Fungal pathogens significantly impact human health, agriculture, and ecosystems, with infections leading to high morbidity and mortality, especially among immunocompromised individuals. The increasing prevalence of antifungal resistance (AFR) exacerbates these challenges, limiting the effectiveness of current treatments. Identifying robust biomarkers associated AFR could accelerate targeted diagnosis, shorten decision time for treatment strategies, and improve patient health. This paper examines traditional avenues of AFR biomarker detection, contrasting them with the increasingly effective role of machine learning (ML) in advancing diagnostic and therapeutic strategies. The integration of ML with technologies such as mass spectrometry, molecular dynamics, and various omics-based approaches often results in the discovery of diverse and novel resistance biomarkers. ML's capability to analyse complex data patterns enhances the identification of resistance biomarkers and potential drug targets, offering innovative solutions to AFR management. This paper highlights the importance of interdisciplinary approaches and continued innovation in leveraging ML to combat AFR, aiming for more effective and targeted treatments for fungal infections.
{"title":"From patterns to prediction: machine learning and antifungal resistance biomarker discovery.","authors":"Veronica Thorn, Jianping Xu","doi":"10.1139/cjm-2024-0248","DOIUrl":"https://doi.org/10.1139/cjm-2024-0248","url":null,"abstract":"<p><p>Fungal pathogens significantly impact human health, agriculture, and ecosystems, with infections leading to high morbidity and mortality, especially among immunocompromised individuals. The increasing prevalence of antifungal resistance (AFR) exacerbates these challenges, limiting the effectiveness of current treatments. Identifying robust biomarkers associated AFR could accelerate targeted diagnosis, shorten decision time for treatment strategies, and improve patient health. This paper examines traditional avenues of AFR biomarker detection, contrasting them with the increasingly effective role of machine learning (ML) in advancing diagnostic and therapeutic strategies. The integration of ML with technologies such as mass spectrometry, molecular dynamics, and various omics-based approaches often results in the discovery of diverse and novel resistance biomarkers. ML's capability to analyse complex data patterns enhances the identification of resistance biomarkers and potential drug targets, offering innovative solutions to AFR management. This paper highlights the importance of interdisciplinary approaches and continued innovation in leveraging ML to combat AFR, aiming for more effective and targeted treatments for fungal infections.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":"71 ","pages":"1-13"},"PeriodicalIF":1.8,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143954560","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Botrytis cinerea is a necrotrophic fungal pathogen responsible for grey mold disease, causing significant crop losses globally. Effective genetic manipulation of this pathogen is crucial for understanding its biology and developing better disease management strategies. However, current transformation methods typically use conidia spores or protoplasts, processes that are labor-intensive, inefficient, and often yield inconsistent results. We developed a novel Agrobacterium-mediated transformation protocol that utilizes B. cinerea mycelia, eliminating the need for sporulation or protoplast generation and simplifying genetic manipulation. Using a newly constructed binary expression vector encoding green fluorescent protein and hygromycin resistance, we transformed four different B. cinerea strains. All transformations resulted in stable integration and robust green fluorescent protein expression, confirmed by quantitative polymerase chain reaction and confocal microscopy. Although transformants exhibited altered colony morphology compared to wild-type strains, they remained viable and stably expressed the integrated transgene, supporting the method's utility for genetic studies in B. cinerea. This streamlined method provides a reliable, efficient, and scalable approach for genetic studies in B. cinerea, significantly enhancing fungal functional genomics research and plant pathology investigations.
