Performance of the Cepheid Methicillin-Resistant Staphylococcus aureus/S. aureus Skin and Soft Tissue Infection PCR Assay on Respiratory Samples from Mechanically Ventilated Patients for S. aureus Screening during the Phase 2 Double-Blind SAATELLITE Study
We investigated the performance of the Xpert methicillin-resistant Staphylococcus aureus (MRSA)/ S. aureus skin and soft tissue (SSTI) quantitative PCR (qPCR) assay in SAATELLITE, a multicenter, double-blind, phase 2 study of suvratoxumab, a monoclonal antibody (MAb) targeting S. aureus alpha-toxin,...
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Published in | Journal of clinical microbiology Vol. 60; no. 7; p. e0034722 |
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Main Authors | , , , , , , , , , , , , , , , , , , , , , , , , , , , |
Format | Journal Article |
Language | English |
Published |
United States
American Society for Microbiology
20.07.2022
|
Subjects | |
Online Access | Get full text |
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Summary: | We investigated the performance of the Xpert methicillin-resistant
Staphylococcus aureus
(MRSA)/
S. aureus
skin and soft tissue (SSTI) quantitative PCR (qPCR) assay in SAATELLITE, a multicenter, double-blind, phase 2 study of suvratoxumab, a monoclonal antibody (MAb) targeting
S. aureus
alpha-toxin, for reducing the incidence of
S. aureus
pneumonia.
We investigated the performance of the Xpert methicillin-resistant
Staphylococcus aureus
(MRSA)/
S. aureus
skin and soft tissue (SSTI) quantitative PCR (qPCR) assay in SAATELLITE, a multicenter, double-blind, phase 2 study of suvratoxumab, a monoclonal antibody (MAb) targeting
S. aureus
alpha-toxin, for reducing the incidence of
S. aureus
pneumonia. The assay was used to detect methicillin-susceptible
S. aureus
(MSSA) and MRSA in lower respiratory tract (LRT) samples from mechanically ventilated patients. LRT culture results were compared with
S. aureus
protein A (
spa
) gene cycle threshold (
C
T
) values. Receiver operating characteristic (ROC) and Youden index were used to determine the
C
T
cutoff for best separation of culture-
S. aureus
-negative and
S. aureus
-positive patients. Of 720 screened subjects, 299 (41.5%) were
S. aureus
positive by qPCR, of whom 209 had culture data: 162 (77.5%) were
S. aureus
positive and 47 (22.5%) were
S. aureus
negative. Culture results were negatively affected by antibiotic use and cross-laboratory variability. An inverse linear correlation was observed between
C
T
values and quantitative
S. aureus
culture results. A
spa C
T
value of 29 (≈2 × 10
3
CFU/mL) served as the best cutoff for separation between culture-negative and culture-positive samples. The associated area under the ROC curve was 83.8% (95% confidence interval [CI], 78 to 90%). Suvratoxumab provided greater reduction in
S. aureus
pneumonia or death than placebo in subjects with low
S. aureus
load (
C
T
≥ 29; relative risk reduction [RRR], 50.0%; 90% CI, 2.7 to 74.4%) versus the total study population (RRR, 25.2%; 90% CI, −4.3 to 46.4%). The qPCR assay was easy to perform, sensitive, and standardized and provided better sensitivity than conventional culture for
S. aureus
detection. Quantitative PCR
C
T
output correlated with suvratoxumab efficacy in reducing
S. aureus
pneumonia incidence or death in
S. aureus
-colonized, mechanically ventilated patients. |
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Bibliography: | ObjectType-Article-2 SourceType-Scholarly Journals-1 ObjectType-Feature-1 content type line 23 ObjectType-Undefined-3 Present address: Li Yu, AveXis, La Jolla, California, USA. Present address: Drieke Vandamme, Aridis Pharmaceuticals, Los Gatos, California, USA. Alexey Ruzin and Olivier Barraud contributed equally to this article. The order was determined by the corresponding author after negotiation. The authors declare a conflict of interest. A.R., L.Y., S.O.A., K.S., P.R., S.C., T. Bellamy, B.R.S., M.M., H.S.J., and M.T.E. are or were employees of AstraZeneca at the time of this study, with stock ownership and/or stock options or interests in the company. B.F. reports personal fees (expert panel, consultancy, steering, and/or advisory board or committee) outside the submitted work from bioMérieux, Aridis, Ashai-Kasai, Polyphor, AM-Pharma, Ferring, Inotrem, Transgene, and Enlivex. D.V. reports grants from IMI. J.T. reports grants from AstraZeneca. O.B. reports nonfinancial and personal fees from MSD France, Roche Diagnostics France, Sanofi Aventis France, bioMérieux, Correvio, Viatris, and Pfizer. P.-F.D. reports institutional funding and/or grants from Abionic, Acombioxin, Adrenomed, Aridis, AtoxBio, Combioxin, Faron, Genentech, GSK, Kenta, MedSpace, Merck, RevImmune, Sphingotec, and Tigenix. A.C.H.P., C.B., C.L., H.G., J.P., J.V., L.V., M.S.-G., P.E., P.-F.L., T. Boulain, and V.H. have nothing to disclose. Present address: Hasan S. Jafri, Aridis Pharmaceuticals, Los Gatos, California, USA. Present address: S. Omar Ali, Viela Bio, Gaithersburg, Maryland, USA. Present address: Susan Colbert, Aridis Pharmaceuticals, Los Gatos, California, USA. Present address: Terramika Bellamy, Aridis Pharmaceuticals, Los Gatos, California, USA. |
ISSN: | 0095-1137 1098-660X 1098-660X |
DOI: | 10.1128/jcm.00347-22 |