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      Evolutionary dynamics of SARS-CoV-2 circulating in Yogyakarta and Central Java, Indonesia: sequence analysis covering furin cleavage site (FCS) region of the spike protein

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          Abstract

          Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is a new virus responsible for the COVID-19 pandemic. The emergence of the new SARS-CoV-2 has been attributed to the possibility of evolutionary dynamics in the furin cleavage site (FCS) region. This study aimed to analyze the sequence of the FCS region in the spike protein of SARS-CoV-2 isolates that circulated in the Special Region of Yogyakarta and Central Java provinces in Indonesia. The RNA solution extracted from nasopharyngeal swab samples of confirmed COVID-19 patients were used and subjected to cDNA synthesis, PCR amplification, sequencing, and analysis of the FCS region. The sequence data from GISAID were also retrieved for further genome analysis. This study included 52 FCS region sequences. Several mutations were identified in the FCS region, i.e., D614G, Q675H, Q677H, S680P, and silent mutation in 235.57 C > T. The most important mutation in the FCS region is D614G. This finding indicated the G614 variant was circulating from May 2020 in those two provinces. Eventually, the G614 variant totally replaced the D614 variant from September 2020. All Indonesian SARS-CoV-2 isolates during this study and those deposited in GISAID showed the formation of five clade clusters from the FCS region, in which the D614 variant is in one specific cluster, and the G614 variant is dispersed into four clusters. The data indicated there is evolutionary advantage of the D614G mutation in the FCS region of the spike protein of SARS-CoV-2 circulating in the Special Region of Yogyakarta and Central Java provinces in Indonesia.

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          MAFFT Multiple Sequence Alignment Software Version 7: Improvements in Performance and Usability

          We report a major update of the MAFFT multiple sequence alignment program. This version has several new features, including options for adding unaligned sequences into an existing alignment, adjustment of direction in nucleotide alignment, constrained alignment and parallel processing, which were implemented after the previous major update. This report shows actual examples to explain how these features work, alone and in combination. Some examples incorrectly aligned by MAFFT are also shown to clarify its limitations. We discuss how to avoid misalignments, and our ongoing efforts to overcome such limitations.
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            MEGA X: Molecular Evolutionary Genetics Analysis across Computing Platforms.

            The Molecular Evolutionary Genetics Analysis (Mega) software implements many analytical methods and tools for phylogenomics and phylomedicine. Here, we report a transformation of Mega to enable cross-platform use on Microsoft Windows and Linux operating systems. Mega X does not require virtualization or emulation software and provides a uniform user experience across platforms. Mega X has additionally been upgraded to use multiple computing cores for many molecular evolutionary analyses. Mega X is available in two interfaces (graphical and command line) and can be downloaded from www.megasoftware.net free of charge.
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              Is Open Access

              The species Severe acute respiratory syndrome-related coronavirus : classifying 2019-nCoV and naming it SARS-CoV-2

              The present outbreak of a coronavirus-associated acute respiratory disease called coronavirus disease 19 (COVID-19) is the third documented spillover of an animal coronavirus to humans in only two decades that has resulted in a major epidemic. The Coronaviridae Study Group (CSG) of the International Committee on Taxonomy of Viruses, which is responsible for developing the classification of viruses and taxon nomenclature of the family Coronaviridae, has assessed the placement of the human pathogen, tentatively named 2019-nCoV, within the Coronaviridae. Based on phylogeny, taxonomy and established practice, the CSG recognizes this virus as forming a sister clade to the prototype human and bat severe acute respiratory syndrome coronaviruses (SARS-CoVs) of the species Severe acute respiratory syndrome-related coronavirus, and designates it as SARS-CoV-2. In order to facilitate communication, the CSG proposes to use the following naming convention for individual isolates: SARS-CoV-2/host/location/isolate/date. While the full spectrum of clinical manifestations associated with SARS-CoV-2 infections in humans remains to be determined, the independent zoonotic transmission of SARS-CoV and SARS-CoV-2 highlights the need for studying viruses at the species level to complement research focused on individual pathogenic viruses of immediate significance. This will improve our understanding of virus–host interactions in an ever-changing environment and enhance our preparedness for future outbreaks.
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                Author and article information

                Contributors
                twibawa@ugm.ac.id
                Journal
                Int Microbiol
                Int Microbiol
                International Microbiology
                Springer International Publishing (Cham )
                1139-6709
                1618-1905
                14 February 2022
                : 1-10
                Affiliations
                [1 ]GRID grid.8570.a, ISNI 0000 0001 2152 4506, Animal Physiology Laboratory, Faculty of Biology, , Universitas Gadjah Mada, ; Yogyakarta, Indonesia
                [2 ]GRID grid.8570.a, ISNI 0000 0001 2152 4506, Master Program in Biotechnology, Postgraduate School, , Universitas Gadjah Mada, ; Yogyakarta, Indonesia
                [3 ]GRID grid.8570.a, ISNI 0000 0001 2152 4506, World Mosquito Program Yogyakarta, Centre for Tropical Medicine, Faculty of Medicine, Public Health and Nursing, , Universitas Gadjah Mada, ; Yogyakarta, Indonesia
                [4 ]GRID grid.8570.a, ISNI 0000 0001 2152 4506, Department of Microbiology, Faculty of Medicine, , Public Health and Nursing, Universitas Gadjah Mada, ; Jl. Farmako, Sekip Utara, Yogyakarta, 55281 Indonesia
                [5 ]GRID grid.8570.a, ISNI 0000 0001 2152 4506, Department of Child Health, Faculty of Medicine, Public Health and Nursing, , Universitas Gadjah Mada, ; Yogyakarta, Indonesia
                [6 ]GRID grid.8570.a, ISNI 0000 0001 2152 4506, Biotechnology Laboratory, Faculty of Biology, , Universitas Gadjah Mada, ; Yogyakarta, Indonesia
                [7 ]GRID grid.8570.a, ISNI 0000 0001 2152 4506, Graduate Program in Biology, Faculty of Biology, , Universitas Gadjah Mada, ; Yogyakarta, Indonesia
                [8 ]GRID grid.8570.a, ISNI 0000 0001 2152 4506, Department of Histology and Cell Biology, Faculty of Medicine, , Public Health and Nursing, Universitas Gadjah Mada, ; Yogyakarta, Indonesia
                Author information
                http://orcid.org/0000-0003-0477-4575
                Article
                239
                10.1007/s10123-022-00239-8
                8853438
                35165816
                ddb62ff6-1c60-4a0d-885d-135372b5ea4b
                © The Author(s), under exclusive licence to Springer Nature Switzerland AG 2022

                This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic.

                History
                : 3 November 2021
                : 21 January 2022
                : 3 February 2022
                Funding
                Funded by: FundRef http://dx.doi.org/10.13039/501100012521, Universitas Gadjah Mada;
                Award ID: -
                Award Recipient :
                Categories
                Original Article

                sars-cov-2,spike protein,d614g mutation,furin cleavage site

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