{"title":"Simplified and efficient <i>Agrobacterium</i>-mediated genetic transformation of <i>Botrytis cinerea</i> using mycelia.","authors":"Fayruza Lalany, Peter Moffett","doi":"10.1139/cjm-2025-0085","DOIUrl":"10.1139/cjm-2025-0085","url":null,"abstract":"<p><p><i>Botrytis cinerea</i> is a necrotrophic fungal pathogen responsible for grey mold disease, causing significant crop losses globally. Effective genetic manipulation of this pathogen is crucial for understanding its biology and developing better disease management strategies. However, current transformation methods typically use conidia spores or protoplasts, processes that are labor-intensive, inefficient, and often yield inconsistent results. We developed a novel <i>Agrobacterium</i>-mediated transformation protocol that utilizes <i>B. cinerea</i> mycelia, eliminating the need for sporulation or protoplast generation and simplifying genetic manipulation. Using a newly constructed binary expression vector encoding green fluorescent protein and hygromycin resistance, we transformed four different <i>B. cinerea</i> strains. All transformations resulted in stable integration and robust green fluorescent protein expression, confirmed by quantitative polymerase chain reaction and confocal microscopy. Although transformants exhibited altered colony morphology compared to wild-type strains, they remained viable and stably expressed the integrated transgene, supporting the method's utility for genetic studies in <i>B. cinerea</i>. This streamlined method provides a reliable, efficient, and scalable approach for genetic studies in <i>B. cinerea</i>, significantly enhancing fungal functional genomics research and plant pathology investigations.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":" ","pages":"1-9"},"PeriodicalIF":1.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145124358","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Waleska Stephanie da Cruz Nizer, Madison Elisabeth Adams, Kira Noelle Allison, Carole Beaulieu, Joerg Overhage
The opportunistic human pathogen Pseudomonas aeruginosa exhibits high pathogenicity and antimicrobial resistance, largely due to its ability to form robust biofilms. In addition to the exopolysaccharides Psl and Pel, extracellular DNA (eDNA) is an important matrix component in P. aeruginosa PAO1 biofilms. It has been shown previously that eDNA is involved in biofilm initiation and integrity as well as antibiotic resistance; however, its involvement in resistance to oxidative stressors such as the widely used disinfectant sodium hypochlorite (NaOCl) is less explored. Here, we examined the function of eDNA in NaOCl resistance of P. aeruginosa PAO1 biofilms. Using different biofilm assays in combination with a PAO1 ∆pslA pelF double mutant, which lacks the exopolysaccharides Psl and Pel, and a Tn-bfmR mutant, which exhibits increased eDNA amounts in biofilms, we were able to show that eDNA contributes to NaOCl resistance in P. aeruginosa PAO1 biofilms, in particular when exopolysaccharides are absent. Interestingly, NaOCl was more effective after DNase treatment against ∆pslA pelF biofilms. These findings indicate that the protective function of eDNA in biofilm resistance is matrix composition-dependent and becomes more pronounced in the absence of Psl and Pel.
{"title":"Extracellular DNA enhances <i>Pseudomonas aeruginosa</i> biofilm resistance to sodium hypochlorite stress.","authors":"Waleska Stephanie da Cruz Nizer, Madison Elisabeth Adams, Kira Noelle Allison, Carole Beaulieu, Joerg Overhage","doi":"10.1139/cjm-2025-0051","DOIUrl":"10.1139/cjm-2025-0051","url":null,"abstract":"<p><p>The opportunistic human pathogen <i>Pseudomonas aeruginosa</i> exhibits high pathogenicity and antimicrobial resistance, largely due to its ability to form robust biofilms. In addition to the exopolysaccharides Psl and Pel, extracellular DNA (eDNA) is an important matrix component in <i>P. aeruginosa</i> PAO1 biofilms. It has been shown previously that eDNA is involved in biofilm initiation and integrity as well as antibiotic resistance; however, its involvement in resistance to oxidative stressors such as the widely used disinfectant sodium hypochlorite (NaOCl) is less explored. Here, we examined the function of eDNA in NaOCl resistance of <i>P. aeruginosa</i> PAO1 biofilms. Using different biofilm assays in combination with a PAO1 ∆<i>pslA pelF</i> double mutant, which lacks the exopolysaccharides Psl and Pel, and a Tn-<i>bfmR</i> mutant, which exhibits increased eDNA amounts in biofilms, we were able to show that eDNA contributes to NaOCl resistance in <i>P. aeruginosa</i> PAO1 biofilms, in particular when exopolysaccharides are absent. Interestingly, NaOCl was more effective after DNase treatment against ∆<i>pslA pelF</i> biofilms<i>.