Candida albicans and C. tropicalis Isolates from the Expired Breathes of Captive Dolphins and Their Environments in an Aquarium

Genotypes of Candida spp. isolated from exhalation of 20 dolphins, 11 water samples from captive pools, and 24 oral cavities of staff members in an aquarium using a combination of multiple drug resistance 1 gene (MDR1) and the internal transcribed spacer (ITS) 1 5.8s-ITS 2 regions of ribosomal RNA gene (ITS rDNA) sequences were studied. The holding ratios of the dolphins, captive pools, and staff members were 70, 90, and 29%, respectively. Isolated pathogenic yeast species common to the dolphins and environments were Candida albicans and C. tropicalis. Identical genotypes in both Candida spp. based on the combination of MDR1 and ITSrDNA were found in some dolphins, between a dolphin and a staff, among dolphins and environments, and among environments. The results indicated the diffusion and exchange of pathogenic yeasts at the aquarium among dolphins and environments. The isolates at the aquarium showed higher rates of resistance to azole antifungals compared to reference isolates.

Besides being highly pathogenic, the above fungal species were isolated from exhalation, although the findings do not support correlations between mycoses-fungal pneumonia and/or disseminations and these organisms [3,34]. In fact, even in healthy dolphins, pathogenic fungal species were isolated from exhalation [35]. Most species of pathogenic fungi 2 Veterinary Medicine International isolated from exhalation were environmental contaminants while C. albicans and other Candida spp. existed as normal fungal residents of mucous membranes [3,35]. Furthermore, these human pathogenic yeast species were isolated from more than 70% of captive dolphins and environmental water samples [19].
According to Buck [19] and Dunn et al. [17], there is no transmission or diffusion of Candida spp. between dolphins and environments. However, there has been no investigation of the correlation between human pathogenic yeast isolates from dolphins and their keeping conditions, including captive pools and staff members, based on molecular biological studies.
The present study aims to investigate the fungal flora of pathogenic yeast species from the exhalation of dolphins, captive pools, staff members, and air in front of the dolphin show stage at the Churaumi Aquarium, Okinawa, Japan, to clarify correlations among the isolates from dolphins, captive environments and staff members using genotypes of multiple drug resistance 1 gene (MDR1) having adequate sites of diversity for strain identification [36] and the internal transcribed spacer (ITS) 1 5.8 s-ITS 2 regions of ribosomal RNA gene (ITS rDNA) sequences recommended as the barcoding gene of pathogenic fungi for differentiation of species [37].  Table 1. The survey was performed with the permission of Churaumi Aquarium, Okinawa, Japan, with a perspective for animal welfare.

Isolation and Identification of Pathogenic Yeasts from
Dolphins. Four exhalations from each animal were collected. Two potato dextrose agar plates supplemented with 100 mg/L of chloramphenicol (CPDA) and two CHROMagar Candida plates (Kanto Chemical Co. Ltd., Tokyo, Japan) were placed approximately 40 cm above the blowhole. One plate per an exhalation was used. The plates were cultured at 25 • C for 1 week, and the sprouted yeast colonies were counted. Colonies were collected according to slight differences in color on CHROMagar Candida plates and in size on CPDA. The collected yeast colonies were cultured on potato dextrose agar slants at 35 • C for 48 hours. Colonies having growth ability at 35 • C were identified on the basis of color on the CHROMagar Candida plates and species-specific polymerase chain reaction (PCR) for detecting topoisomerase II gene (Top II PCR) [43]. When plural isolates from one animal having identical genotype based on MDR1 and ITS rDNA sequences have existed, the isolate was treated as one isolate. Mycelial colonies that grew on the plates were ignored at the present study.

