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1.
Front Immunol ; 12: 717311, 2021.
Article in English | MEDLINE | ID: mdl-34819931

ABSTRACT

Aims: Neutrophil granulocytes are the major cells involved in Chlamydia trachomatis (C. trachomatis)-mediated inflammation and histopathology. A key protein in human intracellular antichlamydial defense is the tryptophan-degrading enzyme indoleamine 2,3-dioxygenase (IDO) which limits the growth of the tryptophan auxotroph Chlamydia. Despite its importance, the role of IDO in the intracellular defense against Chlamydia in neutrophils is not well characterized. Methods: Global gene expression screen was used to evaluate the effect of C. trachomatis serovar D infection on the transcriptome of human neutrophil granulocytes. Tryptophan metabolite concentrations in the Chlamydia-infected and/or interferon-gamma (IFNG)-treated neutrophils were measured by ultra-high-performance liquid chromatography-tandem mass spectrometry (UHPLC-MS/MS). Results: Our results indicate that the C. trachomatis infection had a major impact on neutrophil gene expression, inducing 1,295 genes and repressing 1,510 genes. A bioinformatics analysis revealed that important factors involved in the induction of neutrophil gene expression were the interferon-related transcription factors such as IRF1-5, IRF7-9, STAT2, ICSB, and ISGF3. One of the upregulated genes was ido1, a known infection- and interferon-induced host gene. The tryptophan-degrading activity of IDO1 was not induced significantly by Chlamydia infection alone, but the addition of IFNG greatly increased its activity. Despite the significant IDO activity in IFNG-treated cells, C. trachomatis growth was not affected by IFNG. This result was in contrast to what we observed in HeLa human cervical epithelial cells, where the IFNG-mediated inhibition of C. trachomatis growth was significant and the IFNG-induced IDO activity correlated with growth inhibition. Conclusions: IDO activity was not able to inhibit chlamydial growth in human neutrophils. Whether the IDO activity was not high enough for inhibition or other chlamydial growth-promoting host mechanisms were induced in the infected and interferon-treated neutrophils needs to be further investigated.


Subject(s)
Chlamydia Infections/microbiology , Chlamydia trachomatis/growth & development , Indoleamine-Pyrrole 2,3,-Dioxygenase/metabolism , Neutrophils/enzymology , Tryptophan/metabolism , Chlamydia Infections/enzymology , Chlamydia Infections/immunology , Chlamydia trachomatis/immunology , Chlamydia trachomatis/metabolism , HL-60 Cells , HeLa Cells , Humans , Indoleamine-Pyrrole 2,3,-Dioxygenase/genetics , Interferon-gamma/pharmacology , Metabolome , Neutrophils/drug effects , Transcriptome
2.
Infect Immun ; 88(12)2020 11 16.
Article in English | MEDLINE | ID: mdl-32900818

ABSTRACT

The obligate intracellular pathogen Chlamydia trachomatis is the leading cause of noncongenital blindness and causative agent of the most common sexually transmitted infection of bacterial origin. With a reduced genome, C. trachomatis is dependent on its host for survival, in part due to a need for the host cell to compensate for incomplete bacterial metabolic pathways. However, relatively little is known regarding how C. trachomatis is able to hijack host cell metabolism. In this study, we show that two host glycolytic enzymes, aldolase A and pyruvate kinase, as well as lactate dehydrogenase, are enriched at the C. trachomatis inclusion membrane during infection. Inclusion localization was not species specific, since a similar phenotype was observed with C. muridarum Time course experiments showed that the number of positive inclusions increased throughout the developmental cycle. In addition, these host enzymes colocalized to the same inclusion, and their localization did not appear to be dependent on sustained bacterial protein synthesis or on intact host actin, vesicular trafficking, or microtubules. Depletion of the host glycolytic enzyme aldolase A resulted in decreased inclusion size and infectious progeny production, indicating a role for host glycolysis in bacterial growth. Finally, quantitative PCR analysis showed that expression of C. trachomatis glycolytic enzymes inversely correlated with host enzyme localization at the inclusion. We discuss potential mechanisms leading to inclusion localization of host glycolytic enzymes and how it could benefit the bacteria. Altogether, our findings provide further insight into the intricate relationship between host and bacterial metabolism during Chlamydia infection.


Subject(s)
Chlamydia Infections/metabolism , Chlamydia trachomatis/metabolism , Fructose-Bisphosphate Aldolase/metabolism , Glycolysis , Host Microbial Interactions , Inclusion Bodies/metabolism , L-Lactate Dehydrogenase/metabolism , Pyruvate Kinase/metabolism , Actins/metabolism , Bacterial Outer Membrane/enzymology , Bacterial Outer Membrane/metabolism , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Chlamydia Infections/enzymology , Chlamydia Infections/genetics , Chlamydia muridarum/metabolism , Chlamydia trachomatis/enzymology , Chlamydia trachomatis/growth & development , Chlamydia trachomatis/pathogenicity , Fructose-Bisphosphate Aldolase/genetics , HeLa Cells , Humans , Inclusion Bodies/enzymology , Inclusion Bodies/microbiology , L-Lactate Dehydrogenase/genetics , Microtubules/metabolism , Protein Biosynthesis/drug effects , Pyruvate Kinase/genetics
3.
Infect Immun ; 83(8): 3164-75, 2015 Aug.
Article in English | MEDLINE | ID: mdl-26015483

