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1.
Front Public Health ; 11: 1110903, 2023.
Article in English | MEDLINE | ID: mdl-37383272

ABSTRACT

Background: Streptococcus pneumoniae is the most common bacterium that causes community-acquired pneumonia (CAP) in children. The rate of S. pneumoniae resistance to antibiotics is increasing, particularly in patients with severe CAP. Therefore, the level of antibiotic resistance of S. pneumoniae causing severe CAP in Vietnamese children requires regular monitoring. Methods: This was a cross-sectional descriptive study. Nasopharyngeal aspiration specimens from children were cultured, isolated, and examined for S. pneumoniae. Bacterial strains were assessed for antimicrobial susceptibility, and the minimum inhibitory concentration (MIC) was determined. Results: Eighty-nine strains of S. pneumoniae were isolated from 239 children with severe CAP. The majority of isolates were completely non-susceptible to penicillin (1.1% intermediate, 98.9% resistant) and highly resistant to erythromycin (96.6%) and clarithromycin (88.8%); the rate of resistance to ceftriaxone was 16.9%, with the proportion of intermediate resistance at 46.0%; 100% of strains were susceptible to vancomycin and linezolid. For most antibiotics, MIC50 and MIC90 were equal to the resistance threshold according to the Clinical and Laboratory Standards Institute 2021; penicillin had an eight-fold increase in MIC90 (64 mg/L) and ceftriaxone had a 1.5-fold increase in MIC90 (6 mg/L). Conclusion: Streptococcus pneumoniae isolates described in this study were resistant to many antibiotics. Penicillin should not be the first-line antibiotic of choice, and ceftriaxone at an enhanced dose should be used instead.


Subject(s)
Anti-Bacterial Agents , Drug Resistance, Microbial , Pneumonia, Pneumococcal , Pneumonia , Streptococcus pneumoniae , Child , Humans , Anti-Bacterial Agents/pharmacology , Ceftriaxone , Cross-Sectional Studies , Penicillins , Southeast Asian People , Streptococcus pneumoniae/genetics , Pneumonia, Pneumococcal/drug therapy , Pneumonia, Pneumococcal/genetics , Pneumonia, Pneumococcal/physiopathology , Pneumonia, Pneumococcal/virology
2.
Cells ; 12(6)2023 03 21.
Article in English | MEDLINE | ID: mdl-36980300

ABSTRACT

Community-acquired pneumonia remains a major contributor to global communicable disease-mediated mortality. Neutrophils play a leading role in trying to contain bacterial lung infection, but they also drive detrimental pulmonary inflammation, when dysregulated. Here we aimed at understanding the role of microRNA-223 in orchestrating pulmonary inflammation during pneumococcal pneumonia. Serum microRNA-223 was measured in patients with pneumococcal pneumonia and in healthy subjects. Pulmonary inflammation in wild-type and microRNA-223-knockout mice was assessed in terms of disease course, histopathology, cellular recruitment and evaluation of inflammatory protein and gene signatures following pneumococcal infection. Low levels of serum microRNA-223 correlated with increased disease severity in pneumococcal pneumonia patients. Prolonged neutrophilic influx into the lungs and alveolar spaces was detected in pneumococci-infected microRNA-223-knockout mice, possibly accounting for aggravated histopathology and acute lung injury. Expression of microRNA-223 in wild-type mice was induced by pneumococcal infection in a time-dependent manner in whole lungs and lung neutrophils. Single-cell transcriptome analyses of murine lungs revealed a unique profile of antimicrobial and cellular maturation genes that are dysregulated in neutrophils lacking microRNA-223. Taken together, low levels of microRNA-223 in human pneumonia patient serum were associated with increased disease severity, whilst its absence provoked dysregulation of the neutrophil transcriptome in murine pneumococcal pneumonia.


Subject(s)
MicroRNAs , Pneumonia, Pneumococcal , Animals , Humans , Mice , Inflammation/genetics , Inflammation/microbiology , Inflammation/pathology , Lung/pathology , Mice, Knockout , MicroRNAs/genetics , Pneumonia, Pneumococcal/genetics , Pneumonia, Pneumococcal/microbiology , Pneumonia, Pneumococcal/pathology , Streptococcus pneumoniae
3.
Front Immunol ; 13: 945656, 2022.
Article in English | MEDLINE | ID: mdl-35967431

ABSTRACT

Pneumolysin (PLY) is a bacterial pore forming toxin and primary virulence factor of Streptococcus pneumonia, a major cause of pneumonia. PLY binds cholesterol-rich domains of the endothelial cell (EC) plasma membrane resulting in pore assembly and increased intracellular (IC) Ca2+ levels that compromise endothelial barrier integrity. Caveolae are specialized plasmalemma microdomains of ECs enriched in cholesterol. We hypothesized that the abundance of cholesterol-rich domains in EC plasma membranes confers cellular susceptibility to PLY. Contrary to this hypothesis, we found increased PLY-induced IC Ca2+ following membrane cholesterol depletion. Caveolin-1 (Cav-1) is an essential structural protein of caveolae and its regulation by cholesterol levels suggested a possible role in EC barrier function. Indeed, Cav-1 and its scaffolding domain peptide protected the endothelial barrier from PLY-induced disruption. In loss of function experiments, Cav-1 was knocked-out using CRISPR-Cas9 or silenced in human lung microvascular ECs. Loss of Cav-1 significantly enhanced the ability of PLY to disrupt endothelial barrier integrity. Rescue experiments with re-expression of Cav-1 or its scaffolding domain peptide protected the EC barrier against PLY-induced barrier disruption. Dynamin-2 (DNM2) is known to regulate caveolar membrane endocytosis. Inhibition of endocytosis, with dynamin inhibitors or siDNM2 amplified PLY induced EC barrier dysfunction. These results suggest that Cav-1 protects the endothelial barrier against PLY by promoting endocytosis of damaged membrane, thus reducing calcium entry and PLY-dependent signaling.


