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Journal of clinical microbiology2004; 42(12); 5542-5548; doi: 10.1128/JCM.42.12.5542-5548.2004

Nicoletella semolina gen. nov., sp. nov., a new member of Pasteurellaceae isolated from horses with airway disease.

Abstract: Gram-negative, nonmotile bacteria that are catalase, oxidase, and urease positive are regularly isolated from the airways of horses with clinical signs of respiratory disease. On the basis of the findings by a polyphasic approach, we propose that these strains be classified as Nicoletella semolina gen. nov, sp. nov., a new member of the family Pasteurellaceae. N. semolina reduces nitrate to nitrite but is otherwise biochemically inert; this includes the lack of an ability to ferment glucose and other sugars. Growth is fastidious, and the isolates have a distinctive colony morphology, with the colonies being dry and waxy and looking like a semolina particle that can be moved around on an agar plate without losing their shape. DNA-DNA hybridization data and multilocus phylogenetic analysis, including 16S rRNA gene (rDNA), rpoB, and infB sequencing, clearly placed N. semolina as a new genus in the family Pasteurellaceae. In all the phylogenetic trees constructed, N. semolina is on a distinct branch displaying approximately 5% 16S rDNA, approximately 16% rpoB, and approximately 20% infB sequence divergence from its nearest relative within the family Pasteurellaceae. High degrees of conservation of the 16S rDNA (99.8%), rpoB (99.6%), and infB (99.7%) sequences exist within the species, indicating that N. semolina isolates not only are phenotypically homogeneous but also are genetically homogeneous. The type strain of N. semolina is CCUG43639(T) (DSM16380(T)).
Publication Date: 2004-12-08 PubMed ID: 15583279PubMed Central: PMC535277DOI: 10.1128/JCM.42.12.5542-5548.2004Google Scholar: Lookup
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  • Journal Article
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Summary

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The research presented proposes a new classification, Nicoletella semolina gen. nov, sp. nov., of bacteria commonly found in horses experiencing respiratory issues. Demonstrating unique growth and biochemical behaviors, as well as DNA-DNA hybridization data and multilocus phylogenetic analysis, have led to the inclusion of this organism under the Pasteurellaceae family.

Introduction

  • This study portrays a new genus and species of bacteria, classified as Nicoletella semolina gen. nov, sp. nov., that is frequently isolated from horses with respiratory diseases.
  • The bacteria are Gram-negative, nonmotile and exhibit positive reactions for catalase, oxidase and urease – enzymes that play crucial roles in metabolic processes.

Characteristics of Nicoletella semolina

  • Nicoletella semolina reduces nitrate into nitrites but showcases limited biochemical responsiveness, including its inability to ferment glucose and other sugars. This suggests a distinctive metabolic behavior influencing the pathogenicity and survival of the bacteria.
  • Nicoletella semolina exhibits a unique colony morphology. The bacterial colonies bear a dry, waxy appearance, resembling semolina particles. They can be moved on an agar plate while maintaining their form, indicating a robust physical structure.

Genetic Analysis

  • A comprehensive genetic assessment was carried out to better understand Nicoletella semolina’s classification within the Pasteurellaceae family. DNA from different colonies was hybridized and compared. Divergence rates between the Nicoletella semolina and its nearest relative within Pasteurellaceae were around 5% for 16S rDNA, 16% for rpoB, and 20% for infB.
  • Interestingly, high conservation rates were found among the 16S rDNA (99.8%), rpoB (99.6%), and infB (99.7%) sequences within the same species. This indicates that although Nicoletella semolina shows divergence from its nearest Pasteurellaceae relative, it has a high degree of genetic homogeneity within its species.

Conclusion

  • The unique characteristics, both phenotypically and genotypically, led the researchers to propose Nicoletella semolina as a new genus in the family Pasteurellaceae. This might bring new pathways for studying respiratory issues in horses and further understanding of this bacteria’s role in the pathology.
  • The type strain of Nicoletella semolina, acting as a reference point for future studies, is identified as CCUG43639(T) (DSM16380(T)).

