T. Popova, Rozana Nazarjan, Oksana Nakonečna, Vitalij Gargin
{"title":"香烟对大鼠口腔微生物群的影响","authors":"T. Popova, Rozana Nazarjan, Oksana Nakonečna, Vitalij Gargin","doi":"10.5937/mckg56-41893","DOIUrl":null,"url":null,"abstract":"Objective. The tobacco usage is a risk factor of the variety oral diseases. To date, the effect of this risk factor on the composition of the oral microbial community has been considered by single studies with unclear pathogenic links. One of the possible factors that could be critical is a severe disturbance microbiota of oral cavity under influence of smoking, so the purpose of the present study was to evaluate the microflora of rats exposed to tobacco cigarette smoke. Methods. We compared the composition of the oral microflora of 20 WAG rats were exposed to smoke of tobacco cigarette and 10 control rats using a culture-based methods targeted at microbial taxonomic and functional profile. Differences between groups were analyzed with nonparametric the Kruskal-Wallis H test. Paired data were analyzed using the Wilcoxon test and Friedman's ANOVA test. Data presented are expressed as mean ± standard deviation (SD) numbers of colony-forming units per ml (CFU/ml). Statistical significance was defined as p<0.05. Results. At the experiment 60th day, comparative analysis of the microbiota showed that microbiological composition varied considerably between the two groups. In the rats influenced by cigarette smoke, exposure time-related reductions in commensal microflora were noted. At the end of the experiment, the commensal bacteria were markedly reduced. In contrast, the opportunistic bacterial diversity was increased and represented by Gram-negative microorganisms as the major phyla. Conclusion. We conclude that alterations in the composition, diversity, and function of the oral microbiome occur in association with tobacco smoke components and exposition term. The established risk factors for oral dysbiosis, especially after long-term exposure may contribute to disease development of the oral cavity.","PeriodicalId":39117,"journal":{"name":"Medicinski Casopis","volume":"1 1","pages":""},"PeriodicalIF":0.0000,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Effect of tobacco cigarettes on rats' oral microbiota\",\"authors\":\"T. Popova, Rozana Nazarjan, Oksana Nakonečna, Vitalij Gargin\",\"doi\":\"10.5937/mckg56-41893\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"Objective. The tobacco usage is a risk factor of the variety oral diseases. To date, the effect of this risk factor on the composition of the oral microbial community has been considered by single studies with unclear pathogenic links. One of the possible factors that could be critical is a severe disturbance microbiota of oral cavity under influence of smoking, so the purpose of the present study was to evaluate the microflora of rats exposed to tobacco cigarette smoke. Methods. We compared the composition of the oral microflora of 20 WAG rats were exposed to smoke of tobacco cigarette and 10 control rats using a culture-based methods targeted at microbial taxonomic and functional profile. Differences between groups were analyzed with nonparametric the Kruskal-Wallis H test. Paired data were analyzed using the Wilcoxon test and Friedman's ANOVA test. Data presented are expressed as mean ± standard deviation (SD) numbers of colony-forming units per ml (CFU/ml). Statistical significance was defined as p<0.05. Results. At the experiment 60th day, comparative analysis of the microbiota showed that microbiological composition varied considerably between the two groups. In the rats influenced by cigarette smoke, exposure time-related reductions in commensal microflora were noted. At the end of the experiment, the commensal bacteria were markedly reduced. In contrast, the opportunistic bacterial diversity was increased and represented by Gram-negative microorganisms as the major phyla. Conclusion. We conclude that alterations in the composition, diversity, and function of the oral microbiome occur in association with tobacco smoke components and exposition term. The established risk factors for oral dysbiosis, especially after long-term exposure may contribute to disease development of the oral cavity.\",\"PeriodicalId\":39117,\"journal\":{\"name\":\"Medicinski Casopis\",\"volume\":\"1 1\",\"pages\":\"\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Medicinski Casopis\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.5937/mckg56-41893\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q4\",\"JCRName\":\"Medicine\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Medicinski Casopis","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.5937/mckg56-41893","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q4","JCRName":"Medicine","Score":null,"Total":0}
Effect of tobacco cigarettes on rats' oral microbiota
Objective. The tobacco usage is a risk factor of the variety oral diseases. To date, the effect of this risk factor on the composition of the oral microbial community has been considered by single studies with unclear pathogenic links. One of the possible factors that could be critical is a severe disturbance microbiota of oral cavity under influence of smoking, so the purpose of the present study was to evaluate the microflora of rats exposed to tobacco cigarette smoke. Methods. We compared the composition of the oral microflora of 20 WAG rats were exposed to smoke of tobacco cigarette and 10 control rats using a culture-based methods targeted at microbial taxonomic and functional profile. Differences between groups were analyzed with nonparametric the Kruskal-Wallis H test. Paired data were analyzed using the Wilcoxon test and Friedman's ANOVA test. Data presented are expressed as mean ± standard deviation (SD) numbers of colony-forming units per ml (CFU/ml). Statistical significance was defined as p<0.05. Results. At the experiment 60th day, comparative analysis of the microbiota showed that microbiological composition varied considerably between the two groups. In the rats influenced by cigarette smoke, exposure time-related reductions in commensal microflora were noted. At the end of the experiment, the commensal bacteria were markedly reduced. In contrast, the opportunistic bacterial diversity was increased and represented by Gram-negative microorganisms as the major phyla. Conclusion. We conclude that alterations in the composition, diversity, and function of the oral microbiome occur in association with tobacco smoke components and exposition term. The established risk factors for oral dysbiosis, especially after long-term exposure may contribute to disease development of the oral cavity.