Cargando…

Dynamics of colistin and tobramycin resistance among Enterobacter cloacae during prolonged use of selective decontamination of the digestive tract

BACKGROUND: A high prevalence of colistin resistance among E. cloacae isolates in two intensive care units (ICU) (of 16 and 6 beds) using selective digestive decontamination (SDD) since 1990 instigated a retrospective and prospective investigation to quantify the role of clonal transmission. SDD is...

Descripción completa

Detalles Bibliográficos
Autores principales: Dautzenberg, M. J. D., Bayjanov, J. R., Leverstein-van Hall, M. A., Muller, A. E., Gelinck, L. B. S., Jansen, C. L., Leyten, E. M. S., Ruys, T., Scharringa, J., van der Starre, R. E., Fluit, A. C., Bonten, M. J. M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964641/
https://www.ncbi.nlm.nih.gov/pubmed/29796252
http://dx.doi.org/10.1186/s13756-018-0356-7
_version_ 1783325217329774592
author Dautzenberg, M. J. D.
Bayjanov, J. R.
Leverstein-van Hall, M. A.
Muller, A. E.
Gelinck, L. B. S.
Jansen, C. L.
Leyten, E. M. S.
Ruys, T.
Scharringa, J.
van der Starre, R. E.
Fluit, A. C.
Bonten, M. J. M.
author_facet Dautzenberg, M. J. D.
Bayjanov, J. R.
Leverstein-van Hall, M. A.
Muller, A. E.
Gelinck, L. B. S.
Jansen, C. L.
Leyten, E. M. S.
Ruys, T.
Scharringa, J.
van der Starre, R. E.
Fluit, A. C.
Bonten, M. J. M.
author_sort Dautzenberg, M. J. D.
collection PubMed
description BACKGROUND: A high prevalence of colistin resistance among E. cloacae isolates in two intensive care units (ICU) (of 16 and 6 beds) using selective digestive decontamination (SDD) since 1990 instigated a retrospective and prospective investigation to quantify the role of clonal transmission. SDD is topical application of colistin and tobramycin and systemic use of cefotaxime during the first days of ICU-admission. METHODS: Multi-resistant E. cloacae (MREb) was defined as ESBL production and/or tobramycin non-susceptibility and/or colistin non-susceptibility. Incidence of acquisition and prevalence of carriage with MREb was determined from microbiological culture results. RESULTS: Colistin-resistant E. cloacae was first detected in November 2009 and carriage was demonstrated in 141 patients until October 2014. Mean incidence of MREb acquisition was 4.61 and 1.86 per 1000 days at risk in ICUs 1 and 2, respectively, and the mean monthly prevalence of MREb in both ICUs was 7.0 and 3.1%, respectively, without a discernible trend in time. Conversion rates from carriage of colistin-susceptible to resistant E. cloacae were 0.20 and 0.13 per 1000 patient days, respectively. Whole genome sequencing of 149 isolates revealed eight clusters, with the number of SNPs of the largest two clusters ranging between 0 and 116 for cluster 1 (n = 49 isolates), and 0 and 27 for cluster 2 (n = 36 isolates), among isolates derived between 2009 and 2014. CONCLUSIONS: This study demonstrates a stable low-level endemicity of MREb in two Dutch ICUs with prolonged use of SDD, which was characterized by the persistent presence of two clusters, suggesting incidental clonal transmission. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13756-018-0356-7) contains supplementary material, which is available to authorized users.
format Online
Article
Text
id pubmed-5964641
institution National Center for Biotechnology Information
language English
publishDate 2018
publisher BioMed Central
record_format MEDLINE/PubMed
spelling pubmed-59646412018-05-24 Dynamics of colistin and tobramycin resistance among Enterobacter cloacae during prolonged use of selective decontamination of the digestive tract Dautzenberg, M. J. D. Bayjanov, J. R. Leverstein-van Hall, M. A. Muller, A. E. Gelinck, L. B. S. Jansen, C. L. Leyten, E. M. S. Ruys, T. Scharringa, J. van der Starre, R. E. Fluit, A. C. Bonten, M. J. M. Antimicrob Resist Infect Control Research BACKGROUND: A high prevalence of colistin resistance among E. cloacae isolates in two intensive care units (ICU) (of 16 and 6 beds) using selective digestive decontamination (SDD) since 1990 instigated a retrospective and prospective investigation to quantify the role of clonal transmission. SDD is topical application of colistin and tobramycin and systemic use of cefotaxime during the first days of ICU-admission. METHODS: Multi-resistant E. cloacae (MREb) was defined as ESBL production and/or tobramycin non-susceptibility and/or colistin non-susceptibility. Incidence of acquisition and prevalence of carriage with MREb was determined from microbiological