</i> These findings indicate that the protective function of eDNA in biofilm resistance is matrix composition-dependent and becomes more pronounced in the absence of Psl and Pel.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":" ","pages":"1-10"},"PeriodicalIF":1.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144583079","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Marie Ottenbrite, Gokhan Yilmaz, Maria Chan, John Devenish, Mingsong Kang, Hanhong Dan, Calvin Ho-Fung Lau, Sabrina Capitani, Catherine Carrillo, Kyrylo Bessonov, John H E Nash, Edward Topp, Jiewen Guan
Ingestion of antibiotic-resistant bacteria following antibiotic treatments may lead to the transfer of antimicrobial resistance genes (ARGs) within a disturbed gut microbiota. However, it remains unclear whether and how microbes present in food matrices influence ARG transfer. Thus, a previously established mouse model, which demonstrated the conjugative transfer of a multi-drug resistance plasmid (pIncA/C) from Salmonella Heidelberg (donor) to Salmonella Typhimurium (recipient), was used to assess the effects of food-borne microbes derived from fresh carrots on pIncA/C transfer. Mice were pre-treated with ampicillin, streptomycin, sulfamethazine, or left untreated as a control to facilitate bacterial colonization. Contrary to previous findings where high-density colonization of the donor and recipient bacteria occurred in the absence of food-borne microbes, the presence of these microbes resulted in a low abundance of S. Typhimurium and no detection of S. Typhimurium transconjugants in the fecal samples from any of the mice. However, in mice pre-treated with streptomycin, a significant reduction in microbial species richness allowed for the significant enrichment of Enterobacteriaceae and pIncA/C transfer to bacteria from the genera Escherichia, Enterobacter, Citrobacter, and Proteus. These findings suggest that food-borne microbes may enhance ARG dissemination by influencing the population dynamics of bacterial hosts within a pre-disturbed gut microbiome.
{"title":"Food-borne microbes influence conjugative transfer of antimicrobial resistance plasmids in pre-disturbed gut microbiome.","authors":"Marie Ottenbrite, Gokhan Yilmaz, Maria Chan, John Devenish, Mingsong Kang, Hanhong Dan, Calvin Ho-Fung Lau, Sabrina Capitani, Catherine Carrillo, Kyrylo Bessonov, John H E Nash, Edward Topp, Jiewen Guan","doi":"10.1139/cjm-2024-0168","DOIUrl":"10.1139/cjm-2024-0168","url":null,"abstract":"<p><p>Ingestion of antibiotic-resistant bacteria following antibiotic treatments may lead to the transfer of antimicrobial resistance genes (ARGs) within a disturbed gut microbiota. However, it remains unclear whether and how microbes present in food matrices influence ARG transfer. Thus, a previously established mouse model, which demonstrated the conjugative transfer of a multi-drug resistance plasmid (pIncA/C) from <i>Salmonella</i> Heidelberg (donor) to <i>Salmonella</i> Typhimurium (recipient), was used to assess the effects of food-borne microbes derived from fresh carrots on pIncA/C transfer. Mice were pre-treated with ampicillin, streptomycin, sulfamethazine, or left untreated as a control to facilitate bacterial colonization. Contrary to previous findings where high-density colonization of the donor and recipient bacteria occurred in the absence of food-borne microbes, the presence of these microbes resulted in a low abundance of <i>S</i>. Typhimurium and no detection of <i>S</i>. Typhimurium transconjugants in the fecal samples from any of the mice. However, in mice pre-treated with streptomycin, a significant reduction in microbial species richness allowed for the significant enrichment of <i>Enterobacteriaceae</i> and pIncA/C transfer to bacteria from the genera <i>Escherichia, Enterobacter, Citrobacter</i>, and <i>Proteus</i>. These findings suggest that food-borne microbes may enhance ARG dissemination by influencing the population dynamics of bacterial hosts within a pre-disturbed gut microbiome.