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Comparative analysis of metacyclogenesis and infection curves in different discrete typing units of Trypanosoma cruzi
Chagas disease (CD), caused by the complex life cycle parasite Trypanosoma cruzi , is a global health concern and impacts millions globally. T. cruzi ’s genetic variability is categorized into discrete typing units (DTUs). Despite their widespread presence in the Americas, a comprehensive understand...
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Published in: | Parasitology research (1987) 2024-04, Vol.123 (4), p.181-181, Article 181 |
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description | Chagas disease (CD), caused by the complex life cycle parasite
Trypanosoma cruzi
, is a global health concern and impacts millions globally.
T. cruzi
’s genetic variability is categorized into discrete typing units (DTUs). Despite their widespread presence in the Americas, a comprehensive understanding of their impact on CD is lacking. This study aims to analyze life cycle traits across life cycle stages, unraveling DTU dynamics. Metacyclogenesis curves were generated, inducing nutritional stress in epimastigotes of five DTUs (TcI (MG), TcI (DA), TcII(Y), TcIII, TcIV, and TcVI), resulting in metacyclic trypomastigotes. Infection dynamics in Vero cells from various DTUs were evaluated, exploring factors like amastigotes per cell, cell-derived trypomastigotes, and infection percentage. Statistical analyses, including ANOVA tests, identified significant differences. Varying onset times for metacyclogenesis converged on the 7th day. TcI (MG) exhibited the highest metacyclogenesis potential. TcI (DA) stood out, infecting 80% of cells within 24 h. TcI demonstrated the highest potential in both metacyclogenesis and infection among the strains assessed. Intra-DTU diversity was evident among TcI strains, contributing to a comprehensive understanding of
Trypanosoma cruzi
dynamics and genetic diversity. |
doi_str_mv | 10.1007/s00436-024-08183-4 |
format | article |
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Trypanosoma cruzi
, is a global health concern and impacts millions globally.
T. cruzi
’s genetic variability is categorized into discrete typing units (DTUs). Despite their widespread presence in the Americas, a comprehensive understanding of their impact on CD is lacking. This study aims to analyze life cycle traits across life cycle stages, unraveling DTU dynamics. Metacyclogenesis curves were generated, inducing nutritional stress in epimastigotes of five DTUs (TcI (MG), TcI (DA), TcII(Y), TcIII, TcIV, and TcVI), resulting in metacyclic trypomastigotes. Infection dynamics in Vero cells from various DTUs were evaluated, exploring factors like amastigotes per cell, cell-derived trypomastigotes, and infection percentage. Statistical analyses, including ANOVA tests, identified significant differences. Varying onset times for metacyclogenesis converged on the 7th day. TcI (MG) exhibited the highest metacyclogenesis potential. TcI (DA) stood out, infecting 80% of cells within 24 h. TcI demonstrated the highest potential in both metacyclogenesis and infection among the strains assessed. Intra-DTU diversity was evident among TcI strains, contributing to a comprehensive understanding of
Trypanosoma cruzi
dynamics and genetic diversity.</description><identifier>ISSN: 0932-0113</identifier><identifier>EISSN: 1432-1955</identifier><identifier>DOI: 10.1007/s00436-024-08183-4</identifier><identifier>PMID: 38602595</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Amastigotes ; Animals ; Biomedical and Life Sciences ; Biomedicine ; Brief Report ; Chagas Disease ; Chlorocebus aethiops ; Comparative analysis ; Epimastigotes ; Genetic diversity ; Genetic variability ; genetic variation ; Immunology ; Infections ; Life cycles ; malnutrition ; Medical Microbiology ; Microbiology ; Nutrient deficiency ; parasites ; Phenotype ; Protozoa ; Public health ; Statistical analysis ; Trypanosoma cruzi ; Trypanosoma cruzi - genetics ; Trypomastigotes ; Typing ; Vero Cells</subject><ispartof>Parasitology research (1987), 2024-04, Vol.123 (4), p.181-181, Article 181</ispartof><rights>The Author(s) 2024</rights><rights>2024. The Author(s).</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c459t-6857c6194f351ea94beff1ca3f5f2366cddf79bbdd20dd1ba26e86201b7722be3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,776,780,881,27903,27904</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/38602595$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Cáceres, Tatiana M.</creatorcontrib><creatorcontrib>Cruz-Saavedra, Lissa</creatorcontrib><creatorcontrib>Patiño, Luz Helena</creatorcontrib><creatorcontrib>Ramírez, Juan David</creatorcontrib><title>Comparative analysis of metacyclogenesis and infection curves in different discrete typing units of Trypanosoma cruzi</title><title>Parasitology research (1987)</title><addtitle>Parasitol Res</addtitle><addtitle>Parasitol Res</addtitle><description>Chagas disease (CD), caused by the complex life cycle parasite
Trypanosoma cruzi
, is a global health concern and impacts millions globally.
