To investigate the identity and relationship of the V. parahaemolyticus strains causing these two outbreaks to the pandemic strains, we determined their phenotypic and genotypic properties. V. parahaemolyticus isolates from Puerto Montt were obtained from rectal swabs from 24 patients 6 to 69 years of age with acute diarrhea. The 20 clinical isolates from Antofagasta were provided by the National Institute of Public Health of Chile. Eleven previously well-characterized strains of the pandemic complex, isolated in Southeast Asia, including strain RIMD2210633 (VpKX), whose genome has been sequenced (13), were included for comparison. VpKX was directly obtained from the culture collection. The other bacterial strains of the pandemic group were provided by Mitsuaki Nishibuchi, Center for Southeast Asian Studies, Kyoto University. They are KXV225, VP2, VP47, VP81, 97LVP2, JKY-VP6, AN-5034, AN-8373, OP-424, KXV737. Three other V. parahaemolyticus nonpandemic strains, ATCC17802T (VpD), RIMD 2210856 (VpAQ), 2210086 (VpI), and the V. alginolyticus strain ATCC17749 (Va) were directly obtained from the indicated culture collections. The identification of the isolates used in this study was confirmed by API-20E for enterobacteria (bioMérieux, Inc., Hazelwood, MO), according to the manufacturer’s instructions. The O and K antigens of the V. parahaemolyticus strains were determined by slide agglutination with rabbit antisera obtained from Seiken (Denka Seiken. Co. Ltd. Tokyo, Japan), as described by the supplier.

For PCR, bacterial DNA was extracted from overnight cultures in Luria Bertani broth (supplemented with 1% NaCl) by using the Wizard Genomic DNA Purification kit (Promega, Madison, WI). DNA concentration was assessed by the intensity of the DNA band after agarose gel electrophoresis and staining with ethidium bromide. Known amounts of λ-DNA were used as a standard. PCR assays were performed by using approximately 10 ng per reaction tube, except for AP-PCR, in which 25 ng were employed. Amplifications of the different markers were performed as previously described: tdh and trh (7), orf8 (11), toxRS/new (4), and AP-PCR (11). The AP-PCR patterns were recorded and analyzed with GelCompar II (Applied Maths, Sint-Martens-Latern, Belgium). Genetic distance was calculated on the basis of the number of shared bands between isolates, and similarity matrices were calculated by using the Dice coefficient (14). Clustering was achieved by using the unweighted pair group method with arithmetic mean (UPGMA). Kanagawa and urease tests were performed as described by the U.S. Food and Drug Administration/Bacterial Analysis Manual (15).

Figure

Figure. Representative arbitrarily primed polymerase chain reaction (AP-PCR) patterns for Vibrio parahaemolyticus DNA from strains of the outbreaks in Chile and Southeast Asia and dendrogram illustrating the clustering of the patterns by...

Twenty V. parahaemolyticus isolates obtained from the outbreak in Antofagasta, Chile, in 1998 and 24 from the outbreak of Puerto Montt, Chile, in 2004 were characterized. All of the isolates, excluding 1 from Antofagasta and 6 from Puerto Montt, tested positive for every property of the pandemic clonal complex under analysis (Table). Only 1 isolate from Antofagasta (ATC 230) and 1 from Puerto Montt (PMC 59) differed from the pandemic group in more than 1 property. Five isolates from Puerto Montt diverged from the main group in only 1 of the tested properties; 4 were toxRS/new negative, and 1 was serovar O4:K12. The isolates were also analyzed by their AP-PCR patterns. For this analysis, the patterns for 11 South East Asia isolates of the pandemic clone were initially obtained. All of these isolates could be clustered into only 2 groups when either primer P1 or P3 was employed. The patterns obtained with the isolates from Chile were then compared with those of 3 isolates from Southeast Asia, representing the 2 AP-PCR patterns observed within this last group. Three nonpandemic V. parahaemolyticus strains and 1 V. alginolyticus strain were also included. Every isolate from Chile, except ATC230, clustered with the pandemic isolates when using primer P1 (11) for PCR (Figure A). A similar result was observed with primer P3 (Figure B), although in this case PMC59, the isolate that differed from those in the clonal complex in more than 1 property (Table) clustered with ATC230.

Our results show that the spread of the pandemic clonal complex reached the Southern Hemisphere as early as 1998, only 2 years after the strain abruptly appeared in Calcutta, India, in 1996 (3). The diversity observed among the isolates obtained in Puerto Montt did not appear among those from Antofagasta. Five isolates differed in only 1 property, 1 was from a different serovar, and 4 lacked the toxRS/new sequence. These findings raise the question of whether this diversity was originally present in the introduced pandemic strain or whether it was locally generated. The serovar O4:K12 observed in 1 of these isolates (PMC46) has been previously observed among isolates from southern Thailand (11). How and when the pandemic strain arrived to these remote regions in the Southern Hemisphere, and why it caused the outbreaks during those years, remains a matter for speculation. The outbreak in Puerto Montt was likely triggered by higher than normal temperatures during the summer months in this region, which is normally cool in all seasons and has an average daily superficial water temperature<16°C year round (Dirección Meteorológica de Chile, pers. comm.).