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1.
Proc Biol Sci ; 288(1961): 20211213, 2021 10 27.
Article in English | MEDLINE | ID: mdl-34702078

ABSTRACT

The deep sea has been described as the last major ecological frontier, as much of its biodiversity is yet to be discovered and described. Beaked whales (ziphiids) are among the most visible inhabitants of the deep sea, due to their large size and worldwide distribution, and their taxonomic diversity and much about their natural history remain poorly understood. We combine genomic and morphometric analyses to reveal a new Southern Hemisphere ziphiid species, Ramari's beaked whale, Mesoplodon eueu, whose name is linked to the Indigenous peoples of the lands from which the species holotype and paratypes were recovered. Mitogenome and ddRAD-derived phylogenies demonstrate reciprocally monophyletic divergence between M. eueu and True's beaked whale (M. mirus) from the North Atlantic, with which it was previously subsumed. Morphometric analyses of skulls also distinguish the two species. A time-calibrated mitogenome phylogeny and analysis of two nuclear genomes indicate divergence began circa 2 million years ago (Ma), with geneflow ceasing 0.35-0.55 Ma. This is an example of how deep sea biodiversity can be unravelled through increasing international collaboration and genome sequencing of archival specimens. Our consultation and involvement with Indigenous peoples offers a model for broadening the cultural scope of the scientific naming process.


Subject(s)
Genomics , Whales , Animals , Cell Nucleus , Phylogeny , Whales/anatomy & histology , Whales/genetics
2.
J Bacteriol ; 202(11)2020 05 11.
Article in English | MEDLINE | ID: mdl-32179627

ABSTRACT

Listeria monocytogenes is a Gram-positive pathogen able to cause severe human infections. Its major virulence regulator is the transcriptional activator PrfA, a member of the Crp/Fnr family of transcriptional regulators. To establish a successful L. monocytogenes infection, the PrfA protein needs to be in an active conformation, either by binding the cognate inducer glutathione (GSH) or by possessing amino acid substitutions rendering the protein constitutively active (PrfA*). By a yet unknown mechanism, phosphotransferase system (PTS) sugars repress the activity of PrfA. We therefore took a transposon-based approach to identify the mechanism by which PTS sugars repress PrfA activity. For this, we screened a transposon mutant bank to identify clones able to grow in the presence of glucose-6-phosphate as the sole carbon source. Surprisingly, most of the isolated transposon mutants also carried amino acid substitutions in PrfA. In transposon-free strains, the PrfA amino acid substitution mutants displayed growth, virulence factor expression, infectivity, and DNA binding, agreeing with previously identified PrfA* mutants. Hence, the initial growth phenotype observed in the isolated clone was due to the amino acid substitution in PrfA and unrelated to the loci inactivated by the transposon mutant. Finally, we provide structural evidence for the existence of an intermediately activated PrfA state, which gives new insights into PrfA protein activation.IMPORTANCE The Gram-positive bacterium Listeria monocytogenes is a human pathogen affecting mainly the elderly, immunocompromised people, and pregnant women. It can lead to meningoencephalitis, septicemia, and abortion. The major virulence regulator in L. monocytogenes is the PrfA protein, a transcriptional activator. Using a growth-based selection strategy, we identified mutations in the PrfA protein leading to constitutively active virulence factor expression. We provide structural evidence for the existence of an intermediately activated PrfA state, which gives new insights into PrfA protein activation.


Subject(s)
Bacterial Proteins/metabolism , Listeria monocytogenes/growth & development , Listeria monocytogenes/genetics , Listeria monocytogenes/metabolism , Listeria monocytogenes/pathogenicity , Listeriosis/microbiology , Peptide Termination Factors/metabolism , Bacterial Proteins/genetics , Gene Expression Regulation, Bacterial , Humans , Mutation , Peptide Termination Factors/genetics , Virulence
3.
J Chem Ecol ; 42(9): 970-983, 2016 Sep.
Article in English | MEDLINE | ID: mdl-27613544

ABSTRACT

The vast number of plant secondary metabolites (PSMs) produced by higher plants has generated many efforts to exploit their potential for pest control. We performed a systematic literature search to retrieve relevant publications, and we evaluated these according to PSM groups to derive information about the potential for developing plant-derived rodent repellents. We screened a total of 54 publications where different compounds or plants were tested regarding rodent behavior/metabolism. In the search for widely applicable products, we recommend multi-species systematic screening of PSMs, especially from the essential oil and terpenoid group, as laboratory experiments have uniformly shown the strongest effects across species. Other groups of compounds might be more suitable for the management of species-specific or sex-specific issues, as the effects of some compounds on particular rodent target species or sex might not be present in non-target species or in both sexes. Although plant metabolites have potential as a tool for ecologically-based rodent management, this review demonstrates inconsistent success across laboratory, enclosure, and field studies, which ultimately has lead to a small number of currently registered PSM-based rodent repellents.


