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The global spread of 2019-nCoV: a molecular evolutionary analysis

Identifieur interne : 000029 ( Pmc/Checkpoint ); précédent : 000028; suivant : 000030

The global spread of 2019-nCoV: a molecular evolutionary analysis

Auteurs : Domenico Benvenuto [Italie] ; Marta Giovanetti [Brésil] ; Marco Salemi [États-Unis] ; Mattia Prosperi [États-Unis] ; Cecilia De Flora [Italie] ; Luiz Carlos Junior Alcantara [Brésil] ; Silvia Angeletti [Italie] ; Massimo Ciccozzi [Brésil]

Source :

RBID : PMC:7099638

Abstract

ABSTRACT

The global spread of the 2019-nCoV is continuing and is fast moving, as indicated by the WHO raising the risk assessment to high. In this article, we provide a preliminary phylodynamic and phylogeographic analysis of this new virus. A Maximum Clade Credibility tree has been built using the 29 available whole genome sequences of 2019-nCoV and two whole genome sequences that are highly similar sequences from Bat SARS-like Coronavirus available in GeneBank. We are able to clarify the mechanism of transmission among the countries which have provided the 2019-nCoV sequence isolates from their patients. The Bayesian phylogeographic reconstruction shows that the 2019–2020 nCoV most probably originated from the Bat SARS-like Coronavirus circulating in the Rhinolophus bat family. In agreement with epidemiological observations, the most likely geographic origin of the new outbreak was the city of Wuhan, China, where 2019-nCoV time of the most recent common ancestor emerged, according to molecular clock analysis, around November 25th, 2019. These results, together with previously recorded epidemics, suggest a recurring pattern of periodical epizootic outbreaks due to Betacoronavirus. Moreover, our study describes the same population genetic dynamic underlying the SARS 2003 epidemic, and suggests the urgent need for the development of effective molecular surveillance strategies of Betacoronavirus among animals and Rhinolophus of the bat family.


Url:
DOI: 10.1080/20477724.2020.1725339
PubMed: 32048560
PubMed Central: 7099638


Affiliations:


