Candida species: species distribution and antifungal susceptibility patterns.
We investigated the distribution and antifungal susceptibility of Candida species isolated from various clinical specimens and antifungal susceptibility patterns of bloodstream isolates at Tygerberg Hospital. All consecutive non-duplicate Candida species isolated from March to September 2005 were identified using the germ tube test and a commercial identification kit (Auxacolor 2, Bio-Rad, France). Susceptibility to amphotericin B and fluconazole was determined for all blood isolates (E-test method, AB BIODISK, Sweden). Results were read after 48 hours' incubation and interpreted according to NCCLS M27-A2, 2002. Quality control was performed using Candida albicans ATCC 90028 and Candida tropicalis ATCC 750. Patient data analysis included age, sex, specimen type, diagnosis and ward.
Of a total of 119 Candida isolates, 6 were excluded from the analyses as no patient details could be retrieved.
Seventy-five per cent of isolates were recovered from adults and 25% from children. C. albicans constituted 72%, and NAC 28%, of all Candida isolates from adult patients. In children, C. albicans accounted for 67%, and NAC for 33%, of isolates. The adult surgical intensive care unit (ICU) had the highest number of C. albicans isolates (15.2%). Other wards with a high number of C. albicans isolates included the labour ward and obstetric antenatal clinic (predominantly from urine specimens), the paediatric ICU, and the paediatric infectious diseases ward (predominantly HIV-infected patients). The paediatric infectious disease and oncology wards had the highest figure for NAC: 11.8% and 8.8% respectively.
C. albicans was the most common species isolated when comparing the isolation of C. albicans with NAC from urine (29% v. 17%), blood (16% v. 7%) and pus (8% v. 1%). All bloodstream isolates, including 17 C. albicans, 4 C. parapsilosis, 3 C. tropicalis and 1 C. lucitaniae, tested susceptible to both fluconazole and amphotericin B. Discussion
C. albicans (69%) is the most commonly isolated Candida species at Tygerberg Hospital, followed by C. glabrata (10%); C. parapsilosis (10%); C. tropicalis (4%); C. lusitaniae (2%); C. krusei (2%); and C. lipolytica, C. guilliermondii, C. famata (all 1%), which is consistent with international published data. (3)
Septicaemia was the most common diagnosis on the laboratory request forms. Positive blood culture isolates were mostly isolated from paediatric patients with malignancies where NAC predominated, which is consistent with studies citing that NAC occurs more frequently in leukaemia patients. (4) Candida species were also commonly isolated from urine. Urinary tract infections are usually associated with indwelling urinary catheters, particularly in patients on broad-spectrum antibiotics, although positive cultures may also represent contamination of urine specimens with vaginal flora, particularly in cases of vaginal thrush.
A high number of C. albicans were isolated from the surgical ICU. In contrast with trends among immunocompromised patients, C. albicans remains the predominant strain among ICU patients. (5) Risk factors for candidaemia include exposure to broad-spectrum antibiotics, invasive procedures and prolonged ICU stay.
All blood culture isolates tested susceptible to fluconazole, which is important since it has advantages over amphotericin B, including high oral bioavailability and low incidence of side-effects. Amphotericin B-susceptible results for C. lusitaniae should be interpreted with caution as this species has a higher propensity than other Candida species for developing resistance to amphotericin B. (6)
Accepted 7 January 2008.
(1.) Krcmery V, Barnes AJ. Non-albicans Candida spp causing fungaemia: pathogenicity and antifungal resistance. J Hosp Infect 2002; 50: 243-260.
(2.) Nucci M, Colombo AL. Emergence of resistant Candida in neutropenic patients. Braz J Infect Dis 2002; 6: 96-99.
(3.) Pfaller MA, Diekema DJ, International Fungal Surveillance Participant Group. Twelve years of fluconazole in clinical practice: global trends in species distribution and fluconazole susceptibility of bloodstream isolates of Candida. Clin Microbiol Infect 2004; 10 (Suppl 1): 11-23.
(4.) Richet HM, Andermont A, Tancrede C, Pico JL, Jarvis W. Risk factors for candidaemia in patients with acute lymphocytic leukaemia. Rev Infect Dis 1991; 13: 211-215.
(5.) Eggiman P, Garbino J, Pittet D. Epidemiology of Candida species infection in critically ill non-immunosuppressed patients. Lancet Infect Dis 2003; 3: 685-702.
(6.) Sanglard D, Odds FC. Resistance of Candida species to antifungal agents: molecular mechanisms and clinical consequences. Lancet Infect Dis 2002; 2: 73-85. Accepted 7 January 2008.
Department of Pathology, Division of Medical Microbiology, Stellenbosch University and National Health Laboratory Service, Tygerberg, W Cape
Tracy Arendse, BSc (Med Bioscience), BSc Hons (Med Microbiol)
Heidi Orth, MB ChB, MMed (Microbiol Path)
Corresponding author: H Orth (email@example.com)
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|Title Annotation:||Scientific Letters|
|Author:||Arendse, Tracy; Orth, Heidi|
|Publication:||South African Medical Journal|
|Article Type:||Letter to the editor|
|Date:||Jun 1, 2008|
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