Subject(s)
Plant Extracts/metabolism , Plants/metabolism , Rodent Control/methods , Rodenticides/metabolism , Alkaloids/chemistry , Alkaloids/metabolism , Alkaloids/toxicity , Animals , Glucosinolates/chemistry , Glucosinolates/metabolism , Glucosinolates/toxicity , Oils, Volatile/chemistry , Oils, Volatile/metabolism , Oils, Volatile/toxicity , Phenols/chemistry , Phenols/metabolism , Phenols/toxicity , Plant Extracts/chemistry , Plant Extracts/toxicity , Plants/chemistry , Plants/toxicity , Rodentia/physiology , Rodenticides/chemistry , Rodenticides/toxicity , Secondary Metabolism , Terpenes/chemistry , Terpenes/metabolism , Terpenes/toxicity
4.
Nucleic Acids Res ; 41(13): 6381-90, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23658223

ABSTRACT

The lactose operon of Escherichia coli is a paradigm system for quantitative understanding of gene regulation in prokaryotes. Yet, none of the many mathematical models built so far to study the dynamics of this system considered the fact that the Lac repressor regulates its own transcription by forming a transcriptional roadblock at the O3 operator site. Here we study the effect of autoregulation on intracellular LacI levels and also show that cAMP-CRP binding does not affect the efficiency of autoregulation. We built a mathematical model to study the role of LacI autoregulation in the lactose utilization system. Previously, it has been argued that negative autoregulation can significantly reduce noise as well as increase the speed of response. We show that the particular molecular mechanism, a transcriptional roadblock, used to achieve self-repression in the lac system does neither. Instead, LacI autoregulation balances two opposing states, one that allows quicker response to smaller pulses of external lactose, and the other that minimizes production costs in the absence of lactose.


Subject(s)
Escherichia coli Proteins/metabolism , Escherichia coli/genetics , Gene Expression Regulation, Bacterial , Lac Repressors/metabolism , Lactose/metabolism , Computer Simulation , Escherichia coli/metabolism , Escherichia coli Proteins/biosynthesis , Escherichia coli Proteins/genetics , Homeostasis , Lac Operon , Lac Repressors/biosynthesis , Lac Repressors/genetics , Models, Genetic , RNA, Messenger/metabolism , Transcription, Genetic
5.
Nat Methods ; 6(10): 753-7, 2009 Oct.
Article in English | MEDLINE | ID: mdl-19749762

ABSTRACT

We present the Flp-nick system, which allows introduction of a protein-bound nick at a single genomic site in Saccharomyces cerevisiae and thus mimics a stabilized topoisomerase I-DNA cleavage complex. We took advantage of a mutant Flp recombinase that can introduce a nick at a specific Flp recombinase recognition target site that has been integrated in the yeast genome. The genetic requirement for cells to cope with this insult is the same as for cells treated with camptothecin, which traps topoisomerase I-DNA cleavage complexes genome-wide. Hence, a single protein-bound nick is enough to kill cells if functional repair pathways are lacking. The Flp-nick system can be used to dissect repair, checkpoint and replication fork management pathways activated by a single genomic insult, and it allows the study of events at the damage site, which so far has been impossible to address.


Subject(s)
DNA Breaks, Single-Stranded , DNA Damage/physiology , DNA Nucleotidyltransferases/genetics , DNA Repair/physiology , DNA, Bacterial/genetics , Mutagenesis, Site-Directed/methods , Saccharomyces cerevisiae/genetics
6.
Pest Manag Sci ; 78(4): 1620-1629, 2022 Apr.
Article in English | MEDLINE | ID: mdl-34989096

