Literature DB >> 10678950

Genetic relationships between clinical isolates of Streptococcus pneumoniae, Streptococcus oralis, and Streptococcus mitis: characterization of "Atypical" pneumococci and organisms allied to S. mitis harboring S. pneumoniae virulence factor-encoding genes.

A M Whatmore1, A Efstratiou, A P Pickerill, K Broughton, G Woodard, D Sturgeon, R George, C G Dowson.   

Abstract

The oral streptococcal group (mitis phylogenetic group) currently consists of nine recognized species, although the group has been traditionally difficult to classify, with frequent changes in nomenclature over the years. The pneumococcus (Streptococcus pneumoniae), an important human pathogen, is traditionally distinguished from the most closely related oral streptococcal species Streptococcus mitis and Streptococcus oralis on the basis of three differentiating characteristics: optochin susceptibility, bile solubility, and agglutination with antipneumococcal polysaccharide capsule antibodies. However, there are many reports in the literature of pneumococci lacking one or more of these defining characteristics. Sometimes called "atypical" pneumococci, these isolates can be the source of considerable confusion in the clinical laboratory. Little is known to date about the genetic relationships of such organisms with classical S. pneumoniae isolates. Here we describe these relationships based on sequence analysis of housekeeping genes in comparison with previously characterized isolates of S. pneumoniae, S. mitis, and S. oralis. While most pneumococci were found to represent a closely related group these studies identified a subgroup of atypical pneumococcal isolates (bile insoluble and/or "acapsular") distinct from, though most closely related to, the "typical" pneumococcal isolates. However, a large proportion of isolates, found to be atypical on the basis of capsule reaction alone, did group with typical pneumococci, suggesting that they have either lost capsule production or represent as-yet-unrecognized capsular types. In contrast to typical S. pneumoniae, isolates phenotypically identified as S. mitis and S. oralis, which included isolates previously characterized in taxonomic studies, were genetically diverse. While most of the S. oralis isolates did fall into a well-separated group, S. mitis isolates did not cluster into a well-separated group. During the course of these studies we also identified a number of potentially important pathogenic isolates, which were frequently associated with respiratory disease, that phenotypically and genetically are most closely related to S. mitis but which harbor genes encoding the virulence determinants pneumolysin and autolysin classically associated with S. pneumoniae.

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Year:  2000        PMID: 10678950      PMCID: PMC97291          DOI: 10.1128/IAI.68.3.1374-1382.2000

Source DB:  PubMed          Journal:  Infect Immun        ISSN: 0019-9567            Impact factor:   3.441


  45 in total

Review 1.  Current classification of the oral streptococci.

Authors:  R A Whiley; D Beighton
Journal:  Oral Microbiol Immunol       Date:  1998-08

2.  Identification of Streptococcus pneumoniae with a DNA probe.

Authors:  G A Denys; R B Carey
Journal:  J Clin Microbiol       Date:  1992-10       Impact factor: 5.948

3.  The autolysin-encoding gene (lytA) of Streptococcus pneumoniae displays restricted allelic variation despite localized recombination events with genes of pneumococcal bacteriophage encoding cell wall lytic enzymes.

Authors:  A M Whatmore; C G Dowson
Journal:  Infect Immun       Date:  1999-09       Impact factor: 3.441

4.  Population biology of Streptococcus pneumoniae isolated from oropharyngeal carriage and invasive disease.

Authors:  Christine D M Müller-Graf; Adrian M Whatmore; Samantha J King; Krzysztof Trzcinski; A Paul Pickerill; Neil Doherty; John Paul; David Griffiths; Derek Crook; Christopher G Dowson
Journal:  Microbiology (Reading)       Date:  1999-11       Impact factor: 2.777

5.  Molecular characterization of equine isolates of Streptococcus pneumoniae: natural disruption of genes encoding the virulence factors pneumolysin and autolysin.

Authors:  A M Whatmore; S J King; N C Doherty; D Sturgeon; N Chanter; C G Dowson
Journal:  Infect Immun       Date:  1999-06       Impact factor: 3.441

6.  Changes in occurrence of capsular serotypes of Streptococcus pneumoniae at Boston City Hospital during selected years between 1935 and 1974.