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":" ","pages":"1-11"},"PeriodicalIF":1.8,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143974154","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Nguyen Thi Thuy Tien, Le Thi Ha Thanh, Tran Thi My Linh, Nguyen Quang Duc Tien, Nguyen Hoang Loc
Mango (Mangifera indica L.) is famous for its flavor, aroma, and nutritional value. However, anthracnose caused by Colletotrichum is the most destructive postharvest disease of mango, causing significant economic losses. This study aimed to identify and characterize Colletotrichum species associated with mango anthracnose in Vietnam and evaluate their pathogenicity and cross-infection potential. Through examination of colony characteristics, conidia, and appressorial morphology, along with phylogenetic analysis based on the ITS region and five genetic markers (gapdh, act, tub2, chs-1, and cal), five isolates were classified into three distinct species: C. asianum (MH32, MH24, and MC76), C. fructicola (MC32), and C. laticiphilum (MC81). Notably, C. fructicola and C. laticiphilum are the two species identified for the first time on mangoes in Vietnam. Pathogenicity tests demonstrated that C. fructicola MC32 and C. laticiphilum MC81 caused anthracnose in mango, banana, guava, and tomato. Among the C. asianum isolates, differences in aggressiveness were observed: isolate MH32 caused anthracnose on mango, banana, guava, and tomato; isolate MC76 caused anthracnose on mango, banana, and tomato; and isolate MH24 affected only mango and tomato.
{"title":"Identification, characterization and pathogenicity of <i>Colletotrichum asianum</i>, <i>C</i>. <i>fructicola</i>, and <i>C</i>. <i>laticiphilum</i> causing mango anthracnose in Vietnam.","authors":"Nguyen Thi Thuy Tien, Le Thi Ha Thanh, Tran Thi My Linh, Nguyen Quang Duc Tien, Nguyen Hoang Loc","doi":"10.1139/cjm-2025-0069","DOIUrl":"10.1139/cjm-2025-0069","url":null,"abstract":"<p><p>Mango (<i>Mangifera indica</i> L.) is famous for its flavor, aroma, and nutritional value. However, anthracnose caused by <i>Colletotrichum</i> is the most destructive postharvest disease of mango, causing significant economic losses. This study aimed to identify and characterize <i>Colletotrichum</i> species associated with mango anthracnose in Vietnam and evaluate their pathogenicity and cross-infection potential. Through examination of colony characteristics, conidia, and appressorial morphology, along with phylogenetic analysis based on the ITS region and five genetic markers (<i>gapdh</i>, <i>act</i>, <i>tub2</i>, <i>chs-1</i>, and <i>cal</i>), five isolates were classified into three distinct species: <i>C</i>. <i>asianum</i> (MH32, MH24, and MC76), <i>C</i>. <i>fructicola</i> (MC32), and <i>C</i>. <i>laticiphilum</i> (MC81). Notably, <i>C</i>. <i>fructicola</i> and <i>C</i>. <i>laticiphilum</i> are the two species identified for the first time on mangoes in Vietnam. Pathogenicity tests demonstrated that <i>C</i>. <i>fructicola</i> MC32 and <i>C</i>. <i>laticiphilum</i> MC81 caused anthracnose in mango, banana, guava, and tomato. Among the <i>C</i>. <i>asianum</i> isolates, differences in aggressiveness were observed: isolate MH32 caused anthracnose on mango, banana, guava, and tomato; isolate MC76 caused anthracnose on mango, banana, and tomato; and isolate MH24 affected only mango and tomato.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":" ","pages":"1-19"},"PeriodicalIF":1.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144741274","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Emma J Griffiths, Emil Jurga, Gabriel Wajnberg, Julie A Shay, Rhiannon Cameron, Charlie Barclay, Anoosha Sehar, Damion Dooley, Nithu Sara John, Andrew Scott, Lisa A Johnson, James Robertson, Justin Schonfeld, D Patrick Bastedo, Joshua Tang, Xianhua Yin, Attiq Rehman, Rhiannon L Wallace, Krysty Thomas, Shannon H C Eagle, Tim McAllister, Moussa S Diarra, John H E Nash, Ed Topp, Gary Van Domselaar, Eduardo Taboada, Sandeep Tamber, Tony Kess, Jordyn Broadbent, Dominic Poulin-Laprade, Derek D N Smith, Richard Reid-Smith, Rahat Zaheer, Chad R Laing, Catherine D Carrillo, William W L Hsiao
