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Isolation, Molecular Characterization and Antibiotics Susceptibility Pattern of Methylotrophic Bacteria Occuring in the Human Mouth

Received: 5 January 2017    Accepted: 31 January 2017    Published: 21 March 2017
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Abstract

Methylotrophic bacteria are ubiquitous bacteria that are capable of using one carbon compounds such as methane, methanol, halogenated methane, and methylated amine as sources of carbon and energy for their diverse metabolic activities. Methylotrophic bacteria were isolated from the tongue, and supra- and subgingival plaque in the mouths of volunteers and patients with periodontitis. The isolation, identification, antibiotic susceptibility pattern and molecular characterization of methylotrophic bacteria from 150 volunteers and patients with periodontitis were done using standard method. Nutrient agar fortified with methylamine as a growth factor was used to aid the growth of these bacteria. The result show that a total of twelve (12) bacteria were identified. These are Bacillus licheniformis, Neisseria flava, Neisseria meningitis, Micrococcus flava, Pseudomonas aeruginosa, Streptococcus pneumoniae, Methylobacteria radiotolerance, Methylotrophic thiocynatum, Methylococcus capsulatum, Methylotrophic rubra and Branhamella catarhalis. The antibiotics susceptibility test showed that B. licheniformis, N. meningitis and P. aeruginosa exhibited the highest resistance against the antibiotics. The 12 bacteria were characterized molecularly with Polymerase chain reaction PCR amplified method using primers for the virulence genes of Methylotroph. The mxaF gene of methanol dehy- drogenase MxaF was detected in 3 bacteria: pilc of pilin gene in 3 bacteria, stx1 of shiga toxin nana of neuraminidase and pila of pilin gene was detected in all the bacteria. The results obtained in this research showed that methylotrophs may be responsible for periodontitis and that healthy people are carriers.

Published in International Journal of Microbiology and Biotechnology (Volume 2, Issue 3)
DOI 10.11648/j.ijmb.20170203.13
Page(s) 121-128
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This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited.

Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

Keywords

Isolation, Characterization, Methylotrophic, Bacteria, Mouth

References
[1] Nesvera, J., Pátek, M., Hochmannová, J., Chibisova, E., Sererijski, I., Tsyganov, Y., and Netrusov, A. (2011) Transformation of a new Gram-positive methylotroph, Brevibacterium methylicum, by plasmid DNA. Appl Microbiol Biot 35: 777–780.
[2] Anesti V, McDonald IR, Ramaswamy M, Wade WG, Kelly DP, Wood AP. 2005. Isolation and Molecular Characterization of methylotrophic bacteria occurring in the human mouth. Journal of Environmental Microbiology7: 1227-1238.
[3] Ratcliff, P. A., and Johnson, P. W. (1999) Relationship between oral malodor, gingivitis and periodontitis. J Periodontol 70: 485–489.
[4] Ludmila, C.; Marina, G. K. and Mary, E. L. (2010). The expanding world of methylotrophs. Applied Journal of Microbiology; 63: 477-499.
[5] Brooks, G. F.; Butel, J. S. and Morse, S. A. (2012). Medical Microbiology. 25th edition, Mc Graw Hill, New York, USA. Pp814.
[6] Prats, B. E. (2013). Isolation of Methylotrophs. Applied Journal of Microbiology; 69: 565-572.
[7] Bauer AW, Kirby WMM, Sherris JC, Turck M. (2006). Antibiotic susceptibility testing by a standardized single disk method. America Journal of Clinical Pathology 45: 493-496.
[8] Anzai Y, Kim H, Park JY, Wakabayashi H, Oyaizu H (Jul 2010). "Phylogenetic affiliation of the pseudomonads based on 16S rRNA sequence". Int J Syst Evol Microbiol 50 (4): 1563–89. doi:10.1099/00207713-50-4-1563. PMID 10939664.
[9] Fawole, M. A., and Oso, B. A. (2004): Laboratory Manual of Microbiology, Spectrum Books Limited, Ibadan, Nigeria. pp 127.
[10] Olutiola, P. O., Famurewa, O., and Sontag, H. G. (2000): Introduction to Microbiology, 2nd edition, Heidelberg, Nigeria, pp267.
[11] Prescott, L. M. Harley J. P., Klein, D. A. (2008). General Microbiology, 7th Edition McGraw Hill, New York, USA.
[12] Marchesi JR, Sato T, Weight man AJ, Martin TA, Fry JC, Hiom SJ, Dymock D, Wade WG. (2008). Design an evaluation of useful bacterium-specific PCR primers that amplify genes coding for bacterial 16RrRNA. Applied Environmental Microbiology 64: 795-799.
[13] Christoserdova, L. (2015). Methylotrophs in natural habitats. Applied Journal of Microbiology and Biotechnology. 99 (14): 5763-69.
[14] Greenblat, C. L., Baum, J., Klein, B. Y., Nachshon, S., Koltunov, V., Cano, R. J. (2014). "Micrococcus luteus – Survival in Amber". Microbial Ecology 48 (1): 120–127.
[15] Kim W. (2013). Beloin, Christophe, ed. "Spaceflight Promotes Biofilm Formation by Pseudomonas aeruginosa". Plos One 8 (4): e6237. doi:10.1371/journal.pone.0062437. Retrieved 5 July 2013.
[16] Ludwig, W., Strunk, O., Westram, R., Richter, L., Meier, H., Yadhukumar, et al. (2004) ARB: a software environment for sequence data. Nucleic Acids Res 32: 1363–1371.
[17] Janda, W. M., & Gaydos, C. A., (2007). Neisseria. In P. R. Murray, E. J. Baron, J. H. Jorgensen, M. L. Landry & M. A. Pfaller (Eds.), Manual of Clinical Microbiology (9th ed., pp. 601-620). Washington, D. C.: ASM Press.
[18] Hudault S, Guignot J, Servin AL (2011). "Escherichia coli strains colonizing the gastrointestinal tract protect germ-free mice against Salmonella typhimurium infection". Gut 49 (1): 47–55. doi:10.1136/gut.49.1.47. PMC 1728375. PMID 11413110.
[19] Hutter, G., Schlagenhauf, U., Valenza, G., Horn, M., Burgemeister, S., Claus, H., and Vogel, U. (2013) Molecular analysis of bacteria in periodontitis: evaluation of clone libraries, novel phylotypes and putative pathogens. Microbiology UK 149: 67–75.
[20] Vogt R. L, Dippold L (2015). "Escherichia coli O157: H7 outbreak associated with consumption of ground beef, June–July 2002". Public Health Rep 120 (2): 174–8. PMC 1497708. PMID 15842119.
[21] Munson, M. A., Banerjee, A., Watson, T. F., and Wade, W. G. (2004) Molecular analysis of the microflora associated with dental caries. J Clin Microbiol 42: 3023–3029.
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    Ekundayo S. W., Akinyosoye F. A., Momoh A. O. (2017). Isolation, Molecular Characterization and Antibiotics Susceptibility Pattern of Methylotrophic Bacteria Occuring in the Human Mouth. International Journal of Microbiology and Biotechnology, 2(3), 121-128. https://doi.org/10.11648/j.ijmb.20170203.13

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    ACS Style

    Ekundayo S. W.; Akinyosoye F. A.; Momoh A. O. Isolation, Molecular Characterization and Antibiotics Susceptibility Pattern of Methylotrophic Bacteria Occuring in the Human Mouth. Int. J. Microbiol. Biotechnol. 2017, 2(3), 121-128. doi: 10.11648/j.ijmb.20170203.13

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    AMA Style

    Ekundayo S. W., Akinyosoye F. A., Momoh A. O. Isolation, Molecular Characterization and Antibiotics Susceptibility Pattern of Methylotrophic Bacteria Occuring in the Human Mouth. Int J Microbiol Biotechnol. 2017;2(3):121-128. doi: 10.11648/j.ijmb.20170203.13