Cite This Article

APA
Kuhnert P, Korczak B, Falsen E, Straub R, Hoops A, Boerlin P, Frey J, Mutters R. (2004). Nicoletella semolina gen. nov., sp. nov., a new member of Pasteurellaceae isolated from horses with airway disease. J Clin Microbiol, 42(12), 5542-5548. https://doi.org/10.1128/JCM.42.12.5542-5548.2004

Publication

ISSN: 0095-1137
NlmUniqueID: 7505564
Country: United States
Language: English
Volume: 42
Issue: 12
Pages: 5542-5548

Researcher Affiliations

Kuhnert, Peter
  • Institute of Veterinary Bacteriology, University of Bern, Bern, Switzerland. peter.kuhnert@vbi.unibe.ch
Korczak, Bozena
    Falsen, Enevold
      Straub, Reto
        Hoops, Anneliese
          Boerlin, Patrick
            Frey, Joachim
              Mutters, Reinier

                MeSH Terms

                • Animals
                • Bacterial Proteins / genetics
                • DNA, Ribosomal / analysis
                • Horse Diseases / microbiology
                • Horses
                • Lung Diseases / microbiology
                • Lung Diseases / veterinary
                • Molecular Sequence Data
                • Nucleic Acid Hybridization
                • Pasteurellaceae / classification
                • Pasteurellaceae / genetics
                • Pasteurellaceae / isolation & purification
                • Pasteurellaceae / metabolism
                • Pasteurellaceae Infections / microbiology
                • Pasteurellaceae Infections / veterinary
                • Phylogeny
                • RNA, Ribosomal, 16S / genetics
                • Sequence Analysis, DNA

