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Limited Interactions between Streptococcus Suis and Haemophilus Parasuis in In Vitro Co-Infection Studies
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What this work says
Outgoing claims: the papers this work cites, builds on, or argues with.
inferredcites →https://doi.org/10.1002/1873-3468.12364openalex-snapshot
Initial steps of the pathogenesis of the infection caused by Streptococcus suis : fighting against nonspecific defenses
inferredcites →https://doi.org/10.1016/j.micpath.2008.10.008openalex-snapshot
Studies on the interactions of Haemophilus parasuis with porcine epithelial tracheal cells: Limited role of LOS in apoptosis and pro-inflammatory cytokine release
inferredcites →https://doi.org/10.1016/j.molimm.2015.02.016openalex-snapshot
Haemophilus parasuis induces activation of NF-κB and MAP kinase signaling pathways mediated by toll-like receptors
inferredcites →https://doi.org/10.1016/j.molimm.2015.06.029openalex-snapshot
Haemophilus parasuis infection activates chemokine RANTES in PK-15 cells
inferredcites →https://doi.org/10.1016/j.rvsc.2011.07.006openalex-snapshot
Cloning, expression and characterization of a cell wall surface protein, 6-phosphogluconate dehydrogenase, of Haemophilus parasuis
inferredcites →https://doi.org/10.1016/j.tim.2017.02.005openalex-snapshot
Critical Streptococcus suis Virulence Factors: Are They All Really Critical?
inferredcites →https://doi.org/10.1016/j.tvjl.2013.08.027openalex-snapshot
Advances in the quest for virulence factors of Haemophilus parasuis
inferredcites →https://doi.org/10.1016/j.vetmic.2003.12.001openalex-snapshot
Haemophilus parasuis: new trends on diagnosis, epidemiology and control
inferredcites →https://doi.org/10.1016/j.vetmic.2009.07.031openalex-snapshot
Involvement of NF-κB and MAP-kinases in the transcriptional response of alveolar macrophages to Streptococcus suis
inferredcites →https://doi.org/10.1016/j.vetmic.2011.07.022openalex-snapshot
Haemophilus parasuis serovar 5 Nagasaki strain adheres and invades PK-15 cells
inferredcites →https://doi.org/10.1016/j.vetmic.2013.07.028openalex-snapshot
Genetic diversity of Haemophilus parasuis from sick and healthy pigs
inferredcites →https://doi.org/10.1016/j.vetmic.2013.09.010openalex-snapshot
Subcytolytic effects of suilysin on interaction of Streptococcus suis with epithelial cells
inferredcites →https://doi.org/10.1016/s0166-0934(02)00236-7openalex-snapshot
Establishment and characterization of two new pig cell lines for use in virological diagnostic laboratories
inferredcites →https://doi.org/10.1017/s1466252307001247openalex-snapshot
Streptococcus suisinfections in humans: the Chinese experience and the situation in North America
inferredcites →https://doi.org/10.1038/emi.2014.45openalex-snapshot
Streptococcus suis , an important pig pathogen and emerging zoonotic agent—an update on the worldwide distribution based on serotyping and sequence typing
inferredcites →https://doi.org/10.1051/vetres/2009007openalex-snapshot
Differences in phagocytosis susceptibility inHaemophilus parasuisstrains
inferredcites →https://doi.org/10.1099/jgv.0.000223openalex-snapshot
Sialic acid-dependent interactions between influenza viruses and Streptococcus suis affect the infection of porcine tracheal cells
inferredcites →https://doi.org/10.1099/mic.0.037960-0openalex-snapshot
ApuA, a multifunctional α-glucan-degrading enzyme of Streptococcus suis, mediates adhesion to porcine epithelium and mucus
inferredcites →https://doi.org/10.1128/iai.00056-13openalex-snapshot
Changes in Macrophage Phenotype after Infection of Pigs with Haemophilus parasuis Strains with Different Levels of Virulence
