Evaluation of the Xpert Carba-R assay for quantifying carbapenemase-producing bacterial load in stool samples
Background: The spread of Carbapenemase-producing Organisms (CPO) remains a major threat globally. Within clinical settings, the existing method of determining gene load involves traditional culture to determine bacterial load and polymerase-chain-reaction-based Xpert Carba-R Assay to determine carb...
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sg-ntu-dr.10356-1812392024-11-24T15:39:25Z Evaluation of the Xpert Carba-R assay for quantifying carbapenemase-producing bacterial load in stool samples Chua, Jie Yin Lim, Ze Qin Loy, Dennis Song Qi Koh, Vanessa Thevasagayam, Natascha May Huan, Xiaowei Linn, Kyaw Zaw Marimuthu, Kalisvar Ng, Oon Tek Lee Kong Chian School of Medicine (LKCMedicine) National Centre for Infectious Diseases, Singapore Tan Tock Seng Hospital Medicine, Health and Life Sciences Escherichia coli Feces Background: The spread of Carbapenemase-producing Organisms (CPO) remains a major threat globally. Within clinical settings, the existing method of determining gene load involves traditional culture to determine bacterial load and polymerase-chain-reaction-based Xpert Carba-R Assay to determine carbapenemase gene type. However, there is a need for a fast and accurate method of quantifying CPO colonisation to study the risk of persistent CPO carriage. Objective: This study evaluated the accuracy of Xpert Carba-R Ct value in estimating carbapenamase producing bacterial loads in stool samples. Methods: Stool samples were obtained from an ongoing study investigating the household transmission of CPO in Singapore. Stool samples lacking carbapenemase producing organisms were spiked with organism carrying a single carbapenemase gene (blaKPC, blaNDM, blaVIM, blaOXA-48(-like) or blaIMP-1) and serially diluted before being subjected to Xpert Carba-R assay and traditional culture. Standard curves with regression lines showing correlation between Ct values and plate counts were generated. The standard curves were validated with stool samples collected from patients. Results: The limit of detection of blaNDM, blaKPC, and blaOXA-48 was approximately 103 cfu/mL, while that of blaIMP-1 and blaVIM was approximately 104 cfu/mL. Validation of the blaNDM and blaOXA-48 curves revealed average delta values of 0.56 log(cfu/mL) (95% CI 0.24–0.88) and 0.80 log(cfu/mL) (95% CI 0.53–1.07), respectively. Conclusions: Our validation data for stool positive for blaNDM and blaOXA-48-type suggests that bacterial loads can be estimated within a reasonable range of error. Ministry of Health (MOH) National Medical Research Council (NMRC) Published version This study was financially supported by the Singapore Ministry of Health’s National Medical Research Council (NMRC; https://www.nmrc.gov. sg/) under its NMRC Center Grant Programme: Collaborative Solutions Targeting Antimicrobial Resistance Threats in Health Systems (CoSTARHS) in the form of grants (CG21APR2005 and CoSTAR-HS/ARGSeedFund/2022/04) received by OTN. This study was also financially supported by the Singapore Ministry of Health’s National Medical Research Council in the form of an NMRC Clinician Scientist Award (MOH-000276) received by OTN. This study was also financially supported by the Singapore Ministry of Health’s National Medical Research Council in the form of a NMRC Clinician Scientist Individual Research Grant (MOH-CIRG18nov-0006) received by KM. No additional external funding was received for this study. The funder had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript. 2024-11-19T01:39:16Z 2024-11-19T01:39:16Z 2024 Journal Article Chua, J. Y., Lim, Z. Q., Loy, D. S. Q., Koh, V., Thevasagayam, N. M., Huan, X., Linn, K. Z., Marimuthu, K. & Ng, O. T. (2024). Evaluation of the Xpert Carba-R assay for quantifying carbapenemase-producing bacterial load in stool samples. PLoS ONE, 19(8), e0309089-. https://dx.doi.org/10.1371/journal.pone.0309089 1932-6203 https://hdl.handle.net/10356/181239 10.1371/journal.pone.0309089 39196974 2-s2.0-85202663835 8 19 e0309089 en CG21APR2005 CoSTAR-HS/ARGSeedFund/2022/04 MOH-000276 PLoS ONE © 2024 Chua et al. This is an open access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. application/pdf |