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PMC:7099638

Le document en format XML

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<p>The global spread of the 2019-nCoV is continuing and is fast moving, as indicated by the WHO raising the risk assessment to high. In this article, we provide a preliminary phylodynamic and phylogeographic analysis of this new virus. A Maximum Clade Credibility tree has been built using the 29 available whole genome sequences of 2019-nCoV and two whole genome sequences that are highly similar sequences from Bat SARS-like Coronavirus available in GeneBank. We are able to clarify the mechanism of transmission among the countries which have provided the 2019-nCoV sequence isolates from their patients. The Bayesian phylogeographic reconstruction shows that the 2019–2020 nCoV most probably originated from the Bat SARS-like Coronavirus circulating in the
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bat family. In agreement with epidemiological observations, the most likely geographic origin of the new outbreak was the city of Wuhan, China, where 2019-nCoV time of the most recent common ancestor emerged, according to molecular clock analysis, around November 25
<sup>th</sup>
, 2019. These results, together with previously recorded epidemics, suggest a recurring pattern of periodical epizootic outbreaks due to
<italic>Betacoronavirus</italic>
. Moreover, our study describes the same population genetic dynamic underlying the SARS 2003 epidemic, and suggests the urgent need for the development of effective molecular surveillance strategies of
<italic>Betacoronavirus</italic>
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<italic>Rhinolophus</italic>
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<sup>a</sup>
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<contrib contrib-type="author">
<name>
<surname>De Flora</surname>
<given-names>Cecilia</given-names>
</name>
<xref ref-type="aff" rid="AFF0001">
<sup>a</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Junior Alcantara</surname>
<given-names>Luiz Carlos</given-names>
</name>
<xref ref-type="aff" rid="AFF0002">
<sup>b</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Angeletti</surname>
<given-names>Silvia</given-names>
</name>
<xref ref-type="corresp" rid="AN0001"></xref>
<xref ref-type="aff" rid="AFF0005">
<sup>e</sup>
</xref>
<xref ref-type="author-notes" rid="FT0001">
<sup>*</sup>
</xref>
</contrib>
<contrib contrib-type="author">
<name>
<surname>Ciccozzi</surname>
<given-names>Massimo</given-names>
</name>
<xref ref-type="aff" rid="AFF0002">
<sup>b</sup>
</xref>
<xref ref-type="author-notes" rid="FT0001">
<sup>*</sup>
</xref>
</contrib>
<aff id="AFF0001">
<label>a</label>
<institution>Unit of Medical Statistics and Molecular Epidemiology, University Campus Bio-Medico of Rome</institution>
,
<country>Italy</country>
</aff>
<aff id="AFF0002">
<label>b</label>
<institution>Laboratório de Flavivírus, Instituto Oswaldo Cruz, Fundação Oswaldo Cruz</institution>
, Rio de Janeiro,
<country>Brazil</country>
</aff>
<aff id="AFF0003">
<label>c</label>
<institution>Department of Epidemiology, University of Florida</institution>
, Gainesville, FL,
<country>USA</country>
</aff>
<aff id="AFF0004">
<label>d</label>
<institution>Emerging Pathogens Institute, University of Florida</institution>
, Gainesville, FL,
<country>USA</country>
</aff>
<aff id="AFF0005">
<label>e</label>
<institution>Unit of Clinical Laboratory Science, University Campus Bio-Medico of Rome</institution>
,
<country>Italy</country>
</aff>
</contrib-group>
<author-notes>
<corresp id="AN0001">CONTACT Silvia Angeletti
<email xlink:href="s.angeletti@unicampus.it">s.angeletti@unicampus.it</email>
<institution>Unit of Clinical Laboratory Science, University Campus Bio-Medico of Rome</institution>
,
<country>Italy</country>
</corresp>
<fn id="FT0001">
<label>*</label>
<p>These authors contributed equally to this article</p>
</fn>
</author-notes>
<pub-date pub-type="collection">
<year>2020</year>
</pub-date>
<pub-date pub-type="epub">
<day>12</day>
<month>2</month>
<year>2020</year>
</pub-date>
<volume>0</volume>
<issue>0</issue>
<fpage seq="1">1</fpage>
<lpage>4</lpage>
<permissions>
<copyright-statement>© 2020 Informa UK Limited, trading as Taylor & Francis Group</copyright-statement>
<copyright-year>2020</copyright-year>
<copyright-holder>Informa UK Limited, trading as Taylor & Francis Group</copyright-holder>
<license>
<license-p>This article is made available via the PMC Open Access Subset for unrestricted re-use and analyses in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the COVID-19 pandemic or until permissions are revoked in writing. Upon expiration of these permissions, PMC is granted a perpetual license to make this article available via PMC and Europe PMC, consistent with existing copyright protections.</license-p>
</license>
</permissions>
<self-uri content-type="pdf" xlink:href="YPGH_0_1725339.pdf"></self-uri>
<abstract>
<title>ABSTRACT</title>
<p>The global spread of the 2019-nCoV is continuing and is fast moving, as indicated by the WHO raising the risk assessment to high. In this article, we provide a preliminary phylodynamic and phylogeographic analysis of this new virus. A Maximum Clade Credibility tree has been built using the 29 available whole genome sequences of 2019-nCoV and two whole genome sequences that are highly similar sequences from Bat SARS-like Coronavirus available in GeneBank. We are able to clarify the mechanism of transmission among the countries which have provided the 2019-nCoV sequence isolates from their patients. The Bayesian phylogeographic reconstruction shows that the 2019–2020 nCoV most probably originated from the Bat SARS-like Coronavirus circulating in the
<italic>Rhinolophus</italic>
bat family. In agreement with epidemiological observations, the most likely geographic origin of the new outbreak was the city of Wuhan, China, where 2019-nCoV time of the most recent common ancestor emerged, according to molecular clock analysis, around November 25
<sup>th</sup>
, 2019. These results, together with previously recorded epidemics, suggest a recurring pattern of periodical epizootic outbreaks due to
<italic>Betacoronavirus</italic>
. Moreover, our study describes the same population genetic dynamic underlying the SARS 2003 epidemic, and suggests the urgent need for the development of effective molecular surveillance strategies of
<italic>Betacoronavirus</italic>
among animals and
<italic>Rhinolophus</italic>
of the bat family.</p>
</abstract>
<kwd-group kwd-group-type="author">
<title>KEYWORDS</title>
<kwd>2019-nCoV</kwd>
<kwd>molecular Epidemiology</kwd>
<kwd>phylogeny</kwd>
<kwd>SARS</kwd>
</kwd-group>
<counts>
<fig-count count="1"></fig-count>
<ref-count count="16"></ref-count>
<page-count count="4"></page-count>
</counts>
</article-meta>
</front>
</pmc>
<affiliations>
<list>
<country>
<li>Brésil</li>
<li>Italie</li>
<li>États-Unis</li>
</country>
</list>
<tree>
<country name="Italie">
<noRegion>
<name sortKey="Benvenuto, Domenico" sort="Benvenuto, Domenico" uniqKey="Benvenuto D" first="Domenico" last="Benvenuto">Domenico Benvenuto</name>
</noRegion>
<name sortKey="Angeletti, Silvia" sort="Angeletti, Silvia" uniqKey="Angeletti S" first="Silvia" last="Angeletti">Silvia Angeletti</name>
<name sortKey="De Flora, Cecilia" sort="De Flora, Cecilia" uniqKey="De Flora C" first="Cecilia" last="De Flora">Cecilia De Flora</name>
</country>
<country name="Brésil">
<noRegion>
<name sortKey="Giovanetti, Marta" sort="Giovanetti, Marta" uniqKey="Giovanetti M" first="Marta" last="Giovanetti">Marta Giovanetti</name>
</noRegion>
<name sortKey="Ciccozzi, Massimo" sort="Ciccozzi, Massimo" uniqKey="Ciccozzi M" first="Massimo" last="Ciccozzi">Massimo Ciccozzi</name>
<name sortKey="Junior Alcantara, Luiz Carlos" sort="Junior Alcantara, Luiz Carlos" uniqKey="Junior Alcantara L" first="Luiz Carlos" last="Junior Alcantara">Luiz Carlos Junior Alcantara</name>
</country>
<country name="États-Unis">
<noRegion>
<name sortKey="Salemi, Marco" sort="Salemi, Marco" uniqKey="Salemi M" first="Marco" last="Salemi">Marco Salemi</name>
</noRegion>
<name sortKey="Prosperi, Mattia" sort="Prosperi, Mattia" uniqKey="Prosperi M" first="Mattia" last="Prosperi">Mattia Prosperi</name>
<name sortKey="Prosperi, Mattia" sort="Prosperi, Mattia" uniqKey="Prosperi M" first="Mattia" last="Prosperi">Mattia Prosperi</name>
<name sortKey="Salemi, Marco" sort="Salemi, Marco" uniqKey="Salemi M" first="Marco" last="Salemi">Marco Salemi</name>
</country>
</tree>
</affiliations>
</record>

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