Subject(s)
Bacterial Proteins , Caveolin 1 , Lung , Pneumonia, Pneumococcal , Pneumonia , Streptolysins , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Caveolin 1/genetics , Caveolin 1/metabolism , Cholesterol/metabolism , Endothelium, Vascular/metabolism , Humans , Lung/blood supply , Lung/metabolism , Microvessels/metabolism , Pneumonia/genetics , Pneumonia/metabolism , Pneumonia/microbiology , Pneumonia, Pneumococcal/genetics , Pneumonia, Pneumococcal/metabolism , Pneumonia, Pneumococcal/microbiology , Streptococcus pneumoniae/metabolism , Streptococcus pneumoniae/pathogenicity , Streptolysins/genetics , Streptolysins/metabolism , Vascular Diseases/genetics , Vascular Diseases/metabolism , Vascular Diseases/microbiology
4.
Front Immunol ; 12: 723967, 2021.
Article in English | MEDLINE | ID: mdl-34552589

ABSTRACT

Bruton's tyrosine kinase (Btk) is a cytoplasmic kinase expressed in B cells and myeloid cells. It is essential for B cell development and natural antibody-mediated host defense against bacteria in humans and mice, but little is known about the role of Btk in innate host defense in vivo. Previous studies have indicated that lack of (natural) antibodies is paramount for impaired host defense against Streptococcus (S.) pneumoniae in patients and mice with a deficiency in functional Btk. In the present study, we re-examined the role of Btk in B cells and myeloid cells during pneumococcal pneumonia and sepsis in mice. The antibacterial defense of Btk-/- mice was severely impaired during pneumococcal pneumosepsis and restoration of natural antibody production in Btk-/- mice by transgenic expression of Btk specifically in B cells did not suffice to protect against infection. Btk-/- mice with reinforced Btk expression in MhcII+ cells, including B cells, dendritic cells and macrophages, showed improved antibacterial defense as compared to Btk-/- mice. Bacterial outgrowth in Lysmcre-Btkfl/Y mice was unaltered despite a reduced capacity of Btk-deficient alveolar macrophages to respond to pneumococci. Mrp8cre-Btkfl/Y mice with a neutrophil specific paucity in Btk expression, however, demonstrated impaired antibacterial defense. Neutrophils of Mrp8cre-Btkfl/Y mice displayed reduced release of granule content after pulmonary installation of lipoteichoic acid, a gram-positive bacterial cell wall component relevant for pneumococci. Moreover, Btk deficient neutrophils showed impaired degranulation and phagocytosis upon incubation with pneumococci ex vivo. Taken together, the results of our study indicate that besides regulating B cell-mediated immunity, Btk is critical for regulation of myeloid cell-mediated, and particularly neutrophil-mediated, innate host defense against S. pneumoniae in vivo.


Subject(s)
Agammaglobulinaemia Tyrosine Kinase/metabolism , Immunity, Innate , Myeloid Cells/immunology , Pneumonia, Pneumococcal/immunology , Pneumonia, Pneumococcal/metabolism , Sepsis/metabolism , Agammaglobulinaemia Tyrosine Kinase/genetics , Animals , B-Lymphocytes/metabolism , Disease Models, Animal , Female , Humans , Lipopolysaccharides , Lung/pathology , Macrophages, Alveolar/metabolism , Male , Mice , Mice, Inbred C57BL , Phagocytosis , Pneumonia, Pneumococcal/genetics , Signal Transduction , Streptococcus pneumoniae/physiology , Teichoic Acids
5.
Am J Physiol Lung Cell Mol Physiol ; 320(5): L916-L925, 2021 05 01.
Article in English | MEDLINE | ID: mdl-33655757

ABSTRACT

Idiopathic pulmonary fibrosis (IPF) is a deadly condition characterized by progressive respiratory dysfunction. Exacerbations due to airway infections are believed to promote disease progression, and presence of Streptococcus in the lung microbiome has been associated with the progression of IPF and mortality. The aim of this study was to analyze the effect of lung fibrosis on susceptibility to pneumococcal pneumonia and bacteremia. The effects of subclinical (low dose) infection with Streptococcus pneumoniae were studied in a well characterized fos-related antigen-2 (Fra-2) transgenic (TG) mouse model of spontaneous, progressive pulmonary fibrosis. Forty-eight hours after transnasal infection with S. pneumoniae, bacterial load was assessed in lung tissue, bronchoalveolar lavage (BAL), blood, and spleen. Leukocyte subsets and cytokine levels were analyzed in BAL and blood. Lung compliance and arterial blood gases were assessed. In contrast to wildtype mice, low dose lung infection with S. pneumoniae in Fra-2 TG mice resulted in substantial pneumonia including weight loss, increased lung bacterial load, and bacteremia. BAL alveolar macrophages were reduced in Fra-2 TG mice compared to the corresponding WT mice. Proinflammatory cytokines and chemokines (IL-1ß, IL-6, TNF-α, and CXCL1) were elevated upon infection in BAL supernatant and plasma of Fra-2 TG mice. Lung compliance was decreased in Fra-2 TG mice following low dose infection with S. pneumoniae. Pulmonary fibrosis increases susceptibility to pneumococcal pneumonia and bacteremia possibly via impaired alveolar bacterial clearance.


