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- Publisher Website: 10.3390/microorganisms11010128
- Scopus: eid_2-s2.0-85146812513
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Article: Evaluation of a Lateral Flow Immunoassay for Rapid Detection of CTX-M Producers from Blood Cultures
Title | Evaluation of a Lateral Flow Immunoassay for Rapid Detection of CTX-M Producers from Blood Cultures |
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Authors | |
Keywords | bacteremia beta-lactamases blood culture blood-stream infection cefotaxime resistance CTX-M Enterobacteriaceae extended-spectrum beta-lactamases immunochromatographic assay |
Issue Date | 4-Jan-2023 |
Publisher | MDPI |
Citation | Microorganisms, 2023, v. 11, n. 1 How to Cite? |
Abstract | Bacteremia caused by extended-spectrum β-lactamases-producing Enterobacterales has increased rapidly and is mainly attributed to CTX-M enzymes. This study aimed to evaluate the NG-Test® CTX-M MULTI lateral flow assay (CTX-M LFA) for rapid detection of CTX-M producers in blood cultures (BCs) positive for Gram-negative bacilli in spiked and clinical BCs. Retrospective testing was performed on BC bottles spiked with a collection of well-characterized Enterobacterales isolates producing CTX-M (n = 15) and CTX-M-like (n = 27) β-lactamases. Prospective testing of clinical, non-duplicate BCs (n = 350) was performed in two hospital microbiology laboratories from April 2021 to March 2022 following detection of Gram-negative bacilli by microscopic examination. Results were compared against molecular testing as the reference. In the spiked BCs, the CTX-M LFA correctly detected all CTX-M producers including 5 isolates with hybrid CTX-M variants. However, false-positive results were observed for several CTX-M-like β-lactamases, including OXY-1-3, OXY-2-8, OXY-5-3, FONA-8, -9, -10, 11, 13 and SFO-1. In clinical BCs, the CTX-M LFA showed 100% (95% CI, 96.0–100%) sensitivity and 99.6% (97.9–100%) specificity. In conclusion, this study showed that rapid detection of CTX-M producers in BC broths can be reliably achieved using the CTX-M LFA, thus providing an opportunity for early optimization of antibiotics. |
Persistent Identifier | http://hdl.handle.net/10722/347679 |
DC Field | Value | Language |
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dc.contributor.author | Fang, Hanshu | - |
dc.contributor.author | Lee, Chung Ho | - |
dc.contributor.author | Cao, Huiluo | - |
dc.contributor.author | Jiang, Shuo | - |
dc.contributor.author | So, Simon Yung Chun | - |
dc.contributor.author | Tse, Cindy Wing Sze | - |
dc.contributor.author | Cheng, Vincent Chi Chung | - |
dc.contributor.author | Ho, Pak Leung | - |
dc.date.accessioned | 2024-09-27T00:30:18Z | - |
dc.date.available | 2024-09-27T00:30:18Z | - |
dc.date.issued | 2023-01-04 | - |
dc.identifier.citation | Microorganisms, 2023, v. 11, n. 1 | - |
dc.identifier.uri | http://hdl.handle.net/10722/347679 | - |
dc.description.abstract | Bacteremia caused by extended-spectrum β-lactamases-producing Enterobacterales has increased rapidly and is mainly attributed to CTX-M enzymes. This study aimed to evaluate the NG-Test® CTX-M MULTI lateral flow assay (CTX-M LFA) for rapid detection of CTX-M producers in blood cultures (BCs) positive for Gram-negative bacilli in spiked and clinical BCs. Retrospective testing was performed on BC bottles spiked with a collection of well-characterized Enterobacterales isolates producing CTX-M (n = 15) and CTX-M-like (n = 27) β-lactamases. Prospective testing of clinical, non-duplicate BCs (n = 350) was performed in two hospital microbiology laboratories from April 2021 to March 2022 following detection of Gram-negative bacilli by microscopic examination. Results were compared against molecular testing as the reference. In the spiked BCs, the CTX-M LFA correctly detected all CTX-M producers including 5 isolates with hybrid CTX-M variants. However, false-positive results were observed for several CTX-M-like β-lactamases, including OXY-1-3, OXY-2-8, OXY-5-3, FONA-8, -9, -10, 11, 13 and SFO-1. In clinical BCs, the CTX-M LFA showed 100% (95% CI, 96.0–100%) sensitivity and 99.6% (97.9–100%) specificity. In conclusion, this study showed that rapid detection of CTX-M producers in BC broths can be reliably achieved using the CTX-M LFA, thus providing an opportunity for early optimization of antibiotics. | - |
dc.language | eng | - |
dc.publisher | MDPI | - |
dc.relation.ispartof | Microorganisms | - |
dc.rights | This work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License. | - |
dc.subject | bacteremia | - |
dc.subject | beta-lactamases | - |
dc.subject | blood culture | - |
dc.subject | blood-stream infection | - |
dc.subject | cefotaxime resistance | - |
dc.subject | CTX-M | - |
dc.subject | Enterobacteriaceae | - |
dc.subject | extended-spectrum beta-lactamases | - |
dc.subject | immunochromatographic assay | - |
dc.title | Evaluation of a Lateral Flow Immunoassay for Rapid Detection of CTX-M Producers from Blood Cultures | - |
dc.type | Article | - |
dc.identifier.doi | 10.3390/microorganisms11010128 | - |
dc.identifier.scopus | eid_2-s2.0-85146812513 | - |
dc.identifier.volume | 11 | - |
dc.identifier.issue | 1 | - |
dc.identifier.eissn | 2076-2607 | - |
dc.identifier.issnl | 2076-2607 | - |