For a better understanding of the multidrug resistant Pseudomonas aeruginosa (MDR-PA) epidemiology in mainland China, a nationwide surveillance network of 27 tertiary hospitals was established. Non-duplicate MDR-PA isolates from 254 cases of nosocomial infections, were collected during the period August 2011 to July 2012. Minimum inhibitory concentrations (MICs) of nine antimicrobial agents were determined by broth micro-dilution method according to the CLSI guidelines [M7-A10]. Genotyping analysis was performed by multilocus sequence typing (MLST) and pulsed-field gel electrophoresis (PFGE). The presence of acquired carbapenemases was also determined by molecular approaches for 233 carbapenem-resistant isolates. Carbapenemase genes were detected in 19 (8.2%) isolates, with 13 of these isolates encoding IMP-type enzymes, five with VIM-2 and one with KPC-2. MLST analysis revealed significant genetic diversity among the MDR-PA isolates studied and 91 STs (including 17 novel STs) were identified. However, a long-term outbreak of an emerging extensively drug-resistant (XDR) ST292/PFGE genotype A clone was detected in a hospital from Southwest China. This study has demonstrated that MDR-PA in mainland China have evolved from diverse genetic backgrounds. Evidence of clonal dissemination of the organism and nosocomial outbreaks in some regions, suggest a need to strengthen existing infection control measures.
Pseudomonas aeruginosa is one of the most common nosocomial pathogens, especially among patients in intensive care units, burn centres and cystic fibrosis centres. Given its intrinsic resistance to a large variety of antimicrobials1,2, the antimicrobial drug choices for infections caused by this pathogen are more limited than those for other Gram negative bacilli. Furthermore, P. aeruginosa can acquire resistance determinants by horizontal transfer of mobile genetic elements from other bacteria. Infections caused by multidrug resistant P. aeruginosa (MDR-PA) or extensively drug-resistant (XDR-PA) and pan-drug-resistant P. aeruginosa (PDR-PA)3, are extremely difficult to treat and pose a great challenge to both physicians and patients.
Carbapenems are important antimicrobial agents for the treatment of P. aeruginosa infections. However, increasing resistance to these compounds by P. aeruginosa has restricted their use in many geographical areas1,2,4,5. Although carbapenem resistance in P. aeruginosa may occur through different mechanisms, the acquired carbapenemases are of the utmost concern, as they are characterized by a very wide hydrolytic spectrum and affect almost all β-lactams. The two major groups of carbapenemases commonly found in P. aeruginosa, namely IMP and VIM, are Ambler Class B metallo-β lactamases (MBLs). Ambler class A carbapenemases, such as Klebsiella pneumoniae carbapenemase (KPC), are more frequently reported in Enterobacteriaceae, although they have started to be detected in P. aeruginosa isolates as well6. Given the increasing prevalence of carbapenemases and the limited information available about their prevalence in mainland China, we decided to investigate the frequency of different types of carbapenemases among MDR-PA isolates in this geographic area (Fig. 1).
Although several studies have shown that the P. aeruginosa population structure is typically non-clonal7,8, several other studies have described the presence of MBL-producing clones in hospitals9,10. For a comprehensive understanding of the MDR-PA problem in China, we have established a nationwide surveillance network of 27 tertiary hospitals from diverse geographical areas (Fig. 1) to monitor this pathogen, including antimicrobial susceptibilities, molecular epidemiology, clonal structure and prevalence rate of carbapenemase in nosocomial MDR-PA.
A total of 254 non-duplicate MDR-PA isolates were collected from nosocomial infections from 23 of the 27 participating hospitals (four hospitals did not isolate any). The mean age of these 254 patients was 54.6 ± 21.6 years and 66.1% (168 patients) were male. Among them, 49 patients had skin and soft tissue infection, 44 had bacteraemia and 42 had urinary tract infections. The main clinical wards in which MDR-PA were isolated included surgical (99 patients, 39.0%) and ICU (68 patients, 26.8%), while the medical ward accounted for 18.9% (48 patients) and all other wards combined accounted for 15.4% (39 patients).