The Canadian Genomics Research and Development Initiative for Antimicrobial Resistance (GRDI-AMR) uses a genomics-based approach to understand how health care, food production and the environment contribute to the development of antimicrobial resistance. Integrating genomics contextual data streams across the One Health continuum is challenging because of the diversity in data scope, content and structure. To better enable data harmonization for analyses, a contextual data standard was developed. However, development of standards does not guarantee their use. Implementation strategies are critical for putting standards into practice. This work focuses on the development of implementation strategies to better operationalize data standards across the Canadian federal genomics ecosystem. Results include improved understanding of complex data models that can create challenges for existing systems. Technical implementation strategies included spreadsheet-based solutions, new exchange formats, and direct standards integration into new databases. Data curation exercises highlighted common data collection and sharing issues, which informed improved practices and evaluation procedures. These new practices are contributing to improved data quality and sharing within the GRDI-AMR consortium as evidenced by publicly available datasets. The implementation strategies and lessons learned described in this work are generalizable for other standards and can be applied more broadly within other initiatives.
{"title":"Crossing the streams: improving data quality and integration across the One Health genomics continuum with data standards and implementation strategies.","authors":"Emma J Griffiths, Emil Jurga, Gabriel Wajnberg, Julie A Shay, Rhiannon Cameron, Charlie Barclay, Anoosha Sehar, Damion Dooley, Nithu Sara John, Andrew Scott, Lisa A Johnson, James Robertson, Justin Schonfeld, D Patrick Bastedo, Joshua Tang, Xianhua Yin, Attiq Rehman, Rhiannon L Wallace, Krysty Thomas, Shannon H C Eagle, Tim McAllister, Moussa S Diarra, John H E Nash, Ed Topp, Gary Van Domselaar, Eduardo Taboada, Sandeep Tamber, Tony Kess, Jordyn Broadbent, Dominic Poulin-Laprade, Derek D N Smith, Richard Reid-Smith, Rahat Zaheer, Chad R Laing, Catherine D Carrillo, William W L Hsiao","doi":"10.1139/cjm-2024-0203","DOIUrl":"10.1139/cjm-2024-0203","url":null,"abstract":"<p><p>The Canadian Genomics Research and Development Initiative for Antimicrobial Resistance (GRDI-AMR) uses a genomics-based approach to understand how health care, food production and the environment contribute to the development of antimicrobial resistance. Integrating genomics contextual data streams across the One Health continuum is challenging because of the diversity in data scope, content and structure. To better enable data harmonization for analyses, a contextual data standard was developed. However, development of standards does not guarantee their use. Implementation strategies are critical for putting standards into practice. This work focuses on the development of implementation strategies to better operationalize data standards across the Canadian federal genomics ecosystem. Results include improved understanding of complex data models that can create challenges for existing systems. Technical implementation strategies included spreadsheet-based solutions, new exchange formats, and direct standards integration into new databases. Data curation exercises highlighted common data collection and sharing issues, which informed improved practices and evaluation procedures. These new practices are contributing to improved data quality and sharing within the GRDI-AMR consortium as evidenced by publicly available datasets. The implementation strategies and lessons learned described in this work are generalizable for other standards and can be applied more broadly within other initiatives.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":" ","pages":"1-14"},"PeriodicalIF":1.8,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143000699","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Alexandra Langlois, Antony T Vincent, Renée M Petri, Karoline Lauzon, Dominic Poulin-Laprade
