Literature DB >> 1548238

Phylogeny of 54 representative strains of species in the family Pasteurellaceae as determined by comparison of 16S rRNA sequences.

F E Dewhirst1, B J Paster, I Olsen, G J Fraser.   

Abstract

Virtually complete 16S rRNA sequences were determined for 54 representative strains of species in the family Pasteurellaceae. Of these strains, 15 were Pasteurella, 16 were Actinobacillus, and 23 were Haemophilus. A phylogenetic tree was constructed based on sequence similarity, using the Neighbor-Joining method. Fifty-three of the strains fell within four large clusters. The first cluster included the type strains of Haemophilus influenzae, H. aegyptius, H. aphrophilus, H. haemolyticus, H. paraphrophilus, H. segnis, and Actinobacillus actinomycetemcomitans. This cluster also contained A. actinomycetemcomitans FDC Y4, ATCC 29522, ATCC 29523, and ATCC 29524 and H. aphrophilus NCTC 7901. The second cluster included the type strains of A. seminis and Pasteurella aerogenes and H. somnus OVCG 43826. The third cluster was composed of the type strains of Pasteurella multocida, P. anatis, P. avium, P. canis, P. dagmatis, P. gallinarum, P. langaa, P. stomatis, P. volantium, H. haemoglobinophilus, H. parasuis, H. paracuniculus, H. paragallinarum, and A. capsulatus. This cluster also contained Pasteurella species A CCUG 18782, Pasteurella species B CCUG 19974, Haemophilus taxon C CAPM 5111, H. parasuis type 5 Nagasaki, P. volantium (H. parainfluenzae) NCTC 4101, and P. trehalosi NCTC 10624. The fourth cluster included the type strains of Actinobacillus lignieresii, A. equuli, A. pleuropneumoniae, A. suis, A. ureae, H. parahaemolyticus, H. parainfluenzae, H. paraphrohaemolyticus, H. ducreyi, and P. haemolytica. This cluster also contained Actinobacillus species strain CCUG 19799 (Bisgaard taxon 11), A. suis ATCC 15557, H. ducreyi ATCC 27722 and HD 35000, Haemophilus minor group strain 202, and H. parainfluenzae ATCC 29242. The type strain of P. pneumotropica branched alone to form a fifth group. The branching of the Pasteurellaceae family tree was quite complex. The four major clusters contained multiple subclusters. The clusters contained both rapidly and slowly evolving strains (indicated by differing numbers of base changes incorporated into the 16S rRNA sequence relative to outgroup organisms). While the results presented a clear picture of the phylogenetic relationships, the complexity of the branching will make division of the family into genera a difficult and somewhat subjective task. We do not suggest any taxonomic changes at this time.

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Year:  1992        PMID: 1548238      PMCID: PMC205807          DOI: 10.1128/jb.174.6.2002-2013.1992

Source DB:  PubMed          Journal:  J Bacteriol        ISSN: 0021-9193            Impact factor:   3.490


  32 in total

1.  A phylogenetic definition of the major eubacterial taxa.

Authors:  C R Woese; E Stackebrandt; T J Macke; G E Fox
Journal:  Syst Appl Microbiol       Date:  1985       Impact factor: 4.022

2.  Classification and identification of Actinobacillus actinomycetemcomitans and haemophilus aphrophilus by cluster analysis and deoxyribonucleic acid hybridizations.

Authors:  A C Tanner; R A Visconti; S S Socransky; S C Holt
Journal:  J Periodontal Res       Date:  1982-11       Impact factor: 4.419

3.  Conserved 5S rRNA complement to tRNA is not required for protein synthesis.

Authors:  B Pace; E A Matthews; K D Johnson; C R Cantor; N R Pace
Journal:  Proc Natl Acad Sci U S A       Date:  1982-01       Impact factor: 11.205

4.  Re-investigations of selected bovine and ovine strains previously classified as Pasteurella haemolytica and description of some new taxa within the Pasteurella haemolytica-complex.

Authors:  M Bisgaard; R Mutters
Journal:  Acta Pathol Microbiol Immunol Scand B       Date:  1986-06

5.  A numerical taxonomic study of Actinobacillus, Pasteurella and Yersinia.

Authors:  P H Sneath; M Stevens
Journal:  J Gen Microbiol       Date:  1985-10

6.  Characterization of some previously unclassified "Pasteurella" spp. obtained from the oral cavity of dogs and cats and description of a new species tentatively classified with the family Pasteurellaceae Pohl 1981 and provisionally called taxon 16.

