In-vitro activity of azithromycin against Chlamydia trachomatis

We evaluated the efficacy of azithromycin, erythromycin and doxycycline in controlling in-vitro propagation of Chlamydia trachomatis in HeLa 229 cells. Eight recent clinical isolates of C. trachomatis and two fast-growing strains were tested with inocula of 10 super(3)-10 super(5) inclusion forming...

Ausführliche Beschreibung

Gespeichert in:
Bibliographische Detailangaben
Hauptverfasser: Scieux, C, Bianchi, A, Chappey, B, Vassias, I, Perol, Y
Format: Tagungsbericht
Sprache:eng
Online-Zugang:Volltext
Tags: Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
container_end_page no. A Sul.
container_issue
container_start_page no. A Sul.
container_title
container_volume 25
creator Scieux, C
Bianchi, A
Chappey, B
Vassias, I
Perol, Y
description We evaluated the efficacy of azithromycin, erythromycin and doxycycline in controlling in-vitro propagation of Chlamydia trachomatis in HeLa 229 cells. Eight recent clinical isolates of C. trachomatis and two fast-growing strains were tested with inocula of 10 super(3)-10 super(5) inclusion forming units per well of a 96-well microtitre plate. C. trachomatis) inclusions were detected by an immunoperoxidase-antiperoxidase procedure (PAP), including a genus-specific monoclonal antibody. MIC ranges were 0 multiplied by 064-0 multiplied by 25 mg/l azithromycin, 0 multiplied by 064-0 multiplied by 128 mg/l erythromycin and 0 multiplied by 016-0 multiplied by 064 mg/l doxycyline; MBC ranges were 2-8 mg/l azithromycin, 4-64 mg/l erythromycin and 0 multiplied by 5-8 mg/l doxycycline. Since azithromycin appears to be effective against C. trachomatis , clinical studies in sexually transmitted diseases are indicated.
format Conference Proceeding
fullrecord <record><control><sourceid>proquest</sourceid><recordid>TN_cdi_proquest_miscellaneous_15611632</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><sourcerecordid>15611632</sourcerecordid><originalsourceid>FETCH-proquest_miscellaneous_156116323</originalsourceid><addsrcrecordid>eNqNyjkOwjAQQFEXIBGWO7iii-RgbOgoIhD09NHIccggL-BxkMLpoeAAVP8Vf8IKIYUqd1slZ2xOdBdCaKX3BTtcQvnCnCIHk_GrkceOwxtzn6IfDQYON8BAmde9Az-2CDwnMH30kJGWbNqBI7v6dcHWp-O1PpePFJ-Dpdx4JGOdg2DjQE2ldFVpuZF_jx9s5jwB</addsrcrecordid><sourcetype>Aggregation Database</sourcetype><iscdi>true</iscdi><recordtype>conference_proceeding</recordtype><pqid>15611632</pqid></control><display><type>conference_proceeding</type><title>In-vitro activity of azithromycin against Chlamydia trachomatis</title><source>Oxford University Press Journals Digital Archive legacy</source><creator>Scieux, C ; Bianchi, A ; Chappey, B ; Vassias, I ; Perol, Y</creator><contributor>Ridgway, GL (eds) ; Leigh, DA</contributor><creatorcontrib>Scieux, C ; Bianchi, A ; Chappey, B ; Vassias, I ; Perol, Y ; Ridgway, GL (eds) ; Leigh, DA</creatorcontrib><description>We evaluated the efficacy of azithromycin, erythromycin and doxycycline in controlling in-vitro propagation of Chlamydia trachomatis in HeLa 229 cells. Eight recent clinical isolates of C. trachomatis and two fast-growing strains were tested with inocula of 10 super(3)-10 super(5) inclusion forming units per well of a 96-well microtitre plate. C. trachomatis) inclusions were detected by an immunoperoxidase-antiperoxidase procedure (PAP), including a genus-specific monoclonal antibody. MIC ranges were 0 multiplied by 064-0 multiplied by 25 mg/l azithromycin, 0 multiplied by 064-0 multiplied by 128 mg/l erythromycin and 0 multiplied by 016-0 multiplied by 064 mg/l doxycyline; MBC ranges were 2-8 mg/l azithromycin, 4-64 mg/l erythromycin and 0 multiplied by 5-8 mg/l doxycycline. Since azithromycin appears to be effective against C. trachomatis , clinical studies in sexually transmitted diseases are indicated.</description><identifier>ISSN: 0305-7453</identifier><language>eng</language><ispartof>Journal of antimicrobial chemotherapy, 1990, Vol.25, p.no. A Sul.-no. A Sul.</ispartof><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>309,310,780,784,789,790,23930,23931,25140</link.rule.ids></links><search><contributor>Ridgway, GL (eds)</contributor><contributor>Leigh, DA</contributor><creatorcontrib>Scieux, C</creatorcontrib><creatorcontrib>Bianchi, A</creatorcontrib><creatorcontrib>Chappey, B</creatorcontrib><creatorcontrib>Vassias, I</creatorcontrib><creatorcontrib>Perol, Y</creatorcontrib><title>In-vitro activity of azithromycin against Chlamydia trachomatis</title><title>Journal of antimicrobial chemotherapy</title><description>We evaluated the efficacy of azithromycin, erythromycin and doxycycline in controlling in-vitro propagation of Chlamydia trachomatis in HeLa 229 cells. Eight recent clinical isolates of C. trachomatis and two fast-growing strains were tested with inocula of 10 super(3)-10 super(5) inclusion forming units per well of a 96-well microtitre plate. C. trachomatis) inclusions were detected by an immunoperoxidase-antiperoxidase procedure (PAP), including a genus-specific monoclonal antibody. MIC ranges were 0 multiplied by 064-0 multiplied by 25 mg/l azithromycin, 0 multiplied by 064-0 multiplied by 128 mg/l erythromycin and 0 multiplied by 016-0 multiplied by 064 mg/l doxycyline; MBC ranges were 2-8 mg/l azithromycin, 4-64 mg/l erythromycin and 0 multiplied by 5-8 mg/l doxycycline. Since azithromycin appears to be effective against C. trachomatis , clinical studies in sexually transmitted diseases are indicated.