Hemolytic and urease activities in vibrios isolated from fresh and frozen oysters

Introduction: The present study aimed to survey the Vibrio microbiota of oysters (Crassostrea rhizophorae) obtained from restaurants in Fortaleza, State of Ceará, Brazil, and to identify virulence factors. Methods: The isolated vibrios were submitted to biochemical identification and were tested for hemolytic and urease activities. Results: The isolated strains belonged to 13 species, with predominance of Vibrio mimicus. Of the strain isolates only from fresh samples, 20.5% and 2.8% showed hemolytic and urease activities, respectively. Conclusions: The findings support the little-publicized claim that Vibrio species other than V. parahaemolyticus and V. vulnificus can represent a health risk to public health.

Vibrios are part of the native microbiota of marine environments and organisms.Up to 40% of water-column bacteria are associated with zooplankton.Among these, vibrios have a competitive advantage in the colonization of chitinous exoskeletons 1 .Due to their abundance in the water column, vibrios may be up to a hundred times more concentrated in filter-feeding mollusks than in the immediate environment 2 .
Since vibrios are part of the autochthonous bacterial community colonizing bivalves, it comes as no surprise that they have been implicated in many outbreaks related to oyster consumption.The vibrio species most often associated with disease from consumption of oysters in natura are Vibrio parahaemolyticus, V. vulnificus, and V. cholerae 3 .However, virulence factors similar to those displayed by V. parahaemolyticus are detected in other vibrio species with increasing frequency.Thus, Nishibuchi et al. 4 found that V. hollisae strains from clinical samples can carry the hemolysinencoding gene tdh, a marker of virulence.Other vibrio species isolated from marine organisms have also been shown to be capable of β-hemolysis 5 .
The objective of the present study was to survey the Vibrio microbiota of fresh and frozen oysters (Crassostrea rhizophorae) obtained from restaurants in Fortaleza, and to identify phenotypical virulence factors by testing strains for β-hemolysis and urease activity.
The study was based on 15 samples of fresh oysters and 15 samples of frozen oysters (C.rhizophorae) obtained from two restaurants in Fortaleza City (Northeastern Brazil) between August 2009 and August 2010.Each sample consisted of 10 specimens, for a total of 300 specimens examined.Oysters with closed valves were placed in labeled polyethylene bags and transported in isothermal boxes to the Laboratory of Seafood and Environmental Microbiology (LABOMAR/UFC) for processing.Transportation did not exceed two hours.
The oysters were washed in tap water and vigorously scrubbed, then opened under aseptic conditions for retrieval of the intervalvular tissues and fluid.A 50-gram portion was taken from each sample of 10 specimens and added to 450mL alkaline peptone water (pH 8.5) containing 1% NaCl.The sample was homogenized in a magnetic stirrer (Cole Parmer, Model 51450) for 15min.The homogenate (which corresponded to a 10 -1 dilution) was used to make serial decimal dilutions from 10 -2 to 10 -4 .Subsequently, 0.2mL aliquots of each dilution were spreadplated on thiosulfate-citrate-bile salt-sucrose agar (TCBS-Difco) and incubated at 35°C for 18h.Three yellow or blue-green colonies for each sample were randomly select and cultured in tryptone soy agar (TSA-Difco) supplemented with 1% NaCl.All colonies were submitted to biochemical identification using the key developed by Noguerola and Blanch 6  Eleven Vibrio species were identified in the microbiota of fresh samples, compared with five species in frozen samples (Table 1).Only three species (V.rumoiensis, V. coralliilyticus, and V. litoralis) were isolated from fresh and frozen oysters concomitantly.The species V. mimicus, V. ponticus, V. hepatarius, V. proteolyticus, V. lentus, V. natriegens, V. pelagius I, and V. scophthalmi were isolated from fresh samples only.On the other hand, V. vulnificus and V. diazotrophicus were detected only in the microbiota of frozen samples.
Seven strains (20.5% of total) belonging to five species tested were hemolytic-positive in Wagatsuma agar.Only one (2.8%) of our 35 Vibrio strains was capable of ureolysis (Table 2).None of our strains were both Kanagawa-positive and ureolytic.
The Vibrio diversity was greater in fresh than in frozen samples, suggesting that handling and storage practices have an impact on bacterial diversity and confirming the claim that vibrio proliferation is greater at room temperature than under cold storage.This is supported by Pereira et al. 7 , according to whom prolonged storage of oysters at room temperature favors bacterial multiplication.
The most frequently isolated species were V. mimicus (fresh samples) and V. vulnificus B3 (frozen samples).The former has been reported abundantly in the literature since the early 1980s.Thus, Shandera et al. 8 described the clinical and epidemiological characteristics of infection caused by V. mimicus and concluded that the species should be considered in the differential diagnosis of acute gastroenteritis following ingestion of seafood, especially oysters in natura.
The detection of V. vulnificus in frozen oyster samples does not match the findings of Prapaiwong et al. 9 , who observed the species in fresh samples only.However, Bryan et al. 10 suggested that the effectiveness of rapid freezing of oysters to reduce V. vulnificus levels may be compromised by product handling procedures that permit cold adaptation.The authors emphasize than this adaptive nature to cold temperatures could be important for shellfish industry efforts to reduce the risk of V. vulnificus infection from consuming raw oysters.
The index of isolation of V. vulnificus in our study (11.4%) is disquieting and high enough to make positive samples a potential source of infection.According to Daniels 11 , oysters are the most common vehicle of transmission of V. vulnificus infection, which manifests in the form of gastroenteritis, primary septicemia, or wound infection, accompanied by fever, chills, diarrhea, nausea, vomiting, septic shock, and characteristic skin lesions.
Seven (53.8%) of the 13 vibrio species identified in this study were recently described for the first time: V. scophthalmi, V. rumoiensis, V. lentus, V. hepatarius, V. coralliilyticus, V. ponticus, and V. litoralis.The type strains used to characterize the vibrio species above were isolated from aquatic organisms sampled in coastal areas, marine environments, and/or the fishing industry.Of particular interest is V. lentus, which was first characterized based on 12 strains isolated from Mediterranean oysters 12 .
In view of the importance of determining the level of virulence in vibrio strains isolated from oysters destined for human consumption, all strains (n=35) were tested for their ability to hydrolyze urea and produce hemolysin -two wellestablished indicators of pathogenicity in vibrios.In the present study only fresh oyster samples showed hemolytic activity in Wagatsuma agar and strong positive urease production (Table 2).
Detected phenotypically by the observation of β-hemolysis, the phenomenon Kanagawa is triggered by the expression of the gene tdh, which encodes thermostable direct hemolysin (TDH), a determining factor of virulence in V. parahaemolyticus strains.However, functional TDH production depends on two genes, tdh1 and tdh2, of which only the latter is capable of hemolytic activity 13 .
Although most studies on Kanagawa positivity focus on the species V. parahaemolyticus, other vibrio species may occasionally carry tdh highly homologous to the genes known from V. parahaemolyticus 4 .This was borne out in our study by the finding of β-hemolysis in species other than V. parahaemolyticus.

TABLE 1 -Vibrios isolated from 15 fresh and 15 frozen samples of oyster obtained from restaurants in Fortaleza, State of Ceará, Brazil. Origin of strains Isolated Vibrio species Strains (n) Fresh oyster Frozen oyster
Virulence factors in vibrios isolated from oysters A positive control strain (Kanagawa-positive V. parahaemolyticus IOC 18950) was used.www.scielo.br/rsbmtCostaRA et al -