Virological Characterization of the First 2 COVID-19 Patients Diagnosed in Italy: Phylogenetic Analysis, Virus Shedding Profile From Different Body Sites, and Antibody Response Kinetics
Abstract BackgroundThe pathogenesis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection remains unclear. We report the detection of viral RNA from different anatomical districts and the antibody profile in the first 2 COVID-19 cases diagnosed in Italy. MethodsWe tested for SARS...
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creator | Colavita, Francesca Lapa, Daniele Carletti, Fabrizio Lalle, Eleonora Messina, Francesco Rueca, Martina Matusali, Giulia Meschi, Silvia Bordi, Licia Marsella, Patrizia Nicastri, Emanuele Marchioni, Luisa Mariano, Andrea Scorzolini, Laura Ascoli Bartoli, Tommaso Di Caro, Antonino Ippolito, Giuseppe Capobianchi, Maria Rosaria Castilletti, Concetta |
description | Abstract
BackgroundThe pathogenesis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection remains unclear. We report the detection of viral RNA from different anatomical districts and the antibody profile in the first 2 COVID-19 cases diagnosed in Italy.
MethodsWe tested for SARS-CoV-2 RNA clinical samples, either respiratory and nonrespiratory (ie, saliva, serum, urine, vomit, rectal, ocular, cutaneous, and cervico-vaginal swabs), longitudinally collected from both patients throughout the hospitalization. Serological analysis was carried out on serial serum samples to evaluate IgM, IgA, IgG, and neutralizing antibody levels.
ResultsSARS-CoV-2 RNA was detected since the early phase of illness, lasting over 2 weeks in both upper and lower respiratory tract samples. Virus isolate was obtained from acute respiratory samples, while no infectious virus was rescued from late respiratory samples with low viral RNA load, collected when serum antibodies had been developed. Several other specimens came back positive, including saliva, vomit, rectal, cutaneous, cervico-vaginal, and ocular swabs. IgM, IgA, and IgG were detected within the first week of diagnosis, with IgG appearing earlier and at higher titers. Neutralizing antibodies developed during the second week, reaching high titers 32 days after diagnosis.
ConclusionsOur longitudinal analysis showed that SARS-CoV-2 RNA can be detected in different body samples, which may be associated with broad tropism and different spectra of clinical manifestations and modes of transmission. Profiling antibody response and neutralizing activity can assist in laboratory diagnosis and surveillance actions. |
doi_str_mv | 10.1093/ofid/ofaa403 |
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BackgroundThe pathogenesis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection remains unclear. We report the detection of viral RNA from different anatomical districts and the antibody profile in the first 2 COVID-19 cases diagnosed in Italy.
MethodsWe tested for SARS-CoV-2 RNA clinical samples, either respiratory and nonrespiratory (ie, saliva, serum, urine, vomit, rectal, ocular, cutaneous, and cervico-vaginal swabs), longitudinally collected from both patients throughout the hospitalization. Serological analysis was carried out on serial serum samples to evaluate IgM, IgA, IgG, and neutralizing antibody levels.
ResultsSARS-CoV-2 RNA was detected since the early phase of illness, lasting over 2 weeks in both upper and lower respiratory tract samples. Virus isolate was obtained from acute respiratory samples, while no infectious virus was rescued from late respiratory samples with low viral RNA load, collected when serum antibodies had been developed. Several other specimens came back positive, including saliva, vomit, rectal, cutaneous, cervico-vaginal, and ocular swabs. IgM, IgA, and IgG were detected within the first week of diagnosis, with IgG appearing earlier and at higher titers. Neutralizing antibodies developed during the second week, reaching high titers 32 days after diagnosis.