ABSTRACT

BACKGROUND: Norway rats (Rattus norvegicus) need to be controlled to prevent transmission of pathogens and damages to stored products and material, leading to considerable economic risks and losses. Given increasing resistance in Norway rats, the most persistent, bio-accumulative and toxic anticoagulant rodenticides are widely used for management, which presents hazards to the environment especially for non-target species. We investigated how sanitary measures improved management of Norway rats on 12 paired livestock farms in a region of Germany with a high population of resistant rats for reducing application of rodenticides. We recorded food intake, and tracked activity and resistance frequency during the pre-treatment, treatment and post-treatment periods. RESULTS: In the post-treatment period, farms using sanitary measures had a higher control success with > 13% more bait boxes without feeding than farms not using sanitary measures. In addition, the reoccurrence of rats was delayed by 85 days. With increasing accessibility to buildings and more precise positioning of the boxes, control success improved, especially when rats could not spread from water-bearing ditches through the sewer system, and when rat-hunting animals were present. Resistant animals were more common indoors than outdoors, and there were more resistant rats recorded before and during treatment than in the post-treatment period. CONCLUSION: The control success was substantially higher and reoccurrence was delayed using sanitary measures on farms. Sanitary measures can reduce resistance indirectly due to delayed re-colonization and establishment of resistant populations inside buildings. Hence, sanitary measures help to reduce economic losses, rodenticides required for rat management and environmental risk especially in the resistance area. © 2022 The Authors. Pest Management Science published by John Wiley & Sons Ltd on behalf of Society of Chemical Industry.


Subject(s)
4-Hydroxycoumarins , Rodenticides , 4-Hydroxycoumarins/toxicity , Animals , Anticoagulants/toxicity , Drug Resistance , Farms , Livestock , Rats , Rodent Control , Rodenticides/pharmacology
7.
Cereb Cortex Commun ; 3(4): tgac040, 2022.
Article in English | MEDLINE | ID: mdl-36530950

ABSTRACT

A major goal of neuroscience is to reveal mechanisms supporting collaborative actions of neurons in local and larger-scale networks. However, no clear overall principle of operation has emerged despite decades-long experimental efforts. Here, we used an unbiased method to extract and identify the dynamics of local postsynaptic network states contained in the cortical field potential. Field potentials were recorded by depth electrodes targeting a wide selection of cortical regions during spontaneous activities, and sensory, motor, and cognitive experimental tasks. Despite different architectures and different activities, all local cortical networks generated the same type of dynamic confined to one region only of state space. Surprisingly, within this region, state trajectories expanded and contracted continuously during all brain activities and generated a single expansion followed by a contraction in a single trial. This behavior deviates from known attractors and attractor networks. The state-space contractions of particular subsets of brain regions cross-correlated during perceptive, motor, and cognitive tasks. Our results imply that the cortex does not need to change its dynamic to shift between different activities, making task-switching inherent in the dynamic of collective cortical operations. Our results provide a mathematically described general explanation of local and larger scale cortical dynamic.

8.
Int J Cancer ; 123(8): 1956-63, 2008 Oct 15.
Article in English | MEDLINE | ID: mdl-18688857

ABSTRACT

Meningiomas are the second most common type of brain and CNS tumors by histology. Surgery and radiotherapy are main treatment options, but meningiomas may be impossible to adequately resect or may regrow after surgery. In spite of many experimental attempts, there is no generally accepted chemotherapeutic approach. We have studied in a series of meningiomas the expression of the Toll-like receptor 4 (TLR4), which apart from its major role as a key factor of the innate immune system, is believed to play a role in tumorigenesis. All meningiomas studied expressed TLR4 mRNA and protein at variable degree. Paclitaxel, a ligand of TLR4, exhibited a dose- and time-dependent growth suppression in both monolayer and spheroid meningioma cell cultures. The knockdown of TLR4 with siRNA in meningioma cell cultures abrogated the inhibitory effect of paclitaxel. The suppressive action of paclitaxel on meningioma cell growth was enhanced in the presence of fluvastatin or the mitogen-actvated protein kinase (ERK1/2) inhibitor PD98059. At least part of the growth suppressive effect was mediated by the induction of apoptosis in meningioma cells by paclitaxel alone or in combination with fluvastatin. In conclusion, our in vitro results suggest that paclitaxel alone or in combination with other inhibitors of cell growth (statins, MAPK inhibitors) could provide a potential tool for the treatment of TLR4 expressing meningiomas.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/pharmacology , Meningeal Neoplasms/drug therapy , Meningioma/drug therapy , Meningioma/metabolism , Paclitaxel/pharmacology , Toll-Like Receptor 4/biosynthesis , Adult , Aged , Apoptosis/drug effects , Cell Growth Processes/drug effects , Fatty Acids, Monounsaturated/administration & dosage , Fluvastatin , Humans , Hydroxymethylglutaryl-CoA Reductase Inhibitors/administration & dosage , Immunohistochemistry , Indoles/administration & dosage , Male , Meningeal Neoplasms/immunology , Meningeal Neoplasms/metabolism , Meningeal Neoplasms/pathology , Meningioma/immunology , Meningioma/pathology , Middle Aged , Mitogen-Activated Protein Kinase 1/antagonists & inhibitors , Mitogen-Activated Protein Kinase 3/antagonists & inhibitors , Paclitaxel/administration & dosage , RNA, Small Interfering/genetics , Spheroids, Cellular , Toll-Like Receptor 4/genetics , Tumor Cells, Cultured
9.
J Med Chem ; 61(9): 4165-4175, 2018 05 10.
Article in English | MEDLINE | ID: mdl-29667825

