Leishmania donovani: Isolation and characterization of sodium stibogluconate (Pentostam)-resistant cell lines
Leishmania donovani promastigotes were generated by virtue of their reistance to incrementing concentrations of sodium stibogluconate (Pentostam) under completely defined growth conditions. The PENT0400 and PENT03200 cell lines were isolated after prolonged exposure to 0.4 mg/ml and 3.2 mg/ml Pentos...
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description | Leishmania donovani promastigotes were generated by virtue of their reistance to incrementing concentrations of sodium stibogluconate (Pentostam) under completely defined growth conditions. The PENT0400 and PENT03200 cell lines were isolated after prolonged exposure to 0.4 mg/ml and 3.2 mg/ml Pentostam (Sb concentration), respectively. Whereas the effective concentration of Pentostam which inhibited the growth of wild type cells by 50% (EC
50 value) was 0.1-0.15 mg/ml, the EC
50 values for the PENT0400 and PENT03200 cells were approximately 1 and 4 mg/ml, respectively. The decreased sensitivities of both PENT0400 and PENT03200 cells to Pentostam were maintained after 6 months of continuous culture in the absence of selective pressure, indicating that the Pentostam resistance in the mutant organisms was a stable genetic trait. Interestingly, wild type and PENT03200 cells were equally sensitive to growth inhibition and cytotoxicity caused by SbCl
5 and SbCl
3, as well as to a variety of other cations such as Cd, Zn, and As. Wild type and PENT03200 cells also displayed equivalent growth sensitivities to a spectrum of other antiprotozoal agents, including antimony potassium tartrate, melarsoprol, pyrimethamine, pentamidine, formycin B, and difluoromethylornithine. These results illustrate a potentially useful model system to study Pentostam resistance in
Leishmania and suggest that Pentostam resistance
in vitro may be independent of antimony toxicity |
doi_str_mv | 10.1016/0014-4894(89)90184-7 |
format | Article |
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50 value) was 0.1-0.15 mg/ml, the EC
50 values for the PENT0400 and PENT03200 cells were approximately 1 and 4 mg/ml, respectively. The decreased sensitivities of both PENT0400 and PENT03200 cells to Pentostam were maintained after 6 months of continuous culture in the absence of selective pressure, indicating that the Pentostam resistance in the mutant organisms was a stable genetic trait. Interestingly, wild type and PENT03200 cells were equally sensitive to growth inhibition and cytotoxicity caused by SbCl
5 and SbCl
3, as well as to a variety of other cations such as Cd, Zn, and As. Wild type and PENT03200 cells also displayed equivalent growth sensitivities to a spectrum of other antiprotozoal agents, including antimony potassium tartrate, melarsoprol, pyrimethamine, pentamidine, formycin B, and difluoromethylornithine. These results illustrate a potentially useful model system to study Pentostam resistance in
Leishmania and suggest that Pentostam resistance
in vitro may be independent of antimony toxicity</description><identifier>ISSN: 0014-4894</identifier><identifier>EISSN: 1090-2449</identifier><identifier>DOI: 10.1016/0014-4894(89)90184-7</identifier><identifier>PMID: 2546793</identifier><identifier>CODEN: EXPAAA</identifier><language>eng</language><publisher>San Diego, CA: Elsevier Inc</publisher><subject>Animals ; Antimony Sodium Gluconate - pharmacokinetics ; Antimony Sodium Gluconate - pharmacology ; ANTIPROTOZOAIRE ; ANTIPROTOZOAL AGENTS ; Biological and medical sciences ; Biological Transport ; CELL CULTURE ; Cell Line ; CHEMICAL RESISTANCE ; CULTIVO DE CELULAS ; CULTURE DE CELLULES ; Drug Resistance ; DRUGS ; Fundamental and applied biological