Abstract
Objective: To investigate the common bacterial resistance of clinical isolates in our hospital in the second half of 2011.
Methodology: Pathogens isolated from clinical samples in the second half of 2011 were analyzed and categorized to perform susceptibility tests.
Results: In the gram-negative bacteria, Enterobacteriaceae and non-fermenting gram-negative bacilli accounted for 55.89% and 34.51%. In the gram-positive bacteria, Staphylococcus aureus, Coagulase-negative staphylococci, Enterococcus, Strptococcus pneumonia accounted for 32.85%, 40.39%, 12.41% and 10.22%, respectively. Other species accounted for 4.14%. Klebsiella pneumonia and Pseudomonas aeruginosa were sensitive to cepoperazon, cefepime and imipenem. However,Acinetobacter baumannii was more sensitive to carbapenems antibiotics, which was followed by fourth generation cephalosporins. Klebsiella pneumoniae was extremely sensitive to amikacin, cefepime and imipenem, but was resistant to ampicillin. The detection rates of the broad-spectrum Escherichia coli, Pseudomonasaeruginosa and Klebsiella pneumoniae were 54.51%, 52.08% and 38.65%. The gram negative bacilli were the prevalent clinical pathogens in our hospital in the second half of 2011.
Conclusion: The drug resistance of pathogenic bacteria has increased significantly recently, thus the surveillance of antibacterial agents is necessary, and rational use of antibiotic will be urgently needed to reduce the production and dissemination of drug resistant strains.
Key Words: Antibacterial drugs, Pathogen, Gram-negative bacteria, Bacteria resistance
Introduction
Bacterial resistance has become one of the most important issues in the global medical field. It differs in various regions and is related with many social factors.1 Analysis of the resistance can assist to observe the characteristics and changes of the bacterial resistance. Besides, it can provide real-time reference for the clinical application of antibiotics and enhance the monitoring of the distribution of common bacteria, which can offer epidemiology data and changes of bacterial resistance for clinic, and effectively guide the clinical treatment for pathogen infections.2,3 The analysis of the isolated bacterial resistant in our hospital in the second half of 2011 is presented in this manuscript.
Methodology
Source of bacterial strains: All pathogens were isolated from community-acquired infections of the patients enrolled in our hospital, and the secondary infections after being enrolled were excluded.
Instruments and reagents: Automatic micro-analyzer, ProtoCOL automated microbial analysis system, bacterial identification cards and drug susceptibility test cards4 were bought from Synbiosis (UK) Ltd. and control strains including Staphylococcus aureus ATCC25923, Klebsiella pneumoniae ATCC700603, Escherichia coli ATCC25922, Pseudomonas aeruginosa ATCC27853, Candida albicans ATCC90029 and Enterococcus faeciumATCC33186 were all purchased from Shanghai Chuan Xiang Biotech Co., Ltd.
Drug sensitivity tests: Bacterial identifications and susceptibility tests were performed through Automatic micro-analyzer (British Synbiosis) and ProtoCOL automated microbial analysis system, respectively. Antimicrobial minimum inhibitory concentration (MIC) was carried out by the automatic analyzer. Drug sensitivity tests met the standards of Clinical and Laboratory Standards Institute (CLSI).5
Assay methods: The disc confirmatory tests of ESBLs (extended spectrum β lactamases) of Escherichia coli, Klebsiella pneumonia and Proteus mirabilis were carried out according to CLSI2008. Quality control strains included Escherichia coli ATCC25922 (negative control) and Klebsiella pneumoniae ATCC700603 (positive control). PRSP (penicillin resistant Streptococcus pneumoniae) were detected by Optoching antibacterial tests and Streptococcus pneumoniae monoclonal latex agglutination tests. Drug sensitive test of Streptococcus pneumoniae was carried out by ATB-STREP5-test paper, and Streptococcus pneumoniae were divided into three categories: penicillin-susceptible strains (PSSP), penicillin-intermediate strains (PISP) and penicillin-resistant strains (PRSP).6
Statistical analysis: The results were analyzed by one-way ANOVA for multiple comparisons by SPSS. A P-value < 0.05 was considered significant.
Results
A total of 1096 isolates were collected in the second half of 2011, the sources of the strains included respiratory secretions (68.80%), urine (15.69%), blood (12.14%) and others (3.38%).
