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Published on: March 24, 2023
Ubiquitous Conjugative Mega-Plasmids of Acinetobacter Species and Their Role in Horizontal Transfer of Multi-Drug
Sofia Mindlin1, Olga Maslova1, Alexey Beletsky2
1Institute of Molecular Genetics of National Research Center "Kurchatov Institute", Moscow, Russia.
Abstract:
Conjugative mega-plasmids play a special role in adaptation since they carry a huge number of accessory genes, often allowing the host to develop in new niches. In addition, due to conjugation they are able to effectively spread themselves and participate in the transfer of small mobilizable plasmids. In this work, we present a detailed characterization of a recently discovered family of multiple-drug resistance mega-plasmids of Acinetobacter species, termed group III-4a. We describe the structure of the plasmid backbone region, identify the rep gene and the origin of plasmid replication, and show that plasmids from this group are able not only to move between different Acinetobacter species but also to efficiently mobilize small plasmids containing different mob genes. Furthermore, we show that the population of natural Acinetobacter strains contains a significant number of mega-plasmids and reveal a clear correlation between the living conditions of Acinetobacter strains and the structure of their mega-plasmids. In particular, comparison of the plasmids from environmental and clinical strains shows that the genes for resistance to heavy metals were eliminated in the latter, with the simultaneous accumulation of antibiotic resistance genes by incorporation of transposons and integrons carrying these genes. The results demonstrate that this group of mega-plasmids plays a key role in the dissemination of multi-drug resistance among Acinetobacter species.
Insights
Conjugative mega-plasmids in Acinetobacter species facilitate adaptation and spread of resistance genes. Environmental strains show heavy metal resistance, while clinical strains accumulate antibiotic resistance via transposons and integrons.
Area of Science:
- Microbiology
- Genetics
- Evolutionary Biology
Background:
- Conjugative mega-plasmids are crucial for bacterial adaptation, carrying numerous accessory genes that enable survival in new environments.
- These plasmids facilitate their own spread and the mobilization of smaller plasmids through conjugation.
- Acinetobacter species are significant opportunistic pathogens, and understanding their resistance mechanisms is critical.
Purpose of the Study:
- To characterize a newly discovered family of multi-drug resistance mega-plasmids (group III-4a) in Acinetobacter species.
- To investigate the structural features, replication mechanisms, and transfer capabilities of these mega-plasmids.
- To explore the correlation between the living conditions of Acinetobacter strains and the genetic makeup of their mega-plasmids.
Main Methods:
- Detailed characterization of mega-plasmid structure, including identification of the replication (rep) gene and origin of replication.
- Analysis of plasmid mobility within and between Acinetobacter species.
- Mobilization assays for small plasmids with different mobilization (mob) genes.
- Comparative analysis of mega-plasmids from environmental and clinical Acinetobacter isolates.
Main Results:
- The study details the plasmid backbone structure and identifies key replication genes for group III-4a mega-plasmids.
- These mega-plasmids exhibit inter-species mobility within Acinetobacter and can mobilize small plasmids.
- A significant prevalence of mega-plasmids was observed in natural Acinetobacter populations.
- Clinical strains showed a reduction in heavy metal resistance genes, with a concurrent increase in antibiotic resistance genes acquired via transposons and integrons, unlike environmental strains.
Conclusions:
- Group III-4a mega-plasmids are key players in the adaptation and evolution of Acinetobacter species.
- These mega-plasmids significantly contribute to the dissemination of multi-drug resistance within Acinetobacter populations.
- The observed differences in mega-plasmid content between environmental and clinical strains highlight the role of selective pressures in shaping bacterial resistance.
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