Micaela Mossop, Luca Robinson, Jhih-Hang Jiang, Anton Y Peleg, Luke V Blakeway, Nenad Macesic, Audrey Perry, Stephen Bourke, Fatima R Ulhuq, Tracy Palmer
{"title":"临床囊性纤维化金黄色葡萄球菌分离株的关键基因型和表型特征。","authors":"Micaela Mossop, Luca Robinson, Jhih-Hang Jiang, Anton Y Peleg, Luke V Blakeway, Nenad Macesic, Audrey Perry, Stephen Bourke, Fatima R Ulhuq, Tracy Palmer","doi":"10.1099/jmm.0.001703","DOIUrl":null,"url":null,"abstract":"<p><p><b>Introduction.</b> One third of people with CF in the UK are co-infected by both <i>Staphylococcus aureus</i> and <i>Pseudomonas aeruginosa</i>. Chronic bacterial infection in CF contributes to the gradual destruction of lung tissue, and eventually respiratory failure in this group.<b>Gap Statement.</b> The contribution of <i>S. aureus</i> to cystic fibrosis (CF) lung decline in the presence or absence of <i>P. aeruginosa</i> is unclear. Defining the molecular and phenotypic characteristics of a range of <i>S. aureus</i> clinical isolates will help further understand its pathogenic capabilities.<b>Aim.</b> Our objective was to use molecular and phenotypic tools to characterise twenty-five clinical <i>S. aureus</i> isolates collected from mono- and coinfection with <i>P. aeruginosa</i> from people with CF at the Royal Victoria Infirmary, Newcastle upon Tyne.<b>Methodology.</b> Genomic DNA was extracted and sequenced. Multilocus sequence typing was used to construct phylogeny from the seven housekeeping genes. A pangenome was calculated using Roary, and cluster of Orthologous groups were assigned using eggNOG-mapper which were used to determine differences within core, accessory, and unique genomes. Characterisation of sequence type, clonal complex, <i>agr</i> and <i>spa</i> types was carried out using PubMLST, eBURST, AgrVATE and spaTyper, respectively. Antibiotic resistance was determined using Kirby-Bauer disc diffusion tests. Phenotypic testing of haemolysis was carried out using ovine red blood cell agar plates and mucoid phenotypes visualised using Congo red agar.<b>Results.</b> Clinical strains clustered closely based on <i>agr</i> type, sequence type and clonal complex. COG analysis revealed statistically significant enrichment of COG families between core, accessory and unique pangenome groups. The unique genome was significantly enriched for replication, recombination and repair, and defence mechanisms. The presence of known virulence genes and toxins were high within this group, and unique genes were identified in 11 strains. Strains which were isolated from the same patient all surpassed average nucleotide identity thresholds, however, differed in phenotypic traits. Antimicrobial resistance to macrolides was significantly higher in the coinfection group.<b>Conclusion.</b> There is huge variation in genetic and phenotypic capabilities of <i>S. aureus</i> strains. Further studies on how these may differ in relation to other species in the CF lung may give insight into inter-species interactions.</p>","PeriodicalId":16343,"journal":{"name":"Journal of medical microbiology","volume":"72 6","pages":""},"PeriodicalIF":2.4000,"publicationDate":"2023-06-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Characterisation of key genotypic and phenotypic traits of clinical cystic fibrosis <i>Staphylococcus aureus</i> isolates.\",\"authors\":\"Micaela Mossop, Luca Robinson, Jhih-Hang Jiang, Anton Y Peleg, Luke V Blakeway, Nenad Macesic, Audrey Perry, Stephen Bourke, Fatima R Ulhuq, Tracy Palmer\",\"doi\":\"10.1099/jmm.0.001703\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p><b>Introduction.</b> One third of people with CF in the UK are co-infected by both <i>Staphylococcus aureus</i> and <i>Pseudomonas aeruginosa</i>. Chronic bacterial infection in CF contributes to the gradual destruction of lung tissue, and eventually respiratory failure in this group.<b>Gap Statement.</b> The contribution of <i>S. aureus</i> to cystic fibrosis (CF) lung decline in the presence or absence of <i>P. aeruginosa</i> is unclear. Defining the molecular and phenotypic characteristics of a range of <i>S. aureus</i> clinical isolates will help further understand its pathogenic capabilities.<b>Aim.</b> Our objective was to use molecular and phenotypic tools to characterise twenty-five clinical <i>S. aureus</i> isolates collected from mono- and coinfection with <i>P. aeruginosa</i> from people with CF at the Royal Victoria Infirmary, Newcastle upon Tyne.<b>Methodology.</b> Genomic DNA was extracted and sequenced. Multilocus sequence typing was used to construct phylogeny from the seven housekeeping genes. A pangenome was calculated using Roary, and cluster of Orthologous groups were assigned using eggNOG-mapper which were used to determine differences within core, accessory, and unique genomes. Characterisation of sequence type, clonal complex, <i>agr</i> and <i>spa</i> types was carried out using PubMLST, eBURST, AgrVATE and spaTyper, respectively. Antibiotic resistance was determined using Kirby-Bauer disc diffusion tests. Phenotypic testing of haemolysis was carried out using ovine red blood cell agar plates and mucoid phenotypes visualised using Congo red agar.