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Genome sequencing and analysis of the first spontaneous Nanosilver resistant bacterium Proteus mirabilis strain SCDR1
Amr T M Saeb1, Khalid A Al-Rubeaan1, Mohamed Abouelhoda2,3
1Genetics and Biotechnology Department, Strategic Center for Diabetes Research, College of medicine, King Saud University, Riyadh, Kingdom of Saudi Arabia.
Background:
P. mirabilis is a common uropathogenic bacterium that can cause major complications in patients with long-standing indwelling catheters or patients with urinary tract anomalies. In addition, P. mirabilis is a common cause of chronic osteomyelitis in Diabetic foot ulcer (DFU) patients. We isolated P. mirabilis SCDR1 from a Diabetic ulcer patient. We examined P. mirabilis SCDR1 levels of resistance against Nanosilver colloids, the commercial Nanosilver and silver containing bandages and commonly used antibiotics. We utilized next generation sequencing techniques (NGS), bioinformatics, phylogenetic analysis and pathogenomics in the characterization of the infectious pathogen.
Results:
P. mirabilis SCDR1 was the first Nanosilver resistant isolate collected from a diabetic patient polyclonal infection. P. mirabilis SCDR1 showed high levels of resistance against Nanosilver colloids, Nanosilver chitosan composite and the commercially available Nanosilver and silver bandages. The P. mirabilis -SCDR1 genome size is 3,815,621 bp. with G + C content of 38.44%. P. mirabilis-SCDR1 genome contains a total of 3533 genes, 3414 coding DNA sequence genes, 11, 10, 18 rRNAs (5S, 16S, and 23S), and 76 tRNAs. Our isolate contains all the required pathogenicity and virulence factors to establish a successful infection. P. mirabilis SCDR1 isolate is a potential virulent pathogen that despite its original isolation site, the wound, can establish kidney infection and its associated complications. P. mirabilis SCDR1 contains several mechanisms for antibiotics and metals resistance, including, biofilm formation, swarming mobility, efflux systems, and enzymatic detoxification.
Conclusion:
P. mirabilis SCDR1 is the first reported spontaneous Nanosilver resistant bacterial strain. P. mirabilis SCDR1 possesses several mechanisms that may lead to the observed Nanosilver resistance.
Insights
The first Nanosilver-resistant Proteus mirabilis strain, SCDR1, was isolated from a diabetic foot ulcer. This pathogen exhibits resistance to nanosilver and possesses virulence factors, highlighting potential challenges in treating infections.
Area of Science:
- Microbiology
- Genomics
- Infectious Diseases
Background:
- Proteus mirabilis is a common cause of urinary tract infections and osteomyelitis in diabetic foot ulcer (DFU) patients.
- This study isolated P. mirabilis SCDR1 from a DFU patient, investigating its resistance profiles.
- The pathogen's characteristics were analyzed using advanced genomic and bioinformatics techniques.
Purpose of the Study:
- To characterize the Nanosilver resistance of P. mirabilis SCDR1.
- To perform whole-genome sequencing and analysis of the P. mirabilis SCDR1 isolate.
- To identify potential virulence factors and resistance mechanisms in P. mirabilis SCDR1.
Main Methods:
- Isolation of P. mirabilis SCDR1 from a diabetic ulcer.
- Antimicrobial susceptibility testing against nanosilver colloids, silver bandages, and antibiotics.
- Whole-genome sequencing (Next Generation Sequencing), bioinformatics, phylogenetic analysis, and pathogenomic analysis.
Main Results:
- P. mirabilis SCDR1 demonstrated high resistance to nanosilver colloids, nanosilver chitosan composite, and silver bandages.
- The genome of P. mirabilis SCDR1 (3.8 Mbp, 3533 genes) contains genes for pathogenicity, virulence, and multiple resistance mechanisms.
- Identified resistance mechanisms include biofilm formation, swarming motility, efflux systems, and enzymatic detoxification.
Conclusions:
- P. mirabilis SCDR1 is the first reported spontaneous Nanosilver-resistant bacterial strain.
- The isolate possesses multiple mechanisms contributing to its Nanosilver resistance.
- This finding has implications for managing infections caused by Nanosilver-resistant bacteria, particularly in DFU patients.

