Literature DB >> 7041865

Microbial surface interactions: reduction of the haemagglutination activity of the oral bacterium Fusobacterium nucleatum by absorption with Streptococcus and Bacteroides.

W A Falkler, B W Burger.   

Abstract

Oral strains of Fusobacterium nucleatum showed haemagglutination (HA) of sheep red blood cells and attachment of HA-active F. nucleatum fragments to other microorganisms allowed a means of studying microbial surface interactions. HA-active sonicated fragments (SF) prepared from F. nucleatum were mixed with whole cell suspensions of 48 bacterial strains and, after incubation, the whole cells were separated from the non-absorbed fragments by differential centrifugation. Attachment of F. nucleatum fragments to the cells was indicated by a reduction in the HA activity of the SF in the supernatant fluid remaining after absorption with whole cells. HA activity of the microbial cells used for absorption and the detection of F. nucleatum fragments on these cells by an indirect fluorescent antibody technique provided further evidence of attachment. Of the 48 strains tested, 10 absorbed F. nucleatum HA-active fragments. They included Bacteroides gingivalis, Bacteroides fragilis subsp. distasonis, Bacteroides corrodens, Streptococcus morbillorum, Streptococcus sanguis (Blackburn and JC 74) and Streptococcus mutans AHT, BHT, 10449 and 6715. Chelators revealed that F. nucleatum attached to the microorganisms via a Ca2+-dependent interaction. Sugar inhibition demonstrated that F. nucleatum attached to the microorganisms via a D-galactose-containing moiety on their surface. A reduction in the absorption of F. nucleatum HA-active fragments by Strep. mutans grown in a higher concentration of sucrose was observed.

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Year:  1981        PMID: 7041865     DOI: 10.1016/0003-9969(81)90112-6

Source DB:  PubMed          Journal:  Arch Oral Biol        ISSN: 0003-9969            Impact factor:   2.633


  13 in total

1.  Fap2 of Fusobacterium nucleatum is a galactose-inhibitable adhesin involved in coaggregation, cell adhesion, and preterm birth.

Authors:  S Coppenhagen-Glazer; A Sol; J Abed; R Naor; X Zhang; Y W Han; G Bachrach
Journal:  Infect Immun       Date:  2015-01-05       Impact factor: 3.441

2.  Streptococcus mutans SpaP binds to RadD of Fusobacterium nucleatum ssp. polymorphum.

Authors:  Lihong Guo; Bhumika Shokeen; Xuesong He; Wenyuan Shi; Renate Lux
Journal:  Mol Oral Microbiol       Date:  2017-02-13       Impact factor: 3.563

3.  Coaggregation of Candida dubliniensis with Fusobacterium nucleatum.

Authors:  M A Jabra-Rizk; W A Falkler; W G Merz; J I Kelley; A A Baqui; T F Meiller
Journal:  J Clin Microbiol       Date:  1999-05       Impact factor: 5.948

4.  Characterization of coaggregation between Bacteroides gingivalis T22 and Fusobacterium nucleatum T18.

Authors:  S A Kinder; S C Holt
Journal:  Infect Immun       Date:  1989-11       Impact factor: 3.441

5.  Identification of a Fusobacterium nucleatum PK1594 galactose-binding adhesin which mediates coaggregation with periopathogenic bacteria and hemagglutination.

Authors:  B Shaniztki; D Hurwitz; N Smorodinsky; N Ganeshkumar; E I Weiss
Journal:  Infect Immun       Date:  1997-12       Impact factor: 3.441

6.  Inhibition of coaggregation between Fusobacterium nucleatum and Porphyromonas (Bacteroides) gingivalis by lactose and related sugars.

Authors:  P E Kolenbrander; R N Andersen
Journal:  Infect Immun       Date:  1989-10       Impact factor: 3.441

7.  Coaggregation of Fusobacterium nucleatum, Selenomonas flueggei, Selenomonas infelix, Selenomonas noxia, and Selenomonas sputigena with strains from 11 genera of oral bacteria.

Authors:  P E Kolenbrander; R N Andersen; L V Moore
Journal:  Infect Immun       Date:  1989-10       Impact factor: 3.441

8.  Aggregation of platelets by Fusobacterium necrophorum.

Authors:  L J Forrester; B J Campbell; J N Berg; J T Barrett
Journal:  J Clin Microbiol       Date:  1985-08       Impact factor: 5.948

9.  Comparison of serological reactions of typed Fusobacterium nucleatum strains with those of isolates from humans, canines, and a Macaca mulatta monkey.

Authors:  J W Vincent; W A Falkler; J A Craig
Journal:  J Clin Microbiol       Date:  1983-04       Impact factor: 5.948

10.  Surface structures (peritrichous fibrils and tufts of fibrils) found on Streptococcus sanguis strains may be related to their ability to coaggregate with other oral genera.

Authors:  P S Handley; P L Carter; J E Wyatt; L M Hesketh
Journal:  Infect Immun       Date:  1985-01       Impact factor: 3.441

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