Agricultural practices, specifically the use of antibiotics and other biocides, have repercussions on human, animal, and plant health. The aim of this study was to evaluate the levels of Enterobacteriaceae and Enterococcus, as antibiotic-resistant marker bacteria, in various matrices across the agro-ecosystem of an antibiotic-free swine farm in Quebec (Canada), namely pig feed, feces, manure, agricultural soil, water and sediment from a crossing stream, and soil from nearby forests. Samples were collected in fall 2022, spring and fall 2023, and spring 2024. All samples were subjected to counts of total, cefotaxime-, and ciprofloxacin-resistant Enterobacteriaceae as well as total and vancomycin-resistant Enterococcus spp. The frequency of total and cefotaxime-resistant Enterobacteriaceae along with the vancomycin-resistant Enterococcus decreased with age in pig feces, from weaning to the end of the fattening period. High proportions of the Enterobacteriaceae recovered from feces and environmental samples were resistant to cefotaxime. Application of manure on fields contributed a significant input of Enterococcus, but those resistant to vancomycin were under the detection limit. This study shows the prevalence of antibiotic-resistant bacteria in a farm agro-ecosystem even without the administration of antibiotics to the animals and highlights the complexity of components influencing antimicrobial resistance in the environment.
{"title":"Assessment of viable <i>Enterobacteriaceae</i> and <i>Enterococcus</i> spp. across the agro-ecosystem of an antibiotic-free swine farm.","authors":"Alexandra Langlois, Antony T Vincent, Renée M Petri, Karoline Lauzon, Dominic Poulin-Laprade","doi":"10.1139/cjm-2024-0173","DOIUrl":"10.1139/cjm-2024-0173","url":null,"abstract":"<p><p>Agricultural practices, specifically the use of antibiotics and other biocides, have repercussions on human, animal, and plant health. The aim of this study was to evaluate the levels of <i>Enterobacteriaceae</i> and <i>Enterococcus</i>, as antibiotic-resistant marker bacteria, in various matrices across the agro-ecosystem of an antibiotic-free swine farm in Quebec (Canada), namely pig feed, feces, manure, agricultural soil, water and sediment from a crossing stream, and soil from nearby forests. Samples were collected in fall 2022, spring and fall 2023, and spring 2024. All samples were subjected to counts of total, cefotaxime-, and ciprofloxacin-resistant <i>Enterobacteriaceae</i> as well as total and vancomycin-resistant <i>Enterococcus</i> spp. The frequency of total and cefotaxime-resistant <i>Enterobacteriaceae</i> along with the vancomycin-resistant <i>Enterococcus</i> decreased with age in pig feces, from weaning to the end of the fattening period. High proportions of the <i>Enterobacteriaceae</i> recovered from feces and environmental samples were resistant to cefotaxime. Application of manure on fields contributed a significant input of <i>Enterococcus</i>, but those resistant to vancomycin were under the detection limit. This study shows the prevalence of antibiotic-resistant bacteria in a farm agro-ecosystem even without the administration of antibiotics to the animals and highlights the complexity of components influencing antimicrobial resistance in the environment.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":" ","pages":"1-14"},"PeriodicalIF":1.8,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143064035","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Jéssica Cristina Polveiro Campos, Diego Batista Carneiro de Oliveira, Bruna da Silva Souza, Lucas Felipe de Oliveira, Ezequias Pessoa de Siqueira, Markus Kohlhoff, Anderson Assunção Andrade
