Canadian journal of microbiology最新文献

Pyrimidine base and ribonucleoside salvage metabolism was investigated in Pseudomonas putida ATCC 17536 cells. In ATCC 17536 cell extracts, the pyrimidine ribonucleoside salvage enzymes nucleoside hydrolase and cytosine deaminase activities were measurable, while uridine phosphorylase activity was not. Carbon and nitrogen sources influenced the levels of the salvage pathway enzyme activities in P. putida ATCC 17536. Catabolite repression by a glucose metabolite of nucleoside hydrolase and cytosine deaminase synthesis in ATCC 17536 cells compared to cells grown on the carbon source succinate or ribose was observed, while a nitrogen metabolite appeared to be controlling pyrimidine salvage enzyme synthesis. When glucose was the carbon source, ATCC 17536 cells grown on uracil or 5-methylcytosine as a nitrogen source caused at least a five-fold increase in hydrolase and deaminase synthesis relative to their activities in ammonium sulfate-grown cells. In succinate-grown ATCC 17536 cells, thymine or 5-methylcytosine as a nitrogen catabolite produced at least double the hydrolase or deaminase activity relative to either activity in ammonium sulfate-grown cells. Overall, the pyrimidine base and ribonucleoside salvage enzymes in P. putida ATCC 17536 biovar B cells were regulated by the carbon or nitrogen source with pyrimidine salvage metabolism differing in biovar A and B strains.

Highly pathogenic avian influenza (HPAI) H5N1 has caused the deaths of more than 100 million birds since 2021, and human cases since 1997 have been associated with significant morbidity and mortality. Given recent detections of HPAI H5N1 in dairy cattle and H5N1 RNA detections in pasteurized retail milk in the United States, we established the pan-Canadian Milk Network in April 2024. Through our network of collaborators from across Canada, retail milk was procured longitudinally, approximately every 2 weeks, and sent to a central laboratory to test for the presence of influenza A virus RNA. Between 29 April and 17 July 2024, we tested 109 retail milk samples from all 10 Canadian provinces (NL, NS, PEI, NB, QC, ON, MB, SK, AB, and BC). All samples tested negative for influenza A virus RNA. This nationwide initiative was established for rapid retail milk screening as per the earliest reports of similar undertakings in the United States. Our independent testing results have aligned with reporting from federal retail milk testing initiatives. Despite no known HPAI infections of dairy cattle in Canada to date, H5N1 poses a significant threat to the health of both humans and other animals. By performing routine surveillance of retail milk on a national scale, we have shown that academic networks and initiatives can rapidly establish nationwide emerging infectious disease surveillance that is cost-effective, standardized, scalable, and easily accessible. Our network can serve as an early detection system to help inform containment and mitigation activities if positive samples are identified and can be readily reactivated should HPAI H5N1 or other emerging zoonotic viruses be identified in agricultural or livestock settings, including Canadian dairy cattle.

Whole-genome sequence-based surveillance of bacteria for determinants of antimicrobial resistance (AMR) promises many advantages over traditional, wet-lab approaches. However, adjustments to parameters used to identify genetic determinants from sequencing data can affect results and interpretation of the important determinants in circulation. Using a dataset of whole-genome sequences from 1633 isolates of Salmonella Heidelberg and S. Kentucky collected from surveillance of Canadian poultry production, we queried the genomic data using an in silico AMR detection tool, StarAMR, applying a range of parameter values required for the detection pipeline to test for differences in detection accuracy. We compared the results from each iteration to phenotypic antimicrobial susceptibility results, and generated estimates of sensitivity and specificity using regression models that controlled for the effects of multiple sampling events and variables, and interactions between covariates. Results from our analyses revealed small, yet significant effects of the input parameters on the sensitivity and specificity of the AMR detection tool, and these effects differed based on the serovar and drug class in question. Findings from this study may have implications for the incorporation of whole-genome sequence-based approaches to the surveillance of AMR determinants in bacteria sampled from food products and animals related to food production.

