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Features of formation of Yersinia enterocolitica biofilms
AIM: The work aimed to study the morphology of colonies and their comparison by features of the formation of Yersinia enterocolitica biofilms. MATERIALS AND METHODS: Bacteria were cultured on a Yersinia Selective Agar medium (“CIN-agar”) at 28°C for 24 h. The microorganisms were grown in meat-pepton...
Autores principales: | , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Veterinary World
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431818/ https://www.ncbi.nlm.nih.gov/pubmed/30936667 http://dx.doi.org/10.14202/vetworld.2019.136-140 |
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author | Lenchenko, E. Lozovoy, D. Strizhakov, A. Vatnikov, Yu Byakhova, V. Kulikov, Eu Sturov, N. Kuznetsov, V. Avdotin, V. Grishin, V. |
author_facet | Lenchenko, E. Lozovoy, D. Strizhakov, A. Vatnikov, Yu Byakhova, V. Kulikov, Eu Sturov, N. Kuznetsov, V. Avdotin, V. Grishin, V. |
author_sort | Lenchenko, E. |
collection | PubMed |
description | AIM: The work aimed to study the morphology of colonies and their comparison by features of the formation of Yersinia enterocolitica biofilms. MATERIALS AND METHODS: Bacteria were cultured on a Yersinia Selective Agar medium (“CIN-agar”) at 28°C for 24 h. The microorganisms were grown in meat-peptone broth with 1.0% glucose to measure the absolute values of the optical density of the culture. The optical density of the liquid was determined in a microplate photometric analyzer Immunochem-2100 (HTI, USA) at a wavelength of 490 nm. For the study of biofilms, the specimens were fixed for 3-5 h in pairs of 25.0% solution of glutaraldehyde (according to DV), and pairs of a 1.0% aqueous solution of osmic acid (OSO(4)) were used for contrasting for 2-3 min. The specimens were examined with stereoscopic microscopy “BIOMED MS-1 Stereo” (Russia) and scanning electron microscope “TM 3030 plus” (Holland). RESULTS: With stereoscopic microscopy of the colonies of Y. enterocolitica, the S-forms had an elevated intensely colored center, radial striation along the periphery, smooth edges, d ≤ 1.0 mm. R-form colonies had a dark color and a dry surface, were tuberous and had a dense center with a peripheral ridge, rugged edges, d ≥ 1.5 mm. The optical density of the Y. enterocolitica S-form showed that this type of microorganism belongs to the moderate producers of biofilms since the optical density of the sample (density of the sample - Ds) exceeded the optical density of control (density of the control - Dc) by 3 times. In Y. enterocolitic a R-form (D ≤ 0.197) weakly produced biofilms, the optical density of the sample exceeded the optical density of the control by <2 times. CONCLUSION: The ability to form biofilms, the variability of phenotypic features, and the multiplicity of virulence factors of bacteria significantly reduce the effectiveness of diagnostic studies. The development of accelerated methods of detection and differentiation of the virulent properties of pathogenic bacteria will allow scientifically to substantiate and develop a set of measures aimed at preventing animal diseases and obtaining safe livestock products to prevent human diseases. Thus, we need to pay attention to which forms of colonies do Y. enterocolitic a form on solid nutrient media: S- or R-forms. Through this study, we know that bacteria-forming S-shaped colonies are more capable of forming biofilms than R-forms. It means that they are more pathogenic and can cause persistent infections due to adhesion and biofilm formation. |
format | Online Article Text |
id | pubmed-6431818 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | Veterinary World |
record_format | MEDLINE/PubMed |
spelling | pubmed-64318182019-04-01 Features of formation of Yersinia enterocolitica biofilms Lenchenko, E. Lozovoy, D. Strizhakov, A. Vatnikov, Yu Byakhova, V. Kulikov, Eu Sturov, N. Kuznetsov, V. Avdotin, V. Grishin, V. Vet World Research Article AIM: The work aimed to study the morphology of colonies and their comparison by features of the formation of Yersinia enterocolitica biofilms. MATERIALS AND METHODS: Bacteria were cultured on a Yersinia Selective Agar medium (“CIN-agar”) at 28°C for 24 h. The microorganisms were grown in meat-peptone broth with 1.0% glucose to measure the absolute values of the optical density of the culture. The optical density of the liquid was determined in a microplate photometric analyzer Immunochem-2100 (HTI, USA) at a wavelength of 490 nm. For the study of biofilms, the specimens were fixed for 3-5 h in pairs of 25.0% solution of glutaraldehyde (according to DV), and pairs of a 1.0% aqueous solution of osmic acid (OSO(4)) were used for contrasting for 2-3 min. The specimens were examined with stereoscopic microscopy “BIOMED MS-1 Stereo” (Russia) and scanning electron microscope “TM 3030 plus” (Holland). RESULTS: With stereoscopic microscopy of the colonies of Y. enterocolitica, the S-forms had an elevated intensely colored center, radial striation along the periphery, smooth edges, d ≤ 1.0 mm. R-form colonies had a dark color and a dry surface, were tuberous and had a dense center with a peripheral ridge, rugged edges, d ≥ 1.5 mm. The optical density of the Y. enterocolitica S-form showed that this type of microorganism belongs to the moderate producers of biofilms since the optical density of the sample (density of the sample - Ds) exceeded the optical density of control (density of the control - Dc) by 3 times. In Y. enterocolitic a R-form (D ≤ 0.197) weakly produced biofilms, the optical density of the sample exceeded the optical density of the control by <2 times. CONCLUSION: The ability to form biofilms, the variability of phenotypic features, and the multiplicity of virulence factors of bacteria significantly reduce the effectiveness of diagnostic studies. The development of accelerated methods of detection and differentiation of the virulent properties of pathogenic bacteria will allow scientifically to substantiate and develop a set of measures aimed at preventing animal diseases and obtaining safe livestock products to prevent human diseases. Thus, we need to pay attention to which forms of colonies do Y. enterocolitic a form on solid nutrient media: S- or R-forms. Through this study, we know that bacteria-forming S-shaped colonies are more capable of forming biofilms than R-forms. It means that they are more pathogenic and can cause persistent infections due to adhesion and biofilm formation. Veterinary World 2019-01 2019-01-25 /pmc/articles/PMC6431818/ /pubmed/30936667 http://dx.doi.org/10.14202/vetworld.2019.136-140 Text en Copyright: © Lenchenko, et al http://creativecommons.org/licenses/by/4.0 Open Access. This article is 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, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Lenchenko, E. Lozovoy, D. Strizhakov, A. Vatnikov, Yu Byakhova, V. Kulikov, Eu Sturov, N. Kuznetsov, V. Avdotin, V. Grishin, V. Features of formation of Yersinia enterocolitica biofilms |
title | Features of formation of Yersinia enterocolitica biofilms |
title_full | Features of formation of Yersinia enterocolitica biofilms |
title_fullStr | Features of formation of Yersinia enterocolitica biofilms |
title_full_unstemmed | Features of formation of Yersinia enterocolitica biofilms |
title_short | Features of formation of Yersinia enterocolitica biofilms |
title_sort | features of formation of yersinia enterocolitica biofilms |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6431818/ https://www.ncbi.nlm.nih.gov/pubmed/30936667 http://dx.doi.org/10.14202/vetworld.2019.136-140 |
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