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Published on: July 12, 2013
Distribution and characteristics of SGI1/PGI2 genomic island from Proteus strains in China
Tao Xiao1, Hang Dai1, Binghuai Lu2
1State Key Laboratory of Infectious Disease Prevention and Control, National Institute for Communicable Disease Control and Prevention, Chinese Center for Disease Control and Prevention, Beijing 102206, China; Collaborative Innovation Center for Diagnosis and Treatment of Infectious Diseases, Hangzhou 310003, China; Center for Human Pathogen Collection, China CDC, Beijing, 102206, China.
Abstract:
The emergence of multidrug-resistant Salmonella genomic island 1 (SGI1) and Proteus genomic island (PGI) bearing P. mirabilis present a serious threat to public health. In this study, we screened 288 Proteus isolates recovered from seven provinces in China. Fourteen strains (4.9%) all belonged to P. mirabilis were positive for SGI1/PGI2, including twelve from clinical samples (5.3%) and two from food (3.3%). A Blastn search against GenBank and phylogenetic analyses identified eight different SGI1 variants and one PGI2 variant from the fourteen SGI1/PGI2 variants. All SGI1 variants shared a common backbone and harbored different resistance gene(s), except the sul1 gene at its multidrug-resistant (MDR) region. Among the variants, three novel SGI1 variants, designated as SGI1-PmCA11, SGI1-PmCA14 and SGI1-PmCA46, contained different gene cassettes, which were similar to sequences in plasmids or class 1 integrons of Klebsiella pneumoniae, P. mirabilis, Escherichia coli and Salmonella. Moreover, one novel PGI2, designated as PGI2-PmCA72, had an identical gene cassette to the first class 1 integron from PGI2 (GenBank accession no. MG201402.1) in P. mirabilis, but varied due to missing, replaced, inserted and inverted gene clusters. The four novel SGI1/PGI2 variants contained the cmlA5, dfrA14, blaOXA-10, aadA15, blaOXA-1, catB3 and dfrA16 resistance genes, which have never been reported in SGI1/PGI2 variants. Phenotypically, all fourteen SGI1/PGI2-containing strains showed multidrug resistance. All except four strains were resistant to the first, or the second and/or-third generation cephalosporins. Considering the increasing number and the emergence of new SGI1/PGI2 variants, further surveillance is needed to prevent the spreading of the MDR genomic islands among Proteus isolates from human and food.
Insights
Multidrug-resistant Proteus mirabilis strains carrying novel Salmonella genomic island 1 (SGI1) and Proteus genomic island 2 (PGI2) variants were identified in China. These variants harbor new resistance genes, highlighting the need for surveillance to prevent spread.
Area of Science:
- Microbiology
- Genomics
- Antimicrobial Resistance
Background:
- Emergence of multidrug-resistant (MDR) Proteus mirabilis strains carrying genomic islands like Salmonella genomic island 1 (SGI1) and Proteus genomic island (PGI) poses a significant public health threat.
- Genomic islands are mobile genetic elements that can facilitate the rapid spread of antibiotic resistance genes among bacteria.
Purpose of the Study:
- To screen Proteus isolates for the presence of SGI1 and PGI2.
- To characterize the genetic variants of SGI1 and PGI2 found in P. mirabilis.
- To assess the antimicrobial resistance profiles associated with these genomic islands.
Main Methods:
- Screening of 288 Proteus isolates from various sources in China.
- Identification of SGI1/PGI2-positive strains using molecular methods.
- Blastn searches against GenBank and phylogenetic analyses for variant characterization.
- Determination of antimicrobial resistance phenotypes.
Main Results:
- Fourteen P. mirabilis strains (4.9%) were positive for SGI1/PGI2, with twelve from clinical samples and two from food.
- Eight SGI1 variants and one PGI2 variant were identified, including three novel SGI1 variants (SGI1-PmCA11, SGI1-PmCA14, SGI1-PmCA46) and one novel PGI2 variant (PGI2-PmCA72).
- The novel variants harbored previously unreported resistance genes (cmlA5, dfrA14, blaOXA-10, aadA15, blaOXA-1, catB3, dfrA16) and exhibited multidrug resistance, including resistance to cephalosporins.
Conclusions:
- The study identified novel MDR SGI1 and PGI2 variants in P. mirabilis from China, indicating the continuous evolution and spread of these mobile genetic elements.
- The presence of new resistance genes in these variants underscores the urgent need for enhanced surveillance to monitor and control the dissemination of MDR genomic islands in Proteus populations.
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