</description><issn>0305-7453</issn><fulltext>true</fulltext><rsrctype>conference_proceeding</rsrctype><creationdate>1990</creationdate><recordtype>conference_proceeding</recordtype><recordid>eNqNyjkOwjAQQFEXIBGWO7iii-RgbOgoIhD09NHIccggL-BxkMLpoeAAVP8Vf8IKIYUqd1slZ2xOdBdCaKX3BTtcQvnCnCIHk_GrkceOwxtzn6IfDQYON8BAmde9Az-2CDwnMH30kJGWbNqBI7v6dcHWp-O1PpePFJ-Dpdx4JGOdg2DjQE2ldFVpuZF_jx9s5jwB</recordid><startdate>19900101</startdate><enddate>19900101</enddate><creator>Scieux, C</creator><creator>Bianchi, A</creator><creator>Chappey, B</creator><creator>Vassias, I</creator><creator>Perol, Y</creator><scope>7QL</scope><scope>7T7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>P64</scope></search><sort><creationdate>19900101</creationdate><title>In-vitro activity of azithromycin against Chlamydia trachomatis</title><author>Scieux, C ; Bianchi, A ; Chappey, B ; Vassias, I ; Perol, Y</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-proquest_miscellaneous_156116323</frbrgroupid><rsrctype>conference_proceedings</rsrctype><prefilter>conference_proceedings</prefilter><language>eng</language><creationdate>1990</creationdate><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Scieux, C</creatorcontrib><creatorcontrib>Bianchi, A</creatorcontrib><creatorcontrib>Chappey, B</creatorcontrib><creatorcontrib>Vassias, I</creatorcontrib><creatorcontrib>Perol, Y</creatorcontrib><collection>Bacteriology Abstracts (Microbiology B)</collection><collection>Industrial and Applied Microbiology Abstracts (Microbiology A)</collection><collection>Technology Research Database</collection><collection>Environmental Sciences and Pollution Management</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Scieux, C</au><au>Bianchi, A</au><au>Chappey, B</au><au>Vassias, I</au><au>Perol, Y</au><au>Ridgway, GL (eds)</au><au>Leigh, DA</au><format>book</format><genre>proceeding</genre><ristype>CONF</ristype><atitle>In-vitro activity of azithromycin against Chlamydia trachomatis</atitle><btitle>Journal of antimicrobial chemotherapy</btitle><date>1990-01-01</date><risdate>1990</risdate><volume>25</volume><spage>no. A Sul.</spage><epage>no. A Sul.</epage><pages>no. A Sul.-no. A Sul.</pages><issn>0305-7453</issn><abstract>We evaluated the efficacy of azithromycin, erythromycin and doxycycline in controlling in-vitro propagation of Chlamydia trachomatis in HeLa 229 cells. Eight recent clinical isolates of C. trachomatis and two fast-growing strains were tested with inocula of 10 super(3)-10 super(5) inclusion forming units per well of a 96-well microtitre plate. C. trachomatis) inclusions were detected by an immunoperoxidase-antiperoxidase procedure (PAP), including a genus-specific monoclonal antibody. MIC ranges were 0 multiplied by 064-0 multiplied by 25 mg/l azithromycin, 0 multiplied by 064-0 multiplied by 128 mg/l erythromycin and 0 multiplied by 016-0 multiplied by 064 mg/l doxycyline; MBC ranges were 2-8 mg/l azithromycin, 4-64 mg/l erythromycin and 0 multiplied by 5-8 mg/l doxycycline. Since azithromycin appears to be effective against C. trachomatis , clinical studies in sexually transmitted diseases are indicated.</abstract></addata></record>
fulltext fulltext
identifier ISSN: 0305-7453
ispartof Journal of antimicrobial chemotherapy, 1990, Vol.25, p.no. A Sul.-no. A Sul.
issn 0305-7453
language eng
recordid cdi_proquest_miscellaneous_15611632
source Oxford University Press Journals Digital Archive legacy
title In-vitro activity of azithromycin against Chlamydia trachomatis
url https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2024-12-21T06%3A50%3A50IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest&rft_val_fmt=info:ofi/fmt:kev:mtx:book&rft.genre=proceeding&rft.atitle=In-vitro%20activity%20of%20azithromycin%20against%20Chlamydia%20trachomatis&rft.btitle=Journal%20of%20antimicrobial%20chemotherapy&rft.au=Scieux,%20C&rft.date=1990-01-01&rft.volume=25&rft.spage=no.%20A%20Sul.&rft.epage=no.%20A%20Sul.&rft.pages=no.%20A%20Sul.-no.%20A%20Sul.&rft.issn=0305-7453&rft_id=info:doi/&rft_dat=%3Cproquest%3E15611632%3C/proquest%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=15611632&rft_id=info:pmid/&rfr_iscdi=true