{"title":"从肉鸡养殖场生物膜中分离的芽孢杆菌属菌株的基因组和表型特征透视。","authors":"Virgile Guéneau, Guillermo Jiménez, Mathieu Castex, Romain Briandet","doi":"10.1128/aem.00663-24","DOIUrl":null,"url":null,"abstract":"<p><p>The characterization of surface microbiota living in biofilms within livestock buildings has been relatively unexplored, despite its potential impact on animal health. To enhance our understanding of these microbial communities, we characterized 11 spore-forming strains isolated from two commercial broiler chicken farms. Sequencing of the strains revealed them to belong to three species <i>Bacillus velezensis</i>, <i>Bacillus subtilis</i>, and <i>Bacillus licheniformis</i>. Genomic analysis revealed the presence of antimicrobial resistance genes and genes associated with antimicrobial secretion specific to each species. We conducted a comprehensive characterization of the biofilm formed by these strains under various conditions, and we revealed significant structural heterogeneity across the different strains. A macro-colony interaction model was employed to assess the compatibility of these strains to coexist in mixed biofilms. We identified highly competitive <i>B. velezensis</i> strains, which cannot coexist with other <i>Bacillus</i> spp. Using confocal laser scanning microscopy along with a specific dye for extracellular DNA, we uncovered the importance of extracellular DNA for the formation of <i>B. licheniformis</i> biofilms. Altogether, the results highlight the heterogeneity in both genome and biofilm structure among <i>Bacillus</i> spp. isolated from biofilms present within livestock buildings.IMPORTANCELittle is known about the microbial communities that develop on farms in direct contact with animals. Nonpathogenic strains of <i>Bacillus velezensis</i>, <i>Bacillus subtilis</i>, and <i>Bacillus licheniformis</i> were found in biofilm samples collected from surfaces in contact with animals. Significant genetic and phenotypic diversity was described among these <i>Bacillus</i> strains. The strains do not possess mobile antibiotic resistance genes in their genomes and have a strong capacity to form structured biofilms. Among these species, <i>B. velezensis</i> was noted for its high competitiveness compared with the other <i>Bacillus</i> spp. Additionally, the importance of extracellular DNA in the formation of <i>B. licheniformis</i> biofilms was observed. These findings provide insights for the management of these surface microbiota that can influence animal health, such as the use of competitive strains to minimize the establishment of undesirable bacteria or enzymes capable of specifically deconstructing biofilms.</p>","PeriodicalId":8002,"journal":{"name":"Applied and Environmental Microbiology","volume":null,"pages":null},"PeriodicalIF":3.9000,"publicationDate":"2024-09-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11409695/pdf/","citationCount":"0","resultStr":"{\"title\":\"Insights into the genomic and phenotypic characteristics of <i>Bacillus</i> spp. strains isolated from biofilms in broiler farms.\",\"authors\":\"Virgile Guéneau, Guillermo Jiménez, Mathieu Castex, Romain Briandet\",\"doi\":\"10.1128/aem.00663-24\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>The characterization of surface microbiota living in biofilms within livestock buildings has been relatively unexplored, despite its potential impact on animal health. To enhance our understanding of these microbial communities, we characterized 11 spore-forming strains isolated from two commercial broiler chicken farms. Sequencing of the strains revealed them to belong to three species <i>Bacillus velezensis</i>, <i>Bacillus subtilis</i>, and <i>Bacillus licheniformis</i>. Genomic analysis revealed the presence of antimicrobial resistance genes and genes associated with antimicrobial secretion specific to each species. We conducted a comprehensive characterization of the biofilm formed by these strains under various conditions, and we revealed significant structural heterogeneity across the different strains. A macro-colony interaction model was employed to assess the compatibility of these strains to coexist in mixed biofilms. We identified highly competitive <i>B. velezensis</i> strains, which cannot coexist with other <i>Bacillus</i> spp. Using confocal laser scanning microscopy along with a specific dye for extracellular DNA, we uncovered the importance of extracellular DNA for the formation of <i>B. licheniformis</i> biofilms. Altogether, the results highlight the heterogeneity in both genome and biofilm structure among <i>Bacillus</i> spp. isolated from biofilms present within livestock buildings.IMPORTANCELittle is known about the microbial communities that develop on farms in direct contact with animals. Nonpathogenic strains of <i>Bacillus velezensis</i>, <i>Bacillus subtilis</i>, and <i>Bacillus licheniformis</i> were found in biofilm samples collected from surfaces in contact with animals. Significant genetic and phenotypic diversity was described among these <i>Bacillus</i> strains. The strains do not possess mobile antibiotic resistance genes in their genomes and have a strong capacity to form structured biofilms. Among these species, <i>B. velezensis</i> was noted for its high competitiveness compared with the other <i>Bacillus</i> spp. Additionally, the importance of extracellular DNA in the formation of <i>B. licheniformis</i> biofilms was observed. These findings provide insights for the management of these surface microbiota that can influence animal health, such as the use of competitive strains to minimize the establishment of undesirable bacteria or enzymes capable of specifically deconstructing biofilms.