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1.
Eur J Med Chem ; 143: 1077-1089, 2018 Jan 01.
Article in English | MEDLINE | ID: mdl-29232584

ABSTRACT

A natural product inspired library was synthesized based on 2,3-diarylbenzofuran and 2,3-diaryl-2,3-dihydrobenzofuran scaffolds. The library of forty-eight compounds was prepared by utilizing Pd-catalyzed one-pot multicomponent reactions and ruthenium-catalyzed intramolecular carbenoid C-H insertions. The compounds were evaluated for antibacterial activity in a panel of test systems including phenotypic, biochemical and image-based screening assays. We identified several potent inhibitors that block intracellular replication of pathogenic Chlamydia trachomatis with IC50 ≤ 3 µM. These new C. trachomatis inhibitors can serve as starting points for the development of specific treatments that reduces the global burden of C. trachomatis infections.


Subject(s)
Anti-Bacterial Agents/pharmacology , Benzofurans/pharmacology , Biological Products/pharmacology , Chlamydia trachomatis/drug effects , Small Molecule Libraries/pharmacology , Anti-Bacterial Agents/chemical synthesis , Anti-Bacterial Agents/chemistry , Benzofurans/chemical synthesis , Benzofurans/chemistry , Biological Products/chemical synthesis , Biological Products/chemistry , Cell Survival/drug effects , Dose-Response Relationship, Drug , HeLa Cells , Humans , Microbial Sensitivity Tests , Molecular Structure , Small Molecule Libraries/chemical synthesis , Small Molecule Libraries/chemistry , Stereoisomerism , Structure-Activity Relationship , Tumor Cells, Cultured
2.
Front Microbiol ; 9: 3151, 2018.
Article in English | MEDLINE | ID: mdl-30619216

ABSTRACT

In this study, we describe the application of a transformed Chlamydia trachomatis strain constitutively expressing the red fluorescent protein mCherry, to allow real-time monitoring of the infection cycle and screening for agents that block replication of C. trachomatis. The red fluorescent C. trachomatis strain was detected autonomously without antibody staining and was equally susceptible to doxycycline as the wild type strain. A high-throughput screening assay was developed using the transformed strain and automated fluorescence microscopy. The assay was used in a pilot screen of a 349 compound library containing natural products from Australian flora and fauna. Compounds with anti-chlamydial activity were tested for dose response and toxicity to host cells and two non-toxic compounds had 50% effective concentration (EC50) values in the low micromolar range. Natural products are valuable sources for drug discovery and the identified Chlamydia growth inhibition may be starting points for future drug development. Live cell imaging was used to visualize growth of the red fluorescent C. trachomatis strain over time. The screening assay reduced workload and reagents compared to an assay requiring immunostaining and could further be used to monitor the development of Chlamydia inclusions and anti-chlamydial effect in real time.

3.
Article in English | MEDLINE | ID: mdl-28784680

ABSTRACT

The type II fatty acid synthesis (FASII) pathway is essential for bacterial lipid biosynthesis and continues to be a promising target for novel antibacterial compounds. Recently, it has been demonstrated that Chlamydia is capable of FASII and this pathway is indispensable for Chlamydia growth. Previously, a high-content screen with Chlamydia trachomatis-infected cells was performed, and acylated sulfonamides were identified to be potent growth inhibitors of the bacteria. C. trachomatis strains resistant to acylated sulfonamides were isolated by serial passage of a wild-type strain in the presence of low compound concentrations. Results from whole-genome sequencing of 10 isolates from two independent drug-resistant populations revealed that mutations that accumulated in fabF were predominant. Studies of the interaction between the FabF protein and small molecules showed that acylated sulfonamides directly bind to recombinant FabF in vitro and treatment of C. trachomatis-infected HeLa cells with the compounds leads to a decrease in the synthesis of Chlamydia fatty acids. This work demonstrates the importance of FASII for Chlamydia development and may lead to the development of new antimicrobials.


Subject(s)
Anti-Bacterial Agents/pharmacology , Chlamydia trachomatis/drug effects , Fatty Acid Synthase, Type II/metabolism , Fatty Acid Synthesis Inhibitors/pharmacology , Fatty Acids/biosynthesis , Sulfamethoxazole/pharmacology , Acylation/drug effects , Adamantane/pharmacology , Aminobenzoates/pharmacology , Anilides/pharmacology , Animals , Cell Line, Tumor , Cerulenin/pharmacology , Chlamydia Infections/drug therapy , Chlamydia Infections/microbiology , Chlamydia trachomatis/genetics , Chlamydia trachomatis/metabolism , Chlorocebus aethiops , Fatty Acid Synthase, Type II/genetics , HeLa Cells , Humans , Triclosan/pharmacology , Vero Cells
4.
Actual. psicol. (Impr.) ; 30(120)jun. 2016.
Article in Spanish | LILACS-Express | LILACS | ID: biblio-1505559

ABSTRACT

La evaluación de las actitudes en el ámbito educativo ha sido utilizada como herramienta para prevenir la pérdida de asignaturas y la deserción académica. El objetivo del estudio es realizar el análisis psicométrico del instrumento Actitudes hacia las Matemáticas con el Modelo de Respuesta Graduada de Samejima (MRG). Se contó con una muestra total de 944 estudiantes de primeros semestres de diferentes carreras universitarias. Se realizó el análisis a partir de la TCT y se ajustó el modelo MRG. Se estimaron y analizaron los parámetros de los ítems y se encontró que la mayoría se ajustan al modelo. En conclusión, se encuentra que la escala cuenta con adecuadas propiedades psicométricas. Finalmente, se presentan las bondades del uso del MRG para la evaluación de actitudes.


