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Microbiological Oropharyngeal Patterns in Patients with Different Phenotypes of Chronic Obstructive Pulmonary Disease

Microbiological Oropharyngeal Patterns in Patients with Different Phenotypes of Chronic Obstructive Pulmonary Disease

Karnaushkina M.A., Fedosenko S.V., Sazonov A.E., Petrov V.A., Ovsyannikov D.Yu., Ogorodova L.M.
Key words: COPD; oropharyngeal microbiota; sequencing; COPD phenotypes; severity.
2018, volume 10, issue 2, page 101.

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Persistent bronchial inflammation in chronic obstructive pulmonary disease (COPD) is considered the cause of ventilation disorders and related contamination with conditionally pathogenic microorganisms; the latter can proceed and transform into a full infection, which can aggravate and exacerbate COPD.

The aim of the study was to evaluate the relations between the oropharyngeal microbiota in patients with COPD and the clinical, functional, and prognostic parameters of the disease.

Materials and Methods. 64 patients with COPD were included in the study; the participants were scheduled to visit our clinic on two occasions. In the first visit, their medical history was studied in detail and the major examination procedures were conducted. Those included an assessment of the respiratory function, the 6-minute walk test, the degree of dyspnea by the Medical Research Council scale, body plethysmography, the diffusion capacity of the lungs, and a chest CT scan. The second visit took place 12 months after the first one to assess the changes in the course of the disease. The result was considered negative if, in the second examination, the patient‘s condition was found more severe. Oropharyngeal samples of all patients were sequenced to identify the V3–V4 variable sites of the 16S rRNA gene.

Results. It is found that the microbiological oropharyngeal patterns in COPD patients depend on the source of micro-aspiration. In addition, the changes in the oropharyngeal microbiota correlate with the severity and prognosis of the disease, as well as the patient phenotype. Based on the data obtained by sequencing parts of the 16S rRNA gene, the role of oropharyngeal microbiota in determining the course and prognosis of COPD has been elucidated.

Conclusion. The presented clinical and functional characteristics associated with oropharyngeal microbiota indicate that micro-aspirations from other body compartments not only affect the composition of oropharyngeal microbiota in patients with COPD but also have an important prognostic significance.