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Medicine, Health and Life Sciences Escherichia coli Feces Chua, Jie Yin Lim, Ze Qin Loy, Dennis Song Qi Koh, Vanessa Thevasagayam, Natascha May Huan, Xiaowei Linn, Kyaw Zaw Marimuthu, Kalisvar Ng, Oon Tek Evaluation of the Xpert Carba-R assay for quantifying carbapenemase-producing bacterial load in stool samples |
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Background: The spread of Carbapenemase-producing Organisms (CPO) remains a major threat globally. Within clinical settings, the existing method of determining gene load involves traditional culture to determine bacterial load and polymerase-chain-reaction-based Xpert Carba-R Assay to determine carbapenemase gene type. However, there is a need for a fast and accurate method of quantifying CPO colonisation to study the risk of persistent CPO carriage. Objective: This study evaluated the accuracy of Xpert Carba-R Ct value in estimating carbapenamase producing bacterial loads in stool samples. Methods: Stool samples were obtained from an ongoing study investigating the household transmission of CPO in Singapore. Stool samples lacking carbapenemase producing organisms were spiked with organism carrying a single carbapenemase gene (blaKPC, blaNDM, blaVIM, blaOXA-48(-like) or blaIMP-1) and serially diluted before being subjected to Xpert Carba-R assay and traditional culture. Standard curves with regression lines showing correlation between Ct values and plate counts were generated. The standard curves were validated with stool samples collected from patients. Results: The limit of detection of blaNDM, blaKPC, and blaOXA-48 was approximately 103 cfu/mL, while that of blaIMP-1 and blaVIM was approximately 104 cfu/mL. Validation of the blaNDM and blaOXA-48 curves revealed average delta values of 0.56 log(cfu/mL) (95% CI 0.24–0.88) and 0.80 log(cfu/mL) (95% CI 0.53–1.07), respectively. Conclusions: Our validation data for stool positive for blaNDM and blaOXA-48-type suggests that bacterial loads can be estimated within a reasonable range of error. |
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Lee Kong Chian School of Medicine (LKCMedicine) |
author_facet |
Lee Kong Chian School of Medicine (LKCMedicine) Chua, Jie Yin Lim, Ze Qin Loy, Dennis Song Qi Koh, Vanessa Thevasagayam, Natascha May Huan, Xiaowei Linn, Kyaw Zaw Marimuthu, Kalisvar Ng, Oon Tek |
format |
Article |
author |
Chua, Jie Yin Lim, Ze Qin Loy, Dennis Song Qi Koh, Vanessa Thevasagayam, Natascha May Huan, Xiaowei Linn, Kyaw Zaw Marimuthu, Kalisvar Ng, Oon Tek |
author_sort |
Chua, Jie Yin |
title |
Evaluation of the Xpert Carba-R assay for quantifying carbapenemase-producing bacterial load in stool samples |
title_short |
Evaluation of the Xpert Carba-R assay for quantifying carbapenemase-producing bacterial load in stool samples |
title_full |
Evaluation of the Xpert Carba-R assay for quantifying carbapenemase-producing bacterial load in stool samples |
title_fullStr |
Evaluation of the Xpert Carba-R assay for quantifying carbapenemase-producing bacterial load in stool samples |
title_full_unstemmed |
Evaluation of the Xpert Carba-R assay for quantifying carbapenemase-producing bacterial load in stool samples |
title_sort |
evaluation of the xpert carba-r assay for quantifying carbapenemase-producing bacterial load in stool samples |
publishDate |
2024 |
url |
https://hdl.handle.net/10356/181239 |
_version_ |
1816858938374619136 |