Superficial fungal infections, mainly caused by dermatophytes, are a global public health issue. We evaluated the antifungal activity of six β-amino-ketones against Trichophyton rubrum, a leading agent of superficial mycoses. Among them, 3-(morpholin-4-yl)-1-phenylpropan-1-one (AB1) showed the most potent effect, with a minimum inhibitory concentration (MIC) of 7.81 µg/mL against the T. rubrum reference strain and fungicidal activity against clinical isolates, as demonstrated by minimum fungicidal concentration assays. AB1 was effective against both conidia and hyphae of T. rubrum, while showing limited activity against Candida albicans and the bacteria Escherichia coli and Staphylococcus aureus. Mechanistic studies suggest AB1 targets the fungal plasma membrane, possibly via ergosterol interactions, supported by increased MICs in ergosterol-rich conditions and membrane integrity assays. Confocal microscopy revealed morphological alterations in AB1-treated hyphae, indicative of membrane damage. Transmission electron microscopy confirmed cytoplasmic disorganization and membrane disruption at subinhibitory concentrations. Toxicological assays showed moderate cytotoxicity in human fibroblasts (IC50 = 37.75 µg/mL) and no toxicity in Galleria mellonella larvae at high doses. These findings highlight AB1 as a promising antifungal candidate against Trichophyton spp., with the potential benefit of reduced impact on the host microbiota compared to broad-spectrum antimicrobials.
{"title":"A β-amino-ketone that disrupts the fungal plasma membrane exhibits potent activity against pathogenic <i>Trichophyton</i> species.","authors":"Jéssica Cristina Polveiro Campos, Diego Batista Carneiro de Oliveira, Bruna da Silva Souza, Lucas Felipe de Oliveira, Ezequias Pessoa de Siqueira, Markus Kohlhoff, Anderson Assunção Andrade","doi":"10.1139/cjm-2025-0009","DOIUrl":"10.1139/cjm-2025-0009","url":null,"abstract":"<p><p>Superficial fungal infections, mainly caused by dermatophytes, are a global public health issue. We evaluated the antifungal activity of six β-amino-ketones against <i>Trichophyton rubrum</i>, a leading agent of superficial mycoses. Among them, 3-(morpholin-4-yl)-1-phenylpropan-1-one (<b>AB1</b>) showed the most potent effect, with a minimum inhibitory concentration (MIC) of 7.81 µg/mL against the <i>T. rubrum</i> reference strain and fungicidal activity against clinical isolates, as demonstrated by minimum fungicidal concentration assays. <b>AB1</b> was effective against both conidia and hyphae of <i>T. rubrum</i>, while showing limited activity against <i>Candida albicans</i> and the bacteria <i>Escherichia coli</i> and <i>Staphylococcus aureus</i>. Mechanistic studies suggest <b>AB1</b> targets the fungal plasma membrane, possibly via ergosterol interactions, supported by increased MICs in ergosterol-rich conditions and membrane integrity assays. Confocal microscopy revealed morphological alterations in <b>AB1</b>-treated hyphae, indicative of membrane damage. Transmission electron microscopy confirmed cytoplasmic disorganization and membrane disruption at subinhibitory concentrations. Toxicological assays showed moderate cytotoxicity in human fibroblasts (IC<sub>50</sub> = 37.75 µg/mL) and no toxicity in <i>Galleria mellonella</i> larvae at high doses. These findings highlight <b>AB1</b> as a promising antifungal candidate against <i>Trichophyton</i> spp., with the potential benefit of reduced impact on the host microbiota compared to broad-spectrum antimicrobials.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":" ","pages":"1-11"},"PeriodicalIF":1.8,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144157006","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Dominic Poulin-Laprade, Jordyn Broadbent, Damien Biot-Pelletier, Susanne Kraemer, Emma J Griffiths, Ayush Kumar, Xian-Zhi Li, Catherine D Carrillo, Rahat Zaheer, Tim A McAllister, Sigrun Kullik, Ernesto Liebana, Nicole Ricker, Alexandra Langlois, Richard J Reid-Smith, Sébastien P Faucher, Gabriela Flores-Vargas, Emilie Bédard, J Kimberley Summers, Veronica Jarocki, Thanaporn Thongthum, Carolee A Carson
