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...

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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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repository_id_str
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
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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
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spelling 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