ABSTRACT
Mycobacterium tuberculosis (Mtb) as well as nontuberculous mycobacteria are intracellular pathogens whose treatment is extensive and increasingly impaired due to the rise of mycobacterial drug resistance. The loss of antibiotic efficacy has raised interest in the identification of host-directed therapeutics (HDT) to develop novel treatment strategies for mycobacterial infections. In this study, we identified amiodarone as a potential HDT candidate that inhibited both intracellular Mtb and Mycobacterium avium in primary human macrophages without directly impairing bacterial growth, thereby confirming that amiodarone acts in a host-mediated manner. Moreover, amiodarone induced the formation of (auto)phagosomes and enhanced autophagic targeting of mycobacteria in macrophages. The induction of autophagy by amiodarone is likely due to enhanced transcriptional regulation, as the nuclear intensity of the transcription factor EB, the master regulator of autophagy and lysosomal biogenesis, was strongly increased. Furthermore, blocking lysosomal degradation with bafilomycin impaired the host-beneficial effect of amiodarone. Finally, amiodarone induced autophagy and reduced bacterial burden in a zebrafish embryo model of tuberculosis, thereby confirming the HDT activity of amiodarone in vivo. In conclusion, we have identified amiodarone as an autophagy-inducing antimycobacterial HDT that improves host control of mycobacterial infections. IMPORTANCE: Due to the global rise in antibiotic resistance, there is a strong need for alternative treatment strategies against intracellular bacterial infections, including Mycobacterium tuberculosis (Mtb) and non-tuberculous mycobacteria. Stimulating host defense mechanisms by host-directed therapy (HDT) is a promising approach for treating mycobacterial infections. This study identified amiodarone, an antiarrhythmic agent, as a potential HDT candidate that inhibits the survival of Mtb and Mycobacterium avium in primary human macrophages. The antimycobacterial effect of amiodarone was confirmed in an in vivo tuberculosis model based on Mycobacterium marinum infection of zebrafish embryos. Furthermore, amiodarone induced autophagy and inhibition of the autophagic flux effectively impaired the host-protective effect of amiodarone, supporting that activation of the host (auto)phagolysosomal pathway is essential for the mechanism of action of amiodarone. In conclusion, we have identified amiodarone as an autophagy-inducing HDT that improves host control of a wide range of mycobacteria.
Subject(s)
Amiodarone , Autophagy , Macrophages , Mycobacterium tuberculosis , Tuberculosis , Zebrafish , Amiodarone/pharmacology , Autophagy/drug effects , Animals , Zebrafish/microbiology , Humans , Macrophages/microbiology , Macrophages/immunology , Macrophages/drug effects , Mycobacterium tuberculosis/drug effects , Mycobacterium tuberculosis/growth & development , Tuberculosis/drug therapy , Tuberculosis/microbiology , Disease Models, Animal , Mycobacterium avium/drug effects , Lysosomes/drug effects , Lysosomes/metabolism , Lysosomes/microbiologyABSTRACT
Toll-like receptor 2 (TLR2) belongs to the TLR protein family that plays an important role in the immune and inflammation response system. While TLR2 is predominantly expressed in immune cells, its expression has also been detected in the brain, specifically in microglia and astrocytes. Recent studies indicate that genomic deletion of TLR2 can result in impaired neurobehavioural function. It is currently not clear if the genomic deletion of TLR2 leads to any alterations in the microstructural features of the brain. In the current study, we noninvasively assess microstructural changes in the brain of TLR2-deficient (tlr2-/-) zebrafish using state-of-the art magnetic resonance imaging (MRI) methods at ultrahigh magnetic field strength (17.6 T). A significant increase in cortical thickness and an overall trend towards increased brain volumes were observed in young tlr2-/- zebrafish. An elevated T2 relaxation time and significantly reduced apparent diffusion coefficient (ADC) unveil brain-wide microstructural alterations, potentially indicative of cytotoxic oedema and astrogliosis in the tlr2-/- zebrafish. Multicomponent analysis of the ADC diffusivity signal by the phasor approach shows an increase in the slow ADC component associated with restricted diffusion. Diffusion tensor imaging and diffusion kurtosis imaging analysis revealed diminished diffusivity and enhanced kurtosis in various white matter tracks in tlr2-/- compared with control zebrafish, identifying the microstructural underpinnings associated with compromised white matter integrity and axonal degeneration. Taken together, our findings demonstrate that the genomic deletion of TLR2 results in severe alterations to the microstructural features of the zebrafish brain. This study also highlights the potential of ultrahigh field diffusion MRI techniques in discerning exceptionally fine microstructural details within the small zebrafish brain, offering potential for investigating microstructural changes in zebrafish models of various brain diseases.
