2009
DOI: 10.1128/cvi.00096-09
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Towards a New Reference Test for Surra in Camels

Abstract: Current serological diagnosis of Trypanosoma evansi infection in camels is

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Cited by 34 publications
(19 citation statements)
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“…This rare trypanosome type was isolated for the first time from camels in Kenya and may also occur in Sudan and Ethiopia (Borst et al, 1987;Hagos et al, 2009;Salim et al, 2011). Therefore, it might be of interest (Müller et al, 1992;Nguyen et al, 2012;Rogé et al, 2013;Tran et al, 2009). Of particular interest is GM6 of which a 4 repeat fragment derived from T. evansi (TeGM6-4r) has been expressed in E. coli and incorporated in a lateral flow ICT (Nguyen et al, 2015).…”
Section: Discussionmentioning
confidence: 99%
“…This rare trypanosome type was isolated for the first time from camels in Kenya and may also occur in Sudan and Ethiopia (Borst et al, 1987;Hagos et al, 2009;Salim et al, 2011). Therefore, it might be of interest (Müller et al, 1992;Nguyen et al, 2012;Rogé et al, 2013;Tran et al, 2009). Of particular interest is GM6 of which a 4 repeat fragment derived from T. evansi (TeGM6-4r) has been expressed in E. coli and incorporated in a lateral flow ICT (Nguyen et al, 2015).…”
Section: Discussionmentioning
confidence: 99%
“…They include the ISG family as well as various intracellular proteins such as the trypanosome-derived oligopeptidase B, trypanothion and cystein proteases. In this context, it was recently shown that ISG75 can be used as a diagnostic marker in an experimental setting, albeit the assays performed relied on ELISA rather than on a card agglutination format, and was so far only validated for the detection of animal trypanosomiasis [87].…”
Section: Review Magez and Radwanskamentioning
confidence: 99%
“…Nevertheless, it failed to detect T. evansi type B which lacks or does not express RoTat1.2 (Ngaira et al 2005;Tran et al 2009). Another promising recombinant protein is the invariant surface glycoprotein 75 (ISG75) presenting in approximately 5×10 4 molecules on trypanosome cell surface (Tran et al 2009). However, limited number of available antigen candidates drives an urgent need of identification for novel antigens to improve serological diagnostics of surra.…”
Section: Introductionmentioning
confidence: 99%
“…However, preparation of the lysate antigen requires in vitro (cell culture) or in vivo (experimental animals) systems to produce sufficient number of the parasite, and procedures for antigen preparation has not been completely standardized (Reid and Copeman 2002;OIE 2008;Tran et al 2009). Therefore, development of antibody detection ELISA for surra using defined antigens, such as recombinant proteins, has long been needed.…”
Section: Introductionmentioning
confidence: 99%