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The invasion process of bovine erythrocyte by Babesia divergens: knowledge from an in vitro assay
Babesia divergens is a tick-transmitted apicomplexan parasite for which asexual multiplication in its vertebrate hosts is restricted to erythrocytes. Current knowledge of invasion of these target cells is limited. An efficient in vitro invasion assay was set up to gain access to this information. Pa...
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2011
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117698/ https://www.ncbi.nlm.nih.gov/pubmed/21569363 http://dx.doi.org/10.1186/1297-9716-42-62 |
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author | Sun, Yi Moreau, Emmanuelle Chauvin, Alain Malandrin, Laurence |
author_facet | Sun, Yi Moreau, Emmanuelle Chauvin, Alain Malandrin, Laurence |
author_sort | Sun, Yi |
collection | PubMed |
description | Babesia divergens is a tick-transmitted apicomplexan parasite for which asexual multiplication in its vertebrate hosts is restricted to erythrocytes. Current knowledge of invasion of these target cells is limited. An efficient in vitro invasion assay was set up to gain access to this information. Parasites prepared from infected RBC, lysed by electroporation, and mixed with bovine RBC in a selected synthetic medium (RPMI 1640 supplemented with calcium) were able to establish subsequent cultures with parasitemia ranging from 6 to 14%. Free parasites remaining in the invasion medium could be eliminated by Percoll gradient and culture could be pursued with the freshly invaded erythrocytes. In this way, the invasion time window could be shortened to obtain a synchronised start of the culture or to study the kinetics of invasion. With this assay we demonstrate that 1) erythrocyte invasion by B. divergens is a rapid process since 70% of the invasion-competent parasites invaded the RBC in less than 45 s; 2) all invasion-competent parasites achieved invasion within 10 min of contact; 3) one erythrocyte could be invaded concomitantly by two merozoites; 4) despite a synchronous start, the parasite population evolved heterogeneously resulting in a progressive loss of synchronisation. Western blot analysis of proteins collected from invasion medium were performed with sera from animals experimentally infected with B. divergens and highlighted several proteins. The dose-dependent, inhibitory effects of these sera on B. divergens invasion suggest that these proteins might be involved in the invasion process. Further investigations are required for their characterisation. |
format | Online Article Text |
id | pubmed-3117698 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2011 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-31176982011-06-18 The invasion process of bovine erythrocyte by Babesia divergens: knowledge from an in vitro assay Sun, Yi Moreau, Emmanuelle Chauvin, Alain Malandrin, Laurence Vet Res Research Babesia divergens is a tick-transmitted apicomplexan parasite for which asexual multiplication in its vertebrate hosts is restricted to erythrocytes. Current knowledge of invasion of these target cells is limited. An efficient in vitro invasion assay was set up to gain access to this information. Parasites prepared from infected RBC, lysed by electroporation, and mixed with bovine RBC in a selected synthetic medium (RPMI 1640 supplemented with calcium) were able to establish subsequent cultures with parasitemia ranging from 6 to 14%. Free parasites remaining in the invasion medium could be eliminated by Percoll gradient and culture could be pursued with the freshly invaded erythrocytes. In this way, the invasion time window could be shortened to obtain a synchronised start of the culture or to study the kinetics of invasion. With this assay we demonstrate that 1) erythrocyte invasion by B. divergens is a rapid process since 70% of the invasion-competent parasites invaded the RBC in less than 45 s; 2) all invasion-competent parasites achieved invasion within 10 min of contact; 3) one erythrocyte could be invaded concomitantly by two merozoites; 4) despite a synchronous start, the parasite population evolved heterogeneously resulting in a progressive loss of synchronisation. Western blot analysis of proteins collected from invasion medium were performed with sera from animals experimentally infected with B. divergens and highlighted several proteins. The dose-dependent, inhibitory effects of these sera on B. divergens invasion suggest that these proteins might be involved in the invasion process. Further investigations are required for their characterisation. BioMed Central 2011 2011-05-11 /pmc/articles/PMC3117698/ /pubmed/21569363 http://dx.doi.org/10.1186/1297-9716-42-62 Text en Copyright ©2011 Sun et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Research Sun, Yi Moreau, Emmanuelle Chauvin, Alain Malandrin, Laurence The invasion process of bovine erythrocyte by Babesia divergens: knowledge from an in vitro assay |
title | The invasion process of bovine erythrocyte by Babesia divergens: knowledge from an in vitro assay |
title_full | The invasion process of bovine erythrocyte by Babesia divergens: knowledge from an in vitro assay |
title_fullStr | The invasion process of bovine erythrocyte by Babesia divergens: knowledge from an in vitro assay |
title_full_unstemmed | The invasion process of bovine erythrocyte by Babesia divergens: knowledge from an in vitro assay |
title_short | The invasion process of bovine erythrocyte by Babesia divergens: knowledge from an in vitro assay |
title_sort | invasion process of bovine erythrocyte by babesia divergens: knowledge from an in vitro assay |
topic | Research |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3117698/ https://www.ncbi.nlm.nih.gov/pubmed/21569363 http://dx.doi.org/10.1186/1297-9716-42-62 |
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