Evaluation of a new serological test for the detection of anti-Coxiella and anti-Rickettsia antibodies.

Détails

Ressource 1Télécharger: 5_26432518_Postprint.pdf (839.33 [Ko])
Etat: Serval
Version: Author's accepted manuscript
ID Serval
serval:BIB_2B6BE80D27F1
Type
Article: article d'un périodique ou d'un magazine.
Collection
Publications
Titre
Evaluation of a new serological test for the detection of anti-Coxiella and anti-Rickettsia antibodies.
Périodique
Microbes and Infection
Auteur(s)
Bizzini A., Péter O., Baud D., Edouard S., Meylan P., Greub G.
ISSN
1769-714X (Electronic)
ISSN-L
1286-4579
Statut éditorial
Publié
Date de publication
2015
Peer-reviewed
Oui
Volume
17
Numéro
11-12
Pages
811-816
Langue
anglais
Notes
Publication types: Journal ArticlePublication Status: ppublish
Résumé
Coxiella burnetii and members of the genus Rickettsia are obligate intracellular bacteria. Since cultivation of these organisms requires dedicated techniques, their diagnosis usually relies on serological or molecular biology methods. Immunofluorescence is considered the gold standard to detect antibody-reactivity towards these organisms. Here, we assessed the performance of a new automated epifluorescence immunoassay (InoDiag) to detect IgM and IgG against C. burnetii, Rickettsia typhi and Rickettsia conorii. Samples were tested with the InoDiag assay. A total of 213 sera were tested, of which 63 samples from Q fever, 20 from spotted fever rickettsiosis, 6 from murine typhus and 124 controls. InoDiag results were compared to micro-immunofluorescence. For acute Q fever, the sensitivity of phase 2 IgG was only of 30% with a cutoff of 1 arbitrary unit (AU). In patients with acute Q fever with positive IF IgM, sensitivity reached 83% with the same cutoff. Sensitivity for chronic Q fever was 100% whereas sensitivity for past Q fever was 65%. Sensitivity for spotted Mediterranean fever and murine typhus were 91% and 100%, respectively. Both assays exhibited a good specificity in control groups, ranging from 79% in sera from patients with unrelated diseases or EBV positivity to 100% in sera from healthy patients. In conclusion, the InoDiag assay exhibits an excellent performance for the diagnosis of chronic Q fever but a very low IgG sensitivity for acute Q fever likely due to low reactivity of phase 2 antigens present on the glass slide. This defect is partially compensated by the detection of IgM. Because it exhibits a good negative predictive value, the InoDiag assay is valuable to rule out a chronic Q fever. For the diagnosis of rickettsial diseases, the sensitivity of the InoDiag method is similar to conventional immunofluorescence.
Pubmed
Web of science
Open Access
Oui
Création de la notice
03/01/2016 17:42
Dernière modification de la notice
08/05/2019 16:20
Données d'usage