Evaluation and Validation of a PulseNet Standardized Pulsed-Field Gel Electrophoresis Protocol for Subtyping Vibrio parahaemolyticus : an International Multicenter Collaborative Study

Author:

Kam Kai Man1,Luey Cindy K. Y.1,Parsons Michele B.2,Cooper Kara L. F.2,Nair G. B.3,Alam M.3,Islam M. Atiqul3,Cheung Danny T. L.1,Chu Y. W.1,Ramamurthy T.4,Pazhani G. P.4,Bhattacharya S. K.4,Watanabe H.5,Terajima J.5,Arakawa E.5,Ratchtrachenchai O.-A.6,Huttayananont S.6,Ribot Efrain M.2,Gerner-Smidt Peter2,Swaminathan Bala2

Affiliation:

1. Public Health Laboratory Centre, Kowloon, Hong Kong

2. PulseNet Methods Development and Validation Laboratory, Centers for Disease Control and Prevention, Atlanta, Georgia

3. International Centre for Diarrhoeal Diseases Research, Dhaka, Bangladesh

4. National Institute of Cholera and Enteric Diseases, Kolkata, India

5. National Institute of Infectious Diseases, Tokyo, Japan

6. National Institute of Health, Bangkok, Thailand

Abstract

ABSTRACT The pandemic spread of Vibrio parahaemolyticus is an international public health issue. Because of the outbreak potential of the organism, it is critical to establish an internationally recognized molecular subtyping protocol for V. parahaemolyticus that is both rapid and robust as a means to monitor its further spread and to guide control measures in combination with epidemiologic data. Here we describe the results of a multicenter, multicountry validation of a new PulseNet International standardized V. parahaemolyticus pulsed-field gel electrophoresis (PFGE) protocol. The results are from a composite analysis of 36 well-characterized V. parahaemolyticus isolates from six participating laboratories, and the isolates represent predominant serotypes and various genotypes isolated from different geographic regions and time periods. The discriminatory power is very high, as 34 out of 36 sporadic V. parahaemolyticus strains tested fell into 34 distinguishable PFGE groups when the data obtained with two restriction enzymes (SfiI and NotI) were combined. PFGE was further able to cluster members of known pandemic serogroups. The study also identified quality measures which may affect the performance of the protocol. Nonadherence to the recommended procedure may lead to high background in the PFGE gel patterns, partial digestion, and poor fragment resolution. When these quality measures were implemented, the PulseNet V. parahaemolyticus protocol was found to be both robust and reproducible among the collaborating laboratories.

Publisher

American Society for Microbiology

Subject

Microbiology (medical)

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