Captive Pools and Discharged
Water to the Sea. Samples were collected from eight pools of the aquarium for dolphins, two for manatees (Trichechus manatus), and at a discharging point of all pools to the sea. The relationship among pools and the water system is shown in Table 2.
Pools 1, 2, 3, and 8 communicated with each another and are supplied, seawater directly; this is indicated as water group A. Pools 4, 5, 6, and 7 indicated as water group B, also communicate with each another, and are supplied by sea water, and overflowing water from a fish aquarium. Pools 9 and 10 are supplied by salty well water, indicated as water group C. Seawater in discharge point is indicated as water D.
Water for captive pools is taken 300 m from the shore and at a depth of 20 m. Water exchange by an overflow system works at 8, 4, and 24 times of the volume of water per day at water systems A, B, and C, respectively. A complete change of water is provided 2 or 3 times a week, and this is aided by a scrubbing brush and by using 12% concentration of hydrochloride solution.
Pools 1, 2, and 3 are used for the dolphin show at least 4 times a day, and sometimes the splash sprays on the audience. A special exhibition of training of a dolphin with an artificial tail fin is held at pools 4 and 5 at least twice a day, and the touching of dolphins by registered visitors is allowed every weekend and on holidays. Pools 9 and 10 also have opportunities for registered visitors to feed the manatees.
The inhabiting dolphin members are not fixed. They are placed depending on the programs of dolphin shows, health conditions, and affinities. In contrast, the housing of the manatees is fixed depending on the sex. The dolphins and manatees are nursed and treated by the same staff members. Foot-bathing tubs with hydrochloride are placed at each pool entrance.

Isolation of Pathogenic Yeasts from Water Samples.
Five hundreds milliliter of water samples taken from the surface of the captive pools were filtered with a 0.22 µm pore-sized filter. The filters used for filtration were washed with 5 mL of sterile saline. One milliliter of the saline was put on CPDA and CHROMagar Candida plates and cultured at 25 • C for 7 days. Yeast-form colonies were picked up and maintained on PDA slants at room temperature and identified by Top II PCR [43]. Mycelial colonies that grew on the plates were ignored at the present study.

Oral Pathogenic Yeast Flora of Staff Members.
Twentyfour staff members (11 men, 13 women, 20-50 years old) were studied under personal agreement with informed consent. The survey was performed with the permission of Churaumi Aquarium, Okinawa, Japan. The ethic committee  at the Chiba University judged that the present study had no infringement. A sterile cotton tip was placed on the center of the tongue for 1 minute with rolling movements. The cotton tip was soaked in 2 mL of sterile-distilled water and then stirred vigorously for 10 seconds. One hundred microliters of the water was spread on a CHROMagar Candida plate cultured at 35 • C for up to 7 days in duplicate. The sprouted yeast colonies were picked up and maintained on PDA slants at room temperature and identified by Top II PCR [43].
2.6. Airborne Fungi during Dolphin Show. One hundred liters and/or 500 L air was collected with an air sampler (Gunze, Tokyo, Japan) using an agar strip containing CPDA during the 4 dolphin shows at 11:00, 13:30, 15:00, and 16:00 in February 2007. The agar strips were cultured at 25 • C for 7 days. The yeast colonies were picked up and cultured on PDA slants at 35 • C for 2 and 7 days if the colonies were identified.

DNA Extraction.
Fungal DNA was extracted with a DEXPAT Kit (TaKaRa, Ohtsu, Japan), following the manufacturer's protocol with slight modification, from cultures incubated on PDA slants at 25 • C for 48 to 96 hours. Approximately 100 µL of fungal mass was transferred to a sterilized microtube (1.5 mL) and homogenized with 0.5 mL of DEXPAT solution with a plastic pestle. The mixture was incubated at 100 • C for 10 minutes and centrifuged at 4 Veterinary Medicine International 12,000 pm (13, 201 g) for 10 min. The supernatant was used as the DNA sample.