T. cruzi
’s genetic variability is categorized into discrete typing units (DTUs). Despite their widespread presence in the Americas, a comprehensive understanding of their impact on CD is lacking. This study aims to analyze life cycle traits across life cycle stages, unraveling DTU dynamics. Metacyclogenesis curves were generated, inducing nutritional stress in epimastigotes of five DTUs (TcI (MG), TcI (DA), TcII(Y), TcIII, TcIV, and TcVI), resulting in metacyclic trypomastigotes. Infection dynamics in Vero cells from various DTUs were evaluated, exploring factors like amastigotes per cell, cell-derived trypomastigotes, and infection percentage. Statistical analyses, including ANOVA tests, identified significant differences. Varying onset times for metacyclogenesis converged on the 7th day. TcI (MG) exhibited the highest metacyclogenesis potential. TcI (DA) stood out, infecting 80% of cells within 24 h. TcI demonstrated the highest potential in both metacyclogenesis and infection among the strains assessed. Intra-DTU diversity was evident among TcI strains, contributing to a comprehensive understanding of
Trypanosoma cruzi
dynamics and genetic diversity.</description><subject>Amastigotes</subject><subject>Animals</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brief Report</subject><subject>Chagas Disease</subject><subject>Chlorocebus aethiops</subject><subject>Comparative analysis</subject><subject>Epimastigotes</subject><subject>Genetic diversity</subject><subject>Genetic variability</subject><subject>genetic variation</subject><subject>Immunology</subject><subject>Infections</subject><subject>Life cycles</subject><subject>malnutrition</subject><subject>Medical Microbiology</subject><subject>Microbiology</subject><subject>Nutrient deficiency</subject><subject>parasites</subject><subject>Phenotype</subject><subject>Protozoa</subject><subject>Public health</subject><subject>Statistical analysis</subject><subject>Trypanosoma cruzi</subject><subject>Trypanosoma cruzi - genetics</subject><subject>Trypomastigotes</subject><subject>Typing</subject><subject>Vero Cells</subject><issn>0932-0113</issn><issn>1432-1955</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><recordid>eNqFkstu1TAQhi1ERQ-FF2CBIrFhE-p74hVCR9ykSt2UteU444OrxA52cqT06XGbUi4LuprRzDe_Z8aD0CuC3xGMm_OMMWeyxpTXuCUtq_kTtCOc0ZooIZ6iHVbFx4SwU_Q852uMSSM5f4ZOWSsxFUrs0LKP42SSmf0RKhPMsGafq-iqEWZjVzvEAwS4jZnQVz44sLOPobJLOkIugar3zkGCMBcv2wQzVPM6-XColuDnO62rtE4mxBxHU9m03PgX6MSZIcPLe3uGvn36eLX_Ul9cfv66_3BRWy7UXMtWNFYSxR0TBIziHThHrGFOOMqktH3vGtV1fU9x35POUAmtpJh0TUNpB-wMvd90p6Ubobely2QGPSU_mrTqaLz-OxP8d32IR03KglssRVF4e6-Q4o8F8qzHMiUMgwkQl6wZEUy0bcvZ4yhmDVOimIK--Qe9jksq298oQVmjVKHoRtkUc07gHhonWN9egN4uQJcL0HcXoHkpev3nyA8lv768AGwDckmFA6Tfb_9H9ic4Lr9E</recordid><startdate>20240401</startdate><enddate>20240401</enddate><creator>Cáceres, Tatiana M.</creator><creator>Cruz-Saavedra, Lissa</creator><creator>Patiño, Luz Helena</creator><creator>Ramírez, Juan David</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><scope>C6C</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>7X8</scope><scope>7S9</scope><scope>L.6</scope><scope>5PM</scope></search><sort><creationdate>20240401</creationdate><title>Comparative analysis of metacyclogenesis and infection curves in different discrete typing units of Trypanosoma cruzi</title><author>Cáceres, Tatiana M. ; Cruz-Saavedra, Lissa ; Patiño, Luz Helena ; Ramírez, Juan David</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c459t-6857c6194f351ea94beff1ca3f5f2366cddf79bbdd20dd1ba26e86201b7722be3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Amastigotes</topic><topic>Animals</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brief Report</topic><topic>Chagas Disease</topic><topic>Chlorocebus aethiops</topic><topic>Comparative analysis</topic><topic>Epimastigotes</topic><topic>Genetic