</p>\",\"PeriodicalId\":8002,\"journal\":{\"name\":\"Applied and Environmental Microbiology\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":3.9000,\"publicationDate\":\"2024-09-18\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11409695/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Applied and Environmental Microbiology\",\"FirstCategoryId\":\"99\",\"ListUrlMain\":\"https://doi.org/10.1128/aem.00663-24\",\"RegionNum\":2,\"RegionCategory\":\"生物学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2024/8/19 0:00:00\",\"PubModel\":\"Epub\",\"JCR\":\"Q2\",\"JCRName\":\"BIOTECHNOLOGY & APPLIED MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Applied and Environmental Microbiology","FirstCategoryId":"99","ListUrlMain":"https://doi.org/10.1128/aem.00663-24","RegionNum":2,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2024/8/19 0:00:00","PubModel":"Epub","JCR":"Q2","JCRName":"BIOTECHNOLOGY & APPLIED MICROBIOLOGY","Score":null,"Total":0}
引用次数: 0
摘要
尽管生活在畜舍生物膜中的表面微生物群对动物健康有潜在影响,但对其特征的研究相对较少。为了加深我们对这些微生物群落的了解,我们对从两个商业肉鸡养殖场分离出的 11 株孢子形成菌株进行了鉴定。这些菌株的测序结果表明,它们分别属于韦氏芽孢杆菌、枯草芽孢杆菌和地衣芽孢杆菌三个物种。基因组分析表明,每个菌种都存在抗菌药耐药性基因和与抗菌药分泌相关的基因。我们对这些菌株在各种条件下形成的生物膜进行了全面鉴定,发现不同菌株的生物膜在结构上存在显著的异质性。我们采用了大菌落相互作用模型来评估这些菌株在混合生物膜中共存的兼容性。利用激光共聚焦扫描显微镜和细胞外 DNA 的特异性染料,我们发现了细胞外 DNA 对地衣芽孢杆菌生物膜形成的重要性。总之,这些结果凸显了从畜牧建筑内的生物膜中分离出的芽孢杆菌属在基因组和生物膜结构上的异质性。从与动物接触的表面采集的生物膜样本中发现了非致病性的韦氏芽孢杆菌、枯草芽孢杆菌和地衣芽孢杆菌。在这些芽孢杆菌菌株中发现了显著的遗传和表型多样性。这些菌株的基因组中没有可移动的抗生素耐药性基因,并且具有形成结构化生物膜的强大能力。地衣芽孢杆菌生物膜的形成过程中,细胞外 DNA 起着重要作用。这些发现为管理这些可能影响动物健康的表面微生物群提供了启示,例如使用具有竞争力的菌株来尽量减少不良细菌的建立,或使用能够专门分解生物膜的酶。
Insights into the genomic and phenotypic characteristics of Bacillus spp. strains isolated from biofilms in broiler farms.
The characterization of surface microbiota living in biofilms within livestock buildings has been relatively unexplored, despite its potential impact on animal health. To enhance our understanding of these microbial communities, we characterized 11 spore-forming strains isolated from two commercial broiler chicken farms. Sequencing of the strains revealed them to belong to three species Bacillus velezensis, Bacillus subtilis, and Bacillus licheniformis. Genomic analysis revealed the presence of antimicrobial resistance genes and genes associated with antimicrobial secretion specific to each species. We conducted a comprehensive characterization of the biofilm formed by these strains under various conditions, and we revealed significant structural heterogeneity across the different strains. A macro-colony interaction model was employed to assess the compatibility of these strains to coexist in mixed biofilms. We identified highly competitive B. velezensis strains, which cannot coexist with other Bacillus spp. Using confocal laser scanning microscopy along with a specific dye for extracellular DNA, we uncovered the importance of extracellular DNA for the formation of B. licheniformis biofilms. Altogether, the results highlight the heterogeneity in both genome and biofilm structure among Bacillus spp. isolated from biofilms present within livestock buildings.IMPORTANCELittle is known about the microbial communities that develop on farms in direct contact with animals. Nonpathogenic strains of Bacillus velezensis, Bacillus subtilis, and Bacillus licheniformis were found in biofilm samples collected from surfaces in contact with animals. Significant genetic and phenotypic diversity was described among these Bacillus strains. The strains do not possess mobile antibiotic resistance genes in their genomes and have a strong capacity to form structured biofilms. Among these species, B. velezensis was noted for its high competitiveness compared with the other Bacillus spp. Additionally, the importance of extracellular DNA in the formation of B. licheniformis biofilms was observed. These findings provide insights for the management of these surface microbiota that can influence animal health, such as the use of competitive strains to minimize the establishment of undesirable bacteria or enzymes capable of specifically deconstructing biofilms.
期刊介绍:
Applied and Environmental Microbiology (AEM) publishes papers that make significant contributions to (a) applied microbiology, including biotechnology, protein engineering, bioremediation, and food microbiology, (b) microbial ecology, including environmental, organismic, and genomic microbiology, and (c) interdisciplinary microbiology, including invertebrate microbiology, plant microbiology, aquatic microbiology, and geomicrobiology.