Authors:  M Finland; M W Barnes
Journal:  J Clin Microbiol       Date:  1977-02       Impact factor: 5.948

7.  Genetic diversity of the streptococcal competence (com) gene locus.

Authors:  A M Whatmore; V A Barcus; C G Dowson
Journal:  J Bacteriol       Date:  1999-05       Impact factor: 3.490

8.  Molecular relationships and antimicrobial susceptibilities of viridans group streptococci isolated from blood of neutropenic cancer patients.

Authors:  H Wisplinghoff; R R Reinert; O Cornely; H Seifert
Journal:  J Clin Microbiol       Date:  1999-06       Impact factor: 5.948

9.  Role of the major pneumococcal autolysin in the atypical response of a clinical isolate of Streptococcus pneumoniae.

Authors:  E Díaz; R López; J L García
Journal:  J Bacteriol       Date:  1992-09       Impact factor: 3.490

10.  A scheme for the identification of viridans streptococci.

Authors:  D Beighton; J M Hardie; R A Whiley
Journal:  J Med Microbiol       Date:  1991-12       Impact factor: 2.472

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  114 in total

1.  PCR can add to detection of pneumococcal disease in pneumonic patients receiving antibiotics at admission.

Authors:  J Wheeler; O M Murphy; R Freeman; A M Kearns; M Steward; M J Lee
Journal:  J Clin Microbiol       Date:  2000-10       Impact factor: 5.948

2.  Distribution of the mosaic structured murM genes among natural populations of Streptococcus pneumoniae.

Authors:  S R Filipe; E Severina; A Tomasz
Journal:  J Bacteriol       Date:  2000-12       Impact factor: 3.490

3.  All detectable high-molecular-mass penicillin-binding proteins are modified in a high-level beta-lactam-resistant clinical isolate of Streptococcus mitis.

Authors:  A Amoroso; D Demares; M Mollerach; G Gutkind; J Coyette
Journal:  Antimicrob Agents Chemother       Date:  2001-07       Impact factor: 5.191

4.  Isolation of pneumococcal DNA from nasopharyngeal samples for real-time, quantitative PCR: comparison of three methods.

Authors:  Annika Saukkoriipi; Tarja Kaijalainen; Leena Kuisma; Anu Ojala; Maija Leinonen
Journal:  Mol Diagn       Date:  2003

5.  Amplified fragment length polymorphism fingerprinting is an effective technique to distinguish streptococcus pneumoniae from other Streptococci and an efficient alternative to pulsed-field gel electrophoresis for molecular typing of pneumococci.

Authors:  Chris Neeleman; Corné H W Klaassen; Hanneke A de Valk; Maaike T de Ruiter; Johan W Mouton
Journal:  J Clin Microbiol       Date:  2004-01       Impact factor: 5.948

6.  A homologue of aliB is found in the capsule region of nonencapsulated Streptococcus pneumoniae.

Authors:  Lucy J Hathaway; Patricia Stutzmann Meier; Patrick Bättig; Suzanne Aebi; Kathrin Mühlemann
Journal:  J Bacteriol       Date:  2004-06       Impact factor: 3.490

7.  Use of tuf sequences for genus-specific PCR detection and phylogenetic analysis of 28 streptococcal species.

Authors:  François J Picard; Danbing Ke; Dominique K Boudreau; Maurice Boissinot; Ann Huletsky; Dave Richard; Marc Ouellette; Paul H Roy; Michel G Bergeron
Journal:  J Clin Microbiol       Date:  2004-08       Impact factor: 5.948

8.  An internationally spread clone of Streptococcus pneumoniae evolves from low-level to higher-level penicillin resistance by uptake of penicillin-binding protein gene fragments from nonencapsulated pneumococci.

Authors:  Christoph Hauser; Suzanne Aebi; Kathrin Mühlemann
Journal:  Antimicrob Agents Chemother       Date:  2004-09       Impact factor: 5.191

9.  Evidence of localized prophage-host recombination in the lytA gene, encoding the major pneumococcal autolysin.

Authors:  María Morales; Pedro García; Adela G de la Campa; Josefina Liñares; Carmen Ardanuy; Ernesto García
Journal:  J Bacteriol       Date:  2010-03-19       Impact factor: 3.490

10.  Characterization of LytA-like N-acetylmuramoyl-L-alanine amidases from two new Streptococcus mitis bacteriophages provides insights into the properties of the major pneumococcal autolysin.

Authors:  Patricia Romero; Rubens López; Ernesto García
Journal:  J Bacteriol       Date:  2004-12       Impact factor: 3.490

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