sciences. Psychology ; Gluconates - pharmacology ; GROWTH INHIBITORS ; Human protozoal diseases ; Infectious diseases ; INHIBIDORES DEL CRECIMIENTO ; LEISHMANIA ; Leishmania donovani ; Leishmania donovani - drug effects ; Leishmania donovani - metabolism ; Leshmaniasis ; Medical sciences ; MEDICAMENT ; MEDICAMENTOS ; MEDICAMENTOS CONTRA PROTOZOARIOS ; Parasitic diseases ; Pentostam ; Protozoa ; Protozoal diseases ; RESISTANCE AUX PRODUITS CHIMIQUES ; RESISTENCIA QUIMICA ; RETARDATEUR DE CROISSANCE ; TERAPIA ; THERAPEUTIQUE ; THERAPY ; Tropical medicine</subject><ispartof>Experimental parasitology, 1989-08, Vol.69 (1), p.157-163</ispartof><rights>1989</rights><rights>1990 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c436t-3fc2ffc337f9642d6f0d58ca1ec93c748c775150607b908c7835d3eface17fe13</citedby><cites>FETCH-LOGICAL-c436t-3fc2ffc337f9642d6f0d58ca1ec93c748c775150607b908c7835d3eface17fe13</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://dx.doi.org/10.1016/0014-4894(89)90184-7$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>314,780,784,3550,27924,27925,45995</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=6662792$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/2546793$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Ullman, Buddy</creatorcontrib><creatorcontrib>Carrero-Valenzuela, Elvira</creatorcontrib><creatorcontrib>Coons, Terry</creatorcontrib><title>Leishmania donovani: Isolation and characterization of sodium stibogluconate (Pentostam)-resistant cell lines</title><title>Experimental parasitology</title><addtitle>Exp Parasitol</addtitle><description>Leishmania donovani promastigotes were generated by virtue of their reistance to incrementing concentrations of sodium stibogluconate (Pentostam) under completely defined growth conditions. The PENT0400 and PENT03200 cell lines were isolated after prolonged exposure to 0.4 mg/ml and 3.2 mg/ml Pentostam (Sb concentration), respectively. Whereas the effective concentration of Pentostam which inhibited the growth of wild type cells by 50% (EC
50 value) was 0.1-0.15 mg/ml, the EC
50 values for the PENT0400 and PENT03200 cells were approximately 1 and 4 mg/ml, respectively. The decreased sensitivities of both PENT0400 and PENT03200 cells to Pentostam were maintained after 6 months of continuous culture in the absence of selective pressure, indicating that the Pentostam resistance in the mutant organisms was a stable genetic trait. Interestingly, wild type and PENT03200 cells were equally sensitive to growth inhibition and cytotoxicity caused by SbCl
5 and SbCl
3, as well as to a variety of other cations such as Cd, Zn, and As. Wild type and PENT03200 cells also displayed equivalent growth sensitivities to a spectrum of other antiprotozoal agents, including antimony potassium tartrate, melarsoprol, pyrimethamine, pentamidine, formycin B, and difluoromethylornithine. These results illustrate a potentially useful model system to study Pentostam resistance in
Leishmania and suggest that Pentostam resistance
in vitro may be independent of antimony toxicity</description><subject>Animals</subject><subject>Antimony Sodium Gluconate - pharmacokinetics</subject><subject>Antimony Sodium Gluconate - pharmacology</subject><subject>ANTIPROTOZOAIRE</subject><subject>ANTIPROTOZOAL AGENTS</subject><subject>Biological and medical sciences</subject><subject>Biological Transport</subject><subject>CELL CULTURE</subject><subject>Cell Line</subject><subject>CHEMICAL RESISTANCE</subject><subject>CULTIVO DE CELULAS</subject><subject>CULTURE DE CELLULES</subject><subject>Drug Resistance</subject><subject>DRUGS</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gluconates - pharmacology</subject><subject>GROWTH INHIBITORS</subject><subject>Human