Multiple Drug Resistant Gene 1 (MDR 1) Sequencing.
The DNA was amplified with primers described by Tavanti et al. [36]. The primer sets for C. albicans were MDR1 CAF (5 -TGT TGT GTT TCA CTT TAC CT-3 ) and MDR1 CAR (5 -AGG AGC ACC AAA TAA TGG GA-3 ), and those for C. tropicalis were MDR1 CTF (5 -TGT TGG CAT TCA CCC TTC CT-3 ) and MDR1 CTR (5 -TGG AGC ACC AAA CAA TGG GA-3 ). DNA extract at 2.5 µL, a piece of Ready-to-Go beads (Amersham Pharmacia, Tokyo, Japan), 2.5 µL of 10 pM of the above primers, and 17.5µL of distilled water were mixed. Amplification was performed for an initial denaturing step of 7 min at 94 • C, 30 cycles of 1 min at 94 • C for DNA denaturation, 90 seconds at 55 • C for primer annealing, 90 sec at 72 • C for primer extension, a final extension of 10 min at 72 • C, and a 4 • C soak. The amplified PCR product was confirmed by electrophoresis on 1.0% agarose in 1x/TBE buffer (0.04 M Tris-boric acid, 0.001 M EDTA [pH 8.0]) and ethidium bromide staining. The amplified product was purified with a PCR purification kit (QIAquick PCR Purification Kit, QIAGEN, Hilden, Germany) according to the manufacturer's instructions. Cycle sequencing was performed with BigDye fluorescent-labeled DyeDeoxy protocols (BigDye Terminator ver. 1.01; Amersham Pharmacia, Piscataway, NJ, USA) as follows: 15 sec at 96 • C, 30 sec at 55 • C, and 4 min at 60 • C for 25 cycles, followed by a 4 • C soak. All sequencing reactions were run on an automated DNA sequencer (3100, Applied Biosystems, Foster City, CA, USA) after purification by ethanol precipitation. DNA sequences were aligned by GENETEX-MAC genetic information processing software (Software Development Co., Ltd. Tokyo, Japan).
2.9. ITS rDNA Sequencing. We used the same reaction system as that used for MDR1 detection with a piece of Ready-to-Go beads and the primer set ITS-5 (5 -GGA AGT AAA AGT CGT AAC AAG G-3 ), and ITS-4 (5 -TCC TCC GCT TAT TGA TAT GC-3 ) [38]. Amplification was performed for an initial denaturing step of 4 minutes at 95 • C, 30 cycles of 1 minute at 94 • C for DNA denaturation, 90 seconds at 50-53 • C for primer annealing depending on samples, 2 min at 72 • C for primer extension, a final extension of 10 min at 72 • C, and a 4 • C soak. After confirming the amplified DNA by electrophoresis, being purified using a kit, it was labeled with the primers ITS-5, ITS-4, ITS-2 (5 -GCT GCG TTC TTC ATC GAT GC-3 ) and ITS3 (5 -GCA TCG ATG AAG AAC GCA GC-3 ) [38] as follows: 15 sec at 96 • C, 30 sec at 50 to 55 • C, and 4 min at 60 • C for 25 cycles, followed by a 4 • C soak, and sequenced.
Because yeast is a diploid organism, analysis of MDR 1 and ITS rDNA sequences from both C. albicans and C. tropicalis was based on the data set of only the variable bases or the apparently predominant peak used previously with C. albicans multilocus sequence typing. When showing almost equal peaks, the base was determined as a wobble base using a universal code; K: G+T, M: A+C, R: A+G, S: C+G, W: A+T, and Y: C+T [36, 39, 40].