ABSTRACT

The ability of certain species of Chlamydia to inhibit the biogenesis of phagolysosomes permits their survival and replication within macrophages. The survival of macrophage-adapted chlamydiae correlates with the multiplicity of infection (MOI), and optimal chlamydial growth occurs in macrophages infected at an MOI of ≤1. In this study, we examined the replicative capacity of Chlamydia muridarum in the RAW 264.7 murine macrophage cell line at different MOIs. C. muridarum productively infected these macrophages at low MOIs but yielded few viable elementary bodies (EBs) when macrophages were infected at a moderate (10) or high (100) MOI. While high MOIs caused cytotoxicity and irreversible host cell death, macrophages infected at a moderate MOI did not show signs of cytotoxicity until late in the infectious cycle. Inhibition of host protein synthesis rescued C. muridarum in macrophages infected at a moderate MOI, implying that chlamydial growth was blocked by activated defense mechanisms. Conditioned medium from these macrophages was antichlamydial and contained elevated levels of interleukin 1ß (IL-1ß), IL-6, IL-10, and beta interferon (IFN-ß). Macrophage activation depended on Toll-like receptor 2 (TLR2) signaling, and cytokine production required live, transcriptionally active chlamydiae. A hydroxyl radical scavenger and inhibitors of inducible nitric oxide synthase (iNOS) and cathepsin B also reversed chlamydial killing. High levels of reactive oxygen species (ROS) led to an increase in cathepsin B activity, and pharmacological inhibition of ROS and cathepsin B reduced iNOS expression. Our data demonstrate that MOI-dependent TLR2 activation of macrophages results in iNOS induction via a novel ROS- and cathepsin-dependent mechanism to facilitate C. muridarum clearance.


Subject(s)
Cathepsin B/immunology , Chlamydia Infections/immunology , Chlamydia muridarum/physiology , Macrophages/enzymology , Nitric Oxide/immunology , Reactive Oxygen Species/immunology , Animals , Cathepsin B/genetics , Cell Line , Chlamydia Infections/enzymology , Chlamydia Infections/genetics , Chlamydia Infections/microbiology , Humans , Interleukin-6/immunology , Macrophages/immunology , Macrophages/microbiology , Mice , Nitric Oxide Synthase Type II/genetics , Nitric Oxide Synthase Type II/immunology
4.
Mol Microbiol ; 94(1): 186-201, 2014 Oct.
Article in English | MEDLINE | ID: mdl-25116793

ABSTRACT

Chlamydia trachomatis is an obligate intracellular pathogen responsible for a high burden of human disease. Here, a loss-of-function screen using a set of lentivirally transduced shRNAs identified 14 human host cell factors that modulate C. trachomatis infectivity. Notably, knockdown of dynamin, a host GTPase, decreased C. trachomatis infectivity. Dynamin functions in multiple cytoplasmic locations, including vesicle formation at the plasma membrane and the trans-Golgi network. However, its role in C. trachomatis infection remains unclear. Here we report that dynamin is essential for homotypic fusion of C. trachomatis inclusions but not for C. trachomatis internalization into the host cell. Further, dynamin activity is necessary for lipid transport into C. trachomatis inclusions and for normal re-differentiation from reticulate to elementary bodies. Fragmentation of the Golgi apparatus is proposed to be an important strategy used by C. trachomatis for efficient lipid acquisition and replication within the host. Here we show that a subset of C. trachomatis-infected cells displayed Golgi fragmentation, which was concurrent with increased mitotic accumulation. Golgi fragmentation was dispensable for dynamin-mediated lipid acquisition into C. trachomatis inclusions, irrespective of the cell cycle phase. Thus, our study reveals a critical role of dynamin in host-derived lipid acquisition for C. trachomatis development.


Subject(s)
Chlamydia Infections/enzymology , Chlamydia Infections/microbiology , Chlamydia trachomatis/growth & development , Chlamydia trachomatis/metabolism , Dynamin I/metabolism , Dynamins/metabolism , Lipid Metabolism , Chlamydia Infections/genetics , Chlamydia trachomatis/cytology , Chlamydia trachomatis/genetics , Dynamin I/genetics , Dynamin II , Dynamins/genetics , Golgi Apparatus/metabolism , Golgi Apparatus/microbiology , Humans
5.
J Infect Dis ; 207(7): 1095-104, 2013 Apr.
Article in English | MEDLINE | ID: mdl-23303804