Subject(s)
Fos-Related Antigen-2 , Macrophages, Alveolar , Pneumonia, Pneumococcal , Pulmonary Fibrosis , Streptococcus pneumoniae/metabolism , Animals , Cytokines/genetics , Cytokines/metabolism , Disease Models, Animal , Disease Susceptibility , Fos-Related Antigen-2/genetics , Fos-Related Antigen-2/metabolism , Macrophages, Alveolar/metabolism , Macrophages, Alveolar/microbiology , Macrophages, Alveolar/pathology , Mice , Mice, Transgenic , Pneumonia, Pneumococcal/genetics , Pneumonia, Pneumococcal/metabolism , Pneumonia, Pneumococcal/microbiology , Pneumonia, Pneumococcal/pathology , Pulmonary Fibrosis/genetics , Pulmonary Fibrosis/metabolism , Pulmonary Fibrosis/microbiology , Pulmonary Fibrosis/pathology
6.
Antioxid Redox Signal ; 34(12): 962-978, 2021 04 20.
Article in English | MEDLINE | ID: mdl-32283950

ABSTRACT

Significance:Streptococcus pneumoniae (Spn), a facultative anaerobic Gram-positive human pathogen with increasing rates of penicillin and macrolide resistance, is a major cause of lower respiratory tract infections worldwide. Pneumococci are a primary agent of severe pneumonia in children younger than 5 years and of community-acquired pneumonia in adults. A major defense mechanism toward Spn is the generation of reactive oxygen species, including hydrogen peroxide (H2O2), during the oxidative burst of neutrophils and macrophages. Paradoxically, Spn produces high endogenous levels of H2O2 as a strategy to promote colonization. Recent Advances: Pneumococci, which express neither catalase nor common regulators of peroxide stress resistance, have developed unique mechanisms to protect themselves from H2O2. Spn generates high levels of H2O2 as a strategy to promote colonization. Production of H2O2 moreover constitutes an important virulence phenotype and its cellular activities overlap and complement those of other virulence factors, such as pneumolysin, in modulating host immune responses and promoting organ injury. Critical Issues: This review examines the dual role of H2O2 in pneumococcal pneumonia, from the viewpoint of both the pathogen (defense mechanisms, lytic activity toward competing pathogens, and virulence) and the resulting host-response (inflammasome activation, endoplasmic reticulum stress, and damage to the alveolar-capillary barrier in the lungs). Future Directions: An understanding of the complexity of H2O2-mediated host-pathogen interactions is necessary to develop novel strategies that target these processes to enhance lung function during severe pneumonia.


Subject(s)
Drug Resistance, Bacterial/genetics , Hydrogen Peroxide/metabolism , Pneumonia, Pneumococcal/drug therapy , Streptococcus pneumoniae/metabolism , Bacterial Proteins/genetics , Bacterial Proteins/metabolism , Host-Pathogen Interactions/genetics , Humans , Lung/metabolism , Lung/microbiology , Lung/pathology , Neutrophils/metabolism , Neutrophils/microbiology , Oxidants/metabolism , Pneumonia, Pneumococcal/genetics , Pneumonia, Pneumococcal/microbiology , Pneumonia, Pneumococcal/pathology , Streptococcus pneumoniae/drug effects , Streptococcus pneumoniae/pathogenicity , Streptolysins/genetics , Streptolysins/metabolism
7.
J Immunol ; 205(12): 3390-3399, 2020 12 15.
Article in English | MEDLINE | ID: mdl-33158955

ABSTRACT

Macrophage-inducible C-type lectin (Mincle)-dependent sensing of pathogens triggers proinflammatory immune responses in professional phagocytes that contribute to protecting the host against pathogen invasion. In this study, we examined whether overexpression of Mincle that is designed to improve early pathogen sensing by professional phagocytes would improve lung-protective immunity against Streptococcus pneumoniae in mice. Proteomic profiling of alveolar macrophages of Mincle transgenic (tg) mice stimulated with the Mincle-specific pneumococcal ligand glucosyl-diacylglycerol (Glc-DAG) revealed increased Nlrp3 inflammasome activation and downstream IL-1ß cytokine release that was not observed in Glc-DAG-stimulated Mincle knockout or Nlrp3 knockout macrophages. Along this line, Mincle tg mice also responded with a stronger Nlrp3 expression and early proinflammatory cytokine release after challenge with S. pneumoniae, ultimately leading to fatal pneumonia in the Mincle tg mice. Importantly, Nlrp3 inhibitor treatment of Mincle tg mice significantly mitigated the observed hyperinflammatory response to pneumococcal challenge. Together, we show that overexpression of the pattern recognition receptor Mincle triggers increased Glc-DAG-dependent Nlrp3 inflammasome activation in professional phagocytes leading to fatal pneumococcal pneumonia in mice that is amenable to Nlrp3 inhibitor treatment. These data show that ectopic expression of the Mincle receptor confers increased susceptibility rather than resistance to S. pneumoniae in mice, thus highlighting the importance of an inducible Mincle receptor expression in response to microbial challenge.


Subject(s)
Lectins, C-Type/immunology , Macrophages, Alveolar/immunology , Membrane Proteins/immunology , Pneumonia, Pneumococcal/immunology , Streptococcus pneumoniae/immunology , Animals , Inflammasomes/genetics , Inflammasomes/immunology , Interleukin-1beta/genetics , Interleukin-1beta/immunology , Lectins, C-Type/genetics , Macrophages, Alveolar/pathology , Membrane Proteins/genetics , Mice , Mice, Transgenic , NLR Family, Pyrin Domain-Containing 3 Protein/genetics , NLR Family, Pyrin Domain-Containing 3 Protein/immunology , Pneumonia, Pneumococcal/genetics , Pneumonia, Pneumococcal/pathology
8.
J Clin Invest ; 130(6): 3021-3037, 2020 06 01.
Article in English | MEDLINE | ID: mdl-32364537

ABSTRACT

Patients with respiratory syncytial virus (RSV) infection exhibit enhanced susceptibility to subsequent pneumococcal infections. However, the underlying mechanisms involved in this increased susceptibility remain unclear. Here, we identified potentially novel cellular and molecular cascades triggered by RSV infection to exacerbate secondary pneumococcal pneumonia. RSV infection stimulated the local production of growth arrest-specific 6 (Gas6). The Gas6 receptor Axl was crucial for attenuating pneumococcal immunity in that the Gas6/Axl blockade fully restored antibacterial immunity. Mechanistically, Gas6/Axl interaction regulated the conversion of alveolar macrophages from an antibacterial phenotype to an M2-like phenotype that did not exhibit antibacterial activity, and the attenuation of caspase-1 activation and IL-18 production in response to pneumococcal infection. The attenuated IL-18 production failed to drive both NK cell-mediated IFN-γ production and local NO and TNF-α production, which impair the control of bacterial infection. Hence, the RSV-mediated Gas6/Axl activity attenuates the macrophage-mediated protection against pneumococcal infection. The Gas6/Axl axis could be a potentially novel therapeutic target for RSV-associated secondary bacterial infection.