Genotypings.
The MDR 1 and ITS rDNA sequences from both C. albicans and C. tropicalis were deposited in the GenBank via DDBJ (DNA database of Japan, Mishima, Shizuoka, Japan). The combined sequences of MDR 1 and ITS rDNA sequences were analyzed by the Unweighted Pair Group Method with Arithmetic mean (UPGMA) using GENETYX-MAC ver. 13.0 (GENETYX Corporation, Tokyo, Japan) genetic information processing software and given a serial number of genotype.
2.11. Susceptibility Testing. Susceptibility tests were performed according to the broth microdilution-modified method of the CLSI M27-A3 standard [41,42] accepted standard using RPMI 1640 medium (Sigma, Poole, UK) buffered to pH 7.0 with MOPS (Sigma) and serial concentrations of amphotericin B (AMPH-B), flucytosine (5-FC), itraconazole (ITZ), fluconazole (FLCZ), miconazole (MCZ), and micafungin (MCFG). The latter three antifungals were included even though the method was originally described for use with AMPH-B, 5-FC, and ITZ. The test was performed in 96well round-bottomed plastic plates using 100 mL of RPMI 1640 medium with fungal cells and antifungal substances (Dry plate koubo you, Eiken Co. Ltd., Tokyo, Japan). Data were obtained from duplicate trials. The mean or the lower data were taken. Reading results and the evaluation of the susceptibility categorized as susceptible, doze-dependent susceptible, intermediate, resistant and nonsusceptible on 5-FC, ITZ, FLCZ, and MCFG were followed to CLSI guideline [41,42]. The category for susceptibility extracted from the CLSI guideline was shown in Table 1.
Twelve references isolates each for C. albicans and C. tropicalis stored in our center were added as references for molecular biological studies and the susceptibility test to antifungal substances.

Isolates from Dolphins.
The pathogenic yeasts isolated from exhalation of dolphins were C. albicans, C. tropicalis, and C. glabrata. The total numbers of colonies and identified species are shown in Table 1. Fourteen out of 20 dolphins, corresponding to 70% of the animals, had some kinds of pathogenic yeast species. The holding rates of C. albicans, C. tropicalis, and C. glabrata were 40%, 30%, and 5%, respectively.
Except for dolphin number 1, the rest of the fungalpositive animals had the same species of Candida in investigations of both August 2006 and February 2007 ( Table 2). The genotypes and susceptibility to antifungal drugs of the C. glabrata isolate are not shown in the present study because there was only one isolate throughout the study.
Mycelial fungal species were also obtained from dolphin samples although the number of colonies was 1 or 2 per animal. The filamentous fungal species isolated from the exhalation of dolphins were shown in Table 3.  the summer investigation while the winter investigation resulted in 4 of the 11 sites showing only C. albicans isolates. The total number of colonies was less than 5 regardless of the collecting time or place. Except for Pool No. 10 nursing the male manatees, all water sources were positive for pathogenic yeasts for at least one collection period corresponding to 90.9% (Table 4). Candida albicans from 1 man and 2 women, C. dubliniensis from 1 woman, C. parapsilosis from 1 man, and Cryptococcus albidus from 1 man and 1 woman were isolated from the oral samples of staff members, corresponding to 29.2% (7 out of 24 individuals). The number of colonies per plate was more than 100, regardless of the sample. Except for C. albicans, genotypes and susceptibility to antifungal drugs were not shown in the present study.

Isolates from
Although mycelial fungal species were Aspergillus niger, A. ochraceus, Cladosporium sp., Fusarium sp., Penicillium sp., and Trichoderma sp. identified in the basis of morphology, there was no pathogenic yeast from the air samples collected in the front of the dolphin shows.