Pus was the most common specimen, accounting for 19.3% of all MDR isolates, followed by blood cultures (17.3%), urine (16.5%) and broncho-alveolar lavage fluid (12.6%). The isolates were also obtained from venous catheters (7.5%), ascitic fluid (5.9%), surgery incision (5.9%), bile (5.5%), hydrothorax (4.7%) and cerebrospinal fluid (3.2%). Tissue biopsy specimens, peritoneal dialysate fluid and bone marrow only yielded one or two isolates each (Table 1).
Among the 254 MDR-PA isolates included in this study, 40 (15.7%) isolates were collected from hospital KM, followed by 26 (10.2%) from hospital SD, 17 (6.7%) from hospital JL. A further 14 isolates (5.5%) each were collected from 5 hospitals (SC, ZZ, TJ, Z1, TZ), followed by 13 (5.1%) from hospital XY. The remaining hospitals contributed on average less than 2.5% of the isolates each (Fig. 1). The ICU (15 isolates), neurosurgery (9 isolates), haemodialysis centre (8 isolates) and urology surgery (5 isolates) were the main wards/departments from which MDR-PA isolates were collected from hospital KM. However, such isolates were also collected in other wards e.g. respiratory and gastroenterology wards.
More than 70% of MDR-PA isolates were resistant to piperacillin/tazobactam, cefepime, aztreonam, imipenem, meropenem and ciprofloxacin (Table 2). Colistin was the most active agent (7.9% resistance), followed by amikacin with a resistance rate of 33.5%.
Eighty-six antimicrobial resistance patterns were detected among the 254 MDR-PA isolates. The most common pattern was resistance to piperacillin/tazobactam, cefepime, aztreonam, imipenem, meropenem and ciprofloxacin, but susceptible to ceftazidime, amikacin and colistin (44 isolates, 17.3%). The second most common pattern was resistance to all the agents except colistin (31 isolates, 12.2%). The other antibiotic susceptibility patterns were highly variable, with less than 20 isolates per pattern. The resistance patterns showed no obvious correlation with specimen sources, but with geographical areas. Among 44 isolates sharing the most common pattern, 40 were from KM hospital and were identified as XDR-PA. Furthermore, among 31 isolates of the second most common pattern, 11 isolates were from the SD hospital.
Multilocus sequence typing (MLST) analysis revealed significant genetic diversity among MDR-PA, with 91 sequence types (STs) (17 of which were novel) identified among the 254 isolates studied. All the STs belonged to different singletons. The most common ST was ST292 (47 isolates, 18.5%), followed by ST244 (24 isolates, 9.4%), ST277 (18 isolates, 7.1%), ST235 (13 isolates, 5.1%) and ST699 (10 isolates, 3.9%). Seventeen novel STs identified in the present study have been deposited in the MLST database, with assigned numbers of ST1950, ST1956, ST1960 and ST1963 to ST1976 (Supplementary Table S1).
Pulsed-field gel electrophoresis (PFGE) was performed on all the 47 ST292 (the single most common ST) isolates and these were discriminated into six different genotypes (A–F) (Fig. 2). A high degree of genetic similarity (≥90%) was observed within the 40 isolates collected from KM hospital and belonged to genotype A. The other 7 isolates from 3 hospitals in different cities, belonged to five genotypes (B–F) (Fig. 2).
Nineteen (8.15% overall) carbapenem-non-susceptible P. aeruginosa isolates carried acquired carbapenemase genes and most of them were isolated from east or south of China (Fig. 1). PCR analysis and sequencing identified 13 isolates encoding IMP-type enzymes (10 IMP-9, two encoding IMP-1 and one encoding IMP-10), five isolates encoding VIM-2 and one isolate encoding KPC-2. The IMP-9-encoding gene was the most common, being detected among 10 isolates from six hospitals (Table 3). Carbapenemase producers were isolated more frequently from urinary tract specimens (8/42, 19.0%) than from other specimens (Table 1). All the 19 carbapenemase producing isolates were resistant or intermediate to β-lactam antimicrobials and β-lactam/β-lactamase inhibitors. Among them, 15 isolates were non-susceptible to ciprofloxacin, whilst 12 and 17 were non-susceptible to amikacin and colistin, respectively.
The MLST ST distribution of the 19 carbapenemase producing isolates was scattered, but three patients hospitalized in the same neurosurgery ward in HN hospital (Fig. 2), had urinary tract infection by IMP-9-producing P. aeruginosa each within 45 days and shared the same resistance pattern and belonged to ST357. Three VIM-2-producing isolates from XY Hospital, but collected from different wards, belonged to different sequence types (STs) and also exhibited different resistance patterns (Table 3).
