INVESTIGADORES
DELGADO Monica Alejandra
congresos y reuniones científicas
Título:
The PmrA/PmrB and RcsC/YojN/RcsB systems control expression of the Salmonella O-antigen chain length determinant
Autor/es:
DELGADO, MONICA ALEJANDRA; MOUSLIM, CHAKIB; GROISMAN, EDUARDO A.
Lugar:
Pinamar
Reunión:
Conferencia; X Congreso PABMB; XXXXI Reunión Anual de SAIB and XX Annual meeting of SAN; 2005
Institución organizadora:
SAIB
Resumen:
THE PMRA/PMRB AND RCSC/YOJN/RCSB SYSTEMS
CONTROL EXPRESSION OF THE SALMONELLA OANTIGEN
CHAIN LENGTH DETERMINANT
Delgado MA, Mouslim C, Groisman EA.
Department of Molecular Microbiology, Washington University
School of Medicine, 660 S. Euclid, St. Louis, Missouri, 63110, USA.
E-mail: monaledel@hotmail.com
The lipopolysaccharide (LPS) is the outermost component of the
Gram-negative envelope. It consists of the hydrophobic lipid A, a
short non-repeating core oligosaccharide and a distal polysaccharide
known as O antigen. The cld gene product determines the modal
distribution of chain length on the O-antigen. However, little is
known about how cld expression is regulated. We now report that
the PmrA/PmrB and RcsC/YojN/RcsB two-component systems
independently promote cld transcription. We show that the
response regulators PmrA and RcsB footprint different regions of
the cld promoter but promote transcription using the same start
site. Conditions that promote cld expression increase the amount
of O-antigen L-type in the LPS, leading to heightened resistance to
serum complement. The LPS profile of the rcsB mutant was also
altered in the size of the O-antigen subunits attached to the lipid Acore.
The lipid A structure of a cld null mutant differed from that of
the wild-type strain, suggesting a novel role for the Cld protein in
lipid A modification. The participation of the Cld protein in the
modification of lipid A and in the regulation of O-antigen length
may be the reason cld expression is controlled by multiple regulatory
systems.