ABSTRACT
Bacteria have an extensive adaptive ability to live in close association with eukaryotic hosts, exhibiting detrimental, neutral or beneficial effects on host growth and health. However, the genes involved in niche adaptation are mostly unknown and their functions poorly characterized. Here, we present bacLIFE ( https://github.com/Carrion-lab/bacLIFE ) a streamlined computational workflow for genome annotation, large-scale comparative genomics, and prediction of lifestyle-associated genes (LAGs). As a proof of concept, we analyzed 16,846 genomes from the Burkholderia/Paraburkholderia and Pseudomonas genera, which led to the identification of hundreds of genes potentially associated with a plant pathogenic lifestyle. Site-directed mutagenesis of 14 of these predicted LAGs of unknown function, followed by plant bioassays, showed that 6 predicted LAGs are indeed involved in the phytopathogenic lifestyle of Burkholderia plantarii and Pseudomonas syringae pv. phaseolicola. These 6 LAGs encompassed a glycosyltransferase, extracellular binding proteins, homoserine dehydrogenases and hypothetical proteins. Collectively, our results highlight bacLIFE as an effective computational tool for prediction of LAGs and the generation of hypotheses for a better understanding of bacteria-host interactions.
Subject(s)
Genome, Bacterial , Pseudomonas syringae , Genome, Bacterial/genetics , Pseudomonas syringae/genetics , Workflow , Genomics/methodsABSTRACT
In this study, the authors compared the efficiency of automated robotic and manual injection methods for the CRISPR-RfxCas13d (CasRx) system for mRNA knockdown and Cas9-mediated DNA targeting in zebrafish embryos. They targeted the no tail (TBXTA) gene as a proof-of-principle, evaluating the induced embryonic phenotypes. Both Cas9 and CasRx systems caused loss of function phenotypes for TBXTA. Cas9 protein exhibited a higher percentage of severe phenotypes compared with mRNA, while CasRx protein and mRNA showed similar efficiency. Both robotic and manual injections demonstrated comparable phenotype percentages and mortality rates. The findings highlight the potential of RNA-targeting CRISPR effectors for precise gene knockdown and endorse automated microinjection at a speed of 1.0 s per embryo as a high-throughput alternative to manual methods.
Subject(s)
CRISPR-Cas Systems , Microinjections , Robotics , Zebrafish , Animals , Zebrafish/genetics , Zebrafish/embryology , CRISPR-Cas Systems/genetics , Microinjections/methods , Robotics/methods , RNA Interference , Embryo, Nonmammalian , Gene Knockdown Techniques/methods , Zebrafish Proteins/genetics , RNA, Messenger/geneticsABSTRACT
Ancient environmental samples, including permafrost soils and frozen animal remains, represent an archive with microbial communities that have barely been explored. This yet unexplored microbial world is a genetic resource that may provide us with new evolutionary insights into recent genomic changes, as well as novel metabolic pathways and chemistry. Here, we describe Actinomycetota Micromonospora, Oerskovia, Saccharopolyspora, Sanguibacter and Streptomyces species were successfully revived and their genome sequences resolved. Surprisingly, the genomes of these bacteria from an ancient source show a large phylogenetic distance to known strains and harbour many novel biosynthetic gene clusters that may well represent uncharacterised biosynthetic potential. Metabolic profiles of the strains display the production of known molecules like antimycin, conglobatin and macrotetrolides, but the majority of the mass features could not be dereplicated. Our work provides insights into Actinomycetota isolated from an ancient source, yielding unexplored genomic information that is not yet present in current databases.
Subject(s)
Actinomycetales , Mammoths , Streptomyces , Animals , Phylogeny , Genomics , Streptomyces/genetics , FecesABSTRACT
The incidence of infections due to nontuberculous mycobacteria (NTM) has increased rapidly in recent years, surpassing tuberculosis in developed countries. Due to inherent antimicrobial resistance, NTM infections are particularly difficult to treat with low cure rates. There is an urgent need to understand NTM pathogenesis and to develop novel therapeutic approaches for the treatment of NTM diseases. Zebrafish have emerged as an excellent animal model due to genetic amenability and optical transparency during embryonic development, allowing spatiotemporal visualization of host-pathogen interactions. Furthermore, adult zebrafish possess fully functional innate and adaptive immunity and recapitulate important pathophysiological hallmarks of mycobacterial infection. Here, we report recent breakthroughs in understanding the hallmarks of NTM infections using the zebrafish model.