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  • @article{10.11648/j.ijmb.20170203.13,
      author = {Ekundayo S. W. and Akinyosoye F. A. and Momoh A. O.},
      title = {Isolation, Molecular Characterization and Antibiotics Susceptibility Pattern of Methylotrophic Bacteria Occuring in the Human Mouth},
      journal = {International Journal of Microbiology and Biotechnology},
      volume = {2},
      number = {3},
      pages = {121-128},
      doi = {10.11648/j.ijmb.20170203.13},
      url = {https://doi.org/10.11648/j.ijmb.20170203.13},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijmb.20170203.13},
      abstract = {Methylotrophic bacteria are ubiquitous bacteria that are capable of using one carbon compounds such as methane, methanol, halogenated methane, and methylated amine as sources of carbon and energy for their diverse metabolic activities. Methylotrophic bacteria were isolated from the tongue, and supra- and subgingival plaque in the mouths of volunteers and patients with periodontitis. The isolation, identification, antibiotic susceptibility pattern and molecular characterization of methylotrophic bacteria from 150 volunteers and patients with periodontitis were done using standard method. Nutrient agar fortified with methylamine as a growth factor was used to aid the growth of these bacteria. The result show that a total of twelve (12) bacteria were identified. These are Bacillus licheniformis, Neisseria flava, Neisseria meningitis, Micrococcus flava, Pseudomonas aeruginosa, Streptococcus pneumoniae, Methylobacteria radiotolerance, Methylotrophic thiocynatum, Methylococcus capsulatum, Methylotrophic rubra and Branhamella catarhalis. The antibiotics susceptibility test showed that B. licheniformis, N. meningitis and P. aeruginosa exhibited the highest resistance against the antibiotics. The 12 bacteria were characterized molecularly with Polymerase chain reaction PCR amplified method using primers for the virulence genes of Methylotroph. The mxaF gene of methanol dehy- drogenase MxaF was detected in 3 bacteria: pilc of pilin gene in 3 bacteria, stx1 of shiga toxin nana of neuraminidase and pila of pilin gene was detected in all the bacteria. The results obtained in this research showed that methylotrophs may be responsible for periodontitis and that healthy people are carriers.},
     year = {2017}
    }
    

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  • TY  - JOUR
    T1  - Isolation, Molecular Characterization and Antibiotics Susceptibility Pattern of Methylotrophic Bacteria Occuring in the Human Mouth
    AU  - Ekundayo S. W.
    AU  - Akinyosoye F. A.
    AU  - Momoh A. O.
    Y1  - 2017/03/21
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    N1  - https://doi.org/10.11648/j.ijmb.20170203.13
    DO  - 10.11648/j.ijmb.20170203.13
    T2  - International Journal of Microbiology and Biotechnology
    JF  - International Journal of Microbiology and Biotechnology
    JO  - International Journal of Microbiology and Biotechnology
    SP  - 121
    EP  - 128
    PB  - Science Publishing Group
    SN  - 2578-9686
    UR  - https://doi.org/10.11648/j.ijmb.20170203.13
    AB  - Methylotrophic bacteria are ubiquitous bacteria that are capable of using one carbon compounds such as methane, methanol, halogenated methane, and methylated amine as sources of carbon and energy for their diverse metabolic activities. Methylotrophic bacteria were isolated from the tongue, and supra- and subgingival plaque in the mouths of volunteers and patients with periodontitis. The isolation, identification, antibiotic susceptibility pattern and molecular characterization of methylotrophic bacteria from 150 volunteers and patients with periodontitis were done using standard method. Nutrient agar fortified with methylamine as a growth factor was used to aid the growth of these bacteria. The result show that a total of twelve (12) bacteria were identified. These are Bacillus licheniformis, Neisseria flava, Neisseria meningitis, Micrococcus flava, Pseudomonas aeruginosa, Streptococcus pneumoniae, Methylobacteria radiotolerance, Methylotrophic thiocynatum, Methylococcus capsulatum, Methylotrophic rubra and Branhamella catarhalis. The antibiotics susceptibility test showed that B. licheniformis, N. meningitis and P. aeruginosa exhibited the highest resistance against the antibiotics. The 12 bacteria were characterized molecularly with Polymerase chain reaction PCR amplified method using primers for the virulence genes of Methylotroph. The mxaF gene of methanol dehy- drogenase MxaF was detected in 3 bacteria: pilc of pilin gene in 3 bacteria, stx1 of shiga toxin nana of neuraminidase and pila of pilin gene was detected in all the bacteria. The results obtained in this research showed that methylotrophs may be responsible for periodontitis and that healthy people are carriers.
    VL  - 2
    IS  - 3
    ER  - 

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Author Information
  • Department of Microbiology, The Federal University of Technology, Akure, Nigeria

  • Department of Microbiology, The Federal University of Technology, Akure, Nigeria

  • Department of Biological Sciences (Microbiology Unit), Elizade University, Ilara-Mokin, Nigeria

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