Prevalence of Bartonella spp. Infection in Patients with Sickle Cell Disease

Background: The inherent characteristics of the sickle cell disease (SCD), the most common genetic hematological disorder, increase the propensity of infections. Bartonella spp. are emerging and neglected bacteria. A large spectrum of clinical manifestations has been linked to bartonella bloodstream...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Veröffentlicht in:Vector borne and zoonotic diseases (Larchmont, N.Y.) N.Y.), 2020-07, Vol.20 (7), p.59-512
Hauptverfasser: Soares, Tânia Cristina Benetti, Isaias, Gustavo Alves Brito, Almeida, Amanda Roberta de, Drummond, Marina Rovani, da Silva, Marilene Neves, Lania, Bruno Grosselli, Vieira-Damiani, Gislaine, Saad, Sara Teresinha Olalla, Ericson, Marna Elise, Gupta, Kalpna, Velho, Paulo Eduardo Neves Ferreira
Format: Artikel
Sprache:eng
Schlagworte:
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page 512
container_issue 7
container_start_page 59
container_title Vector borne and zoonotic diseases (Larchmont, N.Y.)
container_volume 20
creator Soares, Tânia Cristina Benetti
Isaias, Gustavo Alves Brito
Almeida, Amanda Roberta de
Drummond, Marina Rovani
da Silva, Marilene Neves
Lania, Bruno Grosselli
Vieira-Damiani, Gislaine
Saad, Sara Teresinha Olalla
Ericson, Marna Elise
Gupta, Kalpna
Velho, Paulo Eduardo Neves Ferreira
description Background: The inherent characteristics of the sickle cell disease (SCD), the most common genetic hematological disorder, increase the propensity of infections. Bartonella spp. are emerging and neglected bacteria. A large spectrum of clinical manifestations has been linked to bartonella bloodstream infection in the last two decades that can cause fatal outcomes, especially in immunodeficient patients. The goal of this study was to evaluate the prevalence of bartonella infection in SCD patients. Materials and Methods: We evaluated Bartonella spp. prevalence in 107 SCD patients. Blood samples and enrichment blood cultures were analyzed by molecular detection of Bartonella spp. DNA. Bartonella DNA was amplified using conventional genus-specific Bartonella PCR which amplifies the Intergenic Transcribed Spacer region and Bartonella henselae- specific nested PCR which amplifies the FtsZ gene. Positive patient DNAs were tested with ssrA conventional PCR. All amplicons were sequenced. Findings: Ten of 107 patients tested positive for B. henselae infection in at least one molecular test. All obtained amplicons were sequenced and similar to B. henselae sequences deposited in GenBank (accession number BX897699). Based on statistical results, bloodstream infection with B. henselae was not associated with animal contact or blood transfusions. Conclusion: We detected B. henselae DNA in 10 (9.3%) SCD studied patients. These patients were notified and treatment was offered to them.