<b>Results.</b> Clinical strains clustered closely based on <i>agr</i> type, sequence type and clonal complex. COG analysis revealed statistically significant enrichment of COG families between core, accessory and unique pangenome groups. The unique genome was significantly enriched for replication, recombination and repair, and defence mechanisms. The presence of known virulence genes and toxins were high within this group, and unique genes were identified in 11 strains. Strains which were isolated from the same patient all surpassed average nucleotide identity thresholds, however, differed in phenotypic traits. Antimicrobial resistance to macrolides was significantly higher in the coinfection group.<b>Conclusion.</b> There is huge variation in genetic and phenotypic capabilities of <i>S. aureus</i> strains. Further studies on how these may differ in relation to other species in the CF lung may give insight into inter-species interactions.</p>\",\"PeriodicalId\":16343,\"journal\":{\"name\":\"Journal of medical microbiology\",\"volume\":\"72 6\",\"pages\":\"\"},\"PeriodicalIF\":2.4000,\"publicationDate\":\"2023-06-01\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"Journal of medical microbiology\",\"FirstCategoryId\":\"3\",\"ListUrlMain\":\"https://doi.org/10.1099/jmm.0.001703\",\"RegionNum\":4,\"RegionCategory\":\"医学\",\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"Q3\",\"JCRName\":\"MICROBIOLOGY\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"Journal of medical microbiology","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.1099/jmm.0.001703","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MICROBIOLOGY","Score":null,"Total":0}
Characterisation of key genotypic and phenotypic traits of clinical cystic fibrosis Staphylococcus aureus isolates.
Introduction. One third of people with CF in the UK are co-infected by both Staphylococcus aureus and Pseudomonas aeruginosa. Chronic bacterial infection in CF contributes to the gradual destruction of lung tissue, and eventually respiratory failure in this group.Gap Statement. The contribution of S. aureus to cystic fibrosis (CF) lung decline in the presence or absence of P. aeruginosa is unclear. Defining the molecular and phenotypic characteristics of a range of S. aureus clinical isolates will help further understand its pathogenic capabilities.Aim. Our objective was to use molecular and phenotypic tools to characterise twenty-five clinical S. aureus isolates collected from mono- and coinfection with P. aeruginosa from people with CF at the Royal Victoria Infirmary, Newcastle upon Tyne.Methodology. Genomic DNA was extracted and sequenced. Multilocus sequence typing was used to construct phylogeny from the seven housekeeping genes. A pangenome was calculated using Roary, and cluster of Orthologous groups were assigned using eggNOG-mapper which were used to determine differences within core, accessory, and unique genomes. Characterisation of sequence type, clonal complex, agr and spa types was carried out using PubMLST, eBURST, AgrVATE and spaTyper, respectively. Antibiotic resistance was determined using Kirby-Bauer disc diffusion tests. Phenotypic testing of haemolysis was carried out using ovine red blood cell agar plates and mucoid phenotypes visualised using Congo red agar.Results. Clinical strains clustered closely based on agr type, sequence type and clonal complex. COG analysis revealed statistically significant enrichment of COG families between core, accessory and unique pangenome groups. The unique genome was significantly enriched for replication, recombination and repair, and defence mechanisms. The presence of known virulence genes and toxins were high within this group, and unique genes were identified in 11 strains. Strains which were isolated from the same patient all surpassed average nucleotide identity thresholds, however, differed in phenotypic traits. Antimicrobial resistance to macrolides was significantly higher in the coinfection group.Conclusion. There is huge variation in genetic and phenotypic capabilities of S. aureus strains. Further studies on how these may differ in relation to other species in the CF lung may give insight into inter-species interactions.
期刊介绍:
Journal of Medical Microbiology provides comprehensive coverage of medical, dental and veterinary microbiology, and infectious diseases. We welcome everything from laboratory research to clinical trials, including bacteriology, virology, mycology and parasitology. We publish articles under the following subject categories: Antimicrobial resistance; Clinical microbiology; Disease, diagnosis and diagnostics; Medical mycology; Molecular and microbial epidemiology; Microbiome and microbial ecology in health; One Health; Pathogenesis, virulence and host response; Prevention, therapy and therapeutics