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  3. Expression Analysis of the Theileria parva Subtelomere-Encoded Variable Secreted Protein Gene Family
 

Expression Analysis of the Theileria parva Subtelomere-Encoded Variable Secreted Protein Gene Family

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BORIS DOI
10.7892/boris.38327
Date of Publication
2009
Publication Type
Article
Division/Institute

Department of Clinica...

Institut für Parasito...

Institut für Patholog...

Contributor
Schmuckli, Jacqueline
Department of Clinical Research and Veterinary Public Health, Molekulare Pathobiologie
Casanova, Carlo
Schmied, Stéfanie
Affentranger, Sarah
Institut für Pathologie, Entzündungspathologie
Departement für Chemie und Biochemie (DCB)
Parvanova, Iana
Kang'a, Simon
Nene, Vishvanath
Katzer, Frank
McKeever, Declan
Müller, Heinz Joachim
Institut für Parasitologie der Universität Bern
Bishop, Richard
Pain, Arnab
Dobbelaere, Dirk,
Department of Clinical Research and Veterinary Public Health, Molekulare Pathobiologie
Rodrigues, Mauricio Martins
Subject(s)

500 - Science::570 - ...

500 - Science::540 - ...

600 - Technology::630...

Series
PLoS ONE
ISSN or ISBN (if monograph)
1932-6203
Publisher
Public Library of Science
Language
English
Publisher DOI
10.1371/journal.pone.0004839
PubMed ID
19325907
Description
Background
The intracellular protozoan parasite Theileria parva transforms bovine lymphocytes inducing uncontrolled proliferation. Proteins released from the parasite are assumed to contribute to phenotypic changes of the host cell and parasite persistence. With 85 members, genes encoding subtelomeric variable secreted proteins (SVSPs) form the largest gene family in T. parva. The majority of SVSPs contain predicted signal peptides, suggesting secretion into the host cell cytoplasm.

Methodology/Principal Findings
We analysed SVSP expression in T. parva-transformed cell lines established in vitro by infection of T or B lymphocytes with cloned T. parva parasites. Microarray and quantitative real-time PCR analysis revealed mRNA expression for a wide range of SVSP genes. The pattern of mRNA expression was largely defined by the parasite genotype and not by host background or cell type, and found to be relatively stable in vitro over a period of two months. Interestingly, immunofluorescence analysis carried out on cell lines established from a cloned parasite showed that expression of a single SVSP encoded by TP03_0882 is limited to only a small percentage of parasites. Epitope-tagged TP03_0882 expressed in mammalian cells was found to translocate into the nucleus, a process that could be attributed to two different nuclear localisation signals.
Conclusions
Our analysis reveals a complex pattern of Theileria SVSP mRNA expression, which depends on the parasite genotype. Whereas in cell lines established from a cloned parasite transcripts can be found corresponding to a wide range of SVSP genes, only a minority of parasites appear to express a particular SVSP protein. The fact that a number of SVSPs contain functional nuclear localisation signals suggests that proteins released from the parasite could contribute to phenotypic changes of the host cell. This initial characterisation will facilitate future studies on the regulation of SVSP gene expression and the potential biological role of these enigmatic proteins.
Handle
https://boris-portal.unibe.ch/handle/20.500.12422/111513
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FileFile TypeFormatSizeLicensePublisher/Copright statementContent
journal.pone.0004839.pdftextAdobe PDF1.21 MBpublishedOpen
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