ABSTRACT

Tubal factor infertility (TFI) represents 36% of female infertility and genital infection by Chlamydia trachomatis (C. trachomatis) is a major cause. Although TFI is associated with host inflammatory responses to bacterial components, the molecular pathogenesis of Chlamydia-induced infertility remains poorly understood. We investigated the hypothesis that activation of specific cysteine proteases, the caspases, during C. trachomatis genital infection causes the disruption of key fertility-promoting molecules required for embryo development and implantation. We analyzed the effect of caspase inhibition on infertility and the integrity of Dicer, a caspase-sensitive, fertility-promoting ribonuclease III enzyme, and key micro-RNAs in the reproductive system. Genital infection with the inflammation- and caspase-inducing, wild-type C. trachomatis serovar L2 led to infertility, but the noninflammation-inducing, plasmid-free strain did not. We confirmed that caspase-mediated apoptotic tissue destruction may contribute to chlamydial pathogenesis. Caspase-1 or -3 deficiency, or local administration of the pan caspase inhibitor, Z-VAD-FMK into normal mice protected against Chlamydia-induced infertility. Finally, the oviducts of infected infertile mice showed evidence of caspase-mediated cleavage inactivation of Dicer and alteration in critical miRNAs that regulate growth, differentiation, and development, including mir-21. These results provide new insight into the molecular pathogenesis of TFI with significant implications for new strategies for treatment and prevention of chlamydial complications.


Subject(s)
Caspase 1/metabolism , Caspase 3/metabolism , Chlamydia trachomatis/pathogenicity , Infertility, Female/microbiology , Infertility, Female/prevention & control , Pregnancy Complications, Infectious/prevention & control , Animals , Apoptosis , Caspase 1/genetics , Caspase 3/genetics , Chlamydia Infections/enzymology , Chlamydia Infections/microbiology , Chlamydia Infections/pathology , Enzyme Activation , Female , HeLa Cells , Humans , Infertility, Female/enzymology , Inflammation/microbiology , Inflammation/pathology , Male , Mice , Mice, Inbred C57BL , Mice, Knockout , Pregnancy , Pregnancy Complications, Infectious/enzymology , Pregnancy Complications, Infectious/microbiology , Pregnancy Complications, Infectious/pathology
6.
PLoS Pathog ; 8(8): e1002842, 2012.
Article in English | MEDLINE | ID: mdl-22876181

ABSTRACT

Bacteria in the genus Chlamydia are major human pathogens that cause an intracellular infection. A chlamydial protease, CPAF, has been proposed as an important virulence factor that cleaves or degrades at least 16 host proteins, thereby altering multiple cellular processes. We examined 11 published CPAF substrates and found that there was no detectable proteolysis when CPAF activity was inhibited during cell processing. We show that the reported proteolysis of these putative CPAF substrates was due to enzymatic activity in cell lysates rather than in intact cells. Nevertheless, Chlamydia-infected cells displayed Chlamydia-host interactions, such as Golgi reorganization, apoptosis resistance, and host cytoskeletal remodeling, that have been attributed to CPAF-dependent proteolysis of host proteins. Our findings suggest that other mechanisms may be responsible for these Chlamydia-host interactions, and raise concerns about all published CPAF substrates and the proposed roles of CPAF in chlamydial pathogenesis.


Subject(s)
Bacterial Proteins/metabolism , Chlamydia Infections/enzymology , Chlamydia trachomatis/physiology , Endopeptidases/metabolism , Host-Pathogen Interactions , Apoptosis/genetics , Bacterial Proteins/genetics , Chlamydia Infections/genetics , Endopeptidases/genetics , Golgi Apparatus/genetics , Golgi Apparatus/metabolism , HeLa Cells , Humans , Proteolysis , Substrate Specificity
7.
PLoS One ; 6(6): e21477, 2011.
Article in English | MEDLINE | ID: mdl-21731762

ABSTRACT

Chlamydia pneumoniae (CP) is an important human pathogen that causes atypical pneumonia and is associated with various chronic inflammatory disorders. Caspase-1 is a key component of the 'inflammasome', and is required to cleave pro-IL-1ß to bioactive IL-1ß. Here we demonstrate for the first time a critical requirement for IL-1ß in response to CP infection. Caspase-1⁻/⁻ mice exhibit delayed cytokine production, defective clearance of pulmonary bacteria and higher mortality in response to CP infection. Alveolar macrophages harbored increased bacterial numbers due to reduced iNOS levels in Caspase-1⁻/⁻ mice. Pharmacological blockade of the IL-1 receptor in CP infected wild-type mice phenocopies Caspase-1-deficient mice, and administration of recombinant IL-1ß rescues CP infected Caspase-1⁻/⁻ mice from mortality, indicating that IL-1ß secretion is crucial for host immune defense against CP lung infection. In vitro investigation reveals that CP-induced IL-1ß secretion by macrophages requires TLR2/MyD88 and NLRP3/ASC/Caspase-1 signaling. Entry into the cell by CP and new protein synthesis by CP are required for inflammasome activation. Neither ROS nor cathepsin was required for CP infection induced inflammasome activation. Interestingly, Caspase-1 activation during CP infection occurs with mitochondrial dysfunction indicating a possible mechanism involving the mitochondria for CP-induced inflammasome activation.


