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. 2017 Oct 3;12(10):e0185504.
doi: 10.1371/journal.pone.0185504. eCollection 2017.

Secretome analysis of Trypanosoma cruzi by proteomics studies

Affiliations

Secretome analysis of Trypanosoma cruzi by proteomics studies

Jean-Yves Brossas et al. PLoS One. .

Abstract

Background: Chagas disease is a debilitating often fatal disease resulting from infection by the protozoan parasite Trypanosoma cruzi. Chagas disease is endemic in 21 countries of the Americas, and it is an emerging disease in other countries as a result of migration. Given the chronic nature of the infection where intracellular parasites persist for years, the diagnosis of T. cruzi by direct detection is difficult, whereas serologic tests though sensitive may yield false-positive results. The development of new rapid test based on the identification of soluble parasitic antigens in serum would be a real innovation in the diagnosis of Chagas disease.

Methods: To identify new soluble biomarkers that may improve diagnostic tests, we investigated the proteins secreted by T. cruzi using mass spectrometric analyses of conditioned culture media devoid of serum collected during the emergence of trypomastigotes from infected Vero cells. In addition, we compared the secretomes of two T. cruzi strains from DTU Tc VI (VD and CL Brener).

Results: Analysis of the secretome collected during the emergence of trypomastigotes from Vero cells led to the identification of 591 T. cruzi proteins. Three hundred sixty three proteins are common to both strains and most belong to different multigenic super families (i.e. TcS, GP63, MASP, and DGF1). Ultimately we have established a list of 94 secreted proteins, common to both DTU Tc VI strains that do not belong to members of multigene families.

Conclusions: This study provides the first comparative analysis of the secretomes from two distinct T. cruzi strains of DTU TcVI. This led us to identify a subset of common secreted proteins that could potentially serve as serum markers for T. cruzi infection. Their potential could now be evaluated, with specific antibodies using sera collected from patients and residents from endemic regions.

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Conflict of interest statement

Competing Interests: The Bruker Society provided support in the form of salary for M. Chapelle. The cooperation with Bruker society does not alter our adherence to PLOS ONE policies on sharing data and materials.

Figures

Fig 1
Fig 1. Overlap between secretomes of two different T. cruzi strains DTU Tc VI.
A total of 591 proteins of T. cruzi were identified. We note that 78 proteins are specific to the CL Brener strain whereas 151 proteins are specific to VD strain. However, 363 proteins are common to both strains.
Fig 2
Fig 2. Functional categories classification of T. cruzi proteins from CL Brener and VD strains.
Proteins were classified into 15 functional categories using literature and UniprotKB annotation. Y-axis, categories are indicated. X-axis shows the percentage of each category for each strain.
Fig 3
Fig 3. Analyse of trans-sialidase (TcS) proteins found in secretome of 2 strains.
Classification of TcS proteins for each strain into 8 group previously described [22]. Groups IV, V and VI are less than I, II, III groups VII and VIII for two strains. On the x-axis, the number of group is indicated. The Y-axis shows the percentage of each TcS identified in our analyses.

References

    1. WHO | 6 February 2015, vol. 90, 6 (pp. 33–44) [Internet]. WHO. [cited 2017 Jan 4]. Available from: http://www.who.int/wer/2015/wer9006/en/
    1. Steverding D. The history of Chagas disease. Parasit Vectors. 2014. July 10;7:317 doi: 10.1186/1756-3305-7-317 - DOI - PMC - PubMed
    1. Messenger LA, Miles MA. Evidence and importance of genetic exchange among field populations of Trypanosoma cruzi. Acta Trop. 2015. November;151:150–5. doi: 10.1016/j.actatropica.2015.05.007 - DOI - PMC - PubMed
    1. Tibayrenc M, Ayala FJ. The population genetics of Trypanosoma cruzi revisited in the light of the predominant clonal evolution model. Acta Trop. 2015. November;151:156–65. doi: 10.1016/j.actatropica.2015.05.006 - DOI - PMC - PubMed
    1. Zingales B, Andrade SG, Briones MRS, Campbell DA, Chiari E, Fernandes O, et al. A new consensus for Trypanosoma cruzi intraspecific nomenclature: second revision meeting recommends TcI to TcVI. Mem Inst Oswaldo Cruz. 2009. November;104(7):1051–4. - PubMed

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