According to previous studies, clonal dissemination of P. aeruginosa is considered to be low7,11,12. In the present study, except for the isolates collected in KM hospital, the MDR-PA isolates exhibited a high genetic diversity and varied resistant patterns. However, it was unusual that all the 40 MDR-PA isolates (40 patients) collected from one hospital (KM) presented the same XDR resistant profiles, belonged to ST292 clone and PFGE genotype A. Clinical records showed that these 40 patients were diagnosed with different infectious diseases and hospitalized in different wards. So we highly suspected that an outbreak of XDR P. aeruginosa was present in KM hospital (Yunnan province) during the surveillance period.
There are very limited clinical reports on P. aeruginosa ST292 lineage worldwide, with some detailed information on this clone available in a study by Lee et al. from Korea13. In contrast to the P. aeruginosa ST292 isolates in the present study (from KM hospital), the ones in the Korean study were carbapenem-susceptible but had reduced susceptibility to colistin13. It is worth noting that the isolates from KM hospital did not produce any carbapenemases. According to previous studies, apart from production of carbapenemases, the major mechanism of carbapenem-resistance in P. aeruginosa is the loss of outer membrane porin OprD and over-expression of efflux pump systems MexAB-OprM16,17. Furthermore, ST292 isolates in the present study had an unusual phenotype, being resistant to cefepime but susceptible to ceftazidime. Previous studies suggested this uncommon phenotype may be due to hyper-expression of the multidrug efflux pump named MexXY-OprM efflux pumps14,15.
However, possible nosocomial outbreaks of carbapenemase-producing P. aeruginosa were actually noted in some other hospitals9,18,19,20. In this study, we detected three ST357 MDR-PA isolates, all from three urinary tract infection patients hospitalized in the same neurosurgery ward in HN within 45 days, suggesting possible clonal dissemination. These strains produced IMP-9 and were only susceptible to colistin. ST357 strains have been detected in other geographical regions, but usually produce IMP-7 in Europe21,22,23 and other IMP enzymes like in Japan24, which is different from the present study.
Recent studies have revealed significant differences in the prevalence and distribution of carbapenemase-producing P. aeruginosa strains from Europe and Asia. In a very recent survey in Europe, performed on 529 carbapenem-non-susceptible P. aeruginosa, 20.0% (106 isolates) were positive for MBL, with the VIM-type enzymes12 predominating. Only two IMP-type enzymes (IMP-15 and IMP-33) were detected in two strains. However, studies in Japan in 2004 and 2006, detected 2.3% and 2.1% MBL-producers, respectively24. A nation-wide survey in mainland China involving 258 P. aeruginosa isolates collected from 2006 to 2007 at 28 hospitals, detected MBL in only 22 isolates (8.5%)11. Thus comparing to the European data12, the carbapenemase prevalence in China and Japan was much lower. In this study, the carbapenemase producing isolates were frequently detected in east and south of China (Fig. 1), regions with larger population densities and considered to be relatively more developed economically than others and hence probably used drugs more often than other regions.
Previous studies show that the prevalence of MBL producers in Europe kept increasing during the years 2009 to 2011, rising from 12.3% to 30.6%12. Based on this background, it is important to adopt and implement continuous surveillance programs for such organisms to assess the effectiveness of current control strategies as well as formulation of new ones. Our study is an important update on the prevalence of carbapenemase producing P. aeruginosa in China. The MBL were detected in only 19 isolates (8.15%) and with IMP-9 the most common carbapenemase, which appears to be an important feature of Chinese strains according to previous studies11,25.
ST235, another recognized international drug-resistant lineage26, is more often associated with worldwide outbreaks of nosocomial infections27,28. In the present study, ST235 was detected in seven hospitals and accounted for 13 isolates (5.1%), but none of them produced carbapenemase. Another potential outbreak case was observed in SD hospital, where ten ST244 P. aeruginosa isolates collected from this hospital exhibited a similar resistant profile (Fig. 1). Interestingly, ST244 is a lineage known world-wide to cause outbreaks of nosocomial infections7,29,30.