ConclusionsOur longitudinal analysis showed that SARS-CoV-2 RNA can be detected in different body samples, which may be associated with broad tropism and different spectra of clinical manifestations and modes of transmission. Profiling antibody response and neutralizing activity can assist in laboratory diagnosis and surveillance actions.</description><identifier>ISSN: 2328-8957</identifier><identifier>EISSN: 2328-8957</identifier><identifier>DOI: 10.1093/ofid/ofaa403</identifier><identifier>PMID: 33527081</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Analysis ; Coronaviruses ; Development and progression ; Diagnosis ; Immunoglobulin A ; Immunoglobulin G ; Major ; Phylogeny ; RNA ; Severe acute respiratory syndrome</subject><ispartof>Open Forum Infectious Diseases, 2020-10, Vol.7 (10), p.ofaa403-ofaa403</ispartof><rights>The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America. 2020</rights><rights>The Author(s) 2020. Published by Oxford University Press on behalf of Infectious Diseases Society of America.</rights><rights>COPYRIGHT 2020 Oxford University Press</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c413t-6dfc6a13c372169b955bfb12afffbfb435b545634a2bfa217bd497e7a2db87d53</citedby><cites>FETCH-LOGICAL-c413t-6dfc6a13c372169b955bfb12afffbfb435b545634a2bfa217bd497e7a2db87d53</cites><orcidid>0000-0001-6027-3009</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499768/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC7499768/$$EHTML$$P50$$Gpubmedcentral$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,860,881,1598,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/33527081$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Colavita, Francesca</creatorcontrib><creatorcontrib>Lapa, Daniele</creatorcontrib><creatorcontrib>Carletti, Fabrizio</creatorcontrib><creatorcontrib>Lalle, Eleonora</creatorcontrib><creatorcontrib>Messina, Francesco</creatorcontrib><creatorcontrib>Rueca, Martina</creatorcontrib><creatorcontrib>Matusali, Giulia</creatorcontrib><creatorcontrib>Meschi, Silvia</creatorcontrib><creatorcontrib>Bordi, Licia</creatorcontrib><creatorcontrib>Marsella, Patrizia</creatorcontrib><creatorcontrib>Nicastri, Emanuele</creatorcontrib><creatorcontrib>Marchioni, Luisa</creatorcontrib><creatorcontrib>Mariano, Andrea</creatorcontrib><creatorcontrib>Scorzolini, Laura</creatorcontrib><creatorcontrib>Ascoli Bartoli, Tommaso</creatorcontrib><creatorcontrib>Di Caro, Antonino</creatorcontrib><creatorcontrib>Ippolito, Giuseppe</creatorcontrib><creatorcontrib>Capobianchi, Maria Rosaria</creatorcontrib><creatorcontrib>Castilletti, Concetta</creatorcontrib><creatorcontrib>INMI COVID-19 Laboratory Team and INMI COVID-19 Study Group</creatorcontrib><title>Virological Characterization of the First 2 COVID-19 Patients Diagnosed in Italy: Phylogenetic Analysis, Virus Shedding Profile From Different Body Sites, and Antibody Response Kinetics</title><title>Open Forum Infectious Diseases</title><addtitle>Open Forum Infect Dis</addtitle><description>Abstract
BackgroundThe pathogenesis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection remains unclear. We report the detection of viral RNA from different anatomical districts and the antibody profile in the first 2 COVID-19 cases diagnosed in Italy.
MethodsWe tested for SARS-CoV-2 RNA clinical samples, either respiratory and nonrespiratory (ie, saliva, serum, urine, vomit, rectal, ocular, cutaneous, and cervico-vaginal swabs), longitudinally collected from both patients throughout the hospitalization. Serological analysis was carried out on serial serum samples to evaluate IgM, IgA, IgG, and neutralizing antibody levels.
ResultsSARS-CoV-2 RNA was detected since the early phase of illness, lasting over 2 weeks in both upper and lower respiratory tract samples. Virus isolate was obtained from acute respiratory samples, while no infectious virus was rescued from late respiratory samples with low viral RNA load, collected when serum antibodies had been developed. Several other specimens came back positive, including saliva, vomit, rectal, cutaneous, cervico-vaginal, and ocular swabs. IgM, IgA, and IgG were detected within the first week of diagnosis, with IgG appearing earlier and at higher titers. Neutralizing antibodies developed during the second week, reaching high titers 32 days after diagnosis.