Consistent Fungal Species between Dolphins and Environments.
The consistent fungal species through the dolphins, the water samples, and staff members were C. albicans and C. tropicalis, as shown in Tables 5 and 6, respectively. The plural isolates from an animal or a site at the same collection period were due to the size of the colony on CPDA and/or CHROMagar Candida, the color on CHROMagar Candida, and the genotype based on the combination of MDR1 and ITS rDNA.
3.4. MDR 1 and ITS rDNA Sequences in C. albicans. The sequences of MDR 1 in C. albicans, consisting of 645 bases, were divided into 16 genotypes with at least 98.8% identity, and those in ITS rDNA, consisting of at least of 447 bases, were divided into 12 genotypes with at least 99.5% identity. Twenty-four genotypes based on combined sequences of MDR 1 and ITS rDNA among C. albicans isolates showed more than 99.2% identity. Although we tried to determine the ITS sequences on isolates IFM 55378, 55281, and 55298 many times, these sequences were impossible to complete, because of extremely overlapping sequence. The accession numbers of the genes and the genotypes were shown in Table 5.
Except for C. albicans isolates derived from the dolphin No. 11 having 2 different genotypes of C. albicans collected at the 2006 summer, there was no dolphin having different genotype simultaneously at the same collecting time. Candida albicans isolates from dolphin numbers 3, 4, and 13 showed different genotypes depending on the collecting seasons. Isolates IFM 55378 derived from the dolphin No. 9 and IFM 55281 from the dolphin No. 16 were treated as exceptions for genotyping analysis, because of lacking ITS rDNA sequences. Candida albicans isolates from the captive pools; numbers 1, 2, and 4 of the same collecting period showed different genotypes, except for the isolate IFM 55298 lacked the genotype of ITS rDNA.
The genotypes A, B, G, and H are common among C. albicans isolates from dolphins and environment. The genotype C is identical between a dolphin and a staff. There was no common genotype between the isolates from the aquarium and the references in C. albicans. There was no common genotype between the isolates from the aquarium and the references in C. albicans.
3.5. MDR 1 and ITS rDNA Sequences in C. tropicalis. The sequences of MDR 1 in C. tropicalis, consisting of 645 bases, were divided into 11 genotypes with at least 97.5% identity, and those in ITS rDNA, consisted of at least 435 bases, were divided into 5 genotypes with at least 94.5% identity. Thirteen genotypes based on combined sequences of MDR 1 and ITS rDNA among C. tropicalis isolates had more than 97.2% identity. In addition, the ITS rDNA sequence of isolate IFM 55379 derived from dolphin No. 10 was not determined and treated as an exception for genotype analysis because of extremely overlapping signals. The accession numbers of the genes and the genotypes were shown in Table 4.
Candida tropicalis isolates from dolphin No. 7 collected in the summer had 2 genotypes and in the winter had independent one. Isolates from dolphin No. 2 were identical irrespective of the collecting time while dolphin No. 14 had different clones depending on the collecting time.  The genotypes A and B are common among C. tropicalis isolates from dolphins and environment. In addition, the genotype A was detected not only in isolates at the aquarium but also in the reference ones.
3.6. Antifungal Susceptibility. The susceptibilities to antifungal agents were shown in Tables 5 and 6. No isolate showed resistance to AMPB among the C. albicans and C. tropicalis isolates from dolphins, environments, and reference.
Three of 15 (20%) from dolphins, 1 of 12 (8.3%) from the environments, and 1 of 12 (8.3%) from the references in C. albicans isolates showed resistance to 5-FC while none of C. tropicalis isolates regardless of origins showed resistance to 5-FC.
Thirteen of 15 (86.7%) from dolphins, 7 of 12 (58.3%) from the environments, and 1 of 3 (33.3%) from the staffs showed resistance or dose-dependent susceptibilities to FLCZ; however there was no isolate that showed resistance to the compound in the reference C. albicans isolates. Eight of 10 (80%) from dolphins, 1 of 6 (16.7%) from the environments, and 3 of 12 (25%) from the reference C. tropicalis isolates showed resistance or dose-dependent susceptibilities to FLCZ.
Twelve of 15 (80.0%) from dolphins, 10 of 12 (83.3%) from the environments, and 1 of 3 (33.3%) from the staffs showed resistance susceptibilities to ITZ; however no isolate showed resistance to the compound in the reference C. albicans isolates. Eight of 10 (80%) from dolphins, 3 of 6 (50%) from the environments, and 6 of 12 (50.0%) from the reference C. tropicalis isolates showed resistance or dosedependent susceptibilities to ITZ.
There was no correlation between resistance or dosedependent susceptibilities to antifungal agents and the genotype of MDR1 or ITS rDNA in either C. albicans or C. tropicalis isolates. In addition, one isolate derived from the captive pool no. 5 collected at the winter 2007 showed extremely resistant to MCFG as 16 µg/mL. The susceptibilities to MCZ were listed as reference data.