Authors:  M Bisgaard; R Mutters
Journal:  Acta Pathol Microbiol Immunol Scand B       Date:  1986-06

7.  Comparative investigations of Pasteurella haemolytica sensu stricto and so-called P. haemolytica isolated from different pathological lesions in pigs.

Authors:  M Bisgaard
Journal:  Acta Pathol Microbiol Immunol Scand B       Date:  1984-08

Review 8.  Biology of Haemophilus ducreyi.

Authors:  W L Albritton
Journal:  Microbiol Rev       Date:  1989-12

9.  Serology of oral Actinobacillus actinomycetemcomitans and serotype distribution in human periodontal disease.

Authors:  J J Zambon; J Slots; R J Genco
Journal:  Infect Immun       Date:  1983-07       Impact factor: 3.441

10.  Characterization and identification of bovine and ovine Pasteurellaceae isolated from the oral cavity and rumen of apparently normal cattle and sheep.

Authors:  M Bisgaard; J E Phillips; W Mannheim
Journal:  Acta Pathol Microbiol Immunol Scand B       Date:  1986-02
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  48 in total

1.  Population structure and genetic diversity of Actinobacillus actinomycetemcomitans strains isolated from localized juvenile periodontitis patients.

Authors:  Jeffrey B Kaplan; Helen C Schreiner; David Furgang; Daniel H Fine
Journal:  J Clin Microbiol       Date:  2002-04       Impact factor: 5.948

Review 2.  Immunopathogenesis of Haemophilus ducreyi infection (chancroid).

Authors:  Stanley M Spinola; Margaret E Bauer; Robert S Munson
Journal:  Infect Immun       Date:  2002-04       Impact factor: 3.441

3.  Rapid divergence of two classes of Haemophilus ducreyi.

Authors:  Emily E Ricotta; Nan Wang; Robin Cutler; Jeffrey G Lawrence; Tricia L Humphreys
Journal:  J Bacteriol       Date:  2011-04-22       Impact factor: 3.490

4.  Genotypic diversity of Haemophilus parasuis field strains.

Authors:  A Olvera; M Calsamiglia; V Aragon
Journal:  Appl Environ Microbiol       Date:  2006-06       Impact factor: 4.792

5.  Multiplex PCR that can distinguish between immunologically cross- reactive serovar 3, 6, and 8 Actinobacillus pleuropneumoniae strains.

Authors:  L Zhou; S C P Jones; Ø Angen; J T Bossé; J H E Nash; J Frey; R Zhou; H C Chen; J S Kroll; A N Rycroft; P R Langford
Journal:  J Clin Microbiol       Date:  2007-12-19       Impact factor: 5.948

6.  Putative vaccine candidates and drug targets identified by reverse vaccinology and subtractive genomics approaches to control Haemophilus ducreyi, the causative agent of chancroid.

Authors:  Alissa de Sarom; Arun Kumar Jaiswal; Sandeep Tiwari; Letícia de Castro Oliveira; Debmalya Barh; Vasco Azevedo; Carlo Jose Oliveira; Siomar de Castro Soares
Journal:  J R Soc Interface       Date:  2018-05       Impact factor: 4.118

7.  Complete genome sequence of Haemophilus somnus (Histophilus somni) strain 129Pt and comparison to Haemophilus ducreyi 35000HP and Haemophilus influenzae Rd.

Authors:  Jean F Challacombe; A J Duncan; Thomas S Brettin; David Bruce; Olga Chertkov; J Chris Detter; Cliff S Han; Monica Misra; Paul Richardson; Roxanne Tapia; Nina Thayer; Gary Xie; Thomas J Inzana
Journal:  J Bacteriol       Date:  2006-12-15       Impact factor: 3.490

8.  Sequence-based classification scheme for the genus Legionella targeting the mip gene.

Authors:  R M Ratcliff; J A Lanser; P A Manning; M W Heuzenroeder
Journal:  J Clin Microbiol       Date:  1998-06       Impact factor: 5.948

9.  Phylogeny of Bacteroides, Prevotella, and Porphyromonas spp. and related bacteria.

Authors:  B J Paster; F E Dewhirst; I Olsen; G J Fraser
Journal:  J Bacteriol       Date:  1994-02       Impact factor: 3.490

10.  Genetic diversity of Actinobacillus pleuropneumoniae assessed by amplified fragment length polymorphism analysis.

Authors:  Branko Kokotovic; Øystein Angen
Journal:  J Clin Microbiol       Date:  2007-10-24       Impact factor: 5.948

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