Purification of Trypanosoma cruzi metacyclic trypomastigotes by ion exchange chromatography in sepharose-DEAE, a novel methodology for host-pathogen interaction studies
Metacyclic trypomastigotes are essential for the understanding of the biology of Trypanosoma cruzi, the agent of Chagas disease. However, obtaining these biological stages in axenic medium is difficult. Techniques based on charge and density of the parasite during different stages have been implemen...
- Autores:
- Tipo de recurso:
- Fecha de publicación:
- 2017
- Institución:
- Universidad del Rosario
- Repositorio:
- Repositorio EdocUR - U. Rosario
- Idioma:
- eng
- OAI Identifier:
- oai:repository.urosario.edu.co:10336/22403
- Acceso en línea:
- https://doi.org/10.1016/j.mimet.2017.08.021
https://repository.urosario.edu.co/handle/10336/22403
- Palabra clave:
- Sepharose
Diethylaminoethyldextran
Sepharose
Animal experiment
Article
Epimastigote
Host pathogen interaction
In vitro study
In vivo study
Ion exchange chromatography
Life cycle
Mouse
Nonhuman
Parasitosis
Priority journal
Trypanosoma cruzi
Trypomastigote
Vero cell line
Animal
Cell line
Chlorocebus aethiops
Host pathogen interaction
Institute for cancer research mouse
Ion exchange chromatography
Isolation and purification
Procedures
Trypanosoma cruzi
Animals
Cell line
Cercopithecus aethiops
Deae-dextran
Host-pathogen interactions
Mice
Sepharose
Trypanosoma cruzi
Vero cells
Chromatography
Culture
Metacyclic trypomastigotes
Sepharose-deae
Trypanosoma cruzi
inbred icr
ion exchange
Chromatography
Mice
- Rights
- License
- Abierto (Texto Completo)
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dc.title.spa.fl_str_mv |
Purification of Trypanosoma cruzi metacyclic trypomastigotes by ion exchange chromatography in sepharose-DEAE, a novel methodology for host-pathogen interaction studies |
title |
Purification of Trypanosoma cruzi metacyclic trypomastigotes by ion exchange chromatography in sepharose-DEAE, a novel methodology for host-pathogen interaction studies |
spellingShingle |
Purification of Trypanosoma cruzi metacyclic trypomastigotes by ion exchange chromatography in sepharose-DEAE, a novel methodology for host-pathogen interaction studies Sepharose Diethylaminoethyldextran Sepharose Animal experiment Article Epimastigote Host pathogen interaction In vitro study In vivo study Ion exchange chromatography Life cycle Mouse Nonhuman Parasitosis Priority journal Trypanosoma cruzi Trypomastigote Vero cell line Animal Cell line Chlorocebus aethiops Host pathogen interaction Institute for cancer research mouse Ion exchange chromatography Isolation and purification Procedures Trypanosoma cruzi Animals Cell line Cercopithecus aethiops Deae-dextran Host-pathogen interactions Mice Sepharose Trypanosoma cruzi Vero cells Chromatography Culture Metacyclic trypomastigotes Sepharose-deae Trypanosoma cruzi inbred icr ion exchange Chromatography Mice |
title_short |
Purification of Trypanosoma cruzi metacyclic trypomastigotes by ion exchange chromatography in sepharose-DEAE, a novel methodology for host-pathogen interaction studies |
title_full |
Purification of Trypanosoma cruzi metacyclic trypomastigotes by ion exchange chromatography in sepharose-DEAE, a novel methodology for host-pathogen interaction studies |
title_fullStr |
Purification of Trypanosoma cruzi metacyclic trypomastigotes by ion exchange chromatography in sepharose-DEAE, a novel methodology for host-pathogen interaction studies |
title_full_unstemmed |
Purification of Trypanosoma cruzi metacyclic trypomastigotes by ion exchange chromatography in sepharose-DEAE, a novel methodology for host-pathogen interaction studies |
title_sort |
Purification of Trypanosoma cruzi metacyclic trypomastigotes by ion exchange chromatography in sepharose-DEAE, a novel methodology for host-pathogen interaction studies |
dc.subject.keyword.spa.fl_str_mv |
Sepharose Diethylaminoethyldextran Sepharose Animal experiment Article Epimastigote Host pathogen interaction In vitro study In vivo study Ion exchange chromatography Life cycle Mouse Nonhuman Parasitosis Priority journal Trypanosoma cruzi Trypomastigote Vero cell line Animal Cell line Chlorocebus aethiops Host pathogen interaction Institute for cancer research mouse Ion exchange chromatography Isolation and purification Procedures Trypanosoma cruzi Animals Cell line Cercopithecus aethiops Deae-dextran Host-pathogen interactions Mice Sepharose Trypanosoma cruzi Vero cells Chromatography Culture Metacyclic trypomastigotes Sepharose-deae Trypanosoma cruzi |
topic |
