Volume 19, Number 3—March 2013
Cryptococcus gattii, Florida, USA, 2011
To the Editor: Cryptococcosis is a systemic mycosis most commonly caused by 2 species of encapsulated yeast: Cryptococcus neoformans and C. gattii. C. gattii is a globally emerging pathogen. In the United States, an outbreak of C. gattii infection caused by molecular type VGII has been ongoing since 2004, primarily in the Pacific Northwest (1). In addition, sporadic cases caused by molecular types VGI and VGIII have been reported in other areas, including North Carolina, Rhode Island, New Mexico, Michigan, Georgia, and Montana (2). We report a case of disseminated C. gattii VGIIb infection in the United States outside of the Pacific Northwest in an otherwise healthy Florida native who had no known travel to C. gattii–endemic areas.
In May 2011, a 50-year-old man sought care for 6 months of progressive pain, swelling, and deformity of the left thigh and stiffness of his left knee. His only recent trauma was a minor left lower extremity injury 2 years earlier when a horse rolled on him. However, he had no fracture, and the injury eventually healed without medical care. He also reported occasional productive coughing and smoking 1 pack of cigarettes per day for 30 years. The patient was born and raised in Pasco County, Florida, and had not traveled outside of Florida in 20 years. He reported working on a dairy farm and having regular exposure to horses and pigs. Imaging showed a possible fracture of his left femur at the same site as the horse-related injury 2 years earlier. Computed tomographic scan of the chest demonstrated mediastinal lymphadenopathy and multiple pulmonary nodules bilaterally.
The man underwent open biopsy and fixation of the left femur fracture. Arthrocentesis was performed on his left knee. The bone and joint fluid were full of India ink–positive encapsulated budding yeast. The serum cryptococcal antigen was 1:4,096 (reference value, negative). An HIV antibody test result was negative, and CD4 count was 800 cells/mL (reference 500–2,600 cells/mL). A lumbar puncture showed normal opening pressure, 27 leukocytes/mL (reference 0–5 cells/mL) (89% lymphocytes [reference 40%–80%]), protein 464 mg/dL (reference 15–45 mg/dL), and glucose 21 mg/dL (reference 40–70 mg/dL). The cerebrospinal fluid (CSF) cryptococcal antigen was 1:4,096 (reference, negative). Magnetic resonance imaging of the brain indicated mild enhancement of the lining of the lateral ventricles and mild dilatation.
C. gattii was isolated from the femur wound (superficial and deep) and CSF. Phenotypic testing was performed at ARUP Laboratories (Salt Lake City, UT, USA). In addition, the isolate was identified by multilocus sequence typing analysis as C. gattii type VGIIb by the Centers for Disease Control and Prevention (Atlanta, GA, USA) (3) (Figure).
The patient was treated with liposomal amphotericin B and 5-flucytosine for 4 weeks for disseminated C. gattii infection with musculoskeletal, central nervous system, and pulmonary involvement. Repeat lumbar puncture revealed a normal opening pressure. CSF studies were not performed on this specimen. The patient gradually improved and was discharged on oral voriconazole (to be continued for 1 year) after 4 weeks of hospitalization. By July 2011, the patient was walking with crutches and had no symptoms other than persistent swelling and pain of his left leg. As of July 2012, he had fully recovered except for some residual pain and weakness in his left leg.
In addition to its newfound endemicity in the US Pacific Northwest, C. gattii is known to be endemic to Australia, Papua New Guinea, South and Southeast Asia, and some parts of Mexico and southern California (4). Its genetic diversity, the global distribution of isolates, and a broad range of hosts contribute to its success as a pathogen. C. gattii can be subdivided into at least 4 molecular types: VGI, VGII, VGIII, and VGIV (5). Most isolates identified from the Pacific Northwest outbreak are molecular type VGII, primarily comprising 3 distinct clonal subtype lineages: VGIIa, VGIIb, and VGIIc (6,7).