doi_str_mv 10.1089/vbz.2019.2545
format Article
fullrecord <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7336878</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>2350906011</sourcerecordid><originalsourceid>FETCH-LOGICAL-c459t-8605b4cfb77888f7cb47089db5810605620244c7fb50fcc37508c64b141069483</originalsourceid><addsrcrecordid>eNqFkc1LBCEAxSWKvo9dQ-jSZTYddXQuQW2fsFBQnUVdp6xZ3XR2o_76HHaL6tJJ8f18vMcDYA-jAUaiPprrj0GJcD0oGWUrYBMzxgvOWb3a3wkqSFXxDbCV0jNCJRaYrYMNkn8QzsUmGN1GO1et9cbC0MBTFbvgbdsqmKbTAbz2jTWdCx46D29V56zvEnxz3RO8c-altXCYYXjmklXJ7oC1RrXJ7i7PbfBwcX4_vCpGN5fXw5NRYSiru0JUiGlqGp0TCNFwoynPVcaaCYyyVpWopNTwRjPUGEM4Q8JUVGOa5ZoKsg2OF77TmZ7YscmhomrlNLqJiu8yKCd_K949yccwl5yQSvDe4HBpEMPrzKZOTlwyfW1vwyzJkjBU5ygYZ_TgD_ocZtHnerKkJapyWoIyVSwoE0NK0TbfYTCS_U4y7yT7nWS_U-b3fzb4pr-GyQBZAP2z8r51VtvY_WP7CeQfniU</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2420656230</pqid></control><display><type>article</type><title>Prevalence of Bartonella spp. Infection in Patients with Sickle Cell Disease</title><source>MEDLINE</source><source>Alma/SFX Local Collection</source><creator>Soares, Tânia Cristina Benetti ; Isaias, Gustavo Alves Brito ; Almeida, Amanda Roberta de ; Drummond, Marina Rovani ; da Silva, Marilene Neves ; Lania, Bruno Grosselli ; Vieira-Damiani, Gislaine ; Saad, Sara Teresinha Olalla ; Ericson, Marna Elise ; Gupta, Kalpna ; Velho, Paulo Eduardo Neves Ferreira</creator><creatorcontrib>Soares, Tânia Cristina Benetti ; Isaias, Gustavo Alves Brito ; Almeida, Amanda Roberta de ; Drummond, Marina Rovani ; da Silva, Marilene Neves ; Lania, Bruno Grosselli ; Vieira-Damiani, Gislaine ; Saad, Sara Teresinha Olalla ; Ericson, Marna Elise ; Gupta, Kalpna ; Velho, Paulo Eduardo Neves Ferreira</creatorcontrib><description>Background: The inherent characteristics of the sickle cell disease (SCD), the most common genetic hematological disorder, increase the propensity of infections. Bartonella spp. are emerging and neglected bacteria. A large spectrum of clinical manifestations has been linked to bartonella bloodstream infection in the last two decades that can cause fatal outcomes, especially in immunodeficient patients. The goal of this study was to evaluate the prevalence of bartonella infection in SCD patients. Materials and Methods: We evaluated Bartonella spp. prevalence in 107 SCD patients. Blood samples and enrichment blood cultures were analyzed by molecular detection of Bartonella spp. DNA. Bartonella DNA was amplified using conventional genus-specific Bartonella PCR which amplifies the Intergenic Transcribed Spacer region and Bartonella henselae- specific nested PCR which amplifies the FtsZ gene. Positive patient DNAs were tested with ssrA conventional PCR. All amplicons were sequenced. Findings: Ten of 107 patients tested positive for B. henselae infection in at least one molecular test. All obtained amplicons were sequenced and similar to B. henselae sequences deposited in GenBank (accession number BX897699). Based on statistical results, bloodstream infection with B. henselae was not associated with animal contact or blood transfusions. Conclusion: We detected B. henselae DNA in 10 (9.3%) SCD studied patients. These patients were notified and treatment was offered to them.</description><identifier>ISSN: 1530-3667</identifier><identifier>EISSN: 1557-7759</identifier><identifier>DOI: 10.1089/vbz.2019.2545</identifier><identifier>PMID: 32013778</identifier><language>eng</language><publisher>United States: Mary Ann Liebert, Inc., publishers</publisher><subject>Amplification ; Anemia, Sickle Cell - complications ; Bartonella ; Bartonella - isolation &amp; purification ; Bartonella Infections - complications ; Bartonella Infections - epidemiology ; Blood transfusion ; Deoxyribonucleic acid ; DNA ; FtsZ gene ; Hematology ; Humans ; Immunodeficiency ; Infections ; Original ; Original Articles ; Patients ; Polymerase Chain Reaction ; Prevalence ; Risk