Subject(s)
Intercellular Signaling Peptides and Proteins/immunology , Macrophages, Alveolar/immunology , Pneumonia, Pneumococcal/immunology , Proto-Oncogene Proteins/immunology , Receptor Protein-Tyrosine Kinases/immunology , Respiratory Syncytial Virus Infections/immunology , Respiratory Syncytial Viruses/immunology , Animals , Cytokines/genetics , Cytokines/immunology , Intercellular Signaling Peptides and Proteins/genetics , Macrophages, Alveolar/microbiology , Macrophages, Alveolar/pathology , Macrophages, Alveolar/virology , Male , Mice , Mice, Knockout , Pneumonia, Pneumococcal/genetics , Pneumonia, Pneumococcal/pathology , Pneumonia, Pneumococcal/virology , Proto-Oncogene Proteins/genetics , Receptor Protein-Tyrosine Kinases/genetics , Respiratory Syncytial Virus Infections/genetics , Respiratory Syncytial Virus Infections/pathology , Axl Receptor Tyrosine Kinase
9.
PLoS Pathog ; 16(4): e1008464, 2020 04.
Article in English | MEDLINE | ID: mdl-32324805

ABSTRACT

Streptococcus pneumoniae is a major human pathogen, causing pneumonia and sepsis. Genetic components strongly influence host responses to pneumococcal infections, but the responsible loci are unknown. We have previously identified a locus on mouse chromosome 7 from a susceptible mouse strain, CBA/Ca, to be crucial for pneumococcal infection. Here we identify a responsible gene, Cd22, which carries a point mutation in the CBA/Ca strain, leading to loss of CD22 on B cells. CBA/Ca mice and gene-targeted CD22-deficient mice on a C57BL/6 background are both similarly susceptible to pneumococcal infection, as shown by bacterial replication in the lungs, high bacteremia and early death. After bacterial infections, CD22-deficient mice had strongly reduced B cell populations in the lung, including GM-CSF producing, IgM secreting innate response activator B cells, which are crucial for protection. This study provides striking evidence that CD22 is crucial for protection during invasive pneumococcal disease.


Subject(s)
B-Lymphocytes/immunology , Pneumococcal Infections/immunology , Sialic Acid Binding Ig-like Lectin 2/immunology , Animals , B-Lymphocytes/microbiology , Bacteremia/genetics , Bacteremia/immunology , Bacteremia/microbiology , Female , Host-Pathogen Interactions , Humans , Male , Mice , Mice, Inbred BALB C , Mice, Inbred C57BL , Mice, Inbred CBA , Pneumococcal Infections/genetics , Pneumococcal Infections/metabolism , Pneumonia, Pneumococcal/genetics , Pneumonia, Pneumococcal/immunology , Pneumonia, Pneumococcal/metabolism , Pneumonia, Pneumococcal/microbiology , Sialic Acid Binding Ig-like Lectin 2/deficiency , Sialic Acid Binding Ig-like Lectin 2/genetics , Streptococcus pneumoniae/pathogenicity
10.
Epidemiology ; 31(2): 259-262, 2020 03.
Article in English | MEDLINE | ID: mdl-31913908

ABSTRACT

Pneumococcal conjugate vaccines target 10 or 13 specific serotypes. To evaluate the overall efficacy of these products, the vaccine-targeted serotypes are typically aggregated into a single group. However, it is often desirable to evaluate variations in effects for different serotypes. These serotype-specific estimates are often based on small counts, resulting in a high degree of uncertainty (i.e., large standard errors and wide confidence intervals). An alternative is to use a hierarchical Bayesian statistical model, which estimates overall effectiveness while simultaneously providing estimates of serotype-specific vaccine effects. These shrunken serotype-specific estimators often have smaller mean squared errors (MSEs) than unbiased versions due to a large decrease in posterior uncertainty. We reanalyzed published data from a randomized controlled trial on the efficacy of 13-valent pneumococcal conjugate vaccine (PCV13) against community-acquired pneumonia caused by vaccine-targeted serotype using a hierarchical model. This model provides a potential framework for obtaining estimates of serotype-specific vaccine effects with reduced MSEs.


Subject(s)
Pneumococcal Vaccines , Pneumonia, Pneumococcal , Serogroup , Bayes Theorem , Humans , Models, Statistical , Pneumococcal Vaccines/therapeutic use , Pneumonia, Pneumococcal/genetics , Pneumonia, Pneumococcal/prevention & control , Randomized Controlled Trials as Topic , Treatment Outcome , Vaccines, Conjugate/therapeutic use
11.
Sci Rep ; 9(1): 19839, 2019 12 27.
Article in English | MEDLINE | ID: mdl-31882693

ABSTRACT

Streptococcus pneumonia, one of the major colonizers in nasopharyngeal adenoids, has been the predominant pathogen causing acute otitis media (AOM) in children. Recent evidence suggests an association between IL-17A-mediated immune response and the clearance of pneumococcal colonization in nasopharyngeal adenoids. Here, we evaluated the expressions of IL-17A and associated genes in hypertrophic adenoid tissues of children with sleep-disordered breathing (SDB) and otitis media with effusion (OME) and their association with pneumococcal carriage. Sixty-six pediatric patients with adenoid hypertrophy were enrolled. During adenoidectomy, nasopharyngeal swab and adenoid tissues were used to determine pneumococcal carriage and IL-17A expression. Our results revealed significantly higher levels of IL-17A and IL-17A:IL-10 mRNA in the SDB patients positive for nasopharyngeal pneumococcal carriage than those negative. However, these differences were not significant in the OME group. These results suggested, in OME patients, prolonged or chronic pneumococcal carriage may occur because of insufficient IL-17A-mediated mucosal clearance, and could further lead to AOM and OME development.