ConclusionsOur longitudinal analysis showed that SARS-CoV-2 RNA can be detected in different body samples, which may be associated with broad tropism and different spectra of clinical manifestations and modes of transmission. Profiling antibody response and neutralizing activity can assist in laboratory diagnosis and surveillance actions.</description><subject>Analysis</subject><subject>Coronaviruses</subject><subject>Development and progression</subject><subject>Diagnosis</subject><subject>Immunoglobulin A</subject><subject>Immunoglobulin G</subject><subject>Major</subject><subject>Phylogeny</subject><subject>RNA</subject><subject>Severe acute respiratory syndrome</subject><issn>2328-8957</issn><issn>2328-8957</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>TOX</sourceid><recordid>eNp9kk1vEzEQhlcIRKvSG2fkGxy6xR_r9S4HpJC2EFGpEYVeLa89Tow2drAdpPDP-u9wSKjKBVmyRzPv-3hsTVW9JPic4J69DdaZsinVYPakOqaMdnXXc_H0UXxUnab0HWNMCOZY9M-rI8Y4Fbgjx9X9nYthDAun1YimSxWVzhDdL5Vd8ChYlJeArlxMGVE0vbmbXdSkR_NSBp8TunBq4UMCg5xHs6zG7Ts0X24LEDxkp9HEl1xy6QyVizYJ3S7BGOcXaB5L72Nhx7AqGGshFiL6EMwW3boMxaG8Kf7shl3uC6R18AnQZ_eHnF5Uz6waE5wezpPq29Xl1-mn-vrm42w6ua51Q1iuW2N1qwjTTFDS9kPP-WAHQpW1tgQN4wNveMsaRQerKBGDaXoBQlEzdMJwdlK933PXm2EFRpcuoxrlOrqVilsZlJP_VrxbykX4KUXT96LtCuDNARDDjw2kLFcuaRhH5SFskqRNxznFTLRFer6XLtQI0nkbClGXZWDldPCw-zI5afuOckK5KIazvUHHkFIE-9AXwXI3IXI3IfIwIUX-6vFbHsR_56EIXu8FYbP-P-o3ebLJTQ</recordid><startdate>20201001</startdate><enddate>20201001</enddate><creator>Colavita, Francesca</creator><creator>Lapa, Daniele</creator><creator>Carletti, Fabrizio</creator><creator>Lalle, Eleonora</creator><creator>Messina, Francesco</creator><creator>Rueca, Martina</creator><creator>Matusali, Giulia</creator><creator>Meschi, Silvia</creator><creator>Bordi, Licia</creator><creator>Marsella, Patrizia</creator><creator>Nicastri, Emanuele</creator><creator>Marchioni, Luisa</creator><creator>Mariano, Andrea</creator><creator>Scorzolini, Laura</creator><creator>Ascoli Bartoli, Tommaso</creator><creator>Di Caro, Antonino</creator><creator>Ippolito, Giuseppe</creator><creator>Capobianchi, Maria Rosaria</creator><creator>Castilletti, Concetta</creator><general>Oxford University Press</general><scope>TOX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>IAO</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6027-3009</orcidid></search><sort><creationdate>20201001</creationdate><title>Virological Characterization of the First 2 COVID-19 Patients Diagnosed in Italy: Phylogenetic Analysis, Virus Shedding Profile From Different Body Sites, and Antibody Response Kinetics</title><author>Colavita, Francesca ; Lapa, Daniele ; Carletti, Fabrizio ; Lalle, Eleonora ; Messina, Francesco ; Rueca, Martina ; Matusali, Giulia ; Meschi, Silvia ; Bordi, Licia ; Marsella, Patrizia ; Nicastri, Emanuele ; Marchioni, Luisa ; Mariano, Andrea ; Scorzolini, Laura ; Ascoli Bartoli, Tommaso ; Di Caro, Antonino ; Ippolito, Giuseppe ; Capobianchi, Maria Rosaria ; Castilletti, Concetta</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c413t-6dfc6a13c372169b955bfb12afffbfb435b545634a2bfa217bd497e7a2db87d53</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Analysis</topic><topic>Coronaviruses</topic><topic>Development and progression</topic><topic>Diagnosis</topic><topic>Immunoglobulin A</topic><topic>Immunoglobulin G</topic><topic>Major</topic><topic>Phylogeny</topic><topic>RNA</topic><topic>Severe acute respiratory syndrome</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Colavita, Francesca</creatorcontrib><creatorcontrib>Lapa, Daniele</creatorcontrib><creatorcontrib>Carletti, Fabrizio</creatorcontrib><creatorcontrib>Lalle, Eleonora</creatorcontrib><creatorcontrib>Messina, Francesco</creatorcontrib><creatorcontrib>Rueca, Martina</creatorcontrib><creatorcontrib>Matusali, Giulia</creatorcontrib><creatorcontrib>Meschi, Silvia</creatorcontrib><creatorcontrib>Bordi, Licia</creatorcontrib><creatorcontrib>Marsella, Patrizia</creatorcontrib><creatorcontrib>Nicastri, Emanuele</creatorcontrib><creatorcontrib>Marchioni, Luisa</creatorcontrib><creatorcontrib>Mariano, Andrea</creatorcontrib><creatorcontrib>Scorzolini, Laura</creatorcontrib><creatorcontrib>Ascoli