In the 1096 isolates, gram negative and gram positive bacteria accounted for 54.20% and 37.50% respectively, fungi accounted for 8.30%. In the gram negative bacteria, the proportion of Enterobacteriaceae was 55.89%, and those of non-fermenting gram negative bacilli and other species were 34.51% and 9.60%, respectively. In the gram positive bacteria, Staphylococcus, Coagulase-negative staphylococci, Enterococcus and Streptococcus pneumonia accounted for 32.85%, 40.39%, 12.41% and 10.22% respectively, other species accounted for 4.14%. The proportions of all the bacteria are shown in Table-I. The main pathogens, including E. coli, Staphylococcus aureus, Klebsiella pneumoniae, Pseudomonas aeruginosa, Candida albicans and Acinetobacter baumannii, occurred following a decreasing frequency.
Table-I.
Pathogen | No. of strains | Proportion (%) |
---|---|---|
Gram negative bacteria | 594 | 54.20 |
Enterobacteriaceae | 332 | 30.29 |
E. coli | 153 | 13.96 |
Klebsiella pneumoniae | 92 | 8.39 |
Others | 87 | 7.94 |
NFGNB | 205 | 18.70 |
Pseudomonas aeruginosa | 74 | 6.75 |
Acinetobacter baumannii | 62 | 5.66 |
Others | 69 | 6.30 |
Others | 57 | 5.20 |
Gram positive bacteria | 411 | 37.50 |
Staphylococcus aureus | 135 | 12.14 |
Coagulase-negative staphylococci | 166 | 15.23 |
Staphylococcus epidermidis | 52 | 4.74 |
Staphylococcus haemolyticus | 51 | 4.65 |
Others | 63 | 5.75 |
Enterococcus | 51 | 4.65 |
Pneumonia hammer | 42 | 3.83 |
Others | 17 | 1.55 |
Fungi | 91 | 8.30 |
Candida albicans | 66 | 6.02 |
Candida glabrata | 18 | 1.64 |
Others | 7 | 0.64 |
Resistance of gram negative bacilli to antibiotics: Top five of the selected gram negative bacilli were Klebsiella pneumoniae, Pseudomonas aeruginosa, Acinetobacter baumannii, Escherichia coli and Proteus mirabilis, respectively. Susceptibility tests showed that Klebsiella pneumoniae was sensitive to amikacin, cefepime and imipenem (the resistance rate <20%), whereas it was highly resistant to ampicillin. The detection rates of ESBLs from Escherchia coli, Pseudomonas aeruginosa and Klebsiella pneumoniae were 54.51%, 52.08% and 38.65%, respectively. Pseudomonas aeruginosa was sensitive to cefepime and imipenem, whereas it exhibited high resistance to cefoperazone/tazobactam and cefotaxime. Acinetobacter baumannii as well as Escherichia coli were resistant to most antibiotics (Table-II).
Table-II.
Antibiotic | Klebsiella pneumoniae (n=92) | Bacillus pyocyaneus (n=74) | Acinetobacter baumannii (n=62) | Escherichia coli (n=153) |
Proteus mirabilis
(n=32) |
---|---|---|---|---|---|
Amikacin | 19.57 | 31.08 | 48.39 | 23.53 | 25.00 |
Ampicillin | 94.57 | 91.89 | 96.78 | 90.20 | 90.63 |
Aztreonam | 61.96 | 85.90 | 67.74 | 71.90 | 34.38 |
Ceftazidime | 34.78 | 33.78 | 79.03 | 70.59 | 40.63 |
Cefotaxime | 33.70 | 29.73 | 75.81 | 57.52 | 43.75 |
Cefoperazone/ Tazobactam | 27.17 | 28.38 | 70.97 | 50.98 | 31.25 |
Cefepime | 19.57 | 18.92 | 38.71 | 33.99 | 21.88 |
Imipenem | 10.87 | 12.16 | 24.19 | 28.76 | 15.63 |
Gentamicin | 29.35 | 28.38 | 62.90 | 66.67 | 46.88 |
Ciprofloxacin | 26.09 | 24.32 | 64.74 | 64.71 | 40.63 |
Levofloxacin | 21.74 | 25.68 | 72.58 | 73.20 | 34.38 |
Resistance of gram-positive cocci to antibiotics: Gram positive cocci mainly consisted of Staphylococcus aureus, Staphylococcus epidermidis and Enterococcus. Staphylococcus aureus was sensitive to fusidic acid, vancomycin and teicoplanin, but showed high resistant rates to β-lactams, macrolides, quinolones and aminoglycosides. Staphylococcus epidermidis was highly resistant to a variety of antibiotics, and Enterococciwas resistant to traditional antibiotics. Susceptibility tests showed the detection rates of MRSA and MRCNS were 60.13% and 85.54%, in which 38 and 39 strains were resistant to fusidic acid and vancomycin, respectively (Table-III).