Subject(s)
Disease Models, Animal , Host-Pathogen Interactions , Mycobacterium Infections, Nontuberculous , Nontuberculous Mycobacteria , Zebrafish , Zebrafish/microbiology , Animals , Mycobacterium Infections, Nontuberculous/microbiology , Nontuberculous Mycobacteria/pathogenicity , Host-Pathogen Interactions/immunology , Humans , Immunity, Innate , Adaptive ImmunityABSTRACT
Non-alcoholic steatohepatitis (NASH) has been associated with hepatocellular carcinoma (HCC) often arising in histologically advanced disease when steatohepatitis is not active (cryptogenic cirrhosis). Our objective was to characterize patients with HCC and active, histologically defined steatohepatitis. Among 394 patients with HCC detected by ultrasound imaging over 8 years and staged by the Barcelona Clinic Liver Cancer (BCLC) criteria, we identified 7 cases (1.7 percent) with HCC occurring in the setting of active biopsy-proven NASH. All were negative for other liver diseases such as hepatitis C, hepatitis B, autoimmune hepatitis, Wilson disease, and hemochromatosis. The patients (4 males and 3 females, age 63 ± 13 years) were either overweight (4) or obese (3); 57 percent were diabetic and 28.5 percent had dyslipidemia. Cirrhosis was present in 6 of 7 patients, but 1 patient had well-differentiated HCC in the setting of NASH without cirrhosis (fibrosis stage 1) based on repeated liver biopsies, the absence of portal hypertension by clinical and radiographic evaluations and by direct surgical inspection. Among the cirrhotic patients, 71.4 percent were clinically staged as Child A and 14.2 percent as Child B. Tumor size ranged from 1.0 to 5.2 cm and 5 of 7 patients were classified as early stage; 46 percent of all nodules were hyper-echoic and 57 percent were <3 cm. HCC was well differentiated in 1/6 and moderately differentiated in 5/6. Alpha-fetoprotein was <100 ng/mL in all patients. HCC in patients with active steatohepatitis is often multifocal, may precede clinically advanced disease and occurs without diagnostic levels of alpha-fetoprotein. Importantly, HCC may occur in NASH in the absence of cirrhosis. More aggressive screening of NASH patients may be warranted.
Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Carcinoma, Hepatocellular/complications , Fatty Liver/complications , Liver Cirrhosis/complications , Liver Neoplasms/complications , Carcinoma, Hepatocellular/pathology , Fatty Liver/pathology , Liver Cirrhosis/pathology , Liver Neoplasms/pathology , Neoplasm StagingABSTRACT
Após a confirmaçao clínica e laboratorial de hiperinsulinismo, o principal problema consiste na localizaçao precisa da lesao no parênquima pancreático, propiciando tratamento cirúrgico adequado. Objetivo. Analisar os métodos utilizados para o diagnóstico e localizaçao pré e intra-operatório dos insulinomas, bem como as técnicas e os resultados do tratamento cirúrgico. Métodos. Foram estudados 59 casos consecutivos de insulinoma submetidos a intervençao cirúrgica. Cada um dos métodos utilizados para a localizaçao pré-operatória dessas lesoes foi avaliado quanto à sua eficiência em confronto com os achados intra-operatórios. A palpaçao do pâncreas, isoladamente ou associada à ultra-sonografia intra-operatória, como métodos de localizaçao dos insulinomas, foi também estudada. Os tipos de intervençao cirúrgica foram analisados quanto aos seus resultados imediatos e tardios. Resultados. Dos 59 insulinomas, 55 eram benignos e quatro, malignos. Dos métodos utilizados para a localizaçao pré-operatória, a ultra-sonografia foi eficiente em 28,1 por cento dos casos, a tomografia computadorizada em 25 por cento, a ultra-sonografia endoscópica em 27,2 por cento, a arteriografia seletiva em 54,1 por cento e a colheita de amostras de sangue portal para dosagem de insulina em 94,4 por cento dos casos. A palpaçao bidigital, durante a intervençao cirúrgica, localizou as lesoes em 54/55 casos (98,2 por cento). A ultra-sonografia intra-operatória foi decisiva em apenas um caso. Cinco doentes apresentavam neoplasia endócrina múltipla tipo I e em todos as lesoes pancreáticas eram múltiplas. Foram efetuadas 29 enucleaçoes e 32 ressecçoes pancreáticas nos doentes com lesoes benignas. Os doentes com lesoes malignas foram submetidos a ressecçoes pancreáticas e quimioterapia. Nao houve mortalidade, porém observaram-se complicaçoes (fístulas) em 29/59 casos. Os resultados foram bons em 98,1 por cento dos doentes com lesoes benignas. Apenas um dos doentes com lesoes malignas. sobreviveu cinco anos. Três doentes portadores de lesoes benignas e submetidos a ressecçoes pancreáticas evoluíram com diabetes tardiamente. Conclusoes. A localizaçao pré-operatória nao é absolutamente necessária desde que a palpaçao bidigital associada a ultra-sonografia intra-operatória permite a localizaçao de todas as lesoes. As enucleaçoes devem ser utilizadas, quando possível, de preferência às ressecçoes pancreáticas nas lesoes benignas.
Subject(s)
Humans , Female , Adolescent , Middle Aged , Child , Adult , Pancreatic Neoplasms/surgery , Insulinoma/surgery , Pancreatic Neoplasms/diagnosis , Surgical Procedures, Operative , Treatment Outcome , Insulin/blood , Insulinoma/diagnosisABSTRACT
Medical involvement in mass casualty incidents rewuires proper planning and preparedness. In disaster situations, legal aspects concerning the dead add to the general problem of a lack of time, place and resources to maintain routine working conditions, and demand authority and competence. The aspects of planning the recovery of the dead, transportation and morgue facilities, establishment of cause of death, identification, and the final disposition of the dead are discussed. The implementation of forensic mass fatality teams is felt to be the right answer for a better planning and coordination.(AU)