Volume 20, Number 7—July 2014
Candida auris–Associated Candidemia, South Africa
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|EID||Magobo RE, Corcoran C, Seetharam S, Govender NP. Candida auris–Associated Candidemia, South Africa. Emerg Infect Dis. 2014;20(7):1250-1251. https://dx.doi.org/10.3201/eid2007.131765|
|AMA||Magobo RE, Corcoran C, Seetharam S, et al. Candida auris–Associated Candidemia, South Africa. Emerging Infectious Diseases. 2014;20(7):1250-1251. doi:10.3201/eid2007.131765.|
|APA||Magobo, R. E., Corcoran, C., Seetharam, S., & Govender, N. P. (2014). Candida auris–Associated Candidemia, South Africa. Emerging Infectious Diseases, 20(7), 1250-1251. https://dx.doi.org/10.3201/eid2007.131765.|
To the Editor: We noted the report by Chowdhary et al. (1) and report Candida auris as a causative agent of candidemia in South Africa, with an estimated prevalence of 0.3% (N.P. Govender et al., unpub. data). First isolated in 2009, C. auris is an emerging species associated with clinical disease (2–6). We analyzed 4 isolates submitted to the National Institute for Communicable Diseases (Johannesburg, South Africa) from 4 patients with candidemia who had been admitted to different public- and private-sector hospitals from October 2012 through October 2013.
Identification of the isolates was undertaken by using ChromAgar Candida medium (Mast Diagnostics, Merseyside, UK), Vitek-2 YST (bioMérieux, Marcy ľEtoile, France), API 20C AUX (bioMérieux), and sequencing of internal transcribed spacer (ITS) and D1/D2 domains of the ribosomal RNA gene (7), followed by microbroth dilution susceptibility testing (8). All isolates were misidentified as C. haemulonii and Rhodotorula glutinis by Vitek-2 YST and API 20C AUX assays, respectively (Table).
Similar to the findings of Chowdhary et al., all isolates assimilated N-acetyl-glucosamine (1). With the use of the CBS-KNAW database, pairwise sequence alignment of ITS region showed 99% sequence homology to Kuwait isolates, and alignment of D1/D2 domain showed 98% homology to the Kuwait/India isolates (9). In a neighbor-joining phylogenetic tree based on ITS sequences, South Africa isolates formed a cluster with India and Kuwait isolates (Technical Appendix [PDF - 69 KB - 2 pages]Figure).
Fluconazole MICs were high for all isolates (Table). Isolates 209 and 224 showed reduced voriconazole susceptibility with MICs of 1 μg/mL and 2 μg/mL, respectively, which is above the epidemiologic cutoff value for 11 Candida species (10). Isolates were susceptible to amphotericin B and echinocandins at low MICs Clinical data were available for 1 patient (Technical Appendix [PDF - 69 KB - 2 pages] Table). Two C. haemulonii isolates were identified during laboratory-based sentinel surveillance for candidemia in South Africa; the ITS region of one isolate was sequenced and the isolate identified as C. auris (N.P. Govender, pers. comm.). In this study, C. auris was misidentified by routinely used tests and was accurately identified by sequencing, in keeping with previous findings (1,3,4,6).
We thank Serisha Naicker for technical assistance.
The work was supported by the National Institute for Communicable Diseases. N.P.G. has received honoraria from MSD (Pty) Ltd South Africa (Merck) and Pfizer for speaking engagements and has received a research grant from Pfizer South Africa.
- Chowdhary A, Sharma C, Duggal S, Agarwal K, Prakash A, Kumar Singh P, New clonal strain of Candida auris, Delhi, India. Emerg Infect Dis. 2013;19:1670–3 .
- Satoh K, Makimura K, Hasumi Y, Nishiyama Y, Uchida K, Yamaguchi H. Candida auris sp. nov., a novel ascomycetous yeast isolated from the external ear canal of an inpatient in a Japanese hospital. Microbiol Immunol. 2009;53:41–4.
- Kim MN, Shin JH, Sung H, Lee K, Kim EC, Roy N, Candida haemulonii and closely related species at 5 university hospitals in Korea: identification, antifungal susceptibility, and clinical features. Clin Infect Dis. 2009;48:e57–61.
- Lee WG, Shin JH, Uh Y, Kang MG, Kim SH, Park KH, First three reported cases of nosocomial fungemia caused by Candida auris. J Clin Microbiol. 2011;49:3139–42.
- Oh BJ, Shin JH, Kim MN, Sung H, Lee K, Joo MY, Biofilm formation and genotyping of Candida haemulonii, Candida pseudohaemulonii, and a proposed new species (Candida auris) isolates from Korea. Med Mycol. 2011;49:98–102.
- Chowdhary A, Kumar VA, Sharma C, Prakash A, Agarwal K, Babu R, Multidrug resistant endemic clonal strain of Candida auris in India. Eur J Clin Microbiol Infect Dis. 2013. Epub ahead of print.
- White TJ, Bruns T, Lee S, Taylor J. Amplification and direct sequencing of fungal ribosomal RNA genes for phylogenetics. In: Innis MA, Gelfand DH, Sninsky JJ, White TJ, editors. PCR protocols: a guide to methods and applications. San Diego: Academic Press; 1990. p. 315–22.
- Clinical and Laboratory Standards Institute. Reference method for broth dilution antifungal susceptibility testing of yeasts; approved standard. 3rd ed. Wayne (PA): The Institute; 2008.
- CBS-KNAW Fungal Biodiversity Centre. Pairwise sequence alignment tool [cited 2013 Nov 1]. http://www.cbs.knaw.nl/Collections/BioloMICSSequences.aspx?file=all.
- 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;50:2846–56.
- Table. Identification and antifungal susceptibility results of 4 Candida auris isolates from 4 male patients with candidemia, South Africa, October 2012–October 2013
Technical AppendixCite This Article
Please use the form below to submit correspondence to the authors or contact them at the following address:
Nelesh P. Govender, National Institute for Communicable Diseases–Centre for Opportunistic, Tropical and Hospital Infections, Private Bag X4, Sandringham, 2132, South Africa
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