Sepharose Diethylaminoethyldextran Sepharose Animal experiment Article Epimastigote Host pathogen interaction In vitro study In vivo study Ion exchange chromatography Life cycle Mouse Nonhuman Parasitosis Priority journal Trypanosoma cruzi Trypomastigote Vero cell line Animal Cell line Chlorocebus aethiops Host pathogen interaction Institute for cancer research mouse Ion exchange chromatography Isolation and purification Procedures Trypanosoma cruzi Animals Cell line Cercopithecus aethiops Deae-dextran Host-pathogen interactions Mice Sepharose Trypanosoma cruzi Vero cells Chromatography Culture Metacyclic trypomastigotes Sepharose-deae Trypanosoma cruzi inbred icr ion exchange Chromatography Mice |
dc.subject.keyword.eng.fl_str_mv |
inbred icr ion exchange Chromatography Mice |
description |
Metacyclic trypomastigotes are essential for the understanding of the biology of Trypanosoma cruzi, the agent of Chagas disease. However, obtaining these biological stages in axenic medium is difficult. Techniques based on charge and density of the parasite during different stages have been implemented, without showing a high efficiency in the purification of metacyclic trypomastigotes. So far, there is no protocol implemented where sepharose-DEAE is used as a resin. Therefore, herein we tested its ability to purify metacyclic trypomastigotes in Liver Infusion Triptose (LIT) medium cultures. A simple, easy-to-execute and effective protocol based on ion exchange chromatography on Sepharose-DEAE resin for the purification of T. cruzi trypomastigotes is described. T. cruzi strains from the Discrete Typing Units (DTUs) I and II were used. The strains were harvested in LIT medium at a concentration of 1 × 107 epimastigotes/mL. We calculated the time of trypomastigotes increment (TTI). Based on the data obtained, Ion exchange chromatography was performed with DEAE-sepharose resin. To verify the purity and viability of the trypomastigotes, a culture was carried out in LIT medium with subsequent verification with giemsa staining. To evaluate if the technique affected the infectivity of trypomastigotes, in vitro assays were performed in Vero cells and in vivo in ICR-CD1 mice. The technique allowed the purification of metacyclic trypomastigotes of other stages of T. cruzi in a percentage of 100%, a greater recovery was observed in cultures of 12 days. There were differences regarding the recovery of metacyclic trypomastigotes for both DTUs, being DTU TcI the one that recovered a greater amount of these forms. The technique did not affect parasite infectivity in vitro or/and in vivo. © 2017 Elsevier B.V. |
publishDate |
2017 |
dc.date.created.spa.fl_str_mv |
2017 |
dc.date.accessioned.none.fl_str_mv |
2020-05-25T23:56:21Z |
dc.date.available.none.fl_str_mv |
2020-05-25T23:56:21Z |
dc.type.eng.fl_str_mv |
article |
dc.type.coarversion.fl_str_mv |
http://purl.org/coar/version/c_970fb48d4fbd8a85 |
dc.type.coar.fl_str_mv |
http://purl.org/coar/resource_type/c_6501 |
dc.type.spa.spa.fl_str_mv |
Artículo |
dc.identifier.doi.none.fl_str_mv |
https://doi.org/10.1016/j.mimet.2017.08.021 |
dc.identifier.issn.none.fl_str_mv |
1677012 |
dc.identifier.uri.none.fl_str_mv |
https://repository.urosario.edu.co/handle/10336/22403 |
url |
https://doi.org/10.1016/j.mimet.2017.08.021 https://repository.urosario.edu.co/handle/10336/22403 |
identifier_str_mv |
1677012 |
dc.language.iso.spa.fl_str_mv |
eng |
language |
eng |
dc.relation.citationEndPage.none.fl_str_mv |
32 |
dc.relation.citationStartPage.none.fl_str_mv |
27 |
dc.relation.citationTitle.none.fl_str_mv |
Journal of Microbiological Methods |
dc.relation.citationVolume.none.fl_str_mv |
Vol. 142 |
dc.relation.ispartof.spa.fl_str_mv |
Journal of Microbiological Methods, ISSN:1677012, Vol.142,(2017); pp. 27-32 |
dc.relation.uri.spa.fl_str_mv |
https://www.scopus.com/inward/record.uri?eid=2-s2.0-85028709682&doi=10.1016%2fj.mimet.2017.08.021&partnerID=40&md5=a200932fa0d0a0952e55a5a66f5bf6fb |
dc.rights.coar.fl_str_mv |
http://purl.org/coar/access_right/c_abf2 |
dc.rights.acceso.spa.fl_str_mv |
Abierto (Texto Completo) |
rights_invalid_str_mv |
Abierto (Texto Completo) http://purl.org/coar/access_right/c_abf2 |
dc.format.mimetype.none.fl_str_mv |
application/pdf |
dc.publisher.spa.fl_str_mv |
Elsevier B.V. |
institution |
Universidad del Rosario |
dc.source.instname.spa.fl_str_mv |
instname:Universidad del Rosario |
dc.source.reponame.spa.fl_str_mv |
reponame:Repositorio Institucional EdocUR |