ABSTRACT

Listeria monocytogenes is a bacterial pathogen that controls much of its virulence through the transcriptional regulator PrfA. In this study, we describe structure-guided design and synthesis of a set of PrfA inhibitors based on ring-fused 2-pyridone heterocycles. Our most effective compound decreased virulence factor expression, reduced bacterial uptake into eukaryotic cells, and improved survival of chicken embryos infected with L. monocytogenes compared to previously identified compounds. Crystal structures identified an intraprotein "tunnel" as the main inhibitor binding site (AI), where the compounds participate in an extensive hydrophobic network that restricts the protein's ability to form functional DNA-binding helix-turn-helix (HTH) motifs. Our studies also revealed a hitherto unsuspected structural plasticity of the HTH motif. In conclusion, we have designed 2-pyridone analogues that function as site-AI selective PrfA inhibitors with potent antivirulence properties.


Subject(s)
Anti-Bacterial Agents/chemistry , Anti-Bacterial Agents/pharmacology , Bacterial Proteins/antagonists & inhibitors , Drug Design , Listeria monocytogenes/drug effects , Listeria monocytogenes/metabolism , Peptide Termination Factors/antagonists & inhibitors , Animals , Bacterial Proteins/chemistry , Bacterial Proteins/metabolism , Chick Embryo , Listeria monocytogenes/pathogenicity , Models, Molecular , Peptide Termination Factors/chemistry , Peptide Termination Factors/metabolism , Protein Conformation , Virulence/drug effects
10.
Integr Zool ; 12(5): 428-436, 2017 Sep.
Article in English | MEDLINE | ID: mdl-27992117

ABSTRACT

Rodents, including common voles (Microtus arvalis) and house mice (Mus musculus) cause immense pre-harvest and post-harvest losses. Therefore, developing methods that mitigate these losses while maintaining their role in ecosystems is a priority. Several plant secondary metabolites (PSM) which significantly reduce food intake of both species under laboratory conditions have been identified. However, before these can be used in rodent pest management, they must be tested under more natural conditions where other food sources are available. In this study, the odors of 4 PSMs were evaluated for their repellent effects in experiments conducted in semi-natural enclosures. Soil treated with PSMs or untreated soil (experimental control) was placed in an underground box containing food (rolled oats). We quantified the number of visits to each box and could demonstrate that all 4 PSMs reduced the number of visits to treatment boxes in both rodent species. For common voles the combination of methyl nonyl ketone + black pepper oil was the most repellent PSM. House mice made fewer visits to all PSM boxes; boxes with the anthraquinone were visited least. Furthermore, house mice consumed less food from boxes containing soil treated with all 4 PSMs. Our results suggest that PSMs are repellent in murid and microtine rodents under semi-field conditions. In addition, the future use of PSM odors for repelling both pest species, especially house mice, seems promising. Further investigations with other PSMs, different concentrations as well as alternative application methods are needed to repel common voles from attractive crops.


Subject(s)
Odorants , Pest Control , Rodentia , Animals , Arvicolinae , Behavior, Animal , Crops, Agricultural
11.
Brain Res ; 1125(1): 147-54, 2006 Dec 13.
Article in English | MEDLINE | ID: mdl-17112483