Subject(s)
Adenoids/metabolism , Interleukin-17/genetics , Nasopharynx/metabolism , Otitis Media with Effusion/genetics , Pneumonia, Pneumococcal/genetics , Sleep Apnea Syndromes/genetics , Adenoids/microbiology , Child , Child, Preschool , Female , Gene Expression Regulation , Humans , Hypertrophy , Immunohistochemistry , Interleukin-17/metabolism , Male , Nasopharynx/microbiology , Nasopharynx/pathology , Otitis Media with Effusion/metabolism , Otitis Media with Effusion/microbiology , Pneumonia, Pneumococcal/metabolism , Pneumonia, Pneumococcal/microbiology , Reverse Transcriptase Polymerase Chain Reaction , Sleep Apnea Syndromes/metabolism , Sleep Apnea Syndromes/microbiology , Streptococcus pneumoniae/physiology
12.
PLoS One ; 14(8): e0221133, 2019.
Article in English | MEDLINE | ID: mdl-31415656

ABSTRACT

BACKGROUND: Antimicrobial resistance (AMR) rates may display seasonal variation. However, it is not clear whether this seasonality is influenced by the seasonal variation of infectious diseases, geographical region or differences in antibiotic prescription patterns. Therefore, we assessed the seasonality of AMR rates in respiratory bacteria. METHODS: Seven electronic databases (Embase.com, Medline Ovid, Cochrane CENTRAL, Web of Science, Core Collection, Biosis Ovid, and Google Scholar), were searched for relevant studies from inception to Jun 25th, 2019. Studies describing resistance rates of Streptococcus pneumoniae and Haemophilus influenzae were included in this review. By using random-effects meta-analysis, pooled odd ratios of seasonal AMR rates were calculated using winter as the reference group. Pooled odd ratios were obtained by antibiotic class and geographical region. RESULTS: We included 13 studies, of which 7 were meta-analyzed. Few studies were done in H. influenzae, thus this was not quantitively analyzed. AMR rates of S. pneumoniae to penicillins were lower in other seasons than in winter with pooled OR = 0.71; 95% CI = 0.65-0.77; I2 = 0.0%, and to all antibiotics with pooled OR = 0.68; 95% CI = 0.60-0.76; I2 = 14.4%. Irrespective of geographical region, the seasonality of AMR rates in S. pneumoniae remained the same. CONCLUSION: The seasonality of AMR rates could result from the seasonality of infectious diseases and its accompanied antibiotic use.


Subject(s)
Anti-Bacterial Agents/therapeutic use , Drug Resistance, Bacterial , Haemophilus Infections , Haemophilus influenzae , Pneumonia, Pneumococcal , Seasons , Streptococcus pneumoniae , Drug Resistance, Bacterial/drug effects , Drug Resistance, Bacterial/genetics , Haemophilus Infections/genetics , Haemophilus Infections/metabolism , Haemophilus Infections/pathology , Haemophilus influenzae/genetics , Haemophilus influenzae/metabolism , Humans , Pneumonia, Pneumococcal/drug therapy , Pneumonia, Pneumococcal/genetics , Pneumonia, Pneumococcal/metabolism , Respiratory System/microbiology , Streptococcus pneumoniae/genetics , Streptococcus pneumoniae/metabolism
13.
Thromb Haemost ; 119(6): 930-940, 2019 Jun.
Article in English | MEDLINE | ID: mdl-30873567

ABSTRACT

Platelet Bruton's tyrosine kinase (Btk) is an essential signalling protein for the collagen receptor glycoprotein VI (GPVI) and podoplanin receptor C-type-lectin-like receptor-2, which are platelet receptors implicated in the maintenance of vascular integrity during inflammation. Moreover, platelets, platelet GPVI and Btk are important for host defence during murine bacterial pneumosepsis. The aim of this study was to determine the role of platelet Btk in vascular integrity and host defence during murine pneumosepsis caused by the common human pathogens Streptococcus pneumoniae and Klebsiella pneumoniae. Using the Cre-loxP system, male platelet-specific Btk-deficient mice (PF4creBtkfl/Y) were created. Similar to platelets from total Btk-deficient mice, platelets from PF4creBtkfl/Y mice showed abrogated aggregation and P-selectin expression when stimulated with the GPVI ligand cross-linked collagen-related peptide. Upon infection with S. pneumoniae, PF4creBtkfl/Y mice showed increased lung bleeding, but unimpaired anti-bacterial defence. During pneumosepsis evoked by K. pneumoniae, platelet Btk deficiency was not associated with lung bleeding and did not impact on host defence, even when platelet function was further compromised by blocking secondary platelet activation by the P2Y12 receptor antagonist clopidogrel. Together, these data indicate that, while platelet Btk is not important for anti-bacterial defence in pneumosepsis, its role in maintaining vascular integrity in the lung depends on the causative pathogen.