Subject(s)
Caspase 1/metabolism , Chlamydia Infections/enzymology , Chlamydia Infections/immunology , Chlamydophila pneumoniae/immunology , Interleukin-1beta/metabolism , Lung/microbiology , Pneumonia, Bacterial/immunology , Animals , Carrier Proteins/metabolism , Caspase 1/deficiency , Chlamydia Infections/complications , Disease Models, Animal , Humans , Immunity, Innate , Inflammasomes/metabolism , Lung/immunology , Lung/pathology , Macrophages, Alveolar/enzymology , Macrophages, Alveolar/microbiology , Mice , Mitochondria/metabolism , Myeloid Differentiation Factor 88/metabolism , NLR Family, Pyrin Domain-Containing 3 Protein , Nitric Oxide Synthase Type II/metabolism , Phagocytosis , Pneumonia, Bacterial/complications , Pneumonia, Bacterial/enzymology , Protein Biosynthesis , Reactive Oxygen Species/metabolism , Survival Analysis , Toll-Like Receptor 2/metabolism
8.
Curr Microbiol ; 63(4): 341-6, 2011 Oct.
Article in English | MEDLINE | ID: mdl-21779937

ABSTRACT

Chlamydiae are obligate intracellular bacteria that cause variety of human diseases. Chlamydia-infected host cells are profoundly resistant to apoptosis induced by many different apoptotic stimuli. The inhibition of apoptosis is thought to be an important immune escape mechanism allowing chlamydiae to productively complete their obligate intracellular growth cycle. Infection with chlamydiae can activate the Raf/MEK/ERK pathway. Because the survival pathway can modulate apoptosis, we used MEK-specific inhibitor U0126 and Raf-specific inhibitor GW5074 to examine the role of Raf/MEK/ERK pathway in chlamydial antiapoptotic activity. Apoptosis was induced by staurosporine (STS) and detected by morphology, DNA fragmentation, caspase-3 activation, and poly (ADP-ribose) polymerase cleavage. Inhibition of the pathway sensitized Chlamydia-infected cells to STS-mediated cell apoptosis. The data indicate that chlamydial antiapoptotic activity involves activation of the Raf/MEK/ERK survival pathway.


Subject(s)
Apoptosis , Chlamydia Infections/enzymology , Chlamydia Infections/microbiology , Chlamydia/physiology , MAP Kinase Signaling System , Mitogen-Activated Protein Kinases/metabolism , raf Kinases/metabolism , Chlamydia Infections/metabolism , Chlamydia Infections/physiopathology , Enzyme Activation , HeLa Cells , Humans
9.
Proc Natl Acad Sci U S A ; 108(17): 7189-93, 2011 Apr 26.
Article in English | MEDLINE | ID: mdl-21482792

ABSTRACT

Chlamydia trachomatis is an obligate intracellular bacterial pathogen that infects hundreds of millions of individuals globally, causing blinding trachoma and sexually transmitted disease. More effective chlamydial control measures are needed, but progress toward this end has been severely hampered by the lack of a tenable chlamydial genetic system. Here, we describe a reverse-genetic approach to create isogenic C. trachomatis mutants. C. trachomatis was subjected to low-level ethyl methanesulfonate mutagenesis to generate chlamydiae that contained less then one mutation per genome. Mutagenized organisms were expanded in small subpopulations that were screened for mutations by digesting denatured and reannealed PCR amplicons of the target gene with the mismatch specific endonuclease CEL I. Subpopulations with mutations were then sequenced for the target region and plaque-cloned if the desired mutation was detected. We demonstrate the utility of this approach by isolating a tryptophan synthase gene (trpB) null mutant that was otherwise isogenic to its parental clone as shown by de novo genome sequencing. The mutant was incapable of avoiding the anti-microbial effect of IFN-γ-induced tryptophan starvation. The ability to genetically manipulate chlamydiae is a major advancement that will enhance our understanding of chlamydial pathogenesis and accelerate the development of new anti-chlamydial therapeutic control measures. Additionally, this strategy could be applied to other medically important bacterial pathogens with no or difficult genetic systems.


Subject(s)
Chlamydia trachomatis/genetics , Mutagenesis , Mutation , Tryptophan Synthase/genetics , Antineoplastic Agents, Alkylating/pharmacology , Chlamydia Infections/enzymology , Chlamydia Infections/genetics , Chlamydia trachomatis/enzymology , Ethyl Methanesulfonate/pharmacology , Humans , Tryptophan Synthase/metabolism
10.
Mol Hum Reprod ; 16(12): 907-15, 2010 Dec.
Article in English | MEDLINE | ID: mdl-20647263

ABSTRACT

Human ectopic pregnancy (EP) remains a common cause of pregnancy-related first trimester death. Nitric oxide (NO) is synthesized from L-arginine by three NO synthases (NOS) in different tissues, including the Fallopian tube. Studies of knockout mouse models have improved our understanding of the function of NOS isoforms in reproduction, but their roles and specific mechanisms in infection-induced tubal dysfunction have not been fully elucidated. Here, we provide an overview of the expression, regulation and possible function of NOS isoforms in the Fallopian tube, highlighting the effects of infection-induced changes in the tubal cellular microenvironment (imbalance of NO production) on tubal dysfunction and the potential involvement of NOS isoforms in tubal EP after Chlamydia trachomatis genital infection. The non-equivalent regulation of tubal NOS isoforms during the menstrual cycle suggests that endogenous ovarian steroid hormones regulate NOS in an isoform-specific manner. The current literature suggests that infection with C. trachomatis induces an inflammatory response that eventually leads to tubal epithelial destruction and functional impairment, caused by a high NO output mediated by inducible NOS (iNOS). Therefore, tissue-specific therapeutic approaches to suppress iNOS expression may help to prevent ectopic implantation in patients with prior C. trachomatis infection of the Fallopian tube.


