Heloisa Silva Inacio, Yasmim Raffaela Soares Santos, Magna Cristina de Paiva, Jaqueline Maria Siqueira Ferreira
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引用次数: 0
Abstract
Serratia marcescens is a gram-negative bacillus commonly found in aquatic environments. This opportunistic human pathogen can form biofilms and acquire resistance to multiple antimicrobial classes, raising public and environmental health concerns. The occurrence of antimicrobial-resistant S. marcescens in aquatic ecosystems is alarming, yet relatively few studies have addressed this topic in depth. To compile and analyse studies on the antimicrobial susceptibility profiles and resistance mechanisms of S. marcescens isolated from aquatic environments. A systematic search was performed in PubMed, Scopus, Web of Science and the Virtual Health Library for articles published between 2019 and 2024, using descriptors related to S. marcescens from aquatic sources. Studies evaluating susceptibility profiles of isolates from water samples were included. Thirteen articles met the inclusion criteria, encompassing 90 isolates from diverse water sources. Resistance to β-lactams was most prevalent, including carbapenems, the most recent compounds in this class. Identified mechanisms included plasmid-mediated genes blaOXA-48, blaTEM-1 and aac(6′)-Ic. Aquatic environments can serve as reservoirs for resistant S. marcescens, posing risks of dissemination to humans and other ecosystems. Continuous monitoring, environmental contamination control and stronger microbiological surveillance policies are crucial to mitigate this emerging public health threat.
粘质沙雷氏菌是一种常见于水生环境的革兰氏阴性杆菌。这种机会性人类病原体可形成生物膜并获得对多种抗菌素类的耐药性,从而引起公众和环境卫生关注。耐药粘质葡萄球菌(S. marcescens)在水生生态系统中的出现令人担忧,但深入研究这一问题的研究相对较少。收集和分析从水生环境中分离的粘质葡萄球菌(S. marcescens)的药敏特征和耐药机制。在PubMed、Scopus、Web of Science和Virtual Health Library中对2019年至2024年间发表的文章进行了系统搜索,使用与水生来源的S. marcescens相关的描述符。包括评估水样中分离株的敏感性谱的研究。13篇文章符合纳入标准,包括来自不同水源的90株分离物。对β-内酰胺类的耐药最为普遍,包括碳青霉烯类,这是该类中最新的化合物。已确定的机制包括质粒介导的基因blaOXA-48、blaem -1和aac(6’)-Ic。水生环境可作为耐药粘质葡萄球菌的宿主,给人类和其他生态系统带来传播风险。持续监测、环境污染控制和更强有力的微生物监测政策对于减轻这一新出现的公共卫生威胁至关重要。
期刊介绍:
The journal is identical in scope to Environmental Microbiology, shares the same editorial team and submission site, and will apply the same high level acceptance criteria. The two journals will be mutually supportive and evolve side-by-side.
Environmental Microbiology Reports provides a high profile vehicle for publication of the most innovative, original and rigorous research in the field. The scope of the Journal encompasses the diversity of current research on microbial processes in the environment, microbial communities, interactions and evolution and includes, but is not limited to, the following:
the structure, activities and communal behaviour of microbial communities
microbial community genetics and evolutionary processes
microbial symbioses, microbial interactions and interactions with plants, animals and abiotic factors
microbes in the tree of life, microbial diversification and evolution
population biology and clonal structure
microbial metabolic and structural diversity
microbial physiology, growth and survival
microbes and surfaces, adhesion and biofouling
responses to environmental signals and stress factors
modelling and theory development
pollution microbiology
extremophiles and life in extreme and unusual little-explored habitats
element cycles and biogeochemical processes, primary and secondary production
microbes in a changing world, microbially-influenced global changes
evolution and diversity of archaeal and bacterial viruses
new technological developments in microbial ecology and evolution, in particular for the study of activities of microbial communities, non-culturable microorganisms and emerging pathogens.