Rhizobia are soil-dwelling proteobacteria that can enter into symbiotic nitrogen-fixing relationships with compatible leguminous plants. Taxonomically, rhizobia are divided into alpha-rhizobia, which belong to the class Alpharoteobacteria, and beta-rhizobia, which belong to the class Betaproteobacteria. To date, all bona fide alpha-rhizobia belong to the order Hyphomicrobiales. However, a recent study suggested that Sphingomonas sediminicola DSM 18106^T is also a rhizobium and is capable of nodulating pea plants (Pisum sativum), which would expand the known taxonomic distribution of alpha-rhizobia to include the order Sphingomonadales. Here, we attempted to replicate the results of that previous study. Resequencing and computational analysis of the genome of S. sediminicola DSM 18106^T failed to identify genes encoding proteins involved in legume nodulation or nitrogen fixation. In addition, experimental plant assays indicated that S. sediminicola DSM 18106^T is unable to nodulate the two cultivars of pea tested in our study, unlike the rhizobium Rhizobium johnstonii 3841^T. Taken together, and in contrast to the previous study, these results suggest that S. sediminicola DSM 18106^T is not capable of inducing root nodule formation on pea, meaning that the taxonomic distribution of all known alpha-rhizobia remains limited to the class Hyphomicrobiales.

On solid substrates, biofilms develop rich wrinkle morphologies during its growth. Based on the thin film buckling theory, we established a local three-dimensional biofilm/substrate buckling model, and explored the effects of mechanical forces, elastic modulus of the substrate, and biofilm thickness on the wrinkle morphology. We simulated the wrinkle evolution in various patterns of Bacillus subtilis biofilm growing on agar substrates with different stiffness and found that the biofilm wrinkling process is the process of internal energy release. The stiffness of the substrate changes the wrinkling time of the biofilm; The biofilm wrinkle morphology (patterns II, III, and IV) U_internal and U_internal/U₀ decrease with nutrient consumption, and the biofilm evolves towards lower energy consumption. In the early stages of biofilm growth (patterns I, II, and III), the harder the agar substrate, the larger the U_friction and U_friction/U₀, which is less conducive to biofilm expansion.

The use of Trichoderma in agriculture as both a biocontrol agent and biofertilizer hinges on its ability to colonize the rhizosphere, promote plant growth, endure adverse environments, compete for space and nutrients, and produce enzymes and secondary metabolites to mycoparasitize and infect other fungus. In humans, Trichoderma exhibits the capacity to infect various bodily tissues, leading to Trichodermosis. There has been a notable increase in cases ranging from superficial to fatal, invasive, and disseminated infections, particularly among immunocompromised individuals. Trichoderma species employ diverse strategies to colonize and survive in various environments, infecting phytopathogens; however, the mechanisms and virulence factors contributing to human infections remain poorly understood. In this mini review, we provide a brief overview and contextualization of the virulence mechanisms employed by Trichoderma in parasitizing other fungi, as well as those implicated in modulating plant immunity and inducing human infections. Furthermore, we discuss the similarity of these virulence factors capable of modulating the mammalian immune system and their potential implications for human infection.

DNA synthesis and assembly techniques have enabled the creation of validated and standardized DNA parts, used for producing proteins, enzymes, and small molecules. However, most DNA parts are governed by Material Transfer Agreements, which restrict sharing and reuse for commercial purposes even in the absence of patents, bottlenecking innovation. DNA synthesis, crucial for producing new parts, also remains expensive and therefore inaccessible to most researchers. With the breakneck pace of digital innovations for designing and learning from biology, a new and more open approach to the physical building and testing of biology is needed. We propose the establishment of an Open Bio Research Alliance, to create and distribute open collections of DNA and other biological parts, combined with regulated and affordable DNA synthesis services. Focusing on Canada's bioeconomy, establishing domestic DNA synthesis infrastructure would not only secure global competitiveness in engineering biology, but also safeguard biosecurity and national sovereignty over critical resources. By harnessing and supporting existing lab automation resources, the Alliance will also help scale the building and testing of engineered biological systems. Leveraging these tools and strategies, Canada is well-positioned to lead the world in open and innovative biotechnology, paving the way for a thriving bioeconomy.

