Abstract

Q fever is a worldwide zoonosis caused by Coxiella burnetii. The disease most frequently manifests clinically as a self-limited febrile illness, as pneumonia (acute Q fever) or as a chronic illness that presents mainly as infective endocarditis. The extreme infectivity of the bacterium results in large outbreaks, and the recent outbreak in the Netherlands underlines its impact on public health. Recent studies on the bacterium have included genome sequencing, the investigation of host-bacterium interactions, the development of cellular and animal models of infection, and the comprehensive analysis of different clinical isolates by whole genome and proteomic approaches. Current approaches for diagnosing Q fever are based on serological methods and PCR techniques, but the diagnosis of early stage disease lacks specificity and sensitivity. Consequently, different platforms have been created to explore Q fever biomarkers. Several studies using a combination of proteomics and recombinant protein screening approaches have been undertaken for the development of diagnostics and vaccines. In this review, we highlight advances in the field of C. burnetii proteomics, focusing mainly on the contribution of these technologies to the development and improvement of Q fever diagnostics.

Highlights

  • Q fever is a worldwide zoonosis caused by Coxiella burnetii

  • Conclusions and future directions The future of diagnostic testing relies upon the develop­ ment of new technologies, and proteomics is rapidly contributing to this area (Table 4)

  • Proteomics is paving the way for serodiagnosis developm­ ent by first selecting seroreactive protein candi­ dates and validating them in recombinant-proteinbased screening systems, such as classic enzyme-linked immuno­sorbent assay (ELISA) and large-scale comprehensive protein arrays

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Summary

8.99 Unknown

9.08 Protein disulfide Membrane MKNRLTALFmAbs, Cb NM II TPE oxidoreductase, LAGTLTAGVAIA unknown role in APSQF pathogenesis. 5.32 GTP-dependent Soluble*† binding of aminoacyltRNA in protein biosynthesis mAbs, TPE Cb NM II, HS, AS (infected/ vaccinated guinea pigs). 6.46 Critical for maintaining integrity of bacterial outer membrane Involved in protein-protein interactions. MRLIKMKIKTLCTPE Cb NM I and II VSSALAALMHS Q-fever (general), LSAPLTWADA AS (immunized guinea pigs) protein microarray

5.61 DNA-dependent Soluble RNA polymerase transcription
6.58 Stress response Soluble*
50 T4SS effector candidates
Limitations
Conclusions and future directions
Findings
61. Murray PR
Full Text
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