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Construction and optimization of a ‘NG Morbidostat’ - An automated continuous-culture device for studying the pathways towards antibiotic resistance in Neisseria gonorrhoeae
To obtain a detailed picture of the dynamics of antibiotic resistance development in Neisseria gonorrhoeae, we built a morbidostat according to the protocol of Toprak et al., adjusted to the specific characteristics required for the growth of N. gonorrhoeae. In this article we describe the adaptatio...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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F1000 Research Limited
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7156024/ https://www.ncbi.nlm.nih.gov/pubmed/32318263 http://dx.doi.org/10.12688/f1000research.18861.2 |
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author | Verhoeven, Els Abdellati, Said Nys, Patrick Laumen, Jolein De Baetselier, Irith Crucitti, Tania Kenyon, Chris |
author_facet | Verhoeven, Els Abdellati, Said Nys, Patrick Laumen, Jolein De Baetselier, Irith Crucitti, Tania Kenyon, Chris |
author_sort | Verhoeven, Els |
collection | PubMed |
description | To obtain a detailed picture of the dynamics of antibiotic resistance development in Neisseria gonorrhoeae, we built a morbidostat according to the protocol of Toprak et al., adjusted to the specific characteristics required for the growth of N. gonorrhoeae. In this article we describe the adaptations, specifications and the difficulties we encountered during the construction and optimization of the NG morbidostat. As a proof of concept, we conducted a morbidostat experiment by increasing concentrations of azithromycin in response to bacterial growth. We started the experiment with two N. gonorrhoeae reference strains WHO-F and WHO-X. These strains were grown in 12 mL GC Broth supplemented with IsoVitaleX™ (1%) and vancomycin, colistin, nystatin, trimethoprim (VCNT) selective supplement for 30 days in a 6% CO (2) environment at 36°C. Samples of the cultures were taken 2-3 times a week and minimal inhibitory concentrations (MICs) of azithromycin were determined using E-test. The initial MICs of WHO-F and WHO-X were 0.125 µg/mL and 0.25 µg/mL, respectively. In less than 30 days, we were able to induce high level azithromycin resistance in N. gonorrhoeae, with a 750 and 1000 fold increase in MIC for WHO-F and WHO-X, respectively. |
format | Online Article Text |
id | pubmed-7156024 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | F1000 Research Limited |
record_format | MEDLINE/PubMed |
spelling | pubmed-71560242020-04-20 Construction and optimization of a ‘NG Morbidostat’ - An automated continuous-culture device for studying the pathways towards antibiotic resistance in Neisseria gonorrhoeae Verhoeven, Els Abdellati, Said Nys, Patrick Laumen, Jolein De Baetselier, Irith Crucitti, Tania Kenyon, Chris F1000Res Method Article To obtain a detailed picture of the dynamics of antibiotic resistance development in Neisseria gonorrhoeae, we built a morbidostat according to the protocol of Toprak et al., adjusted to the specific characteristics required for the growth of N. gonorrhoeae. In this article we describe the adaptations, specifications and the difficulties we encountered during the construction and optimization of the NG morbidostat. As a proof of concept, we conducted a morbidostat experiment by increasing concentrations of azithromycin in response to bacterial growth. We started the experiment with two N. gonorrhoeae reference strains WHO-F and WHO-X. These strains were grown in 12 mL GC Broth supplemented with IsoVitaleX™ (1%) and vancomycin, colistin, nystatin, trimethoprim (VCNT) selective supplement for 30 days in a 6% CO (2) environment at 36°C. Samples of the cultures were taken 2-3 times a week and minimal inhibitory concentrations (MICs) of azithromycin were determined using E-test. The initial MICs of WHO-F and WHO-X were 0.125 µg/mL and 0.25 µg/mL, respectively. In less than 30 days, we were able to induce high level azithromycin resistance in N. gonorrhoeae, with a 750 and 1000 fold increase in MIC for WHO-F and WHO-X, respectively. F1000 Research Limited 2020-01-08 /pmc/articles/PMC7156024/ /pubmed/32318263 http://dx.doi.org/10.12688/f1000research.18861.2 Text en Copyright: © 2020 Verhoeven E et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution Licence, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Method Article Verhoeven, Els Abdellati, Said Nys, Patrick Laumen, Jolein De Baetselier, Irith Crucitti, Tania Kenyon, Chris Construction and optimization of a ‘NG Morbidostat’ - An automated continuous-culture device for studying the pathways towards antibiotic resistance in Neisseria gonorrhoeae |
title | Construction and optimization of a ‘NG Morbidostat’ - An automated continuous-culture device for studying the pathways towards antibiotic resistance in
Neisseria gonorrhoeae
|
title_full | Construction and optimization of a ‘NG Morbidostat’ - An automated continuous-culture device for studying the pathways towards antibiotic resistance in
Neisseria gonorrhoeae
|
title_fullStr | Construction and optimization of a ‘NG Morbidostat’ - An automated continuous-culture device for studying the pathways towards antibiotic resistance in
Neisseria gonorrhoeae
|
title_full_unstemmed | Construction and optimization of a ‘NG Morbidostat’ - An automated continuous-culture device for studying the pathways towards antibiotic resistance in
Neisseria gonorrhoeae
|
title_short | Construction and optimization of a ‘NG Morbidostat’ - An automated continuous-culture device for studying the pathways towards antibiotic resistance in
Neisseria gonorrhoeae
|
title_sort | construction and optimization of a ‘ng morbidostat’ - an automated continuous-culture device for studying the pathways towards antibiotic resistance in
neisseria gonorrhoeae |
topic | Method Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7156024/ https://www.ncbi.nlm.nih.gov/pubmed/32318263 http://dx.doi.org/10.12688/f1000research.18861.2 |
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