                References

                This article includes 27 references
                1. Altschul SF, Gish W, Miller W, Myers EW, Lipman DJ. Basic local alignment search tool.. J Mol Biol 1990 Oct 5;215(3):403-10.
                  pubmed: 2231712doi: 10.1016/s0022-2836(05)80360-2google scholar: lookup
                2. Angen Ø, Ahrens P, Kuhnert P, Christensen H, Mutters R. Proposal of Histophilus somni gen. nov., sp. nov. for the three species incertae sedis 'Haemophilus somnus', 'Haemophilus agni' and 'Histophilus ovis'.. Int J Syst Evol Microbiol 2003 Sep;53(Pt 5):1449-1456.
                  pubmed: 13130032doi: 10.1099/ijs.0.02637-0google scholar: lookup
                3. Angen O, Mutters R, Caugant DA, Olsen JE, Bisgaard M. Taxonomic relationships of the [Pasteurella] haemolytica complex as evaluated by DNA-DNA hybridizations and 16S rRNA sequencing with proposal of Mannheimia haemolytica gen. nov., comb. nov., Mannheimia granulomatis comb. nov., Mannheimia glucosida sp. nov., Mannheimia ruminalis sp. nov. and Mannheimia varigena sp. nov.. Int J Syst Bacteriol 1999 Jan;49 Pt 1:67-86.
                  pubmed: 10028248doi: 10.1099/00207713-49-1-67google scholar: lookup
                4. Christensen H, Bisgaard M. Revised definition of Actinobacillus sensu stricto isolated from animals. A review with special emphasis on diagnosis.. Vet Microbiol 2004 Mar 26;99(1):13-30.
                  pubmed: 15019108doi: 10.1016/j.vetmic.2003.12.002google scholar: lookup
                5. Christensen H, Bisgaard M, Aalbæk B, Olsen JE. Reclassification of Bisgaard taxon 33, with proposal of Volucribacter psittacicida gen. nov., sp. nov. and Volucribacter amazonae sp. nov. as new members of the Pasteurellaceae.. Int J Syst Evol Microbiol 2004 May;54(Pt 3):813-818.
                  pubmed: 15143029doi: 10.1099/ijs.0.02797-0google scholar: lookup
                6. Christensen H, Bisgaard M, Bojesen AM, Mutters R, Olsen JE. Genetic relationships among avian isolates classified as Pasteurella haemolytica, 'Actinobacillus salpingitidis' or Pasteurella anatis with proposal of Gallibacterium anatis gen. nov., comb. nov. and description of additional genomospecies within Gallibacterium gen. nov.. Int J Syst Evol Microbiol 2003 Jan;53(Pt 1):275-287.
                  pubmed: 12656185doi: 10.1099/ijs.0.02330-0google scholar: lookup
                7. Christensen H, Bisgaard M, Olsen JE. Reclassification of equine isolates previously reported as Actinobacillus equuli, variants of A. equuli, Actinobacillus suis or Bisgaard taxon 11 and proposal of A. equuli subsp. equuli subsp. nov. and A. equuli subsp. haemolyticus subsp. nov.. Int J Syst Evol Microbiol 2002 Sep;52(Pt 5):1569-1576.
                  pubmed: 12361259doi: 10.1099/00207713-52-5-1569google scholar: lookup
                8. Church S, Harrigan KE, Irving AE, Peel MM. Endocarditis caused by Pasteurella caballi in a horse.. Aust Vet J 1998 Aug;76(8):528-30.
                9. Dahllöf I, Baillie H, Kjelleberg S. rpoB-based microbial community analysis avoids limitations inherent in 16S rRNA gene intraspecies heterogeneity.. Appl Environ Microbiol 2000 Aug;66(8):3376-80.
                10. Dewhirst FE, Paster BJ, Olsen I, Fraser GJ. Phylogeny of 54 representative strains of species in the family Pasteurellaceae as determined by comparison of 16S rRNA sequences.. J Bacteriol 1992 Mar;174(6):2002-13.
                11. Dewhirst FE, Paster BJ, Olsen I, Fraser GJ. Phylogeny of the Pasteurellaceae as determined by comparison of 16S ribosomal ribonucleic acid sequences.. Zentralbl Bakteriol 1993 Jun;279(1):35-44.
                  pubmed: 7690271doi: 10.1016/s0934-8840(11)80489-5google scholar: lookup
                12. Foster G, Ross HM, Malnick H, Willems A, Hutson RA, Reid RJ, Collins MD. Phocoenobacter uteri gen. nov., sp. nov., a new member of the family Pasteurellaceae Pohl (1979) 1981 isolated from a harbour porpoise (Phocoena phocoena).. Int J Syst Evol Microbiol 2000 Jan;50 Pt 1:135-139.
                  pubmed: 10826796doi: 10.1099/00207713-50-1-135google scholar: lookup
                13. Hedegaard J, Okkels H, Bruun B, Kilian M, Mortensen KK, Nørskov-Lauritsen N. Phylogeny of the genus Haemophilus as determined by comparison of partial infB sequences.. Microbiology (Reading) 2001 Sep;147(Pt 9):2599-2609.
                  pubmed: 11535800doi: 10.1099/00221287-147-9-2599google scholar: lookup
                14. Kilian M. Genus Haemophilus Winslow, Broadhurst, Buchanan, Krumwiede, Rogers and Smith 1917, 561AL. Bergey's manual of systematic bacteriology 2004.
                15. Korczak B, Christensen H, Emler S, Frey J, Kuhnert P. Phylogeny of the family Pasteurellaceae based on rpoB sequences.. Int J Syst Evol Microbiol 2004 Jul;54(Pt 4):1393-1399.
                  pubmed: 15280320doi: 10.1099/ijs.0.03043-0google scholar: lookup
                16. Kuhnert P, Capaul SE, Nicolet J, Frey J. Phylogenetic positions of Clostridium chauvoei and Clostridium septicum based on 16S rRNA gene sequences.. Int J Syst Bacteriol 1996 Oct;46(4):1174-6.
                  pubmed: 8863454doi: 10.1099/00207713-46-4-1174google scholar: lookup
                17. Kuhnert P, Frey J, Lang NP, Mayfield L. Phylogenetic analysis of Prevotella nigrescens, Prevotella intermedia and Porphyromonas gingivalis clinical strains reveals a clear species clustering.. Int J Syst Evol Microbiol 2002 Jul;52(Pt 4):1391-1395.
                  pubmed: 12148655doi: 10.1099/00207713-52-4-1391google scholar: lookup
                18. Mollet C, Drancourt M, Raoult D. rpoB sequence analysis as a novel basis for bacterial identification.. Mol Microbiol 1997 Dec;26(5):1005-11.
                19. Mutters R, Christensen H, Bisgaard M. Genus Pasteurella Trevisian 1887, 94AL, Nom. cons. Opin. 13, Jud. Comm. 1954. Bergey's manual of systematic bacteriology 2003.
                20. Mutters R, Ihm P, Pohl S, Frederiksen W, Mannheim W. Reclassification of the genus Pasteurella Trevisan 1887 on the basis of deoxyribonucleic acid homology, with proposals for the new species Pasteurella dagmatis, Pasteurella canis, Pasteurella stomatis, Pasteurella anatis, and Pastuerella langaa. Int. J. Syst. Bacteriol. 1985 35:309-322.
                21. Mutters R, Mannheim W, Bisgaard M. Taxonomy of the group. Pasteurella and pasteurellosis 1989 p. 3-34.
                22. Nørskov-Lauritsen N, Christensen H, Okkels H, Kilian M, Bruun B. Delineation of the genus Actinobacillus by comparison of partial infB sequences.. Int J Syst Evol Microbiol 2004 May;54(Pt 3):635-644.
                  pubmed: 15143001doi: 10.1099/ijs.0.02785-0google scholar: lookup
                23. Olsen I, Dewhirst FE, Paster BJ, Busse HJ. Family Pasteurellaceae. Bergey's manual of systematic bacteriology 2004.
                24. Olsen I, Moller K. Genus Actinobacillus Brumpt 1919, 849AL. Bergey's manual of systematic bacteriology 2004.
                25. Osawa R, Rainey FA, Fujisawa T, Lang E, Busse HJ, Walsh T, Stackebrandt E. Lonepinella koalarum gen. nov., sp. nov., a new tannin-protein complex degrading bacterium. Syst. Appl. Microbiol. 1995 18:368-373.
                26. Rycroft AN, Garside LH. Actinobacillus species and their role in animal disease.. Vet J 2000 Jan;159(1):18-36.
                  pubmed: 10640409doi: 10.1053/tvjl.1999.0403google scholar: lookup
                27. Schlater LK, Brenner DJ, Steigerwalt AG, Moss CW, Lambert MA, Packer RA. Pasteurella caballi, a new species from equine clinical specimens.. J Clin Microbiol 1989 Oct;27(10):2169-74.