In conclusion, this study has demonstrated that MDR-PA of nosocomial origin in mainland China are of diverse genetic backgrounds, but suspected nosocomial outbreaks were actually noted in KM hospital, which would suggest strengthening the existing infection control measures for containment of MDR strains.
Material and Methods
This study was approved by the Human Research Ethics Committee of Peking Union Medical College Hospital (Beijing, China) [No. PUMCHBC-C-2-Q01-1] and was carried out strictly in accordance with the approved guidelines. Informed consent was obtained from all subjects.
This study was part of a Chinese nationwide prospective surveillance project for investigating the antimicrobial resistance and molecular epidemiology of major MDR bacterial pathogens causing nosocomial infections between August 2011 and July 2012. Twenty-seven hospitals from 26 provinces in mainland China participated in the surveillance voluntarily (see Acknowledgments section for full hospital list) (Fig. 1). Non-duplicate MDR-PA isolates causing nosocomial infections (from either hospitalized patients (≥48 h after admission) or in patients with a history of more than 48-h hospitalization within the last 30 days)31 were consecutively collected in the study (Fig. 1) and isolates from sputum and from screening swabs (for example throat swab and rectal swab) were excluded. For each MDR-PA isolate, clinical data was obtained from medical records by the collecting hospital and completed on a standard electronic report form. All the isolates meeting the inclusion criteria were forwarded to our central laboratory (Department of Clinical Laboratory, Peking Union Medical College Hospital) for confirmative identification, further antibiotic susceptibility testing, carbapenemase screening and genotyping. Isolates were stored at −80 °C prior to testing.
Antimicrobial susceptibility testing
At each participating hospital, antimicrobial susceptibility testing was performed according to local routine workflows. At the central laboratory, the minimum inhibitory concentrations (MICs) of nine antimicrobial agents against MDR-PA were determined for each isolate by broth micro-dilution method according to the Clinical and Laboratory Standards Institute (CLSI) guidelines [M7-A10]. The drugs tested included: aminoglycosides (amikacin), antipseudomonal cephalosporins (ceftazidime and cefepime), carbapenems (imipenem and meropenem), fluoroquinolones (ciprofloxacin), antipseudomonal β-lactams/β-lactamase inhibitors (piperacillin/tazobactam and cefoperazone/sulbactam), monobactams (aztreonam) and polymyxins (colistin). Escherichia coli ATCC 25922 and P. aeruginosa ATCC 27853 were used as quality controls at each run and their MICs were within recommended range. Interpretative criteria were consistent with CLSI document M100-S25.
The central laboratory classified MDR and XDR resistance patterns in P. aeruginosa according to proposed interim definitions32. For the eight antimicrobial categories selected for P. aeruginosa MDR and XDR definition, the isolates were defined as MDR when non-susceptible to ≥1 agent in ≥3 antimicrobial categories; and the isolates were defined as XDR when non-susceptible to ≥1 agent in all but ≤2 antimicrobial categories (i.e. bacterial isolates remain susceptible to only one or two categories)32.
MLST and PFGE typing
DNA extraction and MLST was performed according to the protocol published by Curran et al.33. Standard DNA amplification of the seven housekeeping genes (acsA, aroE, guaA, mutL, nuoD, ppsA and trpE) was performed for all isolates. The PCR products were sequenced in both directions using the DNA analyser ABI 3730XL system (Applied Biosystems, Foster City, CA). The nucleotide sequences were compared to existing sequences in the MLST database (www.pubmlst.org/paeruginosa) for assignment of allelic numbers. The isolates were assigned a ST number according to their allelic profiles. The phylogenetic analysis was performed by the MLST clustering software eBURST v3.0 (http://eburst.mlst.net/). Novel alleles in each novel ST were confirmed twice by sequencing in both directions and then submitted to MLST database.
To further investigate the genetic relationship of the isolates belonging to the most common ST and to have some insight into intra-hospital epidemiology of isolates, PFGE analysis was performed as described by Hu et al.34. Briefly, genomic DNA was digested with 10 U restriction enzyme SpeI (New England BioLabs Inc.) and fragments separated by using CHEF MAPPER system (Bio-Rad, Richmond, USA). Dendrogram and cluster analysis were performed by BioNumerics software. Percentage similarities were identified on a dendrogram derived with the un-weighted pair-group method with arithmetic means (UPGMA) and Dice coefficients. The PFGE patterns of isolates with coefficient of similarity ≥90% were considered to belong to the same genotype35.
