Previous Article | Next Article ![]()
J. Bacteriol., Jan 1995, 11-19, Vol 177, No. 1
S Weber, F Lottspeich and J Kohl
A monoclonal antibody (MAb), MAb 900, which detects a 43-kDa protein
present on Escherichia coli was found. Subsequently, more than 90
organisms, belonging to either the bacterial, archaeal, or eucaryal domain,
were tested for reactivity to this MAb. Of the bacterial and archaeal
domains, almost all species proved to be positive, whereas all organisms
from the eucaryal domain gave negative results. The 43-kDa protein was
purified by affinity chromatography and subsequently analyzed by
microsequencing methods. Two peptide sequences which showed a high degree
of homology (> 99%) to the prokaryotic elongation factor Tu (EF-Tu) were
obtained. Western blot (immunoblot) analysis using both purified EF-Tu and
EF-Tu domains confirmed that the unknown protein was EF-Tu. The
panbacterial distribution of EF-Tu, which is present in large amounts in
every prokaryotic cell, renders this protein a good candidate for a
diagnostic approach. In consequence, we have used the anti-EF-Tu MAb 900 to
design both a dot blot assay and an enzyme-linked immunosorbent assay. From
either blood culture, urine, or gall-bladder fluid, bacterial contamination
could be detected. The sensitivity of these tests is currently 10(4)
bacteria per ml.
Copyright © 1995, American Society for Microbiology
An epitope of elongation factor Tu is widely distributed within the bacterial and archaeal domains
Institut fur Medizinische Mikrobiologie, Medizinische Hochschule Hannover, Germany.
This article has been cited by other articles:
| Appl. Environ. Microbiol. | Infect. Immun. | Eukaryot. Cell |
|---|---|---|
| Mol. Cell. Biol. | J. Virol. | Microbiol. Mol. Biol. Rev. |
| ALL ASM JOURNALS |