Table-III.
Antibiotic | Staphylococcus aureus (n=92) | Staphylococcus epidermidis (n=74) | Enterococcus (n=62) | Streptococcus pneumoniae (n=153) | Staphylococcus haemolyticus (n=32) |
---|---|---|---|---|---|
Penicillin | 95.65 | 95.95 | 96.77 | 96.73 | 93.75 |
Cefazolin | 92.39 | 94.60 | 80.65 | 88.24 | 84.38 |
Gentamicin | 93.48 | 93.24 | 77.42 | 86.27 | 81.25 |
Levofloxacin | 83.70 | 83.78 | 72.58 | 78.43 | 71.88 |
Azithromycin | 91.30 | 94.60 | 82.26 | 86.93 | 90.63 |
Ciprofloxacin | 86.96 | 91.89 | 95.16 | 90.20 | 87.50 |
Cefotaxime Fusidic Acid |
81.52 | 85.16 | 75.81 | 75.82 | 78.13 |
41.30 | 31.08 | 35.48 | 50.98 | 50.00 | |
Vancomycin | 42.39 | 35.14 | 43.55 | 46.35 | 53.13 |
Teicoplanin | 35.87 | 33.78 | 38.71 | 42.48 | 59.38 |
Discussion
The emergences of NDM-1 (New Delhi-Metallo-1) bacteria worldwide that are resistant to most antibiotics have greatly threatened human health.7 In recent years, many antibiotics are becoming invalid confronting multi-resistant bacteria. In China, the occurrences of MRSA, MDRSP and VRE have increased tremendously and covered most of the medical institutions, even Klebsiella pneumoniae (KPC) has also been observed having the same tendency. In future, more super bacteria resisting to most antibiotics like NDM-1 bacteria will emerge.8,9 Therefore, as a primary hospital, it is necessary to be aware of the distribution of common pathogens, monitor the bacterial resistance and analyze the bacterial resistance to common antibiotics.10
The results showed that the resistances of Klebsiella pneumoniae to cefoperazone/tazobactam, cefepime, imipenem, ciprofloxacin, gentamicin and levofloxacin were not very significant. Therefore, according to the principle that antibiotics should be used following a rising sensitivity order, leveofloxacin, ciprofloxacin and cefoperazone/tazobactam could be utilized first as empirical treatment against Klebaiella. Pseudomonas aeruginosa was also sensitive to the above antibiotics, but the degree was lower than that of Klebsiella. The drug resistance mechanism of Pseudomonas aeruginosa is quite complex, which will produce a variety of β-lactamase enzymes and express active efflux system.11 Besides, the decreased permeability of the membrane resulted from the changes of outer membrane protein and penicillin-binding protein contributes to the resistance.12
Therefore, the starting point of antibiotics for Pseudomonas aeruginosa ought to be higher than that for Klebsiella. Acinetobacter baumannii ranked second after Pseudomonas aeruginosa for the infections induced by non-fermenting gram-negative bacteria. Acinetobacter carried various drug resistance genes, which would bring about high risks to nosocomial infection.13 In the presence of the extensively used antibiotics, treating the infections resulted from multi-drug resistant Acinetobacter baumannii is becoming difficult. According to the bacterial resistance in the second half of 2011 in our hospital, Acinetobacter baumannii was sensitive to carbapenem antibiotics followed by second-generation cephalosporins, but it was highly resistant to other antibiotics, which should arouse the attention of primary health care institutions. Enterobacteriaceae bacteria were sensitive to carbapenem antibiotics, fourth generation cephalosporins and glycopeptides. The susceptibility tests showed that the sensitivity rates of E. coli to imipenem and cefepime were both above 70%, whereas it was highly resistant to other antibiotics. However, it is worthy to note that the resistance rates against E. coli in other medical institutions were generally lower than those in our hospital. ESBLs tests showed that the detection rate of ESBLs in E. coli was 54.51%, which may be related to the wide application of third generation cephalosporins, leading to the utilization of CTM-type ESBL produced by E. coli as the superior strain.14
During the second half of 2011, the detection rates of MRSA and MRCNS were 60.13% and 85.54%, respectively. Both the bacteria were resistant to all of the β-lactam antibiotics, and they exhibited an increasing resistance tendency to fluoroquinolones, aminoglycosides and polypeptide antibiotics. In the past year, vancomycin-resistant Staphylococcus aureus emerged in succession and became resistant to fusidic acid and cefepime. Therefore, it has been demonstrated that the resistance to polypeptide antibiotic was severe.15,16