protozoal diseases</subject><subject>Infectious diseases</subject><subject>INHIBIDORES DEL CRECIMIENTO</subject><subject>LEISHMANIA</subject><subject>Leishmania donovani</subject><subject>Leishmania donovani - drug effects</subject><subject>Leishmania donovani - metabolism</subject><subject>Leshmaniasis</subject><subject>Medical sciences</subject><subject>MEDICAMENT</subject><subject>MEDICAMENTOS</subject><subject>MEDICAMENTOS CONTRA PROTOZOARIOS</subject><subject>Parasitic diseases</subject><subject>Pentostam</subject><subject>Protozoa</subject><subject>Protozoal diseases</subject><subject>RESISTANCE AUX PRODUITS CHIMIQUES</subject><subject>RESISTENCIA QUIMICA</subject><subject>RETARDATEUR DE CROISSANCE</subject><subject>TERAPIA</subject><subject>THERAPEUTIQUE</subject><subject>THERAPY</subject><subject>Tropical medicine</subject><issn>0014-4894</issn><issn>1090-2449</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1989</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kF1rFTEQhoMo9bT6B0RhL0Tai9Vkk82HF4IUPwoHFLTXISeZtJHdpCbZgv765riHc-lVJvM-MwwPQi8Jfksw4e8wJqxnUrFzqS4UJpL14hHaEKxwPzCmHqPNEXmKTkv5hTGWZGAn6GQYGReKbtC8hVBuZxOD6VyK6b5V77urkiZTQ4qdia6ztyYbWyGHv2sz-a4kF5a5KzXs0s202BRNhe78O8SaSjXzRZ-hhFbF2lmYpm4KEcoz9MSbqcDzw3uGrj9_-nn5td9--3J1-XHbW0Z57am3g_eWUuEVZ4PjHrtRWkPAKmoFk1aIkYyYY7FTuP0kHR0FbywQ4YHQM_Rm3XuX0-8FStVzKPszTIS0FE1GqggRuIFsBW1OpWTw-i6H2eQ_mmC9t6z3CvVeoZZK_7OsRRt7ddi_7GZwx6GD1pa_PuSmWDP5bKIN5Yhxzgehhoa9WDFvkjY3uSHXPxTGalSyhR_WEJqo-wBZFxsgWnAhg63apfD_Ix8ATpmitw</recordid><startdate>19890801</startdate><enddate>19890801</enddate><creator>Ullman, Buddy</creator><creator>Carrero-Valenzuela, Elvira</creator><creator>Coons, Terry</creator><general>Elsevier Inc</general><general>Elsevier</general><scope>FBQ</scope><scope>IQODW</scope><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>M7N</scope></search><sort><creationdate>19890801</creationdate><title>Leishmania donovani: Isolation and characterization of sodium stibogluconate (Pentostam)-resistant cell lines</title><author>Ullman, Buddy ; Carrero-Valenzuela, Elvira ; Coons, Terry</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c436t-3fc2ffc337f9642d6f0d58ca1ec93c748c775150607b908c7835d3eface17fe13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1989</creationdate><topic>Animals</topic><topic>Antimony Sodium Gluconate - pharmacokinetics</topic><topic>Antimony Sodium Gluconate - pharmacology</topic><topic>ANTIPROTOZOAIRE</topic><topic>ANTIPROTOZOAL AGENTS</topic><topic>Biological and medical sciences</topic><topic>Biological Transport</topic><topic>CELL CULTURE</topic><topic>Cell Line</topic><topic>CHEMICAL RESISTANCE</topic><topic>CULTIVO DE CELULAS</topic><topic>CULTURE DE CELLULES</topic><topic>Drug Resistance</topic><topic>DRUGS</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gluconates - pharmacology</topic><topic>GROWTH INHIBITORS</topic><topic>Human protozoal diseases</topic><topic>Infectious diseases</topic><topic>INHIBIDORES DEL CRECIMIENTO</topic><topic>LEISHMANIA</topic><topic>Leishmania donovani</topic><topic>Leishmania donovani - drug effects</topic><topic>Leishmania donovani - metabolism</topic><topic>Leshmaniasis</topic><topic>Medical sciences</topic><topic>MEDICAMENT</topic><topic>MEDICAMENTOS</topic><topic>MEDICAMENTOS CONTRA PROTOZOARIOS</topic><topic>Parasitic diseases</topic><topic>Pentostam</topic><topic>Protozoa</topic><topic>Protozoal diseases</topic><topic>RESISTANCE AUX PRODUITS CHIMIQUES</topic><topic>RESISTENCIA QUIMICA</topic><topic>RETARDATEUR DE CROISSANCE</topic><topic>TERAPIA</topic><topic>THERAPEUTIQUE</topic><topic>THERAPY</topic><topic>Tropical