Screening of carbapenemase producing isolates
The presence of acquired carbapenemases was determined by genetic approaches for the 233 carbapenem-resistant isolates. Described specific primers and conditions were used to amplify blaVIM, blaIPM, blaKPC, blaNDM, blaNMC, blaSME, blaIMI, blaGES, blaSPM, blaGIM, blaSIM, blaOXA-24, or closely related carbapenemase genes36,37. The positive amplification products were sequenced and the results compared with those available in the GenBank database (www.ncbi.nil.gov/BLAST). Multiple-sequence alignments were performed with the CLC Sequence Viewer (version 7.0.2).
How to cite this article: Fan, X. et al. Diverse Genetic Background of Multidrug-Resistant Pseudomonas aeruginosa from Mainland China and Emergence of an Extensively Drug-Resistant ST292 Clone in Kunming. Sci. Rep. 6, 26522; doi: 10.1038/srep26522 (2016).
Giamarellou, H. & Poulakou, G. Multidrug-resistant Gram-negative infections: what are the treatment options? Drugs 69, 1879–1901 (2009).
Livermore, D. M. Has the era of untreatable infections arrived? J Antimicrob Chemother 64 Suppl 1, i29–36 (2009).
Tan, H. L. et al. Genome Sequence of a Pandrug-Resistant Pseudomonas aeruginosa Strain, YN-1. Genome Announc 2, e01280 (2014).
Jean, S. S. & Hsueh, P. R. High burden of antimicrobial resistance in Asia. Int J Antimicrob Agents 37, 291–295 (2011).
Riera, E. et al. Pseudomonas aeruginosa carbapenem resistance mechanisms in Spain: impact on the activity of imipenem, meropenem and doripenem. J Antimicrob Chemother 66, 2022–2027 (2011).
Pasteran, F. et al. Detection of an international multiresistant clone belonging to sequence type 654 involved in the dissemination of KPC-producing Pseudomonas aeruginosa in Argentina. J Antimicrob Chemother 67, 1291–1293 (2012).
Ji, J. et al. Multilocus sequence typing reveals genetic diversity of carbapenem- or ceftazidime-nonsusceptible Pseudomonas aeruginosa in China. Antimicrob Agents Chemother 57, 5697–5700 (2013).
Johansson, E., Welinder-Olsson, C., Gilljam, M., Pourcel, C. & Lindblad, A. Genotyping of Pseudomonas aeruginosa reveals high diversity, stability over time and good outcome of eradication. J Cyst Fibros 14, 7 (2014).
Pena, C. et al. Nosocomial spread of Pseudomonas aeruginosa producing the metallo-beta-lactamase VIM-2 in a Spanish hospital: clinical and epidemiological implications. Clin Microbiol Infect 13, 1026–1029 (2007).
Viedma, E. et al. VIM-2-producing multidrug-resistant Pseudomonas aeruginosa ST175 clone, Spain. Emerg Infect Dis 18, 1235–1241 (2012).
Wang, J. et al. Molecular epidemiology and mechanisms of carbapenem resistance in Pseudomonas aeruginosa isolates from Chinese hospitals. Int J Antimicrob Agents 35, 486–491 (2010).
Castanheira, M., Deshpande, L. M., Costello, A., Davies, T. A. & Jones, R. N. Epidemiology and carbapenem resistance mechanisms of carbapenem-non-susceptible Pseudomonas aeruginosa collected during 2009–11 in 14 European and Mediterranean countries. J Antimicrob Chemother 69, 1804–1814 (2014).
Lee, J. Y., Song, J. H. & Ko, K. S. Identification of nonclonal Pseudomonas aeruginosa isolates with reduced colistin susceptibility in Korea. Microb Drug Resist 17, 299–304 (2011).
Pena, C. et al. Nosocomial outbreak of a non-cefepime-susceptible ceftazidime-susceptible Pseudomonas aeruginosa strain overexpressing MexXY-OprM and producing an integron-borne PSE-1 betta-lactamase. J Clin Microbiol 47, 2381–2387 (2009).
