April 2009
Volume 50, Issue 13
Free
ARVO Annual Meeting Abstract  |   April 2009
Serotyping Toxoplasma Infections: Correlating Strain Genotype to Severity of Infection
Author Affiliations & Notes
  • C. A. Cordeiro
    Retina, MEEI/HARVARD, Boston, Massachusetts
    Biology, MIT, Cambridge, Massachusetts
  • J. Saeij
    Biology, MIT, Cambridge, Massachusetts
  • F. Orefice
    Uveitis Section, Hospital Sao Geraldo, Hospital das Clinicas da Universidade Federal de Minas Gerais, Belo Horizonte, MG, Brazil
    Division of Uveitis, C.B.C.V. - Centro Brasileiro de Ciencias Visuais, Belo Horizonte, MG, Brazil
  • L. Young
    Retina, MEEI/HARVARD, Boston, Massachusetts
  • Footnotes
    Commercial Relationships  C.A. Cordeiro, None; J. Saeij, None; F. Orefice, None; L. Young, None.
  • Footnotes
    Support  None.
Investigative Ophthalmology & Visual Science April 2009, Vol.50, 6041. doi:
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    • Get Citation

      C. A. Cordeiro, J. Saeij, F. Orefice, L. Young; Serotyping Toxoplasma Infections: Correlating Strain Genotype to Severity of Infection. Invest. Ophthalmol. Vis. Sci. 2009;50(13):6041.

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      © ARVO (1962-2015); The Authors (2016-present)

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Abstract

Purpose: : Toxoplasmosis is one of the most common causes of infectious retinitis. The occurrence of the disease, recurrence, clinical presentation and response to conventional therapy vary significantly among patients. In Europe and North America, the vast majority of infections are caused by type I, II and III strains while in South America other strains are more common. The goal of this study is to devise a non-invasive serological test that can easily and accurately determine the genotype and virulence properties of the Toxoplasma strain.

Methods: : Serological typing is based on the fact that many host antibodies are raised against parasite proteins that are highly polymorphic among distinct strains. We therefore synthesized a cellulose peptide array containing 600 peptides from a large number of polymorphic Toxoplasma proteins. The array was screened serologically to identify those polymorphic peptides that can discriminate between infection with different strain types.

Results: : Initial experiments demonstrated that the peptide array could correctly distinguish type II from type III infections. Furthermore, many new peptides that can discriminate between infection with different strain types were discovered. Interestingly, peptides from proteins known to be associated with higher Toxoplasma virulence could also discriminate sera from mice infected with these virulent strains. We are now testing sera from humans known to be infected with distinct strains to determine the unique serological "fingerprint" of each strain. We will then use this peptide array to correlate Toxoplasma genotype to the severity of toxoplasmic retinitis.

Keywords: uvea • inflammation 
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