Furthermore, Staphylococcus epidermidis is one of the most common Coagulase-negative staphylococci, which can also be isolated from most of the methicillin-resistant Coagulase staphylococcus, and its resistance rate increases yearly.17 The results exhibited that except for fusidic acid and polypeptide antibiotics, the resistance of Staphylococcus epidermidis to other antibiotics was even higher than that of MRSA, the severity of which should not be ignored as a result. As an opportunistic pathogen, Enterococcus led to increasing infections every year, and its drug resistance has become extremely serious according to the results in our hospital. Vancomycin-resistant Enterococci was also observed in our hospital, so it is imperative to enhance the monitoring of the drug resistance. Streptococcus pneumoniae is the major pathogen resulting in community-acquired infections, and its resistance to antibiotics has also aroused wide concern.18 Many respiratory tract infections are triggered by Streptococcus pneumonia. Nevertheless, in the presence of the penicillin-resistant Streptococcus pneumoniae, long-term macrolide antibiotics have to be utilized for the treatment, which enables the Streptococcus pneumoniae to be resistant to macrolide antibiotics increasingly.19,20 The results herein showed that the resistance rates of both azithromycin and quinolones were as high as that of penicillin for Streptococcus pneumoniae. Besides, the resistance values of Streptococcus pneumoniae to β-lactams, quinolones and macrolides antibiotics exceeded the national average levels.21
In summary, it is to reinforce the surveillance of pathogens and their drug resistance to use antibiotics rationally. Clinically, antibiotics should be used according to the results of the susceptibility tests to reduce the prevalence of drug resistant strains, which will allow us to control the increase and spread of bacterial resistance.
Acknowledgment
This work was supported by Youth Science & Technology Foundation of Inner Mongolian Medical University and General Science & Technology Project Foundation of Affiliated Hospital of Inner Mongolian Medical University.
References
- 1.Kottapalli KR, Sarla N, Kikuchi S. In silico insight into two rice chromosomal regions associated with submergence tolerance and resistance to bacterial leaf blight and gall midge. Biotechnol Adv. 2006;24(6):561–589. doi: 10.1016/j.biotechadv.2006.05.003. [DOI] [PubMed] [Google Scholar]
- 2.Velickovic-Radovanovic R, Petrovic J, Kocic B, Antic S, Mitic R. Analysis of antibiotic utilization and bacterial resistance changes in a surgical clinic of Clinical Centre, Nis. J Clin Pharm Ther. 2012;37(1):32–36. doi: 10.1111/j.1365-2710.2010.01241.x. [DOI] [PubMed] [Google Scholar]
- 3.Xie W, Yu K, Pauls KP, Navabi A. Application of Image Analysis in Studies of Quantitative Disease Resistance: Exemplified Using Common Bacterial Blight-Common Bean Pathosystem. Phytopathology. 2012;102(4):434–442. doi: 10.1094/PHYTO-06-11-0175. [DOI] [PubMed] [Google Scholar]
- 4.Gagliotti C, Sarti M, Sabia C, Gargiulo R, Rossolini GM, Carillo C, et al. Accuracy of automated and manual systems for susceptibility testing of Pseudomonas aeruginosa to piperacillin and piperacillin-tazobactam. New Microbiol. 2011;34(1):97–99. [PubMed] [Google Scholar]
- 5.Taylor CR. New revised Clinical and Laboratory Standards Institute Guidelines for Immunohistochemistry and Immunocytochemistry. Appl Immunohistochem Mol Morphol. 2011;19(4):289–290. doi: 10.1097/PAI.0b013e31821b505b. [DOI] [PubMed] [Google Scholar]
- 6.Reinert RR, Al-Lahham A, Lutticken R. In vitro activity of cefditoren against clinical isolates of penicillin-susceptible and penicillin-intermediate strains of Streptococcus pneumoniae isolated in Germany, 1992-1998. J Antimicrob Chemother. 2001;48(2):279–281. doi: 10.1093/jac/48.2.279. [DOI] [PubMed] [Google Scholar]