Subject(s)
Chlamydia Infections/complications , Chlamydia trachomatis , Fallopian Tubes/enzymology , Nitric Oxide Synthase/physiology , Pregnancy Complications, Infectious/enzymology , Pregnancy, Ectopic/microbiology , Animals , Cattle , Chlamydia Infections/enzymology , Fallopian Tube Diseases/enzymology , Fallopian Tube Diseases/microbiology , Fallopian Tube Diseases/pathology , Fallopian Tubes/microbiology , Fallopian Tubes/pathology , Female , Gene Expression Regulation , Humans , Isoenzymes/genetics , Isoenzymes/metabolism , Isoenzymes/physiology , Mice , Nitric Oxide Synthase/genetics , Nitric Oxide Synthase/metabolism , Pregnancy , Pregnancy Complications, Infectious/epidemiology , Pregnancy Complications, Infectious/microbiology , Pregnancy, Ectopic/enzymology , Pregnancy, Ectopic/epidemiology , Rats
11.
Microb Pathog ; 46(6): 289-97, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19306922

ABSTRACT

Interferon-gamma (IFNgamma)-mediated indoleamine 2,3-dioxygenase (IDO) expression, important in innate immunity, immune suppression, and tolerance, can be counteracted by ferrous iron (FeSO(4)). Elevation of intracellular iron levels during stimulation with IFNgamma impeded IFNgamma-induced IDO mRNA and protein expression in HEp-2 cells. Decreased IDO expression was accompanied by decreased tryptophan degradation. Accordingly, IFNgamma-mediated suppressing effects on Chlamydia trachomatis (CT) infection were reduced or even abolished in the presence of FeSO(4). Conversely, lowering intracellular iron levels by deferoxamine (DFO) did not increase IFNgamma-induced IDO expression but potentiated Chlamydia-suppressing effects by lowering intracellular iron availability. Additionally, DFO led to a CT-induced IDO expression in HEp-2 cells not treated with IFNgamma. In summary, this study demonstrates that iron acts as a regulatory element for modulating IDO expression, in addition to its function as an essential element for chlamydial growth. This may represent an important control mechanism of IDO expression at the transcriptional level.


Subject(s)
Chlamydia Infections/enzymology , Chlamydia trachomatis/physiology , Gene Expression Regulation, Enzymologic , Indoleamine-Pyrrole 2,3,-Dioxygenase/genetics , Interferon-gamma/immunology , Ions/metabolism , Cell Line , Chlamydia Infections/genetics , Chlamydia Infections/immunology , Chlamydia Infections/metabolism , Humans , Indoleamine-Pyrrole 2,3,-Dioxygenase/metabolism , Interferon-gamma/genetics , Tryptophan/metabolism
12.
FEMS Microbiol Lett ; 289(2): 233-40, 2008 Dec.
Article in English | MEDLINE | ID: mdl-19016873

ABSTRACT

Chlamydia trachomatis translocates the effector protein Tarp (translocated actin-recruiting phosphoprotein) into the host cell cytoplasm where it is quickly tyrosine phosphorylated. Abl and Src kinases have been implicated in Tarp phosphorylation; however, we observed that the situation is more complex. Chemical inhibition of Src family kinases confirmed a role for these kinases in Tarp phosphorylation. Infection of Src, Yes, Fyn (SYF)-deficient cells showed a dampened, but incompletely blocked, Tarp phosphorylation. Inhibition of Abl in an SYF background still did not completely block Tarp phosphorylation. Consequently, we tested additional kinases and found that Syk, but not Btk or Jak2, is a potent kinase of Tarp in vitro. Inhibition of Syk in an SYF background further blocked Tarp phosphorylation. Under these conditions, inclusion formation still proceeded normally. These data reveal a highly promiscuous substrate property of Tarp and set the stage for further functional characterization of Tarp phosphorylation during host cell infection.