Subject(s)
Agammaglobulinaemia Tyrosine Kinase/metabolism , Blood Platelets/physiology , Klebsiella pneumoniae/physiology , Lung/pathology , Pneumonia, Pneumococcal/metabolism , Sepsis/metabolism , Streptococcus pneumoniae/physiology , Agammaglobulinaemia Tyrosine Kinase/genetics , Animals , Disease Models, Animal , Hemorrhage , Humans , Immunity , Lung/blood supply , Male , Membrane Glycoproteins/metabolism , Mice , Mice, Knockout , Platelet Aggregation/genetics , Platelet Membrane Glycoproteins/metabolism , Pneumonia, Pneumococcal/genetics , Regional Blood Flow , Signal Transduction
14.
Sci Rep ; 9(1): 3324, 2019 03 01.
Article in English | MEDLINE | ID: mdl-30824811

ABSTRACT

Streptococcus pneumoniae (pneumococcus) is the most common respiratory pathogen worldwide. Nasopharyngeal carriage with S. pneumoniae is the major source of lower respiratory tract infection and horizontal spread among children. Investigating nasopharyngeal S. pneumoniae is crucial for clinicians to control pneumococcus disease. Here, we retrospectively analyzed clinical information of 5,960 hospitalized children, focusing on pneumonia children less than five years with positive nasopharyngeal pneumococcal cultures. Nasopharyngeal aspirates (NPAs) were collected between June 2009 and December 2016, which were outside the pneumococcal conjugate vaccine(PCV) period. NPAs were subjected to common bacterial culture and antibiotic susceptibility tests, and serotypes were identified by both multiplex PCR and DNA sequencing. Results clearly revealed that clinical manifestations of the children whose NPAs were S. pneumoniae culture positive were serious, especially in those less than twelve months old. Fifteen different serotypes of nasopharyngeal S. pneumoniae were detected, the most common ones being 19F (35.2%), 6A/B (23.8%), 19A (11.4%), 15B/C (9.3%) and 23F (7.8%). Eight serotypes, accounting for 85.5% of the isolates, corresponded to the PCV13 serotypes. Approximately one-third of all S. pneumoniae strains were susceptible to penicillin. Overall, we consider nasopharyngeal S. pneumoniae culture is beneficial in assessing the situations of pneumonia children. Moreover, PCV13 could be useful in preventing pneumococcal disease in Chongqing, China.


Subject(s)
Nasopharynx/microbiology , Pneumonia, Pneumococcal , Streptococcus pneumoniae , Child, Preschool , China/epidemiology , Female , Humans , Infant , Infant, Newborn , Male , Microbial Sensitivity Tests , Pneumonia, Pneumococcal/epidemiology , Pneumonia, Pneumococcal/genetics , Pneumonia, Pneumococcal/microbiology , Streptococcus pneumoniae/classification , Streptococcus pneumoniae/genetics , Streptococcus pneumoniae/isolation & purification
15.
Eur Cytokine Netw ; 30(4): 123-129, 2019 Dec 01.
Article in English | MEDLINE | ID: mdl-32096473

ABSTRACT

INTRODUCTION: Common Variable Immunodeficiency (CVID) is the most common symptomatic form of primary immunodeficiencies. Current research data show altered B cells, TLRs, and cytokine profile in CVID patients. The aim of this study was to determine levels of IL-1ß and IL-6 in CVID patients in response to TLRs stimulation and the association of these cytokines with subtypes of B cells and response to Pneumovax-23 vaccination. METHOD: Peripheral blood mononuclear cells of CIVD patients were stimulated with and without TLR2 and TLR4 agonist and specific inhibitors including lipopolysaccharide (LPS), lipoteichoic (LTA), and OxPAPC. The levels of IL-1ß and IL-6 were assessed by ELISA in different treatment groups. Finally, association of cytokines levels was assessed among different subtypes of B cells and types of response to Pneumovax-23 vaccine. RESULTS: Secretion of IL-6 and IL-1ß was significantly diminished in CVID patients (p = 0.015 and p = 0.019), but ligand engagement of TLR2 and TLR4 leads to significant increase in IL-6 and IL-1ß production. IL-6 was significantly lower in Pneumovax-23 hypo responder patients (p = 0.05) and significant correlations between the concentration of IL-6 and the number of switched memory and CD21low expressing B cells were found. CONCLUSION: Secretion of IL-6 and IL-1ß is abolished in CVID patients. However, TLR2 and TLR4 are hyper responsive to stimulation with their cognate ligands resulting in the secretion of higher levels of proinflammatory cytokines. This characteristic of CVID TLRs leads to an improvement of cytokine secretion compared to baseline levels. Also, our novel findings about the association concentrations of serum IL-6 and the frequency of with switched memory and CD21low expressing B cells as well as the poor response to Pneumovax-23 should be substantiated by the use of a higher sample size in future studies.


Subject(s)
B-Lymphocyte Subsets/immunology , Common Variable Immunodeficiency/immunology , Gene Expression/drug effects , Interleukin-1beta/immunology , Pneumococcal Vaccines/administration & dosage , Pneumonia, Pneumococcal/prevention & control , Adolescent , Adult , B-Lymphocyte Subsets/drug effects , Case-Control Studies , Common Variable Immunodeficiency/genetics , Common Variable Immunodeficiency/pathology , Female , Gene Expression/immunology , Humans , Interleukin-1beta/genetics , Interleukin-6/genetics , Interleukin-6/immunology , Lipopolysaccharides/pharmacology , Lymphocyte Activation/drug effects , Male , Phosphatidylcholines/pharmacology , Pneumonia, Pneumococcal/genetics , Pneumonia, Pneumococcal/immunology , Pneumonia, Pneumococcal/microbiology , Primary Cell Culture , Streptococcus pneumoniae/immunology , Teichoic Acids/pharmacology , Toll-Like Receptor 2/agonists , Toll-Like Receptor 2/genetics , Toll-Like Receptor 2/immunology , Toll-Like Receptor 4/agonists , Toll-Like Receptor 4/genetics , Toll-Like Receptor 4/immunology , Vaccination/methods
16.
Am J Physiol Lung Cell Mol Physiol ; 315(1): L78-L86, 2018 07 01.
Article in English | MEDLINE | ID: mdl-29565180

