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Identification and characterization of putative secreted antigens from Babesia microti.


ABSTRACT: The need for improved diagnostic reagents to identify human long-term carriers of the zoonotic parasite Babesia microti is evidenced by numerous reported cases of transfusion-acquired infections. This report describes the identification and initial characterization of 27 clones representing seven genes or gene families that were isolated through serological expression cloning by using a technique that we specifically designed to screen for shed antigens. In this screen, sera from B. microti-infected SCID mice, putatively containing secreted or shed antigens from the parasites, were harvested and used to immunize syngeneic immunocompetent mice (BALB/c). After boosting, the sera from the BALB/c mice, containing antibodies against the immunodominant secreted antigens, were used to screen a B. microti genomic expression library. Analyses of the putative peptides encoded by the novel DNA sequences revealed characteristics indicating that these peptides might be secreted. Initial serological data obtained with recombinant proteins and a patient serum panel demonstrated that several of the proteins could be useful in developing diagnostic tests for detection of B. microti antibodies and antigens in serum.

SUBMITTER: Homer MJ 

PROVIDER: S-EPMC149722 | biostudies-literature | 2003 Feb

REPOSITORIES: biostudies-literature

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Identification and characterization of putative secreted antigens from Babesia microti.

Homer Mary J MJ   Lodes Michael J MJ   Reynolds Lisa D LD   Zhang Yanni Y   Douglass John F JF   McNeill Patricia D PD   Houghton Raymond L RL   Persing David H DH  

Journal of clinical microbiology 20030201 2


The need for improved diagnostic reagents to identify human long-term carriers of the zoonotic parasite Babesia microti is evidenced by numerous reported cases of transfusion-acquired infections. This report describes the identification and initial characterization of 27 clones representing seven genes or gene families that were isolated through serological expression cloning by using a technique that we specifically designed to screen for shed antigens. In this screen, sera from B. microti-infe  ...[more]

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