Differential Role of the T6SS in Acinetobacter baumannii Virulence
Guillermo D Repizo1, Stéphanie Gagné1, Marie-Laure Foucault-Grunenwald2
1Bases Moléculaires et Structurales des Systèmes Infectieux, CNRS UMR 5086, Université Lyon 1, Institut de Biologie et Chimie des Protéines, Lyon, France.
Abstract:
Gram-negative bacteria, such as Acinetobacter baumannii, are an increasing burden in hospitals worldwide with an alarming spread of multi-drug resistant (MDR) strains. Herein, we compared a type strain (ATCC17978), a non-clinical isolate (DSM30011) and MDR strains of A. baumannii implicated in hospital outbreaks (Ab242, Ab244 and Ab825), revealing distinct patterns of type VI secretion system (T6SS) functionality. The T6SS genomic locus is present and was actively transcribed in all of the above strains. However, only the A. baumannii DSM30011 strain was capable of killing Escherichia coli in a T6SS-dependent manner, unlike the clinical isolates, which failed to display an active T6SS in vitro. In addition, DSM30011 was able to outcompete ATCC17978 as well as Pseudomonas aeruginosa and Klebsiella pneumoniae, bacterial pathogens relevant in mixed nosocomial infections. Finally, we found that the T6SS of DSM30011 is required for host colonization of the model organism Galleria mellonella suggesting that this system could play an important role in A. baumannii virulence in a strain-specific manner.
Insights
Acinetobacter baumannii strains show varied type VI secretion system (T6SS) activity. Only one non-clinical isolate demonstrated T6SS-mediated killing and virulence, highlighting strain-specific differences in this important pathogen.
Area of Science:
- Microbiology
- Bacterial Pathogenesis
- Molecular Biology
Background:
- Acinetobacter baumannii is a significant hospital-acquired pathogen.
- Multi-drug resistant (MDR) strains pose a growing global health threat.
- The type VI secretion system (T6SS) is a key virulence factor in many bacteria.
Purpose of the Study:
- To compare the functional activity of the T6SS across different A. baumannii strains.
- To investigate the role of T6SS in interbacterial competition and host colonization.
- To determine if T6SS functionality differs between clinical and non-clinical isolates.
Main Methods:
- Genomic analysis and transcriptional profiling of T6SS loci.
- In vitro killing assays against Escherichia coli.
- Competition assays with other relevant bacterial pathogens.
- Galleria mellonella larval infection model to assess virulence.
Main Results:
- All tested A. baumannii strains possessed the T6SS gene locus and showed transcription.
- Only the non-clinical isolate DSM30011 exhibited T6SS-dependent killing of E. coli.
- DSM30011 outcompeted other bacterial pathogens and a type strain.
- T6SS of DSM30011 was essential for Galleria mellonella colonization.
Conclusions:
- T6SS functionality in A. baumannii is strain-specific.
- The T6SS contributes to interbacterial competition and virulence.
- Non-clinical isolates may possess more active T6SS than clinical MDR strains.
- T6SS represents a potential target for therapeutic intervention against A. baumannii.
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