Bartoli, Tommaso</creatorcontrib><creatorcontrib>Di Caro, Antonino</creatorcontrib><creatorcontrib>Ippolito, Giuseppe</creatorcontrib><creatorcontrib>Capobianchi, Maria Rosaria</creatorcontrib><creatorcontrib>Castilletti, Concetta</creatorcontrib><creatorcontrib>INMI COVID-19 Laboratory Team and INMI COVID-19 Study Group</creatorcontrib><collection>Oxford Journals Open Access Collection</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Gale Academic OneFile</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Open Forum Infectious Diseases</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Colavita, Francesca</au><au>Lapa, Daniele</au><au>Carletti, Fabrizio</au><au>Lalle, Eleonora</au><au>Messina, Francesco</au><au>Rueca, Martina</au><au>Matusali, Giulia</au><au>Meschi, Silvia</au><au>Bordi, Licia</au><au>Marsella, Patrizia</au><au>Nicastri, Emanuele</au><au>Marchioni, Luisa</au><au>Mariano, Andrea</au><au>Scorzolini, Laura</au><au>Ascoli Bartoli, Tommaso</au><au>Di Caro, Antonino</au><au>Ippolito, Giuseppe</au><au>Capobianchi, Maria Rosaria</au><au>Castilletti, Concetta</au><aucorp>INMI COVID-19 Laboratory Team and INMI COVID-19 Study Group</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Virological Characterization of the First 2 COVID-19 Patients Diagnosed in Italy: Phylogenetic Analysis, Virus Shedding Profile From Different Body Sites, and Antibody Response Kinetics</atitle><jtitle>Open Forum Infectious Diseases</jtitle><addtitle>Open Forum Infect Dis</addtitle><date>2020-10-01</date><risdate>2020</risdate><volume>7</volume><issue>10</issue><spage>ofaa403</spage><epage>ofaa403</epage><pages>ofaa403-ofaa403</pages><issn>2328-8957</issn><eissn>2328-8957</eissn><abstract>Abstract
BackgroundThe pathogenesis of severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) infection remains unclear. We report the detection of viral RNA from different anatomical districts and the antibody profile in the first 2 COVID-19 cases diagnosed in Italy.
MethodsWe tested for SARS-CoV-2 RNA clinical samples, either respiratory and nonrespiratory (ie, saliva, serum, urine, vomit, rectal, ocular, cutaneous, and cervico-vaginal swabs), longitudinally collected from both patients throughout the hospitalization. Serological analysis was carried out on serial serum samples to evaluate IgM, IgA, IgG, and neutralizing antibody levels.
ResultsSARS-CoV-2 RNA was detected since the early phase of illness, lasting over 2 weeks in both upper and lower respiratory tract samples. Virus isolate was obtained from acute respiratory samples, while no infectious virus was rescued from late respiratory samples with low viral RNA load, collected when serum antibodies had been developed. Several other specimens came back positive, including saliva, vomit, rectal, cutaneous, cervico-vaginal, and ocular swabs. IgM, IgA, and IgG were detected within the first week of diagnosis, with IgG appearing earlier and at higher titers. Neutralizing antibodies developed during the second week, reaching high titers 32 days after diagnosis.
ConclusionsOur longitudinal analysis showed that SARS-CoV-2 RNA can be detected in different body samples, which may be associated with broad tropism and different spectra of clinical manifestations and modes of transmission. Profiling antibody response and neutralizing activity can assist in laboratory diagnosis and surveillance actions.</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>33527081</pmid><doi>10.1093/ofid/ofaa403</doi><orcidid>https://orcid.org/0000-0001-6027-3009</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Coronaviruses Development and progression Diagnosis Immunoglobulin A Immunoglobulin G Major Phylogeny RNA Severe acute respiratory syndrome |
title | Virological Characterization of the First 2 COVID-19 Patients Diagnosed in Italy: Phylogenetic Analysis, Virus Shedding Profile From Different Body Sites, and Antibody Response Kinetics |
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