ABSTRACT

Leptin is a pleiotropic hormone produced by white adipose tissue that regulates appetite and many physiological functions, including the immune response to infection. Genetic leptin deficiency in humans and mice impairs host defenses against respiratory tract infections. Since leptin deficiency is associated with obesity and other metabolic abnormalities, we generated mice that lack the leptin receptor (LepRb) in cells of the myeloid linage (LysM-LepRb-KO) to evaluate its impact in lean metabolically normal mice in a murine model of pneumococcal pneumonia. We observed higher lung and spleen bacterial burdens in LysM-LepRb-KO mice following an intratracheal challenge with Streptococcus pneumoniae. Although numbers of leukocytes recovered from bronchoalveolar lavage fluid did not differ between groups, we did observe higher levels of pulmonary IL-13 and TNFα in LysM-LepRb-KO mice 48 h post infection. Phagocytosis and killing of ingested S. pneumoniae were also impaired in alveolar macrophages (AMs) from LysM-LepRb-KO mice in vitro and were associated with reduced LTB4 and enhanced PGE2 synthesis in vitro. Pretreatment of AMs with LTB4 and the cyclooxygenase inhibitor, indomethacin, restored phagocytosis but not bacterial killing in vitro. These results confirm our previous observations in leptin-deficient ( ob/ob) and fasted mice and demonstrate that decreased leptin action, as opposed to metabolic irregularities associated with obesity or starvation, is responsible for the defective host defense against pneumococcal pneumonia. They also provide novel targets for therapeutic intervention in humans with bacterial pneumonia.


Subject(s)
Lung/immunology , Macrophages/immunology , Phagocytosis , Pneumonia, Pneumococcal/immunology , Receptors, Leptin/immunology , Streptococcus pneumoniae/immunology , Animals , Interleukin-13/genetics , Interleukin-13/immunology , Lung/microbiology , Lung/pathology , Macrophages/microbiology , Macrophages/pathology , Mice , Mice, Knockout , Pneumonia, Pneumococcal/genetics , Pneumonia, Pneumococcal/pathology , Receptors, Leptin/genetics , Tumor Necrosis Factor-alpha/genetics , Tumor Necrosis Factor-alpha/immunology
17.
PLoS One ; 13(3): e0194202, 2018.
Article in English | MEDLINE | ID: mdl-29518136

ABSTRACT

Streptococcus pneumoniae is a leading cause of pneumonia and a significant economic burden. Antibiotic-resistant S. pneumoniae has become more prevalent in recent years and many pneumonia cases are caused by S. pneumoniae that is resistant to at least one antibiotic. The ubiquitin ligase natural killer lytic-associated molecule (NKLAM/RNF19b) plays a role in innate immunity and studies using NKLAM-knockout (NKLAM-KO) macrophages have demonstrated that NKLAM positively affects the transcriptional activity of STAT1. Using an inhalation infection model, we found that NKLAM-KO mice had a significantly higher lung bacterial load than WT mice but had less lung inflammation. Coincidently, NKLAM-KO mice had fewer neutrophils and NK cells in their lungs. NKLAM-KO mice also expressed less iNOS in their lungs as well as less MCP-1, MIP1α, TNFα, IL-12, and IFNγ. Both neutrophils and macrophages from NKLAM-KO mice were defective in killing S. pneumoniae as compared to wild type cells (WT). The phosphorylation of STAT1 and STAT3 in NKLAM-KO lungs was lower than in WT lungs at 24 hours post-infection. NKLAM-KO mice were afforded some protection against a lethal dose of S. pneumoniae compared to WT mice. In summary, our novel data demonstrate a role for E3 ubiquitin ligase NKLAM in modulating innate immunity via the positive regulation of inflammatory cytokine expression and bactericidal activity.


Subject(s)
Immunity, Innate , Macrophages/immunology , Membrane Proteins/deficiency , Pneumonia, Pneumococcal/immunology , Streptococcus pneumoniae/immunology , Animals , Cytokines/genetics , Cytokines/immunology , Disease Models, Animal , Gene Expression Regulation/immunology , Macrophages/microbiology , Macrophages/pathology , Membrane Proteins/immunology , Mice , Mice, Knockout , Pneumonia, Pneumococcal/genetics , STAT1 Transcription Factor/genetics , STAT1 Transcription Factor/immunology , STAT3 Transcription Factor/genetics , STAT3 Transcription Factor/immunology
18.
J Allergy Clin Immunol ; 139(4): 1293-1301.e4, 2017 Apr.
Article in English | MEDLINE | ID: mdl-27609654

ABSTRACT

BACKGROUND: The B-cell receptor transmembrane activator and calcium modulator ligand interactor (TACI) is important for T-independent antibody responses. One in 200 blood donors are heterozygous for the TACI A181E mutation. OBJECTIVE: We sought to investigate the effect on B-cell function of TACI A181E heterozygosity in reportedly healthy subjects and of the corresponding TACI A144E mutation in mice. METHODS: Nuclear factor κB (NF-κB) activation was measured by using the luciferase assay in 293T cells cotransfected with wild-type and mutant TACI. TACI-driven proliferation, isotype switching, and antibody responses were measured in B cells from heterozygous TACI A144E knock-in mice. Mouse mortality was monitored after intranasal pneumococcal challenge. RESULTS: Levels of natural antibodies to the pneumococcal polysaccharide component phosphocholine were significantly lower in A181E-heterozygous than TACI-sufficient Swedish blood donors never immunized with pneumococcal antigens. Although overexpressed hTACI A181E and mTACI A144E acted as dominant-negative mutations in transfectants, homozygosity for A144E in mice resulted in absent TACI expression in B cells, indicating that the mutant protein is unstable when naturally expressed. A144E heterozygous mice, such as TACI+/- mice, expressed half the normal level of TACI on their B cells and exhibited similar defects in a proliferation-inducing ligand-driven B-cell activation, antibody responses to TNP-Ficoll, production of natural antibodies to phosphocholine, and survival after intranasal pneumococcal challenge. CONCLUSION: These results suggest that TACI A181E heterozygosity results in TACI haploinsufficiency with increased susceptibility to pneumococcal infection. This has important implications for asymptomatic TACI A181E carriers.