culture results. RESULTS: Colistin-resistant E. cloacae was first detected in November 2009 and carriage was demonstrated in 141 patients until October 2014. Mean incidence of MREb acquisition was 4.61 and 1.86 per 1000 days at risk in ICUs 1 and 2, respectively, and the mean monthly prevalence of MREb in both ICUs was 7.0 and 3.1%, respectively, without a discernible trend in time. Conversion rates from carriage of colistin-susceptible to resistant E. cloacae were 0.20 and 0.13 per 1000 patient days, respectively. Whole genome sequencing of 149 isolates revealed eight clusters, with the number of SNPs of the largest two clusters ranging between 0 and 116 for cluster 1 (n = 49 isolates), and 0 and 27 for cluster 2 (n = 36 isolates), among isolates derived between 2009 and 2014. CONCLUSIONS: This study demonstrates a stable low-level endemicity of MREb in two Dutch ICUs with prolonged use of SDD, which was characterized by the persistent presence of two clusters, suggesting incidental clonal transmission. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13756-018-0356-7) contains supplementary material, which is available to authorized users. BioMed Central 2018-05-22 /pmc/articles/PMC5964641/ /pubmed/29796252 http://dx.doi.org/10.1186/s13756-018-0356-7 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Dautzenberg, M. J. D.
Bayjanov, J. R.
Leverstein-van Hall, M. A.
Muller, A. E.
Gelinck, L. B. S.
Jansen, C. L.
Leyten, E. M. S.
Ruys, T.
Scharringa, J.
van der Starre, R. E.
Fluit, A. C.
Bonten, M. J. M.
Dynamics of colistin and tobramycin resistance among Enterobacter cloacae during prolonged use of selective decontamination of the digestive tract
title Dynamics of colistin and tobramycin resistance among Enterobacter cloacae during prolonged use of selective decontamination of the digestive tract
title_full Dynamics of colistin and tobramycin resistance among Enterobacter cloacae during prolonged use of selective decontamination of the digestive tract
title_fullStr Dynamics of colistin and tobramycin resistance among Enterobacter cloacae during prolonged use of selective decontamination of the digestive tract
title_full_unstemmed Dynamics of colistin and tobramycin resistance among Enterobacter cloacae during prolonged use of selective decontamination of the digestive tract
title_short Dynamics of colistin and tobramycin resistance among Enterobacter cloacae during prolonged use of selective decontamination of the digestive tract
title_sort dynamics of colistin and tobramycin resistance among enterobacter cloacae during prolonged use of selective decontamination of the digestive tract
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5964641/
https://www.ncbi.nlm.nih.gov/pubmed/29796252
http://dx.doi.org/10.1186/s13756-018-0356-7
work_keys_str_mv AT dautzenbergmjd dynamicsofcolistinandtobramycinresistanceamongenterobactercloacaeduringprolongeduseofselectivedecontaminationofthedigestivetract
AT bayjanovjr dynamicsofcolistinandtobramycinresistanceamongenterobactercloacaeduringprolongeduseofselectivedecontaminationofthedigestivetract
AT leversteinvanhallma dynamicsofcolistinandtobramycinresistanceamongenterobactercloacaeduringprolongeduseofselectivedecontaminationofthedigestivetract
AT mullerae dynamicsofcolistinandtobramycinresistanceamongenterobactercloacaeduringprolongeduseofselectivedecontaminationofthedigestivetract
AT gelincklbs dynamicsofcolistinandtobramycinresistanceamongenterobactercloacaeduringprolongeduseofselectivedecontaminationofthedigestivetract
AT jansencl dynamicsofcolistinandtobramycinresistanceamongenterobactercloacaeduringprolongeduseofselectivedecontaminationofthedigestivetract
AT leytenems dynamicsofcolistinandtobramycinresistanceamongenterobactercloacaeduringprolongeduseofselectivedecontaminationofthedigestivetract
AT ruyst dynamicsofcolistinandtobramycinresistanceamongenterobactercloacaeduringprolongeduseofselectivedecontaminationofthedigestivetract
AT scharringaj dynamicsofcolistinandtobramycinresistanceamongenterobactercloacaeduringprolongeduseofselectivedecontaminationofthedigestivetract
AT vanderstarrere dynamicsofcolistinandtobramycinresistanceamongenterobactercloacaeduringprolongeduseofselectivedecontaminationofthedigestivetract
AT fluitac dynamicsofcolistinandtobramycinresistanceamongenterobactercloacaeduringprolongeduseofselectivedecontaminationofthedigestivetract
AT bontenmjm dynamicsofcolistinandtobramycinresistanceamongenterobactercloacaeduringprolongeduseofselectivedecontaminationofthedigestivetract