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b1ad6f0f-e1f9-44ed-b605-775349559b03786af36b-dc0a-4533-888a-63107cb20baa43fdf989-3583-4ef9-9c24-bc670860a1ce9fc64f6d-a903-48f1-ac2e-4e55fd2ed9af17a80466-5242-4fc9-9c3e-684a255aa4717bc60ffc-f9d0-4307-af47-11ccfc7310aaf18bc79b-499e-40a1-aa38-574d9c284d6c63ed03ff-ad94-4df8-86b3-45a05e61c6d510117161186002020-05-25T23:56:21Z2020-05-25T23:56:21Z2017Metacyclic trypomastigotes are essential for the understanding of the biology of Trypanosoma cruzi, the agent of Chagas disease. However, obtaining these biological stages in axenic medium is difficult. Techniques based on charge and density of the parasite during different stages have been implemented, without showing a high efficiency in the purification of metacyclic trypomastigotes. So far, there is no protocol implemented where sepharose-DEAE is used as a resin. Therefore, herein we tested its ability to purify metacyclic trypomastigotes in Liver Infusion Triptose (LIT) medium cultures. A simple, easy-to-execute and effective protocol based on ion exchange chromatography on Sepharose-DEAE resin for the purification of T. cruzi trypomastigotes is described. T. cruzi strains from the Discrete Typing Units (DTUs) I and II were used. The strains were harvested in LIT medium at a concentration of 1 × 107 epimastigotes/mL. We calculated the time of trypomastigotes increment (TTI). Based on the data obtained, Ion exchange chromatography was performed with DEAE-sepharose resin. To verify the purity and viability of the trypomastigotes, a culture was carried out in LIT medium with subsequent verification with giemsa staining. To evaluate if the technique affected the infectivity of trypomastigotes, in vitro assays were performed in Vero cells and in vivo in ICR-CD1 mice. The technique allowed the purification of metacyclic trypomastigotes of other stages of T. cruzi in a percentage of 100%, a greater recovery was observed in cultures of 12 days. There were differences regarding the recovery of metacyclic trypomastigotes for both DTUs, being DTU TcI the one that recovered a greater amount of these forms. The technique did not affect parasite infectivity in vitro or/and in vivo. © 2017 Elsevier B.V.application/pdfhttps://doi.org/10.1016/j.mimet.2017.08.0211677012https://repository.urosario.edu.co/handle/10336/22403engElsevier B.V.3227Journal of Microbiological MethodsVol. 142Journal of Microbiological Methods, ISSN:1677012, Vol.142,(2017); pp. 27-32https://www.scopus.com/inward/record.uri?eid=2-s2.0-85028709682&doi=10.1016%2fj.mimet.2017.08.021&partnerID=40&md5=a200932fa0d0a0952e55a5a66f5bf6fbAbierto (Texto Completo)http://purl.org/coar/access_right/c_abf2instname:Universidad del Rosarioreponame:Repositorio Institucional EdocURSepharoseDiethylaminoethyldextranSepharoseAnimal experimentArticleEpimastigoteHost pathogen interactionIn vitro studyIn vivo studyIon exchange chromatographyLife cycleMouseNonhumanParasitosisPriority journalTrypanosoma cruziTrypomastigoteVero cell lineAnimalCell lineChlorocebus aethiopsHost pathogen interactionInstitute for cancer research mouseIon exchange chromatographyIsolation and purificationProceduresTrypanosoma cruziAnimalsCell lineCercopithecus aethiopsDeae-dextranHost-pathogen interactionsMiceSepharoseTrypanosoma cruziVero cellsChromatographyCultureMetacyclic trypomastigotesSepharose-deaeTrypanosoma cruziinbred icrion exchangeChromatographyMicePurification of Trypanosoma cruzi metacyclic trypomastigotes by ion exchange chromatography in sepharose-DEAE, a novel methodology for host-pathogen interaction studiesarticleArtículohttp://purl.org/coar/version/c_970fb48d4fbd8a85http://purl.org/coar/resource_type/c_6501Cruz-Saavedra L.Muñoz M.León C.Patarroyo M.A.Arevalo G.Pavia P.Vallejo G.Carranza J.C.Ramírez, Juan DavidORIGINAL1-s2-0-S0167701217302282-main.pdfapplication/pdf911973https://repository.urosario.edu.co/bitstreams/1949299c-6e2a-4365-9c6e-366ba288bdb3/download78775572b3d6e13f05d21a2073e9518cMD51TEXT1-s2-0-S0167701217302282-main.pdf.txt1-s2-0-S0167701217302282-main.pdf.txtExtracted texttext/plain34488https://repository.urosario.edu.co/bitstreams/e4ac19d7-d888-41ac-90a2-b65fe0581325/download9995c5b5c68a47205acd420a47adc8caMD52THUMBNAIL1-s2-0-S0167701217302282-main.pdf.jpg1-s2-0-S0167701217302282-main.pdf.jpgGenerated Thumbnailimage/jpeg4475https://repository.urosario.edu.co/bitstreams/2c9b826c-9aed-4b37-a479-e5885bc4022d/downloadab639f1f6ee427732588abbde6c30510MD5310336/22403oai:repository.urosario.edu.co:10336/224032022-05-02 07:37:16.49091https://repository.urosario.edu.coRepositorio institucional EdocURedocur@urosario.edu.co |