medicine</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ullman, Buddy</creatorcontrib><creatorcontrib>Carrero-Valenzuela, Elvira</creatorcontrib><creatorcontrib>Coons, Terry</creatorcontrib><collection>AGRIS</collection><collection>Pascal-Francis</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Algology Mycology and Protozoology Abstracts (Microbiology C)</collection><jtitle>Experimental parasitology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ullman, Buddy</au><au>Carrero-Valenzuela, Elvira</au><au>Coons, Terry</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Leishmania donovani: Isolation and characterization of sodium stibogluconate (Pentostam)-resistant cell lines</atitle><jtitle>Experimental parasitology</jtitle><addtitle>Exp Parasitol</addtitle><date>1989-08-01</date><risdate>1989</risdate><volume>69</volume><issue>1</issue><spage>157</spage><epage>163</epage><pages>157-163</pages><issn>0014-4894</issn><eissn>1090-2449</eissn><coden>EXPAAA</coden><abstract>Leishmania donovani promastigotes were generated by virtue of their reistance to incrementing concentrations of sodium stibogluconate (Pentostam) under completely defined growth conditions. The PENT0400 and PENT03200 cell lines were isolated after prolonged exposure to 0.4 mg/ml and 3.2 mg/ml Pentostam (Sb concentration), respectively. Whereas the effective concentration of Pentostam which inhibited the growth of wild type cells by 50% (EC
50 value) was 0.1-0.15 mg/ml, the EC
50 values for the PENT0400 and PENT03200 cells were approximately 1 and 4 mg/ml, respectively. The decreased sensitivities of both PENT0400 and PENT03200 cells to Pentostam were maintained after 6 months of continuous culture in the absence of selective pressure, indicating that the Pentostam resistance in the mutant organisms was a stable genetic trait. Interestingly, wild type and PENT03200 cells were equally sensitive to growth inhibition and cytotoxicity caused by SbCl
5 and SbCl
3, as well as to a variety of other cations such as Cd, Zn, and As. Wild type and PENT03200 cells also displayed equivalent growth sensitivities to a spectrum of other antiprotozoal agents, including antimony potassium tartrate, melarsoprol, pyrimethamine, pentamidine, formycin B, and difluoromethylornithine. These results illustrate a potentially useful model system to study Pentostam resistance in
Leishmania and suggest that Pentostam resistance
in vitro may be independent of antimony toxicity</abstract><cop>San Diego, CA</cop><pub>Elsevier Inc</pub><pmid>2546793</pmid><doi>10.1016/0014-4894(89)90184-7</doi><tpages>7</tpages></addata></record> |
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ispartof | Experimental parasitology, 1989-08, Vol.69 (1), p.157-163 |
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source | MEDLINE; Elsevier ScienceDirect Journals Complete |
subjects | Animals Antimony Sodium Gluconate - pharmacokinetics Antimony Sodium Gluconate - pharmacology ANTIPROTOZOAIRE ANTIPROTOZOAL AGENTS Biological and medical sciences Biological Transport CELL CULTURE Cell Line CHEMICAL RESISTANCE CULTIVO DE CELULAS CULTURE DE CELLULES Drug Resistance DRUGS Fundamental and applied biological sciences. Psychology Gluconates - pharmacology GROWTH INHIBITORS Human protozoal diseases Infectious diseases INHIBIDORES DEL CRECIMIENTO LEISHMANIA Leishmania donovani Leishmania donovani - drug effects Leishmania donovani - metabolism Leshmaniasis Medical sciences MEDICAMENT MEDICAMENTOS MEDICAMENTOS CONTRA PROTOZOARIOS Parasitic diseases Pentostam Protozoa Protozoal diseases RESISTANCE AUX PRODUITS CHIMIQUES RESISTENCIA QUIMICA RETARDATEUR DE CROISSANCE TERAPIA THERAPEUTIQUE THERAPY Tropical medicine |
title | Leishmania donovani: Isolation and characterization of sodium stibogluconate (Pentostam)-resistant cell lines |
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