-Kemper transmitted in support of our approach and final wider conclusions that is based not only on her overall life experience and view but also on her coronavirus-dominated experience as medical doctor in emergency service at the hospital ‘Universitätsklinikum Eppendorf’ in Hamburg, Germany. Furthermore, we want to appreciate encouragement and comments on the manuscript by Dr. Elisete Santos Macedo, Prof. Dr. Ashwani Kumar (emeritus at the University of Jaipur, India) and Dr. Nidhi Gupta, all are engaged plant scientists, educators, book writers and members of the FunCROP net and accompanied developing this approach from beginning. Finally, the authors thank Sebastian Schaffer, Nutritional Scientist with special knowledge in anti-oxidant food ingredients and their relevance in aging and as neuroprotective agents, who currently founded ACADELION Scientific and Medical Communications, for his carefully reading and helpful editing of the manuscript.en_US
dc.language.isoen_USen_US
dc.publisherFrontiers Media S.A.en_US
dc.subjectSARS-CoV-2en_US
dc.subjectalternative oxidaseen_US
dc.subjectmTORen_US
dc.subjectmelatoninen_US
dc.subjectredox biologyen_US
dc.subjectrepurposing drugsen_US
dc.subjecttubulinen_US
dc.titleROS/RNS Balancing, Aerobic Fermentation Regulation and Cell Cycle Control - a Complex Early Trait ('CoV-MAC-TED') for Combating SARS-CoV-2-Induced Cell Reprogrammingen_US
dc.typeArticleen_US
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