ArticleVeterinary research2011
The invasion process of bovine erythrocyte by Babesia divergens: knowledge from an in vitro assay.
Article in Veterinary research, 2011. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.
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Who cites it
11 citing papers in PubMed, 19 citations in OpenAlex.
- How to Detect Antibodies AgainstOpen forum infectious diseases · 2024Article
- Experimental Infection of Ticks: An Essential Tool for the Analysis ofPathogens (Basel, Switzerland) · 2021Review
- A framework for signaling throughout the life cycle of Babesia species.Molecular microbiology · 2021Review
- Discovering the Potent Inhibitors AgainstFrontiers in veterinary science · 2021Article
- Kinetics of the invasion and egress processes of Babesia divergens, observed by time-lapse video microscopy.Scientific reports · 2018Article
- The Complexity of Piroplasms Life Cycles.Frontiers in cellular and infection microbiology · 2018Review
- Evaluation of a Major Surface Antigen ofFrontiers in microbiology · 2017Article
- Expression, Purification, and Biological Characterization of Babesia microti Apical Membrane Antigen 1.Infection and immunity · 2015Article
- Morphological and Molecular Descriptors of the Developmental Cycle of Babesia divergens Parasites in Human Erythrocytes.PLoS neglected tropical diseases · 2015Article
- Calcium ions are involved in egress of Babesia bovis merozoites from bovine erythrocytes.The Journal of veterinary medical science · 2015Article
- Babesia divergens and Neospora caninum apical membrane antigen 1 structures reveal selectivity and plasticity in apicomplexan parasite host cell invasion.Protein science : a publication of the Protein Society · 2013Article
Corrections and comments
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Authors and funding
4 authors at 2 institutions in 1 country.
Funding
No grant is acknowledged in the PubMed record.
Abstract
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.
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