diversity</topic><topic>Genetic variability</topic><topic>genetic variation</topic><topic>Immunology</topic><topic>Infections</topic><topic>Life cycles</topic><topic>malnutrition</topic><topic>Medical Microbiology</topic><topic>Microbiology</topic><topic>Nutrient deficiency</topic><topic>parasites</topic><topic>Phenotype</topic><topic>Protozoa</topic><topic>Public health</topic><topic>Statistical analysis</topic><topic>Trypanosoma cruzi</topic><topic>Trypanosoma cruzi - genetics</topic><topic>Trypomastigotes</topic><topic>Typing</topic><topic>Vero Cells</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Cáceres, Tatiana M.</creatorcontrib><creatorcontrib>Cruz-Saavedra, Lissa</creatorcontrib><creatorcontrib>Patiño, Luz Helena</creatorcontrib><creatorcontrib>Ramírez, Juan David</creatorcontrib><collection>Springer Nature OA Free Journals</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>AGRICOLA</collection><collection>AGRICOLA - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Parasitology research (1987)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Cáceres, Tatiana M.</au><au>Cruz-Saavedra, Lissa</au><au>Patiño, Luz Helena</au><au>Ramírez, Juan David</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Comparative analysis of metacyclogenesis and infection curves in different discrete typing units of Trypanosoma cruzi</atitle><jtitle>Parasitology research (1987)</jtitle><stitle>Parasitol Res</stitle><addtitle>Parasitol Res</addtitle><date>2024-04-01</date><risdate>2024</risdate><volume>123</volume><issue>4</issue><spage>181</spage><epage>181</epage><pages>181-181</pages><artnum>181</artnum><issn>0932-0113</issn><eissn>1432-1955</eissn><abstract>Chagas disease (CD), caused by the complex life cycle parasite
Trypanosoma cruzi
, is a global health concern and impacts millions globally.
T. cruzi
’s genetic variability is categorized into discrete typing units (DTUs). Despite their widespread presence in the Americas, a comprehensive understanding of their impact on CD is lacking. This study aims to analyze life cycle traits across life cycle stages, unraveling DTU dynamics. Metacyclogenesis curves were generated, inducing nutritional stress in epimastigotes of five DTUs (TcI (MG), TcI (DA), TcII(Y), TcIII, TcIV, and TcVI), resulting in metacyclic trypomastigotes. Infection dynamics in Vero cells from various DTUs were evaluated, exploring factors like amastigotes per cell, cell-derived trypomastigotes, and infection percentage. Statistical analyses, including ANOVA tests, identified significant differences. Varying onset times for metacyclogenesis converged on the 7th day. TcI (MG) exhibited the highest metacyclogenesis potential. TcI (DA) stood out, infecting 80% of cells within 24 h. TcI demonstrated the highest potential in both metacyclogenesis and infection among the strains assessed. Intra-DTU diversity was evident among TcI strains, contributing to a comprehensive understanding of
Trypanosoma cruzi
dynamics and genetic diversity.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>38602595</pmid><doi>10.1007/s00436-024-08183-4</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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subjects | Amastigotes Animals Biomedical and Life Sciences Biomedicine Brief Report Chagas Disease Chlorocebus aethiops Comparative analysis Epimastigotes Genetic diversity Genetic variability genetic variation Immunology Infections Life cycles malnutrition Medical Microbiology Microbiology Nutrient deficiency parasites Phenotype Protozoa Public health Statistical analysis Trypanosoma cruzi Trypanosoma cruzi - genetics Trypomastigotes Typing Vero Cells |
title | Comparative analysis of metacyclogenesis and infection curves in different discrete typing units of Trypanosoma cruzi |
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