- 7.Walsh TR, Weeks J, Livermore DM, Toleman MA. Dissemination of NDM-1 positive bacteria in the New Delhi environment and its implications for human health: an environmental point prevalence study. Lancet Infect Dis. 2011;11(5):355–362. doi: 10.1016/S1473-3099(11)70059-7. [DOI] [PubMed] [Google Scholar]
- 8.Liu QZ, Wu Q, Zhang YB, Liu MN, Hu FP, Xu XG, et al. Prevalence of clinical methicillin-resistant Staphylococcus aureus (MRSA) with high-level mupirocin resistance in Shanghai and Wenzhou, China. Int J Antimicrob Agents. 2010;35(2):114–118. doi: 10.1016/j.ijantimicag.2009.09.018. [DOI] [PubMed] [Google Scholar]
- 9.Meng X, Dong M, Wang DI, He J, Yang C, Zhu L, et al. Antimicrobial susceptibility patterns of clinical isolates of gram-negative bacteria obtained from intensive care units in a tertiary hospital in Beijing, China. J Chemother. 2011;23(4):207–210. doi: 10.1179/joc.2011.23.4.207. [DOI] [PubMed] [Google Scholar]
- 10.Chiu SK, Lin JC, Wang NC, Peng MY, Chang FY. Impact of underlying diseases on the clinical characteristics and outcome of primary pyomyositis. J Microbiol Immunol Infect. 2008;41(4):286–293. [PubMed] [Google Scholar]
- 11.Walsh TR. Clinically significant carbapenemases: an update. Curr Opin Infect Dis. 2008;21(4):367–371. doi: 10.1097/QCO.0b013e328303670b. [DOI] [PubMed] [Google Scholar]
- 12.O’Daniel PI, Zajicek J, Zhang W, Shi Q, Fisher JF, Mobashery S. Elucidation of the structure of the membrane anchor of penicillin-binding protein 5 of Escherichia coli. J Am Chem Soc. 2010;132(12):4110–4118. doi: 10.1021/ja9094445. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 13.Mezzatesta ML, D’Andrea MM, Migliavacca R, Giani T, Gona F, Nucleo E, et al. Epidemiological characterization and distribution of carbapenem-resistant Acinetobacter baumannii clinical isolates in Italy. Clin Microbiol Infect. 2012;18(2):160–166. doi: 10.1111/j.1469-0691.2011.03527.x. [DOI] [PubMed] [Google Scholar]
- 14.Wang A, Yang Y, Lu Q, Wang Y, Chen Y, Deng L, et al. Occurrence of qnr-positive clinical isolates in Klebsiella pneumoniae producing ESBL or AmpC-type beta-lactamase from five pediatric hospitals in China. FEMS Microbiol Lett. 2008;283(1):112–116. doi: 10.1111/j.1574-6968.2008.01163.x. [DOI] [PubMed] [Google Scholar]
- 15.Thong KL, Junnie J, Liew FY, Yusof MY, Hanifah YA. Antibiograms and molecular subtypes of methicillin-resistant Staphylococcus aureus in local teaching hospital, Malaysia. J Microbiol Biotechnol. 2009;19(10):1265–1270. [PubMed] [Google Scholar]
- 16.Zhanel GG, Adam HJ, Low DE, Blondeau J, Decorby M, Karlowsky JA, et al. Antimicrobial susceptibility of 15,644 pathogens from Canadian hospitals: results of the CANWARD 2007-2009 study. Diagn Microbiol Infect Dis. 2011;69(3):291–306. doi: 10.1016/j.diagmicrobio.2010.10.025. [DOI] [PubMed] [Google Scholar]
- 17.Makki AR, Sharma S, Duggirala A, Prashanth K, Garg P, Das T. Phenotypic and genotypic characterization of coagulase negative staphylococci (CoNS) other than Staphylococcus epidermidis isolated from ocular infections. Invest Ophthalmol Vis Sci. 2011;52(12):9018–9022. doi: 10.1167/iovs.11-7777. [DOI] [PubMed] [Google Scholar]
- 18.Paradisi F, Corti G, Cinelli R. Streptococcus pneumoniae as an agent of nosocomial infection: treatment in the era of penicillin-resistant strains. Clin Microbiol Infect. 2001;4(Suppl 4):34–42. doi: 10.1046/j.1469-0691.2001.00056.x. [DOI] [PubMed] [Google Scholar]
- 19.Diaz-Brito V, Gomes MH, Figueiredo-Dias P, Mota-Miranda A. Leukemoid reaction and fever after polyvalent polysaccharide pneumococcal vaccination. Acta Med Port. 2007;20(3):233–237. [PubMed] [Google Scholar]
- 20.Tremolieres F. Current epidemiology of microbial low respiratory tract infections. Med Mal Infect. 2006;36(11-12):546–554. doi: 10.1016/j.medmal.2006.05.013. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 21.Njunda AL, Assob JC, Nsagha DS, Kamga HL, Awafung MP, Weledji EP. Epidemiological, clinical features and susceptibility pattern of shigellosis in the Buea Health District, Cameroon. BMC Res Notes. 2012;5:54. doi: 10.1186/1756-0500-5-54. [DOI] [PMC free article] [PubMed] [Google Scholar]