Subject(s)
Bacterial Proteins/metabolism , Chlamydia Infections/enzymology , Chlamydia trachomatis/metabolism , Phosphoproteins/metabolism , Protein Kinases/metabolism , Amino Acid Sequence , Animals , Bacterial Proteins/genetics , Cell Line, Tumor , Chlamydia Infections/microbiology , Chlamydia trachomatis/genetics , HeLa Cells , Humans , Mice , Molecular Sequence Data , Phosphoproteins/genetics , Phosphorylation , Protein Kinases/genetics , Sequence Alignment
13.
Ukr Biokhim Zh (1999) ; 80(1): 52-6, 2008.
Article in Ukrainian | MEDLINE | ID: mdl-18710027

ABSTRACT

The system L-arginine-nitrogen oxide plays a significant role in maintenance of the anti-infectious protection of an organism. A condition of the given system and activity of a enzymatic part of antiradical protection in the blood of patients with chlamydiosis has been studied. Obtained data specify an intensification of processes of an oxidizing way of recycling of arginine in an organism of patients. Substantial increase of NO-synthase activity and insignificant activity of arginase in the blood is revealed. The level of nitrite-anion in blood cells of patients authentically increases: 1.7 times in erythrocytes, and 1.4 times in lymphocytes. It is shown, that in patients with chlamydiosis glutathione system is intensified, that is evidenced by an increase glutathione-peroxidase activity and authentic increase of glutathione level. It is assummed that the established features of nitrogen oxide exchange play a significant role in formation of a pathological condition at urogenital chlamydia infections.


Subject(s)
Antioxidants/metabolism , Arginine/blood , Chlamydia Infections/blood , Female Urogenital Diseases/blood , Male Urogenital Diseases/blood , Nitric Oxide/blood , Adult , Chlamydia Infections/enzymology , Chlamydia Infections/metabolism , Erythrocytes/enzymology , Erythrocytes/metabolism , Female , Female Urogenital Diseases/enzymology , Female Urogenital Diseases/metabolism , Female Urogenital Diseases/microbiology , Humans , Male , Male Urogenital Diseases/enzymology , Male Urogenital Diseases/metabolism , Male Urogenital Diseases/microbiology , Middle Aged
14.
J Cell Biol ; 182(1): 117-27, 2008 Jul 14.
Article in English | MEDLINE | ID: mdl-18625845

ABSTRACT

Chlamydiae replicate in a vacuole within epithelial cells and commonly induce cell damage and a deleterious inflammatory response of unknown molecular pathogenesis. The chlamydial protease-like activity factor (CPAF) translocates from the vacuole to the cytosol, where it cleaves several cellular proteins. CPAF is synthesized as an inactive precursor that is processed and activated during infection. Here, we show that CPAF can be activated in uninfected cells by experimentally induced oligomerization, reminiscent of the activation mode of initiator caspases. CPAF activity induces proteolysis of cellular substrates including two novel targets, cyclin B1 and PARP, and indirectly results in the processing of pro-apoptotic BH3-only proteins. CPAF activation induces striking morphological changes in the cell and, later, cell death. Biochemical and ultrastructural analysis of the cell death pathway identify the mechanism of cell death as nonapoptotic. Active CPAF in uninfected human cells thus mimics many features of chlamydial infection, implicating CPAF as a major factor of chlamydial pathogenicity, Chlamydia-associated cell damage, and inflammation.


Subject(s)
Bacterial Proteins/metabolism , Chlamydia/enzymology , Chlamydia/pathogenicity , Endopeptidases/metabolism , Amino Acid Motifs , Apoptosis Regulatory Proteins/metabolism , Bacterial Proteins/chemistry , Cell Death , Cell Line , Cell Shape , Chlamydia/ultrastructure , Chlamydia Infections/enzymology , Endopeptidases/chemistry , Humans , Protein Processing, Post-Translational
15.
Am J Obstet Gynecol ; 198(1): 132.e1-7, 2008 Jan.
Article in English | MEDLINE | ID: mdl-17714681

ABSTRACT

OBJECTIVE: The objective of the study was to explore the mechanisms of local innate immunity induction and modulation in pregnant women with bacterial vaginosis (BV). STUDY DESIGN: A total of 200 singleton pregnant women in early gestation (12 +/- 4 weeks) with BV (Nugent 7-10) without concurrent vaginal infections with Trichomonas vaginalis, Chlamydia trachomatis, Neisseria gonorrhoeae, syphilis, and yeast. Concentrations of vaginal interleukin (IL)-1beta and IL-8, the number of neutrophils, and the levels of sialidase and prolidase hydrolytic enzymes were determined in vaginal fluid. RESULTS: Concentrations of vaginal IL-1beta had a strong positive correlation with levels of sialidase (P < .001) and prolidase (P < .001). Conversely, such enzymes were negatively correlated with the ratio of IL-8/IL-1beta (both P < .001) and were not significantly associated with concentrations of IL-8. Notably, the number of vaginal neutrophils had a negative correlation with sialidase (P = .007). CONCLUSION: The strong induction of IL-1beta in BV-positive women appears to be associated with the production of the hydrolytic enzymes sialidase and prolidase by BV-associated bacteria. However, these 2 enzymes may inhibit the expected amplification of the proinflammatory IL-1beta cascade as evaluated by the down-regulation of the IL-8/IL-1beta ratio. A blunted response to IL-1beta signals may cause the poor rise of neutrophils, which is peculiar to BV. This impairment of local defense may contribute to increased susceptibility to adverse outcomes in BV-positive pregnant women.