ABSTRACT

The serine/threonine kinase Raf-1 is involved in the regulation of tumor cell survival, proliferation and metastasis formation, and has therefore emerged as a promising target for cancer therapy. In addition, Raf-1 activity mediates proliferation of endothelial cells thereby promoting angiogenesis and invasive growth of various tumors, including highly vascularized malignant glioblastoma. The aim of this study was to evaluate the effects of small inhibitory RNA (siRNA) directed against Raf-1 on viability, proliferation and motility in glioma cells and cerebral endothelial cells. Half-quantitative RT-PCR and Western blotting revealed efficient siRNA-mediated Raf-1 down regulation in glioma cells (U373, U251) and in human cerebral microvascular endothelial cells (HCMEC). Surprisingly, Raf-1 gene silencing failed to affect cell survival, proliferation or migration activity in the glioblastoma cell lines. In HCMEC, however, pronounced decrease of cell survival and significant inhibition of tube formation was achieved by Raf-1 siRNA compared to non-functional siRNA or vehicle controls. In conclusion, Raf-1 silencing appears as a potential therapeutic strategy to inhibit brain tumor angiogenesis and thereby outgrowth of highly vascularized glioblastoma multiforme, whereas direct cytotoxic effects of Raf-1 knockdown in tumor cells may vary.


Subject(s)
Cerebral Cortex/cytology , Endothelial Cells/drug effects , Proto-Oncogene Proteins c-raf/metabolism , RNA, Small Interfering/pharmacology , Analysis of Variance , Blotting, Northern/methods , Blotting, Western/methods , Cell Movement/drug effects , Cell Proliferation/drug effects , Cell Survival/drug effects , Cell Survival/physiology , Cells, Cultured , Fibrosarcoma/metabolism , Fibrosarcoma/pathology , Glioblastoma/metabolism , Glioblastoma/pathology , Humans , Mutation/physiology , Proto-Oncogene Proteins c-raf/genetics , RNA, Messenger/biosynthesis , Reverse Transcriptase Polymerase Chain Reaction/methods , Time Factors
12.
Cell Chem Biol ; 23(3): 404-14, 2016 Mar 17.
Article in English | MEDLINE | ID: mdl-26991105

ABSTRACT

The transcriptional activator PrfA, a member of the Crp/Fnr family, controls the expression of some key virulence factors necessary for infection by the human bacterial pathogen Listeria monocytogenes. Phenotypic screening identified ring-fused 2-pyridone molecules that at low micromolar concentrations attenuate L. monocytogenes cellular uptake by reducing the expression of virulence genes. These inhibitors bind the transcriptional regulator PrfA and decrease its affinity for the consensus DNA-binding site. Structural characterization of this interaction revealed that one of the ring-fused 2-pyridones, compound 1, binds at two separate sites on the protein: one within a hydrophobic pocket or tunnel, located between the C- and N-terminal domains of PrfA, and the second in the vicinity of the DNA-binding helix-turn-helix motif. At both sites the compound interacts with residues important for PrfA activation and helix-turn-helix formation. Ring-fused 2-pyridones represent a new class of chemical probes for studying virulence in L. monocytogenes.


Subject(s)
Bacterial Proteins/metabolism , Listeria monocytogenes/drug effects , Listeria monocytogenes/pathogenicity , Peptide Termination Factors/metabolism , Pyridones/pharmacology , Bacterial Proteins/genetics , Binding Sites/drug effects , Caco-2 Cells , Cell Line , Dose-Response Relationship, Drug , HeLa Cells , Humans , Models, Molecular , Peptide Termination Factors/genetics , Pyridones/chemistry , Structure-Activity Relationship , Virulence/drug effects
13.
Sci Rep ; 5: 12186, 2015 Jul 17.
Article in English | MEDLINE | ID: mdl-26184971

ABSTRACT

Gene regulatory cascades (GRCs) are common motifs in cellular molecular networks. A given logical function in these cascades, such as the repression of the activity of a transcription factor, can be implemented by a number of different regulatory mechanisms. The potential consequences for the dynamic performance of the GRC of choosing one mechanism over another have not been analysed systematically. Here, we report the construction of a synthetic GRC in Escherichia coli, which allows us for the first time to directly compare and contrast the dynamics of four different regulatory mechanisms, affecting the transcription, translation, stability, or activity of a transcriptional repressor. We developed a biologically motivated mathematical model which is sufficient to reproduce the response dynamics determined by experimental measurements. Using the model, we explored the potential response dynamics that the constructed GRC can perform. We conclude that dynamic differences between regulatory mechanisms at an individual step in a GRC are often concealed in the overall performance of the GRC, and suggest that the presence of a given regulatory mechanism in a certain network environment does not necessarily mean that it represents a single optimal evolutionary solution.


Subject(s)
Gene Expression Regulation, Bacterial , Gene Regulatory Networks , Models, Biological , Bacterial Proteins/genetics , Computer Simulation , Escherichia coli/genetics , Genes, Reporter , Protein Biosynthesis , RNA Stability , Transcription, Genetic
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