John E Moore, John McCaughan, Jacqueline C Rendall, Beverley C Millar
{"title":"囊性纤维化成人非铜绿假单胞菌的微生物学:帮助确定非铜绿假单胞菌在CF肺病理中的临床意义的标准","authors":"John E Moore, John McCaughan, Jacqueline C Rendall, Beverley C Millar","doi":"10.3389/bjbs.2022.10468","DOIUrl":null,"url":null,"abstract":"<p><p><b>Introduction:</b> There is a paucity of reports on non-<i>aeruginosa Pseudomonas</i> (NAPs) in cystic fibrosis, hence this study wished 1). to examine the diversity/frequency of NAPs in an adult CF population, 2) to compare/contrast the microbiology and genomics of NAPs to <i>P. aeruginosa</i> and 3) to propose clinical and laboratory criteria to help determine their clinical significance in CF lung pathology. <b>Materials and Methods:</b> Microbiological data was examined from 100 adult patients with cystic fibrosis from birth to present (31/12/2021), equating to 2455 patient years. 16S rDNA phylogenetic relatedness of NAPs was determined, as well as bioinformatical comparison of whole genomes of <i>P. aeruginosa</i> against <i>P. fluorescens</i>. <b>Results:</b> Ten species were isolated from this patient cohort during this time period, with three species, i.e., <i>P. fluorescens, P. putida</i> and <i>P. stutzeri</i>, accounting for the majority (87.5%) of non-<i>aeruginosa</i> reports. This is the first report of the isolation of <i>P. fragi, P. nitroreducens, P. oryzihabitans</i> and <i>P. veronii</i> in patients with cystic fibrosis. The mean time to first detection of any non-<i>aeruginosa</i> species was 183 months (15.25 years) [median = 229 months (19.1 years)], with a range from 11 months to 338 months (28.2 years). Several of the NAPs were closely related to <i>P. aeruginosa</i>. <b>Discussion:</b> NAPs were isolated infrequently and were transient colonisers of the CF airways, in those patients with CF in which they were isolated. A set of ten clinical and laboratory criteria are proposed to provide key indicators, as to the clinical importance of the non-<i>aeruginosa</i> species isolated.</p>","PeriodicalId":2,"journal":{"name":"ACS Applied Bio Materials","volume":null,"pages":null},"PeriodicalIF":4.6000,"publicationDate":"2022-06-08","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9302546/pdf/","citationCount":"1","resultStr":"{\"title\":\"The Microbiology of Non-<i>aeruginosa Pseudomonas</i> Isolated From Adults With Cystic Fibrosis: Criteria to Help Determine the Clinical Significance of Non-<i>aeruginosa Pseudomonas</i> in CF Lung Pathology.\",\"authors\":\"John E Moore, John McCaughan, Jacqueline C Rendall, Beverley C Millar\",\"doi\":\"10.3389/bjbs.2022.10468\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Introduction:</b> There is a paucity of reports on non-<i>aeruginosa Pseudomonas</i> (NAPs) in cystic fibrosis, hence this study wished 1). to examine the diversity/frequency of NAPs in an adult CF population, 2) to compare/contrast the microbiology and genomics of NAPs to <i>P. aeruginosa</i> and 3) to propose clinical and laboratory criteria to help determine their clinical significance in CF lung pathology. <b>Materials and Methods:</b> Microbiological data was examined from 100 adult patients with cystic fibrosis from birth to present (31/12/2021), equating to 2455 patient years. 16S rDNA phylogenetic relatedness of NAPs was determined, as well as bioinformatical comparison of whole genomes of <i>P. aeruginosa</i> against <i>P. fluorescens</i>. <b>Results:</b> Ten species were isolated from this patient cohort during this time period, with three species, i.e., <i>P. fluorescens, P. putida</i> and <i>P. stutzeri</i>, accounting for the majority (87.5%) of non-<i>aeruginosa</i> reports. This is the first report of the isolation of <i>P. fragi, P. nitroreducens, P. oryzihabitans</i> and <i>P. veronii</i> in patients with cystic fibrosis. The mean time to first detection of any non-<i>aeruginosa</i> species was 183 months (15.25 years) [median = 229 months (19.1 years)], with a range from 11 months to 338 months (28.2 years). Several of the NAPs were closely related to <i>P. aeruginosa</i>. <b>Discussion:</b> NAPs were isolated infrequently and were transient colonisers of the CF airways, in those patients with CF in which they were isolated. A set of ten clinical and laboratory criteria are proposed to provide key indicators, as to the clinical importance of the non-<i>aeruginosa</i> species isolated.</p>\",\"PeriodicalId\":2,\"journal\":{\"name\":\"ACS Applied Bio Materials\",\"volume\":null,\"pages\":null},\"PeriodicalIF\":4.6000,\"publicationDate\":\"2022-06-08\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9302546/pdf/\",\"citationCount\":\"1\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"ACS Applied Bio Materials\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.3389/bjbs.2022.10468\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"2022/1/1 0:00:00\",\"PubModel\":\"eCollection\",\"JCR\":\"Q2\",\"JCRName\":\"MATERIALS SCIENCE, BIOMATERIALS\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"ACS Applied Bio Materials","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.3389/bjbs.2022.10468","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2022/1/1 0:00:00","PubModel":"eCollection","JCR":"Q2","JCRName":"MATERIALS SCIENCE, BIOMATERIALS","Score":null,"Total":0}
The Microbiology of Non-aeruginosa Pseudomonas Isolated From Adults With Cystic Fibrosis: Criteria to Help Determine the Clinical Significance of Non-aeruginosa Pseudomonas in CF Lung Pathology.
Introduction: There is a paucity of reports on non-aeruginosa Pseudomonas (NAPs) in cystic fibrosis, hence this study wished 1). to examine the diversity/frequency of NAPs in an adult CF population, 2) to compare/contrast the microbiology and genomics of NAPs to P. aeruginosa and 3) to propose clinical and laboratory criteria to help determine their clinical significance in CF lung pathology. Materials and Methods: Microbiological data was examined from 100 adult patients with cystic fibrosis from birth to present (31/12/2021), equating to 2455 patient years. 16S rDNA phylogenetic relatedness of NAPs was determined, as well as bioinformatical comparison of whole genomes of P. aeruginosa against P. fluorescens. Results: Ten species were isolated from this patient cohort during this time period, with three species, i.e., P. fluorescens, P. putida and P. stutzeri, accounting for the majority (87.5%) of non-aeruginosa reports. This is the first report of the isolation of P. fragi, P. nitroreducens, P. oryzihabitans and P. veronii in patients with cystic fibrosis. The mean time to first detection of any non-aeruginosa species was 183 months (15.25 years) [median = 229 months (19.1 years)], with a range from 11 months to 338 months (28.2 years). Several of the NAPs were closely related to P. aeruginosa. Discussion: NAPs were isolated infrequently and were transient colonisers of the CF airways, in those patients with CF in which they were isolated. A set of ten clinical and laboratory criteria are proposed to provide key indicators, as to the clinical importance of the non-aeruginosa species isolated.