Subject(s)
Dipeptidases/metabolism , Immunity, Innate/physiology , Interleukin-1beta/metabolism , Neuraminidase/metabolism , Pregnancy Complications, Infectious/immunology , Vaginosis, Bacterial/immunology , Adolescent , Adult , Analysis of Variance , Biomarkers/metabolism , Chlamydia Infections/enzymology , Chlamydia Infections/immunology , Cohort Studies , Female , Gonorrhea/diagnosis , Gonorrhea/immunology , Humans , Pregnancy , Pregnancy Complications, Infectious/enzymology , Pregnancy Complications, Infectious/microbiology , Pregnancy Outcome , Pregnancy Trimester, First , Prenatal Care , Probability , Risk Assessment , Severity of Illness Index , Statistics, Nonparametric , Trichomonas Vaginitis/enzymology , Trichomonas Vaginitis/immunology , Vaginosis, Bacterial/enzymology , Vaginosis, Bacterial/microbiology
16.
Infect Immun ; 75(12): 5924-9, 2007 Dec.
Article in English | MEDLINE | ID: mdl-17893134

ABSTRACT

Diseases associated with Chlamydia infection, such as pelvic inflammatory disease and ectopic pregnancy, are due to inflammation-mediated tissue damage and scarring that occur after chronic or repeated infections. The inflammatory chemokine interleukin-8 (IL-8) is produced by Chlamydia-infected cells through an endogenous mechanism of activation, independent of soluble factors in the supernatant. The host signaling pathways necessary for this response are not understood, but the mitogen-activated protein kinase (MAPK) extracellular signal-regulated kinase (ERK) has been shown to be activated at similar times as IL-8 mRNA up-regulation. The purpose of this study was to elucidate the MAPK pathways necessary to induce the endogenous IL-8 response to Chlamydia trachomatis infection of epithelial cells. IL-8 induced by infection with C. trachomatis L2 was shown to be dependent on ERK and independent of p38 and Jun N-terminal MAPK by use of chemical inhibitors of the signaling pathways. Persistent ERK activation during IL-8 mRNA production at 24 h postinfection was necessary to maintain the response. C. trachomatis serovar D also induced IL-8 in an ERK-dependent manner. We concluded that IL-8 induced during infection of epithelial cells is dependent on continual activation of ERK by C. trachomatis.


Subject(s)
Chlamydia Infections/enzymology , Chlamydia trachomatis/immunology , Extracellular Signal-Regulated MAP Kinases/metabolism , Interleukin-8/immunology , MAP Kinase Signaling System/immunology , Animals , Cell Line , Chlamydia Infections/immunology , Chlamydia Infections/microbiology , Chlamydia trachomatis/growth & development , Chlamydia trachomatis/metabolism , Enzyme Activation , Extracellular Signal-Regulated MAP Kinases/genetics , HeLa Cells , Humans , Interleukin-8/biosynthesis , Mice
17.
Infect Immun ; 74(10): 5513-21, 2006 Oct.
Article in English | MEDLINE | ID: mdl-16988226

ABSTRACT

Matrix metalloproteinases (MMP) are a family of host-derived enzymes involved in the turnover of extracellular matrix molecules. We have previously reported enhanced expression of matrix metalloproteinases in Chlamydia muridarum urogenital tract infection of female mice. Kinetics and patterns of MMP expression as well as enhanced expression in susceptible strains of mice in the prior study implied a role for MMP in pathogenesis. To explore this further, we infected a susceptible strain of mice (C3H/HeN) with C. muridarum and treated two groups of mice with either one of two chemical inhibitors of MMP (MMPi; captopril and a chemically modified tetracycline) and reserved infected sham-treated mice as controls. Neither of the treatments affected shedding of viable chlamydiae from the lower urogenital tract, but the administration of either MMPi protected mice from the formation of hydrosalpinx-a surrogate marker of oviduct occlusion and infertility. Interestingly, the mechanism of protection for mice treated with chemically modified tetracycline 3, appeared to be related to prevention of ascending upper genital tract infection. These results imply that MMP are involved in pathogenesis of chlamydial infection in this model by mediating ascension of the infection into the upper genital tract.


Subject(s)
Chlamydia Infections/prevention & control , Chlamydia muridarum , Female Urogenital Diseases/prevention & control , Matrix Metalloproteinase Inhibitors , Animals , Captopril/administration & dosage , Chlamydia Infections/enzymology , Chlamydia Infections/pathology , Chronic Disease , Female , Female Urogenital Diseases/enzymology , Female Urogenital Diseases/microbiology , Hydroxamic Acids/administration & dosage , Mice , Mice, Mutant Strains , Oligopeptides/administration & dosage , Tetracycline/administration & dosage
18.
J Med Microbiol ; 55(Pt 7): 947-952, 2006 Jul.
Article in English | MEDLINE | ID: mdl-16772424

ABSTRACT

Chlamydia pneumoniae is the aetiological cause of a wide variety of chronic inflammatory diseases and may be associated with neurological disease. Microbiological and immunological aspects of the interaction between C. pneumoniae and the central nervous system (CNS) are not well understood because of the lack of a suitable infection model for neuronal studies. In the present study, an in vitro C. pneumoniae infection model was developed in the established microglial cell line EOC 20. Infection of the cells resulted in obvious induction of proinflammatory cytokines. The infection also selectively induced matrix metalloproteinase-9 (MMP-9) but not MMP-2. Moreover, beta interferon, which is known to modulate CNS disease, inhibited induction of MMP-9 following C. pneumoniae infection. These results support the view that C. pneumoniae infection may be associated with marked alteration of the ability of microglial cells to enhance cytokine production as well as induction of an MMP.