The One Health (OH) approach recognizes the interconnectedness of the health of people, animals, plants/crops and ecosystems, and is central to addressing antimicrobial resistance (AMR). The 7th Environmental Dimension of Antimicrobial Resistance Conference (EDAR7), held in Montreal in May 2024, exemplified this approach by convening international experts and stakeholders to discuss AMR research and policy progress. EDAR7 workshop #8 focused on (1) barriers to establishing effective OH AMR research programs, (2) gaps in OH AMR research priorities, and (3) potential solutions/approaches or "tools" to ensure programs develop in accordance with OH principles and generate insightful data that maximizes limited resources. Key workshop outcomes included identifying critical principles for OH AMR research programs and highlighting the pivotal role of sustainable data management strategies. Additionally, the importance of considering AMR policy and risk assessment needs when planning and designing research was emphasized. Discussions explored specific tools and approaches that support the standardized and harmonized collection and analysis of data, and associated challenges of integrating genomics data into current risk assessments and models. Synthesis of the workshop's discussions outlined critical considerations that interdisciplinary OH AMR research programs and networks should prioritize to enhance the impact of their outputs.
{"title":"Requirements and considerations for effective implementation of integrated One Health antimicrobial resistance research.","authors":"Dominic Poulin-Laprade, Jordyn Broadbent, Damien Biot-Pelletier, Susanne Kraemer, Emma J Griffiths, Ayush Kumar, Xian-Zhi Li, Catherine D Carrillo, Rahat Zaheer, Tim A McAllister, Sigrun Kullik, Ernesto Liebana, Nicole Ricker, Alexandra Langlois, Richard J Reid-Smith, Sébastien P Faucher, Gabriela Flores-Vargas, Emilie Bédard, J Kimberley Summers, Veronica Jarocki, Thanaporn Thongthum, Carolee A Carson","doi":"10.1139/cjm-2024-0194","DOIUrl":"10.1139/cjm-2024-0194","url":null,"abstract":"<p><p>The One Health (OH) approach recognizes the interconnectedness of the health of people, animals, plants/crops and ecosystems, and is central to addressing antimicrobial resistance (AMR). The 7th Environmental Dimension of Antimicrobial Resistance Conference (EDAR7), held in Montreal in May 2024, exemplified this approach by convening international experts and stakeholders to discuss AMR research and policy progress. EDAR7 workshop #8 focused on (1) barriers to establishing effective OH AMR research programs, (2) gaps in OH AMR research priorities, and (3) potential solutions/approaches or \"tools\" to ensure programs develop in accordance with OH principles and generate insightful data that maximizes limited resources. Key workshop outcomes included identifying critical principles for OH AMR research programs and highlighting the pivotal role of sustainable data management strategies. Additionally, the importance of considering AMR policy and risk assessment needs when planning and designing research was emphasized. Discussions explored specific tools and approaches that support the standardized and harmonized collection and analysis of data, and associated challenges of integrating genomics data into current risk assessments and models. Synthesis of the workshop's discussions outlined critical considerations that interdisciplinary OH AMR research programs and networks should prioritize to enhance the impact of their outputs.</p>","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":" ","pages":"1-17"},"PeriodicalIF":1.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144483235","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
{"title":"11th International Symposium on Avian Influenza.","authors":"Andrew S Lang, Michelle Wille","doi":"10.1139/cjm-2025-0196","DOIUrl":"https://doi.org/10.1139/cjm-2025-0196","url":null,"abstract":"","PeriodicalId":9381,"journal":{"name":"Canadian journal of microbiology","volume":"71 ","pages":"1-3"},"PeriodicalIF":1.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145198388","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"生物学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}