Biofilm analyses and exoproduct release by clinical and environmental isolates of Burkholderia pseudomallei from Brazil

IF 1.9 4区 医学 Q3 PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH Asian Pacific journal of tropical medicine Pub Date : 2023-07-01 DOI:10.4103/1995-7645.378565
G. Guedes, Crister J Ocadaque, A. Freitas, R. Pinheiro, G. Riello, S. Bandeira, R. Cordeiro, M. Rocha, J. Sidrim, D. Castelo-Branco
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Abstract

To characterize biofilm production by clinical (n=21) and environmental (n=11) isolates of Burkholderia pseudomallei and evaluate the production of proteases, hemolysins and siderophores. Initially, the 32 strains were evaluated for biofilm production in Müller-Hinton broth-1% glucose (MH-1% glucose) and BHI broth-1% glucose, using the crystal violet staining technique. Subsequently, growing (48 h) and mature (72 h) biofilms were evaluated by confocal microscopy. Finally, the production of proteases, hemolysins and siderophores by planktonic aggregates, growing biofilms and mature biofilms was evaluated. All isolates produced biofilms, but clinical isolates had significantly higher biomass in both MH-1% glucose (P<0.001) and BHI-glucose 1% (P=0.005). The structural analyses by confocal microscopy showed thick biofilms, composed of multiple layers of cells, homogeneously arranged, with mature biofilms of clinical isolates presenting higher biomass (P=0.019) and thickness of the entire area (P=0.029), and lower roughness coefficient (P=0.007) than those of environmental isolates. Protease production by growing biofilms was significantly greater than that of planktonic (P<0.001) and mature biofilms (P<0.001). Hemolysin release by planktonic aggregates was higher than that of biofilms (P<0.001). Regarding siderophores, mature biofilms presented higher production than growing biofilms (P<0.001) and planktonic aggregates (P<0.001). Clinical isolates have higher production of biofilms than their environmental counterparts; protease and siderophores seem important for growth and maintenance of Burkholderia pseudomallei biofilms.
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巴西假槌伯克霍尔德菌临床和环境分离株的生物膜分析和胞外产物释放
通过临床(n=21)和环境(n=11)分离的假马氏伯克氏菌来表征生物膜的产生,并评估蛋白酶、溶血素和铁载体的产生。首先,采用结晶紫染色技术,对32株菌株在1%葡萄糖的m ller- hinton肉汤(MH-1%葡萄糖)和1%葡萄糖的BHI肉汤中产生生物膜的情况进行了评估。随后,用共聚焦显微镜观察生长(48 h)和成熟(72 h)的生物膜。最后,对浮游聚集体、生长生物膜和成熟生物膜的蛋白酶、溶血素和铁载体的产量进行了评价。所有分离株均产生生物膜,但临床分离株在MH-1%葡萄糖(P<0.001)和bhi -1%葡萄糖(P=0.005)中生物量均显著高于临床分离株。共聚焦显微镜结构分析显示,临床分离菌株成熟生物膜的生物量(P=0.019)和面积厚度(P=0.029)均高于环境分离菌株,且生物膜厚度(P=0.007)较低。生长生物膜的蛋白酶产量显著高于浮游生物(P<0.001)和成熟生物膜(P<0.001)。浮游聚集体溶血素释放量高于生物膜(P<0.001)。在铁载体方面,成熟生物膜的产量高于生长生物膜(P<0.001)和浮游聚集体(P<0.001)。临床分离株的生物膜产量高于环境分离株;蛋白酶和铁载体似乎对假杆菌伯克霍尔德菌生物膜的生长和维持很重要。
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来源期刊
Asian Pacific journal of tropical medicine
Asian Pacific journal of tropical medicine PUBLIC, ENVIRONMENTAL & OCCUPATIONAL HEALTH-TROPICAL MEDICINE
CiteScore
4.00
自引率
9.70%
发文量
1936
审稿时长
3-8 weeks
期刊介绍: Asian Pacific Journal of Tropical Medicine (ISSN 1995-7645 CODEN: APJTB6), a publication of Editorial office of Hainan Medical University,is a peer-reviewed print + online Monthly journal. The journal''s full text is available online at http://www.apjtm.org/. The journal allows free access (Open Access) to its contents and permits authors to self-archive final accepted version of the articles on any OAI-compliant institutional / subject-based repository. APJTM aims to provide an academic communicating platform for international physicians, medical scientists, allied health scientists and public health workers, especially those of the Asia-Pacific region and worldwide on tropical medicine, infectious diseases and public health, and to meet the growing challenges of understanding, preventing and controlling the dramatic global emergence and re-emergence of infectious diseases in the Asia-Pacific. The journal is proud to have an international and diverse editorial board that will assist and facilitate the publication of articles that reflect a global view on tropical medicine, infectious diseases and public health, as well as emphasizing our focus on supporting the needs of public health practitioners. The APJTM will allow us to seek opportunities to work with others who share our aim, and to enhance our work through partnership, and to uphold the standards of our profession and contribute to its advancement.
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