Subject(s)
Central Nervous System Diseases/microbiology , Chlamydia Infections/immunology , Chlamydophila pneumoniae/immunology , Microglia/microbiology , Animals , Central Nervous System Diseases/enzymology , Central Nervous System Diseases/genetics , Central Nervous System Diseases/immunology , Chlamydia Infections/enzymology , Chlamydia Infections/genetics , Chlamydia Infections/microbiology , Cytokines/biosynthesis , Cytokines/immunology , Enzyme-Linked Immunosorbent Assay , Interferon-beta/pharmacology , Matrix Metalloproteinase 9/biosynthesis , Matrix Metalloproteinase 9/genetics , Matrix Metalloproteinase Inhibitors , Mice , RNA, Messenger/biosynthesis , RNA, Messenger/genetics , Reverse Transcriptase Polymerase Chain Reaction
19.
Immunology ; 117(2): 213-9, 2006 Feb.
Article in English | MEDLINE | ID: mdl-16423057

ABSTRACT

To determine the role of matrix metalloproteinase-7 (MMP-7) in the pathogenesis of chlamydial infection, C57BL/6 wild-type (WT) and MMP-7 knockout (KO) mice were infected intravaginally with Chlamydia trachomatis mouse pneumonitis (MoPn). Over a period of 6 weeks postinfection, various organs were cultured for C. trachomatis. Other infected animals were mated to assess their fertility status. No significant differences were observed between WT and KO mice in the number of animals with positive vaginal cultures, length of time of C. trachomatis shedding, or the number of C. trachomatis inclusion-forming units (IFU) recovered from their genital tracts. Likewise, the number of animals with hydrosalpinx, and the fertility rates and the number of embryos per mouse, were similar in WT and KO mice. Cultures from the spleen, lungs, kidneys and large intestine yielded similar numbers of IFU from WT and KO mice. However, the number of C. trachomatis IFU recovered from the small intestine of KO mice was significantly higher than that recovered from the small intestine of WT mice at 2 weeks postinfection. Because MMP-7 KO mice are deficient in active intestinal alpha-defensins, the results suggest that these components play a role in regulating colonization of the gastrointestinal tract by Chlamydia. By contrast, MMP-7 is dispensable in the progression and resolution of the genital tract infection.


Subject(s)
Chlamydia Infections/enzymology , Chlamydia trachomatis/isolation & purification , Genital Diseases, Female/enzymology , Matrix Metalloproteinase 7/physiology , Animals , Antibodies, Bacterial/biosynthesis , Chlamydia Infections/immunology , Chlamydia trachomatis/immunology , Disease Progression , Female , Genital Diseases, Female/immunology , Immunoglobulin A/biosynthesis , Immunoglobulin G/biosynthesis , Infertility, Female/immunology , Infertility, Female/microbiology , Matrix Metalloproteinase 7/genetics , Mice , Mice, Inbred C57BL , Mice, Knockout , Organ Culture Techniques , Vagina/microbiology
20.
Infect Immun ; 74(1): 73-80, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16368959

ABSTRACT

Members of the genus Chlamydia are obligate intracellular pathogens that have a unique biphasic developmental cycle and interactions with host cells. Many genes that dictate host infection tropism and, putatively, pathogenic manifestations of disease are clustered in a hypervariable region of the genome termed the plasticity zone (PZ). Comparative genomics studies have determined that an uncharacterized family of PZ genes encoding orthologs of eukaryotic and prokaryotic members of the phospholipase D (PLD) enzyme family varies among chlamydiae. Here, we show that the PZ PLD (pzPLD) of Chlamydia trachomatis are transcribed during both normal and persistent infection and that the corresponding PLD proteins are predominantly localized in reticulate bodies on the inner leaflet of the inclusion membrane. Further, we show that strains of chlamydiae encoding the pzPLD, but not a strain lacking these genes, are inhibited by primary alcohols, potent PLD inhibitors, during growth in HeLa 229 cells. This inhibitory effect is amplified approximately 5,000-fold during recovery from persistent infection. These findings suggest that the chlamydial pzPLD may be important, strain-specific, pathogenesis factors in vivo.


Subject(s)
Alcohols/pharmacology , Chlamydia trachomatis/enzymology , Chlamydia trachomatis/immunology , Complement System Proteins/genetics , Phospholipase D/genetics , Chlamydia Infections/enzymology , Chlamydia Infections/immunology , Chlamydia Infections/microbiology , Chlamydia trachomatis/drug effects , Chlamydia trachomatis/growth & development , HeLa Cells , Humans , Inclusion Bodies/metabolism , Intracellular Membranes/metabolism , Species Specificity
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