Open AccessDetection of Shiga‐like toxin on the outer membranes of Shigella species and Escherichia coli K‐12
Author(s) -
Sharma Kusum,
TimcenkoYoussef Lidija,
Palchaudhuri Sunil
Publication year - 1988
Publication title -
fems microbiology letters
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.899
H-Index - 151
eISSN - 1574-6968
pISSN - 0378-1097
DOI - 10.1111/j.1574-6968.1988.tb02806.x
Subject(s) - shigella dysenteriae , bacterial outer membrane , shigella flexneri , shiga toxin , escherichia coli , microbiology and biotechnology , biology , shiga like toxin , periplasmic space , toxin , plasmid , colicin , biochemistry , gene
Outer membranes of Shigella species and E. coli K‐12 carrying large invasive plasmids and isogenic non‐invasive strains without plasmids were analyzed by SDS‐PAGE. The immunoblotting analysis of the outer membrane proteins of these bacteria was performed with monoclonal antibody (mAb) made against A and B subunits of Shiga‐like toxin (SLT). The SLT was detected in the outer membranes of S. dysenteriae 1 IDBM11, S. sonnei PNS20, S. flexneri M90T, S. dysenteriae 60R, and E. coli K‐12 strain AB2463. The two other E. coli K‐12 strains, C600 and 933J were included as controls for low and high toxin producers respectively. The outer membrane protein band of molecular weight 70 kDa was common to all bacterial strains studied. The most prominent band of 70 kDa protein was seen to be present in the high toxin producing plasmidless strain of S. dysenteriae 60R and the lysogenic strain of E. coli 933J. The invasive strains of S. dysenteriae 1 and S. flexneri M90T which carry the large invasive plasmids showed the least prominent band of 70 kDa protein. The immunoblotting analysis of Shiga‐toxin partially purified from the S. dysenteriae 60R strain revealed the absence of 70 kDa band on SDS‐PAGE, instead the two dissociated subunits were seen. Furthermore, periplasmic Shiga‐toxin proteins also showed the complete dissociation into A and B subunits. However, under the same denaturing conditions, the 70 kDa protein band cross‐reacting with mAb against A and B subunits was still present in the outer membranes of all different strains.