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Emergence of Colistin-Resistant Acinetobacter junii in China
Zhiren Wang1, Xuanyang Fan1, Shuyi Wang1
1Department of Clinical Laboratory, Peking University People's Hospital, Beijing 100044, China.
Abstract:
The increasing number of multidrug-resistant Gram-negative bacteria presents a serious threat to global health. However, colistin-resistant Acinetobacter junii has rarely been reported. We identified a colistin-resistant A. junii clinical isolate, AJ6079, in blood. The colony of AJ6079 presented a dry phenotype, and it was difficult to form a bacterial suspension, whilst transmission electron microscopy revealed that AJ6079 possessed a thick outer membrane. The phenotypic and genomic comparisons were conducted with one colistin-susceptible A. junii, which had the same antibiotic susceptibility profile except for colistin, and had the same KL25 capsule biosynthesis locus. The AJ6079 exhibited a slower growth rate, indicating that colistin-resistant A. junii possesses a higher fitness cost. The genome of AJ6079 had a G+C content of 38.7% and contained one 3,362,966 bp circular chromosome with no plasmid or mobile colistin resistance (mcr) gene. Comparative genomic analysis revealed that the AJ6079 contained several previously unreported point mutations in colistin-resistance-related genes involving amino acid substitutions in PmrB (N5K, G147C), LpxA (I107F, H131Y), and LpxD (F20I, K263R), which might be correlated with colistin resistance in A. junii. Further research is needed for verification as the genetic background was not exactly the same between the two isolates.
Insights
A rare colistin-resistant Acinetobacter junii clinical isolate was identified. This multidrug-resistant bacterium exhibited a dry colony phenotype, thick outer membrane, and novel mutations in resistance-related genes, suggesting a potential fitness cost.
Area of Science:
- Microbiology
- Genomics
- Antimicrobial Resistance
Background:
- Multidrug-resistant Gram-negative bacteria pose a significant global health threat.
- Colistin resistance in Acinetobacter junii is infrequently reported, making it an emerging concern.
- The study focuses on a specific clinical isolate, AJ6079, to understand resistance mechanisms.
Purpose of the Study:
- To characterize a colistin-resistant Acinetobacter junii clinical isolate.
- To investigate the phenotypic and genomic features associated with colistin resistance.
- To identify potential genetic mutations contributing to colistin resistance in this species.
Main Methods:
- Phenotypic analysis including colony morphology and bacterial suspension formation.
- Transmission electron microscopy to examine outer membrane structure.
- Comparative whole-genome sequencing and analysis of resistance-related genes.
- Growth rate determination to assess fitness cost.
Main Results:
- A colistin-resistant Acinetobacter junii isolate (AJ6079) was identified from a blood sample.
- AJ6079 displayed a dry colony phenotype, difficulty in suspension, and a thickened outer membrane.
- Genomic analysis revealed novel point mutations in PmrB, LpxA, and LpxD, potentially linked to colistin resistance.
- The resistant isolate exhibited a slower growth rate, indicating a potential fitness cost.
Conclusions:
- Novel point mutations in colistin-resistance-related genes may confer resistance in Acinetobacter junii.
- The colistin-resistant isolate shows phenotypic differences and a potential fitness cost.
- Further research is required to validate these findings and elucidate the precise mechanisms of colistin resistance.
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