Factors ; Sequences ; Sickle cell disease ; Spacer region ; Statistical methods</subject><ispartof>Vector borne and zoonotic diseases (Larchmont, N.Y.), 2020-07, Vol.20 (7), p.59-512</ispartof><rights>2020, Mary Ann Liebert, Inc., publishers</rights><rights>Copyright Mary Ann Liebert, Inc. Jul 2020</rights><rights>Copyright 2020, Mary Ann Liebert, Inc., publishers 2020 Mary Ann Liebert, Inc., publishers</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c459t-8605b4cfb77888f7cb47089db5810605620244c7fb50fcc37508c64b141069483</citedby><cites>FETCH-LOGICAL-c459t-8605b4cfb77888f7cb47089db5810605620244c7fb50fcc37508c64b141069483</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/32013778$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Soares, Tânia Cristina Benetti</creatorcontrib><creatorcontrib>Isaias, Gustavo Alves Brito</creatorcontrib><creatorcontrib>Almeida, Amanda Roberta de</creatorcontrib><creatorcontrib>Drummond, Marina Rovani</creatorcontrib><creatorcontrib>da Silva, Marilene Neves</creatorcontrib><creatorcontrib>Lania, Bruno Grosselli</creatorcontrib><creatorcontrib>Vieira-Damiani, Gislaine</creatorcontrib><creatorcontrib>Saad, Sara Teresinha Olalla</creatorcontrib><creatorcontrib>Ericson, Marna Elise</creatorcontrib><creatorcontrib>Gupta, Kalpna</creatorcontrib><creatorcontrib>Velho, Paulo Eduardo Neves Ferreira</creatorcontrib><title>Prevalence of Bartonella spp. Infection in Patients with Sickle Cell Disease</title><title>Vector borne and zoonotic diseases (Larchmont, N.Y.)</title><addtitle>Vector Borne Zoonotic Dis</addtitle><description>Background: The inherent characteristics of the sickle cell disease (SCD), the most common genetic hematological disorder, increase the propensity of infections. Bartonella spp. are emerging and neglected bacteria. A large spectrum of clinical manifestations has been linked to bartonella bloodstream infection in the last two decades that can cause fatal outcomes, especially in immunodeficient patients. The goal of this study was to evaluate the prevalence of bartonella infection in SCD patients. Materials and Methods: We evaluated Bartonella spp. prevalence in 107 SCD patients. Blood samples and enrichment blood cultures were analyzed by molecular detection of Bartonella spp. DNA. Bartonella DNA was amplified using conventional genus-specific Bartonella PCR which amplifies the Intergenic Transcribed Spacer region and Bartonella henselae- specific nested PCR which amplifies the FtsZ gene. Positive patient DNAs were tested with ssrA conventional PCR. All amplicons were sequenced. Findings: Ten of 107 patients tested positive for B. henselae infection in at least one molecular test. All obtained amplicons were sequenced and similar to B. henselae sequences deposited in GenBank (accession number BX897699). Based on statistical results, bloodstream infection with B. henselae was not associated with animal contact or blood transfusions. Conclusion: We detected B. henselae DNA in 10 (9.3%) SCD studied patients. These patients were notified and treatment was offered to them.</description><subject>Amplification</subject><subject>Anemia, Sickle Cell - complications</subject><subject>Bartonella</subject><subject>Bartonella - isolation &amp; purification</subject><subject>Bartonella Infections - complications</subject><subject>Bartonella Infections - epidemiology</subject><subject>Blood transfusion</subject><subject>Deoxyribonucleic acid</subject><subject>DNA</subject><subject>FtsZ gene</subject><subject>Hematology</subject><subject>Humans</subject><subject>Immunodeficiency</subject><subject>Infections</subject><subject>Original</subject><subject>Original Articles</subject><subject>Patients</subject><subject>Polymerase Chain Reaction</subject><subject>Prevalence</subject><subject>Risk Factors</subject><subject>Sequences</subject><subject>Sickle cell disease</subject><subject>Spacer region</subject><subject>Statistical