Development of a rapid and simple immunochromatographic assay to identify Vibrio parahaemolyticus.

Abstract:

:To rapidly and simply determine whether or not bacterial colonies growing on agar were Vibrio parahaemolyticus, we developed an immunochromatographic assay (VP-ICA) using two different monoclonal antibodies (designated mAb-VP34 and mAb-VP109) against the delta subunit of V. parahaemolyticus-F0F1 ATP synthase. The epitopes recognized by mAb-VP34 and mAb-VP109 were mapped to sequences of eight ((47)LLTSSFSA(54)) and six amino acid residues ((16)FDFAVD(21)), respectively. An amino acid sequence similarity search of the NCBI database using BLASTP showed that both epitopic amino acid sequences were present together only in V. parahaemolyticus. When 124 V. parahaemolyticus strains and 94 strains of 27 other Vibrio species or 35 non-Vibrio species were tested using the VP-ICA, the VP-ICA identified V. parahaemolyticus with 100% accuracy. The VP-ICA rapidly and simply identified the pathogen directly from a single agar colony within 30 min, indicating that VP-ICA will greatly reduce labor and time required to identify V. parahaemolyticus compared with conventional biochemical tests.

journal_name

J Microbiol Methods

authors

Sakata J,Kawatsu K,Iwasaki T,Kumeda Y

doi

10.1016/j.mimet.2015.06.009

subject

Has Abstract

pub_date

2015-09-01 00:00:00

pages

23-9

eissn

0167-7012

issn

1872-8359

pii

S0167-7012(15)00187-6

journal_volume

116

pub_type

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