Isolating Rates for Pathogenic Yeasts from Dolphins.
According to Buck et al., the holding rates of Candida spp. in free-ranging dolphins were as follows: C. albicans, 7.0%; C. tropicalis, 14.3%; and Candida sp., 14.3% [35]. At the present study, the holding rates of Candida spp. in dolphins and captive-pools were 70% and 90.9%, respectively, which were higher than those of free-ranging dolphins. Similarly, anther report by Buck et al. [35] demonstrated that the captive environments of dolphins showed a higher incidence, over 70%, in feces and pool waters of captive bottlenosed dolphins (Tursiops truncatus). It suggested that the data from various aquariums or institutions might vary depending on the nursing conditions and the climates of the aquarium. Further studies will confirm the average data of the holding ratio of pathogenic yeast species in captive dolphins and their nursing environments with considerations of age, sex, and physiological data.

Relationship between Fungal Exhalation and Health.
The relationship between fungal exhalation phenomena from blowholes and health condition has not been confirmed [3,19], although many veterinarians, animal-keepers, and nurses in aquariums in Japan consider the isolations of Candida spp. from exhalation as being indicative of illness or weakness in dolphins [34]. We agree that a small numbers   Although some pathogenic mycelial fungal species such as Aspergillus niger, Aspergillus spp., Phoma sp., Curvularia lunata, Aspergillus sp., Schizophyllum commune, Aureobasidium pullulans, and Fusarium sp. were isolated from exhalation from blowholes, there was no correlation on the health of dolphins. We should wait for the accumulation of data on the fungal flora from exhalation and body conditions including blood and other physiological examinations, for judging the existence of the correlation.

Seasonal Characteristics on the Isolates.
Interestingly, water source-derived C. tropicalis isolates disappeared in the winter, suggesting that C. tropicalis might have some difficulty surviving in winter conditions, and even in subtropical areas. The average temperatures of the environment and captive pools in February were 19.2 • C and 22.2 • C, while those in August were 31.4 • C and 28.8 • C, respectively. It is considered that the differences in water temperature might be one of the factors for the existence of C. tropicalis. Future investigations may confirm this phenomenon.

Genotypes.
Genotypes based on MDR 1 seemed to be suitable for molecular epidemiological study in a confined area due to adequate sites of diversity [36,39]. On the other hand, genotypes of ITS rDNA could be useful for the identification of some intraspecies diversity and strain differentiations [44], and could show correlations to geographic, regional, and/or host-dependent genotypes of pathogenic fungi determined by multiple gene analysis [45]. Furthermore, the combination of 2 genes; MDR 1 and ITS rDNA, could indicate more detailed diversity of the genotypes of Candida spp. than those by MDR 1 or ITS rDNA alone. Then we discussed on the distributions of genotypes for C. albicans and C. tropicalis isolated in the aquarium based on the combined genotypes of MDR 1 and ITS rDNA. In the basis of these combinations, we could demonstrate the existences of coincident pathogenic yeast species and their genotypes in both C. albicans and C. tropicalis between or among dolphins, captive-pools and a staff member although Buck have denied the possibility that pathogenic yeasts are dispersed to other dolphins and environments [19]. Especially, the common genotype of C. albicans to both a dolphin and a staff member might be exchanged between them since the animal has been receiving medicine and surgical treatments from the staff member working as a veterinarian.
Interestingly, the genotype of C. albicans isolated from dolphin No. 5 which suddenly died of bacterial colitis and pneumonia was detected in the isolate from dolphin No. 3 and captive pools numbers 1, 2, and 4. Those of C. tropicalis isolated from the same dolphin No. 5 have also been detected in the isolate from dolphin No. 10, from captive pools No. 5 and 6, and from drained seawater. The animal might be a dispersal source for both C. albicans and C. tropicalis to other animals as well as to the environment. The source of pathogenic yeasts might be related to the environmental water since common genotypes among the dolphins and pool water samples were found in C. albicans and C. tropicalis isolates. Isolates from captive pools free of dolphins had the same genotypes of Candida spp. isolates as the dolphins. Nevertheless, any systematic relationship of the water supply could not be found between pathogenic yeast species and captive pools or seawater. Exchanges of dolphins, common staff members for dolphins and manatees, and/or the influence of the audience might play roles in the dispersing, exchanging and introducing pathogenic yeasts. Further studies and detailed molecular profiles of the isolates may confirm the principle sources of the pathogenic yeasts. The coincidence of genotypes in dolphins and in environmental isolates to the reference isolates of C. tropicalis suggested that such genotypes might be introduced from audiences or from sea water, and/or be very common in the world.