The Cryptococcus neoformans and Cryptococcus gattii species complexes are the etiological agents of cryptococcosis, a disease responsible for 181 000 deaths annually worldwide due to late diagnosis and limited treatment options. Studies focusing on the identification of new substances with antifungal activity, such as essential oils (EOs), are urgently needed. While the antifungal effects of EO have already been suggested, their mechanism of action at the molecular level still requires evaluation. In this work, we assessed the molecular changes induced by the exposure of Cryptococus neoformans (H99) and Cryptococcus deuterogatti (R265) to lavender essential oil (LEO) using a morphological and proteomics approach. The identified proteins were categorized by Gene Ontology according to biological processes and molecular functions, and Kyoto Encyclopedia of Genes and Genomes pathway analysis was also conducted. Our findings indicate that LEO creates a stressful environment in both strains; however, the response to this stimulus differs between the two species. In C. neoformans, changes were observed in energy metabolism and pathways related to alternative sources of energy and oxidative stress response. In C. deuterogatti, changes were identified in pathways related to cellular architecture, implying that the cell underwent morphological changes such as membrane and cell wall stiffening.

This study investigates the composition, structure, and predictive associated functions of epilithic bacteria living in the biofilms of a freshwater (FWR) and a mixed-saline (MSR) tropical river. High-throughput sequencing revealed a 69% overlap in species richness between the two sites. Cyanobacteria were dominant in freshwater, while heterotrophic classes like Alphaproteobacteria and Betaproteobacteria were prevalent in the mixed-saline biofilm. Predictive functional analysis (FAPROTAX) indicated greater diversity in MSR, favoring organic matter degradation and nutrient cycling, with more bacterial OTUs involved in chemoheterotrophy and hydrogen oxidation (Wilcoxon, p > 0.001). In contrast, FWR had a higher abundance of OTUs linked to phototrophy and degradation of aromatic compounds and plastics (Wilcoxon, p > 0.001). Key microbial interactions were revealed between phototrophic cyanobacteria and heterotrophs such as Fulvivirga (Cytophagia), suggesting a pivotal role for this genus in the carbon cycle. Additionally, bacterial species known for their ability to remove chlorine from pollutants, such as Acidovorax, Acinetobacter, Comamonas, Curvibacter, Sediminibacterium, or bacterial species belonging to the Sphingomonadaceae family were more diverse and abundant in FWR site. These findings point to promising bioremediation potential driven by biofilm community activities, particularly in tropical freshwater environments impacted by organochlorine contaminants.

This study investigated the cecal microbiome of broilers raised under specific antimicrobial feeding programs (AFPs). A total of 2304 day-old Ross-708 male (M, n = 1152) and female (F, n = 1152) chicks were distributed into 48 floor pens which were allocated to one of three AFPs: Conventional, raised without medically important antibiotics (RWMIA), and raised without antibiotics (RWA). At 28 (D28) and 41 (D41) days of age, cecal contents were collected for culture dependent and independent analyses. At both 28 and 41 days, Enterococcus was more abundant in RWA-raised broilers than other groups with the most abundance of this bacterium being found in female birds (P < 0.05). At D41, the most abundant Eimeria tenella counts was observed in RWA-raised broiler ceca (P < 0.05). Sex effects were observed on the abundances of four of the 248 identified antimicrobial resistance genes while abundances of 10 were modulated by AFPs (P < 0.05). Ceca of females birds showed more tssB than males, and ceca of RWMIA-raised birds contained the highest abundance of chuY genes regardless of sex. This study showed that in a specific feeding program, cecal resistome can be affected by chicken's sex contributing to understand the AMR related to the AMU.