Subject(s)
Pneumonia, Pneumococcal/genetics , Transmembrane Activator and CAML Interactor Protein/genetics , Animals , Enzyme-Linked Immunosorbent Assay , Female , Flow Cytometry , Gene Knock-In Techniques , HEK293 Cells , Haploinsufficiency , Heterozygote , Humans , Lymphocyte Activation/immunology , Male , Mice , Mice, Inbred C57BL , Pneumonia, Pneumococcal/immunology , Polymerase Chain Reaction , Transmembrane Activator and CAML Interactor Protein/immunology
19.
Future Microbiol ; 11: 1167-77, 2016 09.
Article in English | MEDLINE | ID: mdl-27546231

ABSTRACT

AIM: To evaluate efficacy of sublingual flagellin to treat acute pneumonia. MATERIALS & METHODS: Mice were treated sublingually with flagellin and challenged intranasally with a lethal dose of pneumococcus. Flagellins lacking TLR5 or NLRC4 activation domains were used to assess their contribution to protection. RESULTS: Sublingual flagellin protected mice in a TLR5-dependent, NLRC4-independent fashion. Neutrophils were required for protection. Flagellin-stimulated lung epithelial cells recapitulated the lung's transcriptional profile suggesting they could be targeted by flagellin in vivo. CONCLUSION: Ligation of TLR5, a pathogen recognition receptor not naturally engaged by pneumococcus, protects mice from invasive pneumonia when administered via sublingual route. This can be a highly cost-effective alternative therapy against pneumonia.


Subject(s)
Bacterial Proteins/immunology , CARD Signaling Adaptor Proteins/immunology , Calcium-Binding Proteins/immunology , Flagellin/immunology , Pneumonia, Pneumococcal/immunology , Pneumonia, Pneumococcal/prevention & control , Streptococcus pneumoniae/immunology , Toll-Like Receptor 5/immunology , Administration, Sublingual , Animals , Bacterial Proteins/administration & dosage , Bacterial Proteins/chemistry , Bacterial Proteins/genetics , Bacterial Vaccines/administration & dosage , Bacterial Vaccines/chemistry , Bacterial Vaccines/genetics , Bacterial Vaccines/immunology , CARD Signaling Adaptor Proteins/genetics , Calcium-Binding Proteins/genetics , Female , Flagellin/administration & dosage , Flagellin/chemistry , Flagellin/genetics , Humans , Lung/immunology , Lung/microbiology , Mice , Mice, Inbred BALB C , Neutrophils/immunology , Pneumonia, Pneumococcal/genetics , Pneumonia, Pneumococcal/microbiology , Protein Domains , Streptococcus pneumoniae/genetics , Toll-Like Receptor 5/genetics
20.
Sci Rep ; 6: 26964, 2016 06 01.
Article in English | MEDLINE | ID: mdl-27247105

ABSTRACT

Streptococcus pneumoniae is the most common bacterial etiology of pneumococcal pneumonia in adults worldwide. Genomic plasticity, antibiotic resistance and extreme capsular antigenic variation complicates the design of effective therapeutic strategies. Polyamines are ubiquitous small cationic molecules necessary for full expression of pneumococcal virulence. Polyamine transport system is an attractive therapeutic target as it is highly conserved across pneumococcal serotypes. In this study, we compared an isogenic deletion strain of S. pneumoniae TIGR4 in polyamine transport operon (ΔpotABCD) with the wild type in a mouse model of pneumococcal pneumonia. Our results show that the wild type persists in mouse lung 24 h post infection while the mutant strain is cleared by host defense mechanisms. We show that intact potABCD is required for survival in the host by providing resistance to neutrophil killing. Comparative proteomics analysis of murine lungs infected with wild type and ΔpotABCD pneumococci identified expression of proteins that could confer protection to wild type strain and help establish infection. We identified ERM complex, PGLYRP1, PTPRC/CD45 and POSTN as new players in the pathogenesis of pneumococcal pneumonia. Additionally, we found that deficiency of polyamine transport leads to up regulation of the polyamine synthesis genes speE and cad in vitro.


Subject(s)
Bacterial Proteins/genetics , Carrier Proteins/genetics , Immune Evasion , Neutrophils/immunology , Pneumonia, Pneumococcal/genetics , Polyamines/metabolism , Streptococcus pneumoniae/metabolism , Animals , Bacterial Proteins/metabolism , Biological Transport , Carrier Proteins/metabolism , Cell Adhesion Molecules/genetics , Cell Adhesion Molecules/immunology , Cytokines/genetics , Cytokines/immunology , DNA-Binding Proteins/genetics , DNA-Binding Proteins/immunology , Gene Expression Regulation , Immunity, Innate , Leukocyte Common Antigens/genetics , Leukocyte Common Antigens/immunology , Lung/immunology , Lung/microbiology , Mice , Mice, Inbred C57BL , Neutrophils/microbiology , Operon , Pneumonia, Pneumococcal/immunology , Pneumonia, Pneumococcal/microbiology , Streptococcus pneumoniae/genetics , Streptococcus pneumoniae/pathogenicity , Transcription Factors/genetics , Transcription Factors/immunology
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