Temperate climate niche for cryptococcus gattii in Northern Europe.
We investigated 112 decayed wood samples collected from inside trunk hollows of 52 living trees belonging to 5 families during April-May 2011 in Nijmegen, the Netherlands. The trees sampled were chestnut (Castanea sativa, n = 24), Douglas fir (Pseudotsuga menziesii, n = 17), oak (Quercus macranthera, n = 6), walnut (Juglans regia, n = 3), and mulberry (Morus alba, n = 2). The main criterion in selecting a tree for sampling was advanced age and presence of large trunk hollows variably sheltered from sunlight. The sampled sites had no bird nests and were apparently free from avian excreta. The decayed wood samples were collected with an in-house swabbing technique by using simplified Staib niger seed agar as described (4). The plates were incubated at 30[degrees]C and periodically observed up to 7 days for isolation of C. gattii and C. neoformans. Suspected colonies of Cryptococcus spp. were purified by dilution plating and identified by their morphologic and biochemical profiles, including development of blue color on L-canavanine-glycine bromothymol blue medium.
Identity of the isolates was confirmed by sequencing the internal trascribed spacer and D1/D2 regions, and they were genotyped by using amplified fragment-length polymorphism (AFLP) fingerprinting and multilocus sequence typing (MLST). The MLST loci CAP10, CAP59, GPD1, IGS, LAC1, MPD1, PLB1, SOD1, TEF1 a, and URA5 of the environmental C. gattii isolates were amplified and sequenced, and data were compared with MLST data from a large C. gattii population study (5) and with a recently published set of clinical, animal, and environmental C. gattii isolates from Mediterranean Europe and the Netherlands (Figure) (3,6,7). In addition, the mating type was determined with PCR by using mating type-specific primers for the STE12a and a alleles (8).
Four strains of C. neoformans species complex were isolated from the 112 decayed wood samples examined from 52 trees. One strain that originated from an oak tree (Q. macranthera), was identified as C. neoformans var. grubii. The remaining 3 strains, all originating from different hollows in a Douglas fir tree, were identified as C. gattii genotype AFLP4/VGI and mating type a. The strains were deposited at the CBS-KNAW (Centraalbureau voor Schimmelcultures/Royal Netherlands Academy of Arts and Sciences) Fungal Biodiversity Centre (accession nos. CBS12349, CBS12355, and 12356), and the sequences were deposited in GenBank (accession nos. JN982044-JN982073).
MLST analysis showed that the C. gattii isolates in our study are more closely related to the clinical isolate from the Netherlands (6) and to the clinical and environmental C. gattii isolates (AFLP4/VGI) reported from the Netherlands and other countries in Europe than to isolates from outside Europe (3,7,8). The autochthonous C. gattii AFLP4/VGI isolate, CBS2502 (earlier identified as C. neoformans) isolate from the Netherlands was recovered postmortem in 1957 from the lungs of a pregnant woman with cryptococcosis (6). This patient came from a low socioeconomic strata, was unlikely to have traveled outside the Netherlands, and probably acquired the infection indigenously from an environmental source (6).
Furthermore, genotype AFLP4/VGI appears to be the genotype of C. gattii prevalent in Europe (3,7,8). Outside Europe, C. gattii has been reported from Douglas fir trees in Vancouver Island, British Columbia, Canada; however, those isolates represented another molecular type, i.e., AFLP6/VGII (9). Genotype AFLP 4/VGI C. gattii isolates have been implicated in human infections in that region, but to our knowledge, no environmental isolates have been found until now.
Our detection of C. gattii in the environment and its previous isolation from a clinical case in the Netherlands suggests that this pathogen is endemic to the temperate climate of northern Europe. This suggestion agrees with the concept emerging from a decade of investigations in Canada and the Pacific Northwest that the geographic distribution of C. gattii extends to the temperate region, albeit with another AFLP genotype (1,9,10). Further environmental studies are likely to show a wider spectrum of host trees and higher environmental prevalence of C. gattii in this continent than what appears in the literature.
This work was supported partly by Department of Science and Technology, Government of India (F. no. SR/SO/HS62/2008) and by Labland BV, Wijchen, the Netherlands, with a research fellowship for A.C.
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Anuradha Chowdhary, Harbans S. Randhawa, Teun Boekhout, Ferry Hagen, Corne H. Klaassen, and Jacques F. Meis
Author affiliations: University of Delhi, Delhi, India (A. Chowdhary, H.S. Randhawa); Centraalbureau voor Schimmelcultures Fungal Biodiversity Center, Utrecht, the Netherlands (T. Boekhout); Canisius Wilhelmina Hospital, Nijmegen, the Netherlands (F. Hagen, C.H. Klaassen, J.F. Meis); and Radboud University Nijmegen Medical Centre, Nijmegen (J.F. Meis)
Address for correspondence: Jacques F. Meis, Department of Medical Microbiology and Infectious Diseases, Canisius Wilhelmina Hospital, Weg door Jonkerbos 100, 6532 SZ Nijmegen, the Netherlands; email: j.meis@cwz. nl
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|Author:||Chowdhary, Anuradha; Randhawa, Harbans S.; Boekhout, Teun; Hagen, Ferry; Klaassen, Corne H.; Meis, J|
|Publication:||Emerging Infectious Diseases|
|Article Type:||Letter to the editor|
|Date:||Jan 1, 2012|
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