Cecilia Sahl, Agnes Andersson, Natalie Larsson, Magnus Paulsson, Oonagh Shannon, Lisa I Påhlman
{"title":"囊性纤维化病原体木糖氧化无色杆菌抑制铜绿假单胞菌的生物膜形成。","authors":"Cecilia Sahl, Agnes Andersson, Natalie Larsson, Magnus Paulsson, Oonagh Shannon, Lisa I Påhlman","doi":"10.1099/jmm.0.002051","DOIUrl":null,"url":null,"abstract":"<p><p><b>Background.</b> <i>Achromobacter xylosoxidans</i> and <i>Pseudomonas aeruginosa</i> are two pathogens that cause persistent airway infections in individuals with cystic fibrosis (CF). The persistence of <i>P. aeruginosa</i> is partly due to a high capacity to form biofilms and the ability to exert antagonism against other bacteria. Loss of microbial diversity in conjunction with chronic <i>P. aeruginosa</i> colonization is strongly correlated with low lung function in CF. <i>A. xylosoxidans</i> and <i>P. aeruginosa</i> are frequently co-isolated in CF airway cultures. This study aims to investigate the reciprocal effects on growth inhibition and biofilm formation between <i>P. aeruginosa</i> and <i>A. xylosoxidans in vitro</i>.<b>Method.</b> Six isolates of <i>A. xylosoxidans</i>, isolated from three CF patients in early and late stages of a chronic infection, were cultured together with a CF isolate of <i>P. aeruginosa</i>. Biofilm formation was assessed using a microtiter assay and crystal violet staining. Quantitative PCR was used to quantify species proportions in biofilms. Growth curves were performed to compare planktonic growth rates.<b>Results.</b> Three <i>A. xylosoxidans</i> isolates, all of which were from early-stage infections, inhibited biofilm formation of <i>P. aeruginosa</i>. The inhibition was concentration-dependent and required the interaction of live bacteria during the early stages of biofilm development. The inhibitory effect was not caused by nutrient depletion of the planktonic cells. The selected <i>A. xylosoxidans</i> isolate had a stronger capacity to adhere to plastic surfaces compared to the <i>P. aeruginosa</i> isolate.<b>Conclusions</b> <i>. A. xylosoxidans</i> can inhibit <i>P. aeruginosa</i> biofilm formation <i>in vitro</i>. The observed effect requires active interactions between live cells during the attachment stage of biofilm formation, possibly due to differences in adhesion capacity.</p>","PeriodicalId":94093,"journal":{"name":"Journal of medical microbiology","volume":"74 8","pages":""},"PeriodicalIF":2.0000,"publicationDate":"2025-08-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12316436/pdf/","citationCount":"0","resultStr":"{\"title\":\"The cystic fibrosis pathogen <i>Achromobacter xylosoxidans</i> inhibits biofilm formation of <i>Pseudomonas aeruginosa</i>.\",\"authors\":\"Cecilia Sahl, Agnes Andersson, Natalie Larsson, Magnus Paulsson, Oonagh Shannon, Lisa I Påhlman\",\"doi\":\"10.1099/jmm.0.002051\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Background.</b> <i>Achromobacter xylosoxidans</i> and <i>Pseudomonas aeruginosa</i> are two pathogens that cause persistent airway infections in individuals with cystic fibrosis (CF). The persistence of <i>P. aeruginosa</i> is partly due to a high capacity to form biofilms and the ability to exert antagonism against other bacteria. Loss of microbial diversity in conjunction with chronic <i>P. aeruginosa</i> colonization is strongly correlated with low lung function in CF. <i>A. xylosoxidans</i> and <i>P. aeruginosa</i> are frequently co-isolated in CF airway cultures. This study aims to investigate the reciprocal effects on growth inhibition and biofilm formation between <i>P. aeruginosa</i> and <i>A. xylosoxidans in vitro</i>.<b>Method.</b> Six isolates of <i>A. xylosoxidans</i>, isolated from three CF patients in early and late stages of a chronic infection, were cultured together with a CF isolate of <i>P. aeruginosa</i>. Biofilm formation was assessed using a microtiter assay and crystal violet staining. Quantitative PCR was used to quantify species proportions in biofilms. Growth curves were performed to compare planktonic growth rates.<b>Results.</b> Three <i>A. xylosoxidans</i> isolates, all of which were from early-stage infections, inhibited biofilm formation of <i>P. aeruginosa</i>. The inhibition was concentration-dependent and required the interaction of live bacteria during the early stages of biofilm development. The inhibitory effect was not caused by nutrient depletion of the planktonic cells. The selected <i>A. xylosoxidans</i> isolate had a stronger capacity to adhere to plastic surfaces compared to the <i>P. aeruginosa</i> isolate.<b>Conclusions</b> <i>. A. xylosoxidans</i> can inhibit <i>P. aeruginosa</i> biofilm formation <i>in vitro</i>. The observed effect requires active interactions between live cells during the attachment stage of biofilm formation, possibly due to differences in adhesion capacity.</p>\",\"PeriodicalId\":94093,\"journal\":{\"name\":\"Journal of medical microbiology\",\"volume\":\"74 8\",\"pages\":\"\"},\"PeriodicalIF\":2.0000,\"publicationDate\":\"2025-08-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12316436/pdf/\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of medical microbiology\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.1099/jmm.0.002051\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of medical microbiology","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1099/jmm.0.002051","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
The cystic fibrosis pathogen Achromobacter xylosoxidans inhibits biofilm formation of Pseudomonas aeruginosa.
Background.Achromobacter xylosoxidans and Pseudomonas aeruginosa are two pathogens that cause persistent airway infections in individuals with cystic fibrosis (CF). The persistence of P. aeruginosa is partly due to a high capacity to form biofilms and the ability to exert antagonism against other bacteria. Loss of microbial diversity in conjunction with chronic P. aeruginosa colonization is strongly correlated with low lung function in CF. A. xylosoxidans and P. aeruginosa are frequently co-isolated in CF airway cultures. This study aims to investigate the reciprocal effects on growth inhibition and biofilm formation between P. aeruginosa and A. xylosoxidans in vitro.Method. Six isolates of A. xylosoxidans, isolated from three CF patients in early and late stages of a chronic infection, were cultured together with a CF isolate of P. aeruginosa. Biofilm formation was assessed using a microtiter assay and crystal violet staining. Quantitative PCR was used to quantify species proportions in biofilms. Growth curves were performed to compare planktonic growth rates.Results. Three A. xylosoxidans isolates, all of which were from early-stage infections, inhibited biofilm formation of P. aeruginosa. The inhibition was concentration-dependent and required the interaction of live bacteria during the early stages of biofilm development. The inhibitory effect was not caused by nutrient depletion of the planktonic cells. The selected A. xylosoxidans isolate had a stronger capacity to adhere to plastic surfaces compared to the P. aeruginosa isolate.Conclusions. A. xylosoxidans can inhibit P. aeruginosa biofilm formation in vitro. The observed effect requires active interactions between live cells during the attachment stage of biofilm formation, possibly due to differences in adhesion capacity.