methods</subject><issn>1530-3667</issn><issn>1557-7759</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2020</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqFkc1LBCEAxSWKvo9dQ-jSZTYddXQuQW2fsFBQnUVdp6xZ3XR2o_76HHaL6tJJ8f18vMcDYA-jAUaiPprrj0GJcD0oGWUrYBMzxgvOWb3a3wkqSFXxDbCV0jNCJRaYrYMNkn8QzsUmGN1GO1et9cbC0MBTFbvgbdsqmKbTAbz2jTWdCx46D29V56zvEnxz3RO8c-altXCYYXjmklXJ7oC1RrXJ7i7PbfBwcX4_vCpGN5fXw5NRYSiru0JUiGlqGp0TCNFwoynPVcaaCYyyVpWopNTwRjPUGEM4Q8JUVGOa5ZoKsg2OF77TmZ7YscmhomrlNLqJiu8yKCd_K949yccwl5yQSvDe4HBpEMPrzKZOTlwyfW1vwyzJkjBU5ygYZ_TgD_ocZtHnerKkJapyWoIyVSwoE0NK0TbfYTCS_U4y7yT7nWS_U-b3fzb4pr-GyQBZAP2z8r51VtvY_WP7CeQfniU</recordid><startdate>20200701</startdate><enddate>20200701</enddate><creator>Soares, Tânia Cristina Benetti</creator><creator>Isaias, Gustavo Alves Brito</creator><creator>Almeida, Amanda Roberta de</creator><creator>Drummond, Marina Rovani</creator><creator>da Silva, Marilene Neves</creator><creator>Lania, Bruno Grosselli</creator><creator>Vieira-Damiani, Gislaine</creator><creator>Saad, Sara Teresinha Olalla</creator><creator>Ericson, Marna Elise</creator><creator>Gupta, Kalpna</creator><creator>Velho, Paulo Eduardo Neves Ferreira</creator><general>Mary Ann Liebert, Inc., publishers</general><general>Mary Ann Liebert, Inc</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QL</scope><scope>7SS</scope><scope>7U9</scope><scope>C1K</scope><scope>H94</scope><scope>M7N</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20200701</creationdate><title>Prevalence of Bartonella spp. Infection in Patients with Sickle Cell Disease</title><author>Soares, Tânia Cristina Benetti ; Isaias, Gustavo Alves Brito ; Almeida, Amanda Roberta de ; Drummond, Marina Rovani ; da Silva, Marilene Neves ; Lania, Bruno Grosselli ; Vieira-Damiani, Gislaine ; Saad, Sara Teresinha Olalla ; Ericson, Marna Elise ; Gupta, Kalpna ; Velho, Paulo Eduardo Neves Ferreira</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-8605b4cfb77888f7cb47089db5810605620244c7fb50fcc37508c64b141069483</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2020</creationdate><topic>Amplification</topic><topic>Anemia, Sickle Cell - complications</topic><topic>Bartonella</topic><topic>Bartonella - isolation &amp; purification</topic><topic>Bartonella Infections - complications</topic><topic>Bartonella Infections - epidemiology</topic><topic>Blood transfusion</topic><topic>Deoxyribonucleic acid</topic><topic>DNA</topic><topic>FtsZ gene</topic><topic>Hematology</topic><topic>Humans</topic><topic>Immunodeficiency</topic><topic>Infections</topic><topic>Original</topic><topic>Original Articles</topic><topic>Patients</topic><topic>Polymerase Chain Reaction</topic><topic>Prevalence</topic><topic>Risk Factors</topic><topic>Sequences</topic><topic>Sickle cell disease</topic><topic>Spacer region</topic><topic>Statistical methods</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Soares, Tânia Cristina Benetti</creatorcontrib><creatorcontrib>Isaias, Gustavo Alves Brito</creatorcontrib><creatorcontrib>Almeida, Amanda Roberta de</creatorcontrib><creatorcontrib>Drummond, Marina Rovani</creatorcontrib><creatorcontrib>da Silva, Marilene Neves</creatorcontrib><creatorcontrib>Lania, Bruno Grosselli</creatorcontrib><creatorcontrib>Vieira-Damiani, Gislaine</creatorcontrib><creatorcontrib>Saad, Sara Teresinha Olalla</creatorcontrib><creatorcontrib>Ericson, Marna Elise</creatorcontrib><creatorcontrib>Gupta, Kalpna</creatorcontrib><creatorcontrib>Velho, Paulo Eduardo Neves Ferreira</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Entomology Abstracts (Full archive)</collection><collection>Virology and AIDS Abstracts</collection><collection>Environmental Sciences and Pollution Management</collection><collection>AIDS and Cancer Research Abstracts</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Vector borne and zoonotic diseases (Larchmont, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Soares, Tânia Cristina Benetti</au><au>Isaias, Gustavo Alves Brito</au><au>Almeida, Amanda Roberta de</au><au>Drummond, Marina Rovani</au><au>da Silva, Marilene Neves</au><au>Lania, Bruno Grosselli</au><au>Vieira-Damiani, Gislaine</au><au>Saad, Sara Teresinha Olalla</au><au>Ericson, Marna Elise</au><au>Gupta, Kalpna</au><au>Velho, Paulo Eduardo Neves Ferreira</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevalence of Bartonella spp. Infection in Patients with Sickle Cell Disease</atitle><jtitle>Vector borne and zoonotic diseases (Larchmont, N.Y.)