  1. Chuchalin A.G., Avdeev S.N., Aysanov Z.R., Belevskiy A.S., Leshchenko I.V., Meshcheryakova N.N., Ovcharenko S.I., Shmelev E.I. Russian respiratory society. Federal guidelines on diagnosis and treatment of chronic obstructive pulmonary disease. Russian Pulmonology 2014; 3: 15–36, https://doi.org/10.18093/0869-0189-2014-0-3-15-54.
  2. Global Initiative for Chronic Obstructive Lung Disease. Global strategy for diagnosis, management, and prevention of COPD. Updated 2015.
  3. Fedosenko S.V., Ogorodova L.M., Popenko A.S., Petrov V.A., Tyakht A.V., Saltykova I.V., Kamaltynova E.M., Deev I.A., Kulikov E.S., Kirillova N.A., Govorun V.M., Kostryukova E.S., Karnaushkina M.A. The qualitative and quantitative characteristics of content of oro-pharyngeal microbiota of patients with chronic obstructive disease of lungs. Lechenie i profilaktika 2015; 2(14): 92–99.
  4. Avdeev S.N. Symptoms and quality of life in patients with chronic obstructive pulmonary disease: are there patient-defined outcomes or predictive factors? Russian Pulmonology 2016; 26(2): 231–237, https://doi.org/10.18093/0869-0189-2016-26-2-231-237.
  5. Chambers D.C., Gellatly S.L., Hugenholtz P., Hansbro P.M. JTD special edition ‘Hot Topics in COPD’ — the microbiome in COPD. J Thorac Dis 2014; 6(11): 1525–1531, https://doi.org/10.3978/j.issn.2072-1439.2014.11.08.
  6. Charlson E.S., Bittinger K., Haas A.R., Fitzgerald A.S., Frank I., Yadav A., Bushman F.D., Collman R.G. Topographical continuity of bacterial populations in the healthy human respiratory tract. Am J Respir Crit Care Med 2011; 184: 957–963, https://doi.org/10.1164/rccm.201104-0655oc.
  7. Górecka D., Puścińska E. Microbiome of the lung. Pneumonol Alergol Pol 2014; 82(6): 481–485, https://doi.org/10.5603/PiAP.2014.0063.
  8. Park H., Shin J.W., Park S.G., Kim W. Microbial communities in the upper respiratory tract of patients with asthma and chronic obstructive pulmonary disease. PLoS One 2014; 9(10): e109710, https://doi.org/10.1371/journal.pone.0109710.
  9. Molyneaux P.L., Mallia P., Cox M.J., Footitt J., Willis-Owen S.A., Homola D., Trujillo-Torralbo M.B., Elkin S., Kon O.M., Cookson W.O., Moffatt M.F., Johnston S.L. Outgrowth of the bacterial airway microbiome following rhinovirus exacerbation of chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2013; 188(10): 1224–1231, https://doi.org/10.1164/rccm.201302-0341oc.
  10. Patel A.R., Hurst J.R. Extrapulmonary comorbidities in chronic obstructive pulmonary disease: state of the art. Expert Rev Respir Med 2011; 5(5): 647–662, https://doi.org/10.1586/ers.11.62.
  11. Hurst J.R. Upper airway. 3: Sinonasal involvement in chronic obstructive pulmonary disease. Thorax 2010; 65(1): 85–90, https://doi.org/10.1136/thx.2008.112888.
  12. Paulson J.N., Olson N.D., Wagner J., Talukder H., Pop M., Bravo H.C. Statistical analysis for sparse high-throughput sequencing, https://doi.org/10.18129/B9.bioc.metagenomeSeq.
  13. Faust K., Sathirapongsasuti J.F., Izard J., Segata N., Gevers D., Raes J., Huttenhower C. Microbial co-occurrence relationships in the human microbiome. PLoS Comput Biol 2012; 8(7): e1002606, https://doi.org/10.1371/journal.pcbi.1002606.
  14. Pragman A.A., Kim H.B., Reilly C.S., Wendt C., Isaacson R.E. The lung microbiome in moderate and severe chronic obstructive pulmonary disease. PloS One 2012; 7(10): e47305, https://doi.org/10.1371/journal.pone.0047305.
  15. Sze M.A., Dimitriu P.A., Hayashi S., Elliott W.M., McDonough J.E., Gosselink J.V., Cooper J., Sin D.D., Mohn W.W., Hogg J.C. The lung tissue microbiome in chronic obstructive pulmonary disease. Am J Respir Crit Care Med 2012; 185(10): 1073–1080, https://doi.org/10.1164/rccm.201111-2075oc.
  16. Sin D., Sze M., Hogg J. Bacterial microbiome of lungs in COPD. Int J Chron Obstruct Pulmon Dis 2014; 9: 229–238, https://doi.org/10.2147/copd.s38932.
  17. Huang Y.J., Sethi S., Murphy T., Nariya S., Boushey H.A., Lynch S.V. Airway microbiome dynamics in exacerbations of chronic obstructive pulmonary disease. J Clin Microbiol 2014; 52(8): 2813–2823, https://doi.org/10.1128/jcm.00035-14.
  18. Ghannoum M.A., Jurevic R.J., Mukherjee P.K., Cui F., Sikaroodi M., Naqvi A., Gillevet P.M. Characterization of the oral fungal microbiome (mycobiome) in healthy individuals. PLoS Pathog 2010; 6(1): e1000713, https://doi.org/10.1371/journal.ppat.1000713.
  19. Hsiao W.W., Li K.L., Liu Z., Jones C., Fraser-Liggett C.M., Fouad A.F. Microbial transformation from normal oral microbiota to acute endodontic infections. BMC Genomics 2012; 13: 345, https://doi.org/10.1186/1471-2164-13-345.
  20. Pei Z., Yang L., Peek R.M., Jr Levine S.M., Pride D.T., Blaser M.J. Bacterial biota in reflux esophagitis and Barrett’s esophagus. World J Gastroenterol 2005; 11(46): 7277–7283, https://doi.org/10.3748/wjg.v11.i46.7277.
  21. Sakae T.M., Pizzichini M.M., Teixeira P.J., Silva R.M., Trevisol D.J., Pizzichini E. Exacerbations of COPD and symptoms of gastroesophageal reflux: a systematic review and meta-analysis. J Bras Pneumol 2013; 39(3): 259–271, https://doi.org/10.1590/s1806-37132013000300002.
Karnaushkina M.A., Fedosenko S.V., Sazonov A.E., Petrov V.A., Ovsyannikov D.Yu., Ogorodova L.M. Microbiological Oropharyngeal Patterns in Patients with Different Phenotypes of Chronic Obstructive Pulmonary Disease. Sovremennye tehnologii v medicine 2018; 10(2): 101, https://doi.org/10.17691/stm2018.10.2.11


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