Hocquet, D., Nordmann, P., El Garch, F., Cabanne, L. & Plesiat, P. Involvement of the MexXY-OprM efflux system in emergence of cefepime resistance in clinical strains of Pseudomonas aeruginosa. Antimicrob Agents Chemother 50, 1347–1351 (2006).
Shen, J., Pan, Y. & Fang, Y. Role of the Outer Membrane Protein OprD2 in Carbapenem-Resistance Mechanisms of Pseudomonas aeruginosa. Plos One 10, e0139995 (2015).
Choudhury, D. et al. Transcriptional analysis of MexAB-OprM efflux pumps system of Pseudomonas aeruginosa and its role in carbapenem resistance in a tertiary referral hospital in India. Plos One 10, e0133842 (2015).
Gibb, A. P. et al. Nosocomial outbreak of carbapenem-resistant Pseudomonas aeruginosa with a new blaIMP allele, blaIMP-7 . Antimicrob Agents Chemother 46, 255–258 (2002).
Lolans, K., Queenan, A. M., Bush, K., Sahud, A. & Quinn, J. P. First nosocomial outbreak of Pseudomonas aeruginosa producing an integron-borne metallo-beta-lactamase (VIM-2) in the United States. Antimicrob Agents Chemother 49, 3538–3540 (2005).
Mudau, M. et al. Outbreak of multi-drug resistant Pseudomonas aeruginosa bloodstream infection in the haematology unit of a South African Academic Hospital. Plos One 8, e55985 (2013).
Hammerum, A. M. et al. Characterisation of an IMP-7-producing ST357 Pseudomonas aeruginosa isolate detected in Denmark using whole genome sequencing. Int J Antimicrob Agents 45, 200–201 (2015).
Hrabak, J. et al. Regional spread of Pseudomonas aeruginosa ST357 producing IMP-7 metallo-beta-lactamase in Central Europe. J Clin Microbiol 49, 474–475 (2011).
Nemec, A., Krizova, L., Maixnerova, M. & Musilek, M. Multidrug-resistant epidemic clones among bloodstream isolates of Pseudomonas aeruginosa in the Czech Republic. Res Microbiol 161, 234–242 (2010).
Mano, Y. et al. Molecular analysis of the integrons of metallo-beta-lactamase-producing Pseudomonas aeruginosa isolates collected by nationwide surveillance programs across Japan. BMC Microbiol 15, 41 (2015).
Xiong, J. et al. blaIMP-9 and its association with large plasmids carried by Pseudomonas aeruginosa isolates from the People’s Republic of China. Antimicrob Agents Chemother 50, 355–358 (2006).
Ranellou, K. et al. Detection of Pseudomonas aeruginosa isolates of the international clonal complex 11 carrying the blaPER-1 extended-spectrum beta-lactamase gene in Greece. J Antimicrob Chemother 67, 357–361 (2012).
Maatallah, M. et al. Population structure of Pseudomonas aeruginosa from five Mediterranean countries: evidence for frequent recombination and epidemic occurrence of CC235. Plos One 6, e25617 (2011).
Viedma, E. et al. Nosocomial spread of colistin-only-sensitive sequence type 235 Pseudomonas aeruginosa isolates producing the extended-spectrum beta-lactamases GES-1 and GES-5 in Spain. Antimicrob Agents Chemother 53, 4930–4933 (2009).
Chen, Y., Sun, M., Wang, M., Lu, Y. & Yan, Z. Dissemination of IMP-6-producing Pseudomonas aeruginosa ST244 in multiple cities in China. Eur J Clin Microbiol Infect Dis 33, 1181–1187 (2014).
Sefraoui, I., Berrazeg, M., Drissi, M. & Rolain, J. M. Molecular epidemiology of carbapenem-resistant Pseudomonas aeruginosa clinical strains isolated from western Algeria between 2009 and 2012. Microb Drug Resist 20, 156–161 (2014).
Revelas, A. Healthcare - associated infections: A public health problem. Niger Med J 53, 59–64 (2012).
Magiorakos, A. P. et al. Multidrug-resistant, extensively drug-resistant and pandrug-resistant bacteria: an international expert proposal for interim standard definitions for acquired resistance. Clin Microbiol Infect 18, 268–281 (2012).
