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Infection and Immunity, February 2000, p. 948-952, Vol. 68, No. 2
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
Molecular Characterization of a New Variant of Toxin-Coregulated
Pilus Protein (TcpA) in a Toxigenic Non-O1/Non-O139 Strain of
Vibrio cholerae
Bisweswar
Nandi,1
Ranjan K.
Nandy,1
Ana C. P.
Vicente,2 and
Asoke C.
Ghose1,*
Department of Microbiology, Bose Institute,
Calcutta 700 054, India,1 and Department
of Genetics, Instituto Oswaldo Cruz, Rio de Janeiro,
Brazil2
Received 13 August 1999/Returned for modification 8 October
1999/Accepted 17 November 1999
A toxigenic non-O1/non-O139 strain of Vibrio cholerae
(10259) was found to contain a new variant of the toxin-coregulated pilus (TCP) protein gene (tcpA) as determined by PCR and
Southern hybridization experiments. Nucleotide sequence analysis data
of the new tcpA gene in strain 10259 (O53) showed it to be
about 74 and 72% identical to those of O1 classical and El Tor biotype strains, respectively. The predicted amino acid sequence of the 10259 TcpA protein shared about 81 and 78% identity with the corresponding sequences of classical and El Tor TcpA strains, respectively. An
antiserum raised against the TCP of a classical strain, O395, although
it recognized the TcpA protein of strain 10259 in an immunoblotting
experiment, exhibited considerably less protection against 10259 challenge compared to that observed against the parent strain.
Incidentally, the tcpA sequences of two other toxigenic non-O1/non-O139 strains (V2 and S7, both belonging to the serogroup O37) were determined to be almost identical to that of classical tcpA. Further, tcpA of another toxigenic
non-O1/non-O139 strain V315-1 (O nontypeable) was closely related to
that of El Tor tcpA. Analysis of these results with those
already available in the literature suggests that there are at least
four major variants of the tcpA gene in V. cholerae which probably evolved in parallel from a common
ancestral gene. Existence of highly conserved as well as hypervariable
regions within the sequence of the TcpA protein would also predict that
such evolution is under the control of considerable selection pressure.
*
Corresponding author. Mailing address: Department of
Microbiology, Bose Institute, P-1/12, CIT scheme VII-M, Calcutta 700 054, India. Phone: 033-337-9416/9544/9219. Fax: 91-33-334-3886. E-mail:
acghosh{at}boseinst.ernet.in.
Infection and Immunity, February 2000, p. 948-952, Vol. 68, No. 2
0019-9567/00/$04.00+0
Copyright © 2000, American Society for Microbiology. All rights reserved.
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