                Citations

                This article has been cited 8 times.
                1. Bond S, McMullen C, Timsit E, Léguillette R. Topography of the respiratory, oral, and guttural pouch bacterial and fungal microbiotas in horses.. J Vet Intern Med 2023 Jan;37(1):349-360.
                  doi: 10.1111/jvim.16612pubmed: 36607177google scholar: lookup
                2. Simões J, Batista M, Tilley P. The Immune Mechanisms of Severe Equine Asthma-Current Understanding and What Is Missing.. Animals (Basel) 2022 Mar 16;12(6).
                  doi: 10.3390/ani12060744pubmed: 35327141google scholar: lookup
                3. Zhu Y, Chen S, Yi Z, Holyoak R, Wang T, Ding Z, Li J. Nasopharyngeal Microbiomes in Donkeys Shedding Streptococcus equi Subspecies equi in Comparison to Healthy Donkeys.. Front Vet Sci 2021;8:645627.
                  doi: 10.3389/fvets.2021.645627pubmed: 33969039google scholar: lookup
                4. Payette F, Charlebois A, Fairbrother JH, Beauchamp G, Leclere M. Nicoletella semolina in the airways of healthy horses and horses with severe asthma.. J Vet Intern Med 2021 May;35(3):1612-1619.
                  doi: 10.1111/jvim.16140pubmed: 33942932google scholar: lookup
                5. Gomez DE, Arroyo LG, Lillie B, Weese JS. Nasal bacterial microbiota during an outbreak of equine herpesvirus 1 at a farm in southern Ontario.. Can J Vet Res 2021 Jan;85(1):3-11.
                  pubmed: 33390647
                6. Ataei Kachooei S, Ranjbar MM, Ataei Kachooei S. Evaluation of Pasteurella multocida serotype B:2 resistance to immune serum and complement system.. Vet Res Forum 2017 Summer;8(3):179-184.
                  pubmed: 29085604
                7. Nørskov-Lauritsen N. Classification, identification, and clinical significance of Haemophilus and Aggregatibacter species with host specificity for humans.. Clin Microbiol Rev 2014 Apr;27(2):214-40.
                  doi: 10.1128/CMR.00103-13pubmed: 24696434google scholar: lookup
                8. McConachie EL, Hart KA, Whelchel DD, Schroeder EL, Schott HC 2nd, Sanchez S. Pulmonary disease potentially associated with Nicoletella semolina in 3 young horses.. J Vet Intern Med 2014 May-Jun;28(3):939-43.
                  doi: 10.1111/jvim.12349pubmed: 24689696google scholar: lookup