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PMID: 6425421 Published · ppublish English Journal Article Research Support, U.S. Gov't, P.H.S.

Ability of monomeric peptidoglycan fragments from Neisseria gonorrhoeae to damage human fallopian-tube mucosa.

The Journal of infectious diseases ·Vol. 149 ·No. 3 ·1984-03-00 ·Pages 378-86

Melly MA, McGee ZA, Rosenthal RS

Abstract

Purified disaccharide peptide monomers obtained from Neisseria gonorrhoeae by enzymatic digestion of gonococcal peptidoglycan damaged the mucosa of human fallopian tubes in organ culture. Two peptidoglycan fragments were tested: a nonreducing, anhydromuramyl-containing monomer (the principal fragment shed by growing gonococci) and the analogous reducing, muramidase-derived monomer. The damage produced by either of these peptidoglycan monomers resulted in sloughing of ciliated cells from the mucosa and resembled the damage observed in active gonococcal infection and that produced by filter-sterilized toxic supernatant fluids from gonococcal-infected organ cultures. The minimal toxic dose of peptidoglycan monomers was 0.75 micrograms/ml. Neither lipopolysaccharide, sodium dodecyl sulfate, nor Triton X-100, possible contaminants from the monomer-purification procedures, was present in sufficient quantity to account for the damage. Both of the gonococcal peptidoglycan monomers may be present in vivo and thus may play a role in the pathogenesis of gonococcal infection.

MeSH Terms
Cilia/physiology Dose-Response Relationship, Drug Endotoxins/analysis Fallopian Tubes/physiology,ultrastructure Female Humans Microscopy, Electron, Scanning Mucous Membrane/ultrastructure Neisseria gonorrhoeae/analysis Organ Culture Techniques Peptidoglycan/analysis,toxicity
Chemicals
Endotoxins Peptidoglycan
Authors & Affiliations
3 authors, click to expand affiliations / ORCID
Melly M A
McGee Z A
Rosenthal R S
Article Info
Journal
The Journal of infectious diseases
Abbr.
J Infect Dis
ISSN
0022-1899
Published
1984-03-00
Pages
378-86
Language
English
Region
United States
NLM ID
0413675
Subset
IM
Grants
NIAID NIH HHS · AI-13488 · United States
NIAID NIH HHS · AI-14826 · United States
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