BMC Infectious Diseases | |
Surveillance of the prevalence, antibiotic susceptibility, and genotypic characterization of invasive candidiasis in a teaching hospital in China between 2006 to 2011 | |
Yingmei Liu1  Xiaoli Li1  Yuyu Zhang1  Bin Cao1  Lin Wu1  Fang Li1  | |
[1] Department of Infectious Diseases and Clinical Microbiology, Beijing Chao-Yang Hospital, Capital Medical University, Beijing 100020, China | |
关键词: Genotyping; Antifungal susceptibility; Epidemiology; Invasive Candida; | |
Others : 1146631 DOI : 10.1186/1471-2334-13-353 |
|
received in 2012-10-01, accepted in 2013-07-15, 发布年份 2013 | |
【 摘 要 】
Background
Invasive candidiasis is an important nosocomial infection associated with high mortality among immunosuppressive or critically ill patients. We described the incidence of invasive candidiasis in our hospital over 6 years and showed the antifungal susceptibility and genotypes of the isolated yeast.
Method
The yeast species were isolated on CHROMagar Candida medium and identified using an yeast identification card, followed by analysis of the D1/D2 domain of 26S rDNA. The susceptibilities of the isolates to flucytosine, amphotericin B, fluconazole, itraconazole, and voriconazole were tested using the ATB FUNGUS 3 system, and that to caspofungin was tested using E-test strips. C. albicans was genotyped using single-strand conformation polymorphism of CAI (Candida albicans I) microsatellite DNA combined with GeneScan data.
Results
From January 2006 to December 2011, a total of 259 isolates of invasive Candida spp. were obtained from 253 patients, among them 6 patients had multiple positive samples. Ninety-one stains were from blood and 168 from sterile fluids, accounting for 6.07% of all pathogens isolated in our hospital. Most of these strains were C. albicans (41.29% in blood/59.06% in sterile body fluids), followed by C. tropicalis (18.06%/25.72%), C. parapsilosis (17.42%/5.43%), C. glabrata (11.61%/3.99%) and other Candida spp. (11.61%/5.80%). Most Candida spp. were isolated from the ICU. The new species-specific CLSI candida MIC breakpoints were applied to these date. Resistance to fluconazole occurred in 6.6% of C. albicans isolates, 10.6% of C. tropicalis isolates and 15.0% of C. glabrata isolates. For the 136 C. albicans isolates, 54 CAI patterns were recognized. The C. albicans strains from blood or sterile body fluids showed no predominant CAI genotypes. C. albicans isolates from different samples from the same patient had the same genotype.
Conclusions
Invasive candidiasis has been commonly encountered in our hospital in the past 6 years, with increasing frequency of non-C. albicans. Resistance to fluconazole was highly predictive of resistance to voriconazole. CAI SSCP genotyping showed that all C. albicans strains were polymorphic. Invasive candidiasis were commonly endogenous infection.
【 授权许可】
2013 Li et al.; licensee BioMed Central Ltd.
【 预 览 】
Files | Size | Format | View |
---|---|---|---|
20150403141934817.pdf | 469KB | download | |
Figure 3. | 38KB | Image | download |
Figure 2. | 57KB | Image | download |
Figure 1. | 55KB | Image | download |
【 图 表 】
Figure 1.
Figure 2.
Figure 3.
【 参考文献 】
- [1]Pfaller MA, Diekema DJ: Epidemiology of invasive candidiasis: a persistent public health problem. Clin Microbiol Rev 2007, 20:133-163.
- [2]Hidron AI, Edwards JR, Patel J, Horan TC, Sievert DM, Pollock DA: NHSN annual update: antimicrobial-resistant pathogens associated with healthcare-associated infections: annual summary of data reported to the National Healthcare Safety Network at the Centers for Disease Control and Prevention, 2006–2007. Infect Control Hosp Epidemiol 2008, 29:996-1011.