The assessment of attitudes in education has been used as a tool for preventing the loss of subjects and the desertion. The aim of the study is to perform a psychometric analysis of the "Attitudes towards Mathematics" scale with Samejima´s graded response model (MRG). The sample was of 944 students from different university careers. To analyze the TCT and the MRG model was used. In conclusion, the scale has good psychometric quality. Finally, the benefits of using the MRG for assessing attitudes are presented.

5.
Mol Biol Cell ; 26(10): 1918-34, 2015 May 15.
Article in English | MEDLINE | ID: mdl-25788290

ABSTRACT

SINC, a new type III secreted protein of the avian and human pathogen Chlamydia psittaci, uniquely targets the nuclear envelope of C. psittaci-infected cells and uninfected neighboring cells. Digitonin-permeabilization studies of SINC-GFP-transfected HeLa cells indicate that SINC targets the inner nuclear membrane. SINC localization at the nuclear envelope was blocked by importazole, confirming SINC import into the nucleus. Candidate partners were identified by proximity to biotin ligase-fused SINC in HEK293 cells and mass spectrometry (BioID). This strategy identified 22 candidates with high confidence, including the nucleoporin ELYS, lamin B1, and four proteins (emerin, MAN1, LAP1, and LBR) of the inner nuclear membrane, suggesting that SINC interacts with host proteins that control nuclear structure, signaling, chromatin organization, and gene silencing. GFP-SINC association with the native LEM-domain protein emerin, a conserved component of nuclear "lamina" structure, or with a complex containing emerin was confirmed by GFP pull down. Our findings identify SINC as a novel bacterial protein that targets the nuclear envelope with the capability of globally altering nuclear envelope functions in the infected host cell and neighboring uninfected cells. These properties may contribute to the aggressive virulence of C. psittaci.


Subject(s)
Bacterial Proteins/metabolism , Chlamydophila psittaci/metabolism , Nuclear Envelope/microbiology , Chlamydophila psittaci/pathogenicity , HEK293 Cells , HeLa Cells , Humans , Mass Spectrometry , Nuclear Envelope/metabolism
6.
Pathog Dis ; 69(3): 213-22, 2013 Dec.
Article in English | MEDLINE | ID: mdl-23873765

ABSTRACT

Among chlamydial virulence factors are the type III secretion (T3S) system and its effectors. T3S effectors target host proteins to benefit the infecting chlamydiae. The assortment of effectors, each with a unique function, varies between species. This variation likely contributes to differences in host specificity and disease severity. A dozen effectors of Chlamydia trachomatis have been identified; however, estimates suggest that more exist. A T3S prediction algorithm, SVM-based Identification and Evaluation of Virulence Effectors (SIEVE), along with a Yersinia surrogate secretion system helped to identify a new T3S substrate, CT082, which rather than functioning as an effector associates with the chlamydial envelope after secretion. SIEVE was modified to improve/expand effector predictions to include all sequenced genomes. Additional adjustments were made to the existing surrogate system whereby the N terminus of putative effectors was fused to a known effector lacking its own N terminus and was tested for secretion. Expansion of effector predictions by cSIEVE and modification of the surrogate system have also assisted in identifying a new T3S substrate from C. psittaci. The expanded predictions along with modifications to improve the surrogate secretion system have enhanced our ability to identify novel species-specific effectors, which upon characterization should provide insight into the unique pathogenic properties of each species.


Subject(s)
Bacterial Secretion Systems/physiology , Chlamydia trachomatis/metabolism , Proteomics , Animals , Cell Membrane/metabolism , Chlamydia trachomatis/genetics , Chlamydia trachomatis/pathogenicity , Gene Expression , Gene Order , Guinea Pigs , Mutation , Protein Transport , Proteomics/methods , Species Specificity , Substrate Specificity , Yersinia pseudotuberculosis/genetics , Yersinia pseudotuberculosis/metabolism
7.
J Bacteriol ; 193(14): 3690, 2011 Jul.
Article in English | MEDLINE | ID: mdl-21571992

ABSTRACT

Chlamydia pecorum is an obligate intracellular bacterial pathogen that causes diverse disease in a wide variety of economically important mammals. We report the finished complete genome sequence of C. pecorum E58, the type strain for the species.


Subject(s)
Cattle Diseases/microbiology , Chlamydia Infections/virology , Chlamydia/genetics , Chlamydia/isolation & purification , Genome, Bacterial , Animals , Base Sequence , Cattle , Chlamydia/classification , Chlamydia Infections/microbiology , Molecular Sequence Data , Sequence Analysis, DNA
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