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Antimicrobial resistance in Antarctica: is it still a pristine environment?

Although the rapid spread of antimicrobial resistance (AMR), particularly in relation to clinical settings, is causing concern in many regions of the globe, remote, extreme environments, such as Antarctica, are thought to be relatively free from the negative impact of human activities. In fact, Anta...

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Autores principales: Hwengwere, K., Paramel Nair, H., Hughes, K. A., Peck, L. S., Clark, M. S., Walker, C. A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072757/
https://www.ncbi.nlm.nih.gov/pubmed/35524279
http://dx.doi.org/10.1186/s40168-022-01250-x
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author Hwengwere, K.
Paramel Nair, H.
Hughes, K. A.
Peck, L. S.
Clark, M. S.
Walker, C. A.
author_facet Hwengwere, K.
Paramel Nair, H.
Hughes, K. A.
Peck, L. S.
Clark, M. S.
Walker, C. A.
author_sort Hwengwere, K.
collection PubMed
description Although the rapid spread of antimicrobial resistance (AMR), particularly in relation to clinical settings, is causing concern in many regions of the globe, remote, extreme environments, such as Antarctica, are thought to be relatively free from the negative impact of human activities. In fact, Antarctica is often perceived as the last pristine continent on Earth. Such remote regions, which are assumed to have very low levels of AMR due to limited human activity, represent potential model environments to understand the mechanisms and interactions underpinning the early stages of evolution, de novo development, acquisition and transmission of AMR. Antarctica, with its defined zones of human colonisation (centred around scientific research stations) and large populations of migratory birds and animals, also has great potential with regard to mapping and understanding the spread of early-stage zoonotic interactions. However, to date, studies of AMR in Antarctica are limited. Here, we survey the current literature focussing on the following: i).. Dissection of human-introduced AMR versus naturally occurring AMR, based on the premise that multiple drug resistance and resistance to synthetic antibiotics not yet found in nature are the results of human contamination; ii).. The potential role of endemic wildlife in AMR spread. There is clear evidence for greater concentrations of AMR around research stations, and although data show reverse zoonosis of the characteristic human gut bacteria to endemic wildlife, AMR within birds and seals appears to be very low, albeit on limited samplings. Furthermore, areas where there is little, to no, human activity still appear to be free from anthropogenically introduced AMR. However, a comprehensive assessment of AMR levels in Antarctica is virtually impossible on current data due to the wide variation in reporting standards and methodologies used and poor geographical coverage. Thus, future studies should engage directly with policymakers to promote the implementation of continent-wide AMR reporting standards. The development of such standards alongside a centralised reporting system would provide baseline data to feedback directly into wastewater treatment policies for the Antarctic Treaty Area to help preserve this relatively pristine environment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01250-x.
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spelling pubmed-90727572022-05-06 Antimicrobial resistance in Antarctica: is it still a pristine environment? Hwengwere, K. Paramel Nair, H. Hughes, K. A. Peck, L. S. Clark, M. S. Walker, C. A. Microbiome Review Although the rapid spread of antimicrobial resistance (AMR), particularly in relation to clinical settings, is causing concern in many regions of the globe, remote, extreme environments, such as Antarctica, are thought to be relatively free from the negative impact of human activities. In fact, Antarctica is often perceived as the last pristine continent on Earth. Such remote regions, which are assumed to have very low levels of AMR due to limited human activity, represent potential model environments to understand the mechanisms and interactions underpinning the early stages of evolution, de novo development, acquisition and transmission of AMR. Antarctica, with its defined zones of human colonisation (centred around scientific research stations) and large populations of migratory birds and animals, also has great potential with regard to mapping and understanding the spread of early-stage zoonotic interactions. However, to date, studies of AMR in Antarctica are limited. Here, we survey the current literature focussing on the following: i).. Dissection of human-introduced AMR versus naturally occurring AMR, based on the premise that multiple drug resistance and resistance to synthetic antibiotics not yet found in nature are the results of human contamination; ii).. The potential role of endemic wildlife in AMR spread. There is clear evidence for greater concentrations of AMR around research stations, and although data show reverse zoonosis of the characteristic human gut bacteria to endemic wildlife, AMR within birds and seals appears to be very low, albeit on limited samplings. Furthermore, areas where there is little, to no, human activity still appear to be free from anthropogenically introduced AMR. However, a comprehensive assessment of AMR levels in Antarctica is virtually impossible on current data due to the wide variation in reporting standards and methodologies used and poor geographical coverage. Thus, future studies should engage directly with policymakers to promote the implementation of continent-wide AMR reporting standards. The development of such standards alongside a centralised reporting system would provide baseline data to feedback directly into wastewater treatment policies for the Antarctic Treaty Area to help preserve this relatively pristine environment. SUPPLEMENTARY INFORMATION: The online version contains supplementary material available at 10.1186/s40168-022-01250-x. BioMed Central 2022-05-06 /pmc/articles/PMC9072757/ /pubmed/35524279 http://dx.doi.org/10.1186/s40168-022-01250-x Text en © The Author(s) 2022 https://creativecommons.org/licenses/by/4.0/Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/ (https://creativecommons.org/publicdomain/zero/1.0/) ) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
spellingShingle Review
Hwengwere, K.
Paramel Nair, H.
Hughes, K. A.
Peck, L. S.
Clark, M. S.
Walker, C. A.
Antimicrobial resistance in Antarctica: is it still a pristine environment?
title Antimicrobial resistance in Antarctica: is it still a pristine environment?
title_full Antimicrobial resistance in Antarctica: is it still a pristine environment?
title_fullStr Antimicrobial resistance in Antarctica: is it still a pristine environment?
title_full_unstemmed Antimicrobial resistance in Antarctica: is it still a pristine environment?
title_short Antimicrobial resistance in Antarctica: is it still a pristine environment?
title_sort antimicrobial resistance in antarctica: is it still a pristine environment?
topic Review
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9072757/
https://www.ncbi.nlm.nih.gov/pubmed/35524279
http://dx.doi.org/10.1186/s40168-022-01250-x
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