Attention for Sample
Collection. Attention to plural isolates from the same animal at the same sampling period might be important. Although the differences in the colonies were slight with regard to size on CPDA or color on CHROMagar Candida, the clones showed different genotypes and/or susceptibilities to antifungal agents as detected in the C. albicans isolates IFM 55273 and IFM 55274 derived from dolphin No.11 isolated at the August 2006. Therefore, at least 2 or more colonies, depending on size and/or color, should be selected for identification, molecular biological analysis, and susceptibilities to antifungal drugs.

Risk to Be
Audience. The fishy smell in the auditorium of the dolphin show indicates a possible spread of the breath, including pathogenic yeasts, to the audience, in spite of the fact that such pathogenic yeast isolates from air samples collected in the front of the dolphin shows were not detected. This suggests that the possibility of inhaling or being exposed to pathogenic Candida spp. from the exhalation of dolphins is relatively low. Nevertheless, it seems dangerous to approach the blowholes to a distance closer than 40 cm. For example, activities such as kissing or touching dolphins and, for pregnant women, swimming with dolphins should be approached with caution. The exact distance from the blowholes of dolphins from where it would be free of yeast-blow needs to be measured. Although there was no record of fungal infection caused by inhalation of the exhalation of dolphins, an immunocompromised person should be strongly urged to avoid such close contact with dolphins.

Characteristics on the Susceptibilities to Antifungal Drugs.
The high ratio in isolations of pathogenic yeasts derived from the dolphins compared with the reference strains was the same as that in human oral fungal flora with HIV-infected or immunocompromised hosts [46,47]. Frequent administrations of antibiotics and steroids might be one of the explanations, but data regarding the parameters concerning stress and immunosupression, defense mechanisms against microorganisms, and drug metabolisms in the animals, even in normal immune data or blood chemical profiles, are not yet sufficient for meaningful discussion, although the correlation between the occurrence of lobomycosis and immune status of the dolphins was reported in Floridan bottlenose dolphins [10,[48][49][50][51].
Furthermore, the higher incidences of resistance to azolerelated antifungal agents in the isolates from dolphins and environments might be related to the sodium chloride in sea water, a speculation drawn from the correlations among resistance to chemical compounds, pathogenicity, and sodium chloride [52].

Correlation between the Genotype and Resistance to
Antifungal Agents. According to Tavanti et al., MDR 1 alone cannot define the relationship between genotypes and profiles of antifungal agents [36]. In the present study, no correlation was found between resistance or dosedependents susceptibilities to azole-related antifungal agents and the genotypes of MDR1 and/or ITS rDNA in either C. albicans or C. tropicalis, since an identical genotype based on MDR1 and ITS rDNA sequences has shown different profiles of susceptibilities to azole-related antifungal agents, regardless of origin. The reference isolates, giving a higher ratio of resistant isolates, could not help in determining the specific genotypes based on the combination of MDR1 and ITS rDNA sequences.

Conclusions
The detection of common genotypes on Candida spp. among dolphins, environments, and staff members pointed to the dissemination of pathogens at the aquarium. Thus, it seemed to be important to consider the effects on audiences from dolphins and the reverse relations for controls of zoonotic infections. In addition, the sequence of MDR 1 showed adequate numbers of variations, indicating that the gene might be useful for molecular epidemiological studies.