Literature DB >> 113174

The biology of the gonococcus.

S A Morse.   

Abstract

Gonorrhea has been known since antiquity. Today, this disease is the most commonly reported infectious disease in the U.S. The natural environment of the etiological agent, Neisseria gonorrhoeae, is man. In this host, the organism usually parasitizes mucosal surfaces populated by columnar epithelial cells. Under certain conditions, the gonococcus may disseminate or spread to adjacent organs. The gonococcus is well adapted to its environment and is a successful parasite. Until recently, gonococci were uniformly sensitive to penicilin. However, a plasmid encoding beta-lactamase has been identified in some isolates. Most strains exhibit specific requirements for various amino acids, vitamins, purines, and pyrimidines. Only glucose, pyruvate, and lactate are utilized as sources of energy. Glucose is dissimilated by a combination of the Entner-Doudoroff and pentose phosphate pathways. A tricarboxylic acid cycle is also present and active under certain conditions. Structurally, the cell envelope of the gonococcus resembles that of a typical Gram-negative bacterium. Gonococci are highly autolytic, especially in older cultures or after depletion of the energy source. Autolysis is not due solely to peptidoglycan hydrolysis, but appears to involve a destabilization of the outer membrane as well. Cell surface components such as pili, lipopolysaccharide, outer membrane proteins, and a capsule are associated with the virulence and pathogenicity of this organism.

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Year:  1978        PMID: 113174     DOI: 10.3109/10408417909083071

Source DB:  PubMed          Journal:  CRC Crit Rev Microbiol        ISSN: 0045-6454


  16 in total

1.  Deciphering the Function of New Gonococcal Vaccine Antigens Using Phenotypic Microarrays.

Authors:  Benjamin I Baarda; Sarah Emerson; Philip J Proteau; Aleksandra E Sikora
Journal:  J Bacteriol       Date:  2017-08-08       Impact factor: 3.490

2.  Effect of dilution rate on lipopolysaccharide and serum resistance of Neisseria gonorrhoeae grown in continuous culture.

Authors:  S A Morse; C S Mintz; S K Sarafian; L Bartenstein; M Bertram; M A Apicella
Journal:  Infect Immun       Date:  1983-07       Impact factor: 3.441

3.  Cytoplasmic membrane proteins of spectinomycin-susceptible and -resistant strains of Neisseria gonorrhoeae.

Authors:  M A Miller; C S Schärli; J Mills
Journal:  J Bacteriol       Date:  1980-07       Impact factor: 3.490

4.  Interaction of Escherichia coli with different fimbriae and polymorphonuclear leukocytes.

Authors:  B Björkstén; T Wadström
Journal:  Infect Immun       Date:  1982-10       Impact factor: 3.441

5.  Antigenic Variation in Bacterial Pathogens.

Authors:  Guy H Palmer; Troy Bankhead; H Steven Seifert
Journal:  Microbiol Spectr       Date:  2016-02

6.  Metabolic responses of Neisseria gonorrhoeae to human serum and myeloid cells. Adaptation to host defenses?

Authors:  M S Cohen; B E Britigan
Journal:  Antonie Van Leeuwenhoek       Date:  1987       Impact factor: 2.271

7.  Terminal branching of the respiratory electron transport chain in Neisseria meningitidis.

Authors:  E K Yu; I W DeVoe
Journal:  J Bacteriol       Date:  1980-06       Impact factor: 3.490

8.  Cloning and characterization of the meningococcal polyphosphate kinase gene: production of polyphosphate synthesis mutants.

Authors:  C R Tinsley; E C Gotschlich
Journal:  Infect Immun       Date:  1995-05       Impact factor: 3.441

9.  Neisseria gonorrhoeae cell envelope: permeability to hydrophobic molecules.

Authors:  P G Lysko; S A Morse
Journal:  J Bacteriol       Date:  1981-02       Impact factor: 3.490

10.  L-cysteine oxidase activity in the membrane of Neisseria meningitidis.

Authors:  E K Yu; I W DeVoe
Journal:  J Bacteriol       Date:  1981-01       Impact factor: 3.490

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