- [3]Pappas PG, Kauffman CA, Andes D, Benjamin DK Jr, Calandra TF, Edwards JE Jr: Clinical practice guidelines for the management of candidiasis: 2009 update by the Infectious Diseases Society of America. Clin Infect Dis 2009, 48:503-535.
- [4]Yenigün Koçak B, Kuloğlu F, Doğan Çelik A, Akata F: Evaluation of epidemiological characteristics and risk factors of candidemia in adult patients in a tertiary-care hospital. Mikrobiyol Bul 2011, 45:489-503.
- [5]Arnold HM, Micek ST, Shorr AF, Zilberberg MD, Labelle AJ, Kothari S: Hospital resource utilization and costs of inappropriate treatment of candidemia. Pharmacotherapy 2010, 30:361-368.
- [6]Chen LY, Liao SY, Kuo SC, Chen SJ, Chen YY, Wang FD: Changes in the incidence of candidaemia during 2000–2008 in a tertiary medical centre in northern Taiwan. J Hosp Infect 2011, 78:50-53.
- [7]Chow JK, Golan Y, Ruthazer R, Karchmer AW, Carmeli Y, Lichtenberg D: Factors associated with candidemia caused by non-albicans Candida species versus Candida albicans in the intensive care unit. Clin Infect Dis 2008, 46:1206-1213.
- [8]Sipsas NV, Kontoyiannis DP: Invasive fungal infections in patients with cancer in the Intensive Care Unit. Int J Antimicrob Agents 2012, 39:464-471.
- [9]Panackal AA, Gribskov JL, Staab JF, Kirby KA, Rinaldi M, Marr KA: Clinical significance of azole antifungal drug cross-resistance in Candida glabrata. J Clin Microbiol 2006, 44:1740-1743.
- [10]Spreghini E, Orlando F, Sanguinetti M, Posteraro B, Giannini D, Manso E: Comparative Effects of Micafungin, Caspofungin, and Anidulafungin against a Difficult-To-Treat Fungal Opportunistic Pathogen, Candida glabrata. Antimicrob Agents Chemother 2012, 56:1215-1222.
- [11]Kurtzman CP, Robnett CJ: Identification of clinically important ascomycetous yeasts based on nucleotide divergence in the 5′ end of the large-subunit (26S) ribosomal DNA gene. J Clin Microbiol 1997, 35:1216-1223.
- [12]Pfaller MA, Diekema DJ: Progress in antifungal susceptibility testing of Candida spp. by use of clinical and laboratory standards institute broth microdilution methods, 2010 to 2012. J Clin Microbiol 2012, 50:2846-2856.
- [13]Li J, Bai FY: Single-strand conformation polymorphism of microsatellite for rapid strain typing of Candida albicans. Med Mycol 2007, 45(7):629-635.
- [14]Sampaio P, Gusmao L, Correia A, Alves C, Rodrigues AG, Pina-Vaz C: New microsatellite multiplex PCR for Candida albicans strain typing reveals microevolutionary changes. J Clin Microbiol 2005, 43:3869-3876.
- [15]Garner JS, Jarvis WR, Emori TG: CDC definations for nosocomial infections. Am J Infect Control 1988, 16:128-140.
- [16]Pereira GH, Muller PR, Szeszs MW, Levin AS, Melhem MS: Five-year evaluation of bloodstream yeast infections in a tertiary hospital: the predominance of non-C. albicans Candida species. Med Mycol 2010, 48:839-842.
- [17]Vincent JL, Rello J, Marshall J, Silva E, Anzueto A, Martin CD: International study of the prevalence and outcomes of infection in intensive care units. JAMA 2009, 302:2323-2329.
- [18]Lockhart SR, Iqbal N, Ahlquist AM, Farley MM, Harrison LH, Bolden CB: Species identification and antifungal susceptibility of candida bloodstream isolates from population-based surveillance in two US cities from 2008–2011. J Clin Microbiol 2012, 50:3435-3442.
