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Using MALDI-TOF-MS to test Staphylococcus aureus–infected vitreous

PURPOSE: This study aimed to establish a method for testing Staphylococcus aureus in the vitreous of endophthalmitis with matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF-MS), which is simple, fast, and sensitive. METHODS: S. aureus at different numbers was eit...

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Autores principales: Song, Zhenyu, Liu, Xiuping, Zhu, Minyu, Tan, Yiwei, Wu, Kaili
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Molecular Vision 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509445/
https://www.ncbi.nlm.nih.gov/pubmed/28744092
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author Song, Zhenyu
Liu, Xiuping
Zhu, Minyu
Tan, Yiwei
Wu, Kaili
author_facet Song, Zhenyu
Liu, Xiuping
Zhu, Minyu
Tan, Yiwei
Wu, Kaili
author_sort Song, Zhenyu
collection PubMed
description PURPOSE: This study aimed to establish a method for testing Staphylococcus aureus in the vitreous of endophthalmitis with matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF-MS), which is simple, fast, and sensitive. METHODS: S. aureus at different numbers was either mixed with homogenized vitreous or inoculated in porcine eyes for culturing, followed by homogenization. The homogenized vitreous samples, with or without centrifugation, were stained with Gram and Coomassie Blue (CBB) dyes and cultured with blood agar. The pellet of the vitreous mixture was analyzed with MALDI-TOF-MS. RESULTS: The minimum detectable levels of S. aureus in H(2)O and in the pellet of homogenized vitreous were 9.0 × 10(3) (positive rate, 22.2%) and 1.0 × 10(4) CFU/μl (positive rate, 11.1%), respectively. In the vitreous samples inoculated with S. aureus and cultured for 12 h, the number of S. aureus increased in a dose-dependent manner to the number of bacteria in the inoculate. In the supernatant of the homogenized vitreous, there were traces of bacteria identified with Gram staining. On the blood agar plates, the supernatant grew a few colonies, while the pellet grew intensive colonies. The vitreous fragments that were stained with CBB were displayed in the supernatants, in small numbers, and in the pellets. When the inoculated number was 1.0 × 10(4) CFU/μl or higher, the bacteria in the vitreous pellets could be identified in all samples (100%, n = 9). However, bacteria could be detected in only two out of nine spots of pellets (22.2%) if the number of inoculated S. aureus was 1.0 × 10(3) CFU/μl. CONCLUSIONS: A method for testing S. aureus directly from vitreous samples of endophthalmitis by the combination of easy extraction methods and a MALDI-TOF- MS assay was provided. This rapid identification method is easily adaptable for use in clinical routine and can help reduce the delay in diagnosis, allowing for earlier therapeutic intervention in patients.
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spelling pubmed-55094452017-07-25 Using MALDI-TOF-MS to test Staphylococcus aureus–infected vitreous Song, Zhenyu Liu, Xiuping Zhu, Minyu Tan, Yiwei Wu, Kaili Mol Vis Research Article PURPOSE: This study aimed to establish a method for testing Staphylococcus aureus in the vitreous of endophthalmitis with matrix-assisted laser desorption/ionization time of flight mass spectrometry (MALDI-TOF-MS), which is simple, fast, and sensitive. METHODS: S. aureus at different numbers was either mixed with homogenized vitreous or inoculated in porcine eyes for culturing, followed by homogenization. The homogenized vitreous samples, with or without centrifugation, were stained with Gram and Coomassie Blue (CBB) dyes and cultured with blood agar. The pellet of the vitreous mixture was analyzed with MALDI-TOF-MS. RESULTS: The minimum detectable levels of S. aureus in H(2)O and in the pellet of homogenized vitreous were 9.0 × 10(3) (positive rate, 22.2%) and 1.0 × 10(4) CFU/μl (positive rate, 11.1%), respectively. In the vitreous samples inoculated with S. aureus and cultured for 12 h, the number of S. aureus increased in a dose-dependent manner to the number of bacteria in the inoculate. In the supernatant of the homogenized vitreous, there were traces of bacteria identified with Gram staining. On the blood agar plates, the supernatant grew a few colonies, while the pellet grew intensive colonies. The vitreous fragments that were stained with CBB were displayed in the supernatants, in small numbers, and in the pellets. When the inoculated number was 1.0 × 10(4) CFU/μl or higher, the bacteria in the vitreous pellets could be identified in all samples (100%, n = 9). However, bacteria could be detected in only two out of nine spots of pellets (22.2%) if the number of inoculated S. aureus was 1.0 × 10(3) CFU/μl. CONCLUSIONS: A method for testing S. aureus directly from vitreous samples of endophthalmitis by the combination of easy extraction methods and a MALDI-TOF- MS assay was provided. This rapid identification method is easily adaptable for use in clinical routine and can help reduce the delay in diagnosis, allowing for earlier therapeutic intervention in patients. Molecular Vision 2017-07-07 /pmc/articles/PMC5509445/ /pubmed/28744092 Text en Copyright © 2017 Molecular Vision. http://creativecommons.org/licenses/by-nc-nd/3.0/ 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 work is properly cited, used for non-commercial purposes, and is not altered or transformed.
spellingShingle Research Article
Song, Zhenyu
Liu, Xiuping
Zhu, Minyu
Tan, Yiwei
Wu, Kaili
Using MALDI-TOF-MS to test Staphylococcus aureus–infected vitreous
title Using MALDI-TOF-MS to test Staphylococcus aureus–infected vitreous
title_full Using MALDI-TOF-MS to test Staphylococcus aureus–infected vitreous
title_fullStr Using MALDI-TOF-MS to test Staphylococcus aureus–infected vitreous
title_full_unstemmed Using MALDI-TOF-MS to test Staphylococcus aureus–infected vitreous
title_short Using MALDI-TOF-MS to test Staphylococcus aureus–infected vitreous
title_sort using maldi-tof-ms to test staphylococcus aureus–infected vitreous
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5509445/
https://www.ncbi.nlm.nih.gov/pubmed/28744092
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