</jtitle><addtitle>Vector Borne Zoonotic Dis</addtitle><date>2020-07-01</date><risdate>2020</risdate><volume>20</volume><issue>7</issue><spage>59</spage><epage>512</epage><pages>59-512</pages><issn>1530-3667</issn><eissn>1557-7759</eissn><abstract>Background: The inherent characteristics of the sickle cell disease (SCD), the most common genetic hematological disorder, increase the propensity of infections. Bartonella spp. are emerging and neglected bacteria. A large spectrum of clinical manifestations has been linked to bartonella bloodstream infection in the last two decades that can cause fatal outcomes, especially in immunodeficient patients. The goal of this study was to evaluate the prevalence of bartonella infection in SCD patients. Materials and Methods: We evaluated Bartonella spp. prevalence in 107 SCD patients. Blood samples and enrichment blood cultures were analyzed by molecular detection of Bartonella spp. DNA. Bartonella DNA was amplified using conventional genus-specific Bartonella PCR which amplifies the Intergenic Transcribed Spacer region and Bartonella henselae- specific nested PCR which amplifies the FtsZ gene. Positive patient DNAs were tested with ssrA conventional PCR. All amplicons were sequenced. Findings: Ten of 107 patients tested positive for B. henselae infection in at least one molecular test. All obtained amplicons were sequenced and similar to B. henselae sequences deposited in GenBank (accession number BX897699). Based on statistical results, bloodstream infection with B. henselae was not associated with animal contact or blood transfusions. Conclusion: We detected B. henselae DNA in 10 (9.3%) SCD studied patients. These patients were notified and treatment was offered to them.</abstract><cop>United States</cop><pub>Mary Ann Liebert, Inc., publishers</pub><pmid>32013778</pmid><doi>10.1089/vbz.2019.2545</doi><tpages>454</tpages><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1530-3667
ispartof Vector borne and zoonotic diseases (Larchmont, N.Y.), 2020-07, Vol.20 (7), p.59-512
issn 1530-3667
1557-7759
language eng
recordid cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_7336878
source MEDLINE; Alma/SFX Local Collection
subjects Amplification
Anemia, Sickle Cell - complications
Bartonella
Bartonella - isolation & purification
Bartonella Infections - complications
Bartonella Infections - epidemiology
Blood transfusion
Deoxyribonucleic acid
DNA
FtsZ gene
Hematology
Humans
Immunodeficiency
Infections
Original
Original Articles
Patients
Polymerase Chain Reaction
Prevalence
Risk Factors
Sequences
Sickle cell disease
Spacer region
Statistical methods
title Prevalence of Bartonella spp. Infection in Patients with Sickle Cell Disease
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-28T23%3A56%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Prevalence%20of%20Bartonella%20spp.%20Infection%20in%20Patients%20with%20Sickle%20Cell%20Disease&rft.jtitle=Vector%20borne%20and%20zoonotic%20diseases%20(Larchmont,%20N.Y.)&rft.au=Soares,%20T%C3%A2nia%20Cristina%20Benetti&rft.date=2020-07-01&rft.volume=20&rft.issue=7&rft.spage=59&rft.epage=512&rft.pages=59-512&rft.issn=1530-3667&rft.eissn=1557-7759&rft_id=info:doi/10.1089/vbz.2019.2545&rft_dat=%3Cproquest_pubme%3E2350906011%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=2420656230&rft_id=info:pmid/32013778&rfr_iscdi=true