- [19]Wang H, Xiao M, Chen SC, Kong F, Sun ZY, Liao K, Lu J, Shao HF, Yan Y, Fan H, Hu ZD, Chu YZ, Hu TS, Ni YX, Zou GL, Xu YC: In Vitro Susceptibilities of Yeast Species to Fluconazole and Voriconazole as Determined by the 2010 National China Hospital Invasive Fungal Surveillance Net (CHIF-NET) study. J Clin Microbiol 2012, 50:3952-3959.
- [20]Pfaller MA, Diekema D, Gibbs D, Newell V, Ellis D, Tullio V: Results from the ARTEMIS DISK Global Antifungal Surveillance Study, 1997 to 2007: a 10.5-year analysis of susceptibilities of Candida species to fluconazole and voriconazole as determined by CLSI standardized disk diffusion. J Clin Microbiol 2010, 48:1366-1377.
- [21]Kao AS, Brandt ME, Pruitt WR, Conn LA, Perkins BA, Stephens DS: The epidemiology of candidemia in two United States cities:results of a population-based active surveillance. Clin Infect Dis 1999, 29:1164-1170.
- [22]Lyon GM, Karatela S, Sunay S, Adiri Y: Antifungal susceptibility testing of Candida isolates from the Candida surveillance study. J Clin Microbiol 2010, 48:1270-1275.
- [23]Mean M, Marchetti O, Calandra T: Bench-to-bedside review: Candida infections in the intensive care unit. Crit Care 2008, 12:204. BioMed Central Full Text
- [24]Wu JQ, Zhu LP, Ou XT, Xu B, Hu XP, Wang X, Weng XH: Epidemiology and risk factors for non-Candida albicans candidemia in non-neutropenic patients at a Chinese teaching hospital. Med Mycol 2011, 49:552-555.
- [25]Cuenca-Estrella M, Gomez-Lopez A, Mellado E, Monzon A, Buitrago MJ, Rodriguez-Tudela JL: Activity profile in vitro of micafungin against Spanish clinical isolates of common and emerging species of yeasts and molds. Antimicrob Agents Chemother 2009, 53:2192-2195.
- [26]Manzoni P, Leonessa M, Galletto P, Latino MA, Arisio R, Maule M: Routine use of fluconazole prophylaxis in a neonatal intensive care unit does not select natively fluconazole-resistant Candida subspecies. Pediatr Infect Dis J 2008, 27:731-737.
- [27]Liu Y, Kang Y, Yokoyama K, Gonoi T, Mikami Y: Molecular differentiation and antifungal susceptibility of Candida albicans isolated from patients with respiratory infections in Guiyang Medical College Hospital, China. Nihon Ishinkin Gakkai Zasshi 2009, 50:175-178.
- [28]Seneviratne CJ, Wong SS, Yuen KY, Meurman JH, Parnanen P, Vaara M: Antifungal susceptibility and virulence attributes of bloodstream isolates of Candida from Hong Kong and Finland. Mycopathologia 2011, 172:389-395.
- [29]Tortorano AM, Prigitano A, Dho G, Grancini A, Passera M: Antifungal susceptibility profiles of Candida isolates from a prospective survey of invasive fungal infections in Italian intensive care units. J Med Microbiol 2012, 61:389-393.
- [30]Chen TC, Chen YH, Chen YC, Lu PL: Fluconazole exposure rather than clonal spreading is correlated with the emergence of Candida glabrata with cross-resistance to triazole antifungal agents. Kaohsiung J Med Sci 2012, 28:306-315.
- [31]Hattori H, Iwata T, Nakagawa Y, Kawamoto F, Tomita Y, Kikuchi A: Genotype analysis of Candida albicans isolates obtained from different body locations of patients with superficial candidiasis using PCRs targeting 25S rDNA and ALT repeat sequences of the RPS. J Dermatol Sci 2006, 42:31-46.