Curran, B., Jonas, D., Grundmann, H., Pitt, T. & Dowson, C. G. Development of a multilocus sequence typing scheme for the opportunistic pathogen Pseudomonas aeruginosa. J Clin Microbiol 42, 5644–5649 (2004).
Hu, H. & Manos, J. Pulsed-field gel electrophoresis of Pseudomonas aeruginosa. Methods Mol Biol 1301, 157–170 (2015).
Ciofi Degli Atti, M. et al. An outbreak of extremely drug-resistant Pseudomonas aeruginosa in a tertiary care pediatric hospital in Italy. BMC Infect Dis 14, 494 (2014).
Yigit, H. et al. Novel carbapenem-hydrolyzing beta-lactamase, KPC-1, from a carbapenem-resistant strain of Klebsiella pneumoniae. Antimicrob Agents Chemother 45, 1151–1161 (2001).
Queenan, A. M. & Bush, K. Carbapenemases: the versatile beta-lactamases. Clin Microbiol Rev 20, 440–458 (2007).
The authors thank Professor Yu-Pei Zhao (Peking Union Medical College Hospital, Beijing, China) for the great support in organising this study. The authors are also grateful to all of the 27 hospitals that participated in this study. They are The First People’s Hospital of Kunming, Kunming (KM); Shandong Provincial Hospital, Jinan (SD); Jilin Province People’s Hospital, Changchun (JL); Sichuan Provincial People’s Hospital, Chengdu (SC); The First Affiliated Hospital of Zhengzhou University, Zhengzhou (ZZ); Tongji Hospital, Wuhan (TJ); The First Affiliated Hospital of Zhejiang University, Hangzhou (Z1); Tianjin Medical University General Hospital, Tianjin (TZ); Xiangya Hospital, Changsha (XY); Guiping People’s Hospital, Guiping (GP); Haikou People’s Hospital, Haikou (HN); The First Affiliated Hospital of PLA General Hospital, Beijing (ZR); Shengjing Hospital of China Medical University, Shengyang (SJ); Shenzhen People’s Hospital, Shenzhen (SZ); The Second Hospital of Hebei Medical University, Shijiazhuang (HB); Neimenggu Xinganleague People’s hospital, Xinganleague (XA); Sir Run Run Shaw Hospital, Hangzhou (ZS); The First Affiliated Hospital of Shanxi Medical University, Taiyuan (SX); The First Teaching Hospital of Xinjiang Medical University, Wulumuqi (XJ); San Er Ling Yi Hospital, Hanzhong (HZ); Qinghai Provincial People’s Hospital, Xining (QR); The First Affiliated Hospital of Harbin Medical University, Harbin (H1); Ningxia People’s Hospital, Yinchuan (NX); The Second Affiliated Hospital of Nanchang University, Nanchang (NC); Gansu Provincial hospital, Lanzhou (GS); The First Affiliated Hospital of Anhui Medical University, Hefei (AH); Qinghai Red Cross Hospital, Xining (QH). This work was supported by the Research Special Fund for Public Welfare Industry of Health [grant no. 201402001]. The funders had no role in study design, data collection and interpretation, or the decision to submit the work for publication.
The authors declare no competing financial interests.
Electronic supplementary material
About this article
Cite this article
Fan, X., Wu, Y., Xiao, M. et al. Diverse Genetic Background of Multidrug-Resistant Pseudomonas aeruginosa from Mainland China and Emergence of an Extensively Drug-Resistant ST292 Clone in Kunming. Sci Rep 6, 26522 (2016) doi:10.1038/srep26522
First Italian outbreak of VIM-producing Serratia marcescens in an adult polyvalent intensive care unit, August-October 2018: A case report and literature review
World Journal of Clinical Cases (2019)
First Italian outbreak of VIM-producing Serratia marcescens in an adult polyvalent intensive care unit, August-October 2018: A case report and literature review
World Journal of Clinical Cases (2019)
Dissemination of Carbapenem-Resistance among Multidrug Resistant Pseudomonas aeruginosa carrying Metallo-Beta-Lactamase Genes, including the Novel bla IMP - 65 Gene in Thailand
Infection & Chemotherapy (2019)
Molecular epidemiology of Pseudomonas aeruginosa isolated from infected ICU patients: a French multicenter 2012–2013 study
European Journal of Clinical Microbiology & Infectious Diseases (2019)