The case reported here involved C. gattii (VGIIb) outside the Pacific Northwest or other regions to which it is known to be endemic. Although the source of this patient’s infection remains unknown, his previous horse-related injury is intriguing as a possible source (8). All 4 isolates from horses in the Centers for Disease Control and Prevention’s collection are molecular type VGIIb (S.R. Lockhart, unpub. data). Other infections have been reported to seed the body and proliferate in areas of prior injury (9); this patient could have inhaled the cryptococcal yeast during exposure to horses, which then disseminated and seeded his prior injury site.
Clinically, infection caused by C. gattii outbreak strains (VGIIa/b/c) is characterized primarily by pulmonary complaints and pneumonia, with or without meningitis (10); other strains, such as VGI, occur as CNS disease (10). The patient reported here showed mainly musculoskeletal complaints, although involvement of the CNS and pulmonary systems was later found. Continued surveillance for C. gattii outside the Pacific Northwest will help shed more light on the spectrum of clinical manifestations. In the United States, C. gattii is likely to be seen increasingly outside the Pacific Northwest and other regions to which it is endemic.
- Datta K, Bartlett KH, Baer R, Byrnes E, Galanis E, Heitman J, Spread of Cryptococcus gattii into Pacific Northwest region of the United States. Emerg Infect Dis. 2009;15:1185–91.
- Brandt ME, Hutwagner LC, Klug LA, Baughman WS, Rimland D, Graviss EA, Molecular subtype distribution of Cryptococcus neoformans in four areas of the United States. Cryptococcal Disease Active Surveillance Group. J Clin Microbiol. 1996;34:912–7 .
- Meyer W, Aanensen DM, Boekhout T, Cogliati M, Diaz MR, Esposto MC, Consensus multi-locus sequence typing scheme for Cryptococcus neoformans and Cryptococcus gattii. Med Mycol. 2009;47:561–70.
- Harris J, Lockhart S, Chiller T. Cryptococcus gattii: where do we go from here? Med Mycol. 2012;50:113–29.
- Bovers M, Hagen F, Kuramae EE, Boekhout T. Six monophyletic lineages identified within Cryptococcus neoformans and Cryptococcus gattii by multi-locus sequence typing. Fungal Genet Biol. 2008;45:400–21.
- Kidd SE, Hagen F, Tscharke RL, Huynh M, Bartlett KH, Fyfe M, A rare genotype of Cryptococcus gattii caused the cryptococcosis outbreak on Vancouver Island (British Columbia, Canada). Proc Natl Acad Sci U S A. 2004;101:17258–63.
- Byrnes EJ III, Bildfell R, Frank SA, Mitchell TG, Marr KA, Heitman J. Molecular evidence that the range of the Vancouver Island outbreak of Cryptococcus gattii infection expanded into the Pacific Northwest in the United States. J Infect Dis. 2009;199:1081–6.
- Duncan C, Stephen C, Campbell J. Clinical characteristics and predictors of mortality for Cryptococcus gattii infection in dogs and cats of southwestern British Columbia. Can Vet J. 2006;47:993–8.
- Chan ED, Kong PM, Fennelly K, Dwyer AP, Iseman MD. Vertebral osteomyelitis due to infection with nontuberculous Mycobacterium species after blunt trauma to the back: 3 examples of the principle of locus minoris resistentiae. Clin Infect Dis. 2001;32:1506–10.
- Centers for Disease Control and Prevention. Emergence of Cryptococcus gattii—Pacific Northwest, 2004–2010. MMWR Morb Mortal Wkly Rep. 2010;59:865–8.
- Figure. . . Neighbor-joining dendrogram of FL isolate (B9588, in boldface) with other US isolates showing that the FL isolate is identical to the VGIIb isolates from the US Pacific Northwest....
Suggested citation for this article: Kunadharaju R, Choe U, Harris JR, Lockhart SR, Greene JN. Cryptococcus gattii, Florida, USA, 2011 [letter]. Emerg Infect Dis [Internet]. 2013 Mar [date cited]. http://dx.doi.org/10.3201/eid1903.121399
Please use the form below to submit correspondence to the authors or contact them at the following address:
John N. Greene, Infectious Diseases and Hospital Epidemiologist, Moffitt Cancer Center, University of South Florida Morsani College of Medicine, 12092 Magnolia Dr, FOB-3, Tampa, FL 33612-9497, USA
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