inferredcites →https://doi.org/10.1128/iai.00297-08openalex-snapshot
Host-Pathogen Interactions ofActinobacillus pleuropneumoniaewith Porcine Lung and Tracheal Epithelial Cells
inferredcites →https://doi.org/10.1128/iai.00818-13openalex-snapshot
Capsular Sialic Acid of Streptococcus suis Serotype 2 Binds to Swine Influenza Virus and Enhances Bacterial Interactions with Virus-Infected Tracheal Epithelial Cells
inferredcites →https://doi.org/10.1128/iai.05734-11openalex-snapshot
Streptococcus suis Capsular Polysaccharide Inhibits Phagocytosis through Destabilization of Lipid Microdomains and Prevents Lactosylceramide-Dependent Recognition
inferredcites →https://doi.org/10.1128/iai.72.3.1441-1449.2004openalex-snapshot
Invasion of Porcine Brain Microvascular Endothelial Cells by Streptococcus suis Serotype 2
inferredcites →https://doi.org/10.1128/jcm.23.6.1022-1025.1986openalex-snapshot
Some antigenic properties of Haemophilus parasuis and a proposal for serological classification
inferredcites →https://doi.org/10.1139/o09-170openalex-snapshot
Structure determination of Streptococcus suis serotype 2 capsular polysaccharide
inferredcites →https://doi.org/10.1186/1297-9716-42-72openalex-snapshot
Characterization of porcine dendritic cell response to Streptococcus suis
inferredcites →https://doi.org/10.1186/1746-6148-10-86openalex-snapshot
Transcriptional approach to study porcine tracheal epithelial cells individually or dually infected with swine influenza virus and Streptococcus suis
inferredcites →https://doi.org/10.1186/s12917-017-1041-4openalex-snapshot
A robust PCR for the differentiation of potential virulent strains of Haemophilus parasuis
inferredcites →https://doi.org/10.1186/s13104-015-1581-2openalex-snapshot
Interactions of Streptococcus suis serotype 2 with human meningeal cells and astrocytes
inferredcites →https://doi.org/10.1186/s13567-017-0417-6openalex-snapshot
Genotyping and investigating capsular polysaccharide synthesis gene loci of non-serotypeable Streptococcus suis isolated from diseased pigs in Canada
inferredcites →https://doi.org/10.1371/journal.pone.0006072openalex-snapshot
Rapid Evolution of Virulence and Drug Resistance in the Emerging Zoonotic Pathogen Streptococcus suis
inferredcites →https://doi.org/10.1371/journal.pone.0044746openalex-snapshot
Immune Receptors Involved in Streptococcus suis Recognition by Dendritic Cells
inferredcites →https://doi.org/10.1371/journal.pone.0149132openalex-snapshot
Characterization and Vaccine Potential of Outer Membrane Vesicles Produced by Haemophilus parasuis
inferredcites →https://doi.org/10.1371/journal.pone.0150908openalex-snapshot
Population Structure and Antimicrobial Resistance Profiles of Streptococcus suis Serotype 2 Sequence Type 25 Strains
inferredcites →https://doi.org/10.1371/journal.pone.0168903openalex-snapshot
Characterization of Chinese Haemophilus parasuis Isolates by Traditional Serotyping and Molecular Serotyping Methods
inferredcites →https://doi.org/10.2217/fmb-2016-0028openalex-snapshot
Biological Activities of Suilysin: Role in Streptococcus Suis Pathogenesis
inferredcites →https://doi.org/10.2217/fmb.11.149openalex-snapshot
Virulence Factors Involved in the Pathogenesis of the Infection Caused by the Swine Pathogen and Zoonotic Agent Streptococcus Suis
inferredcites →https://doi.org/10.3201/eid1712.110609openalex-snapshot
Lineage and Virulence ofStreptococcus suisSerotype 2 Isolates from North America
inferredcites →https://doi.org/10.3390/pathogens5030045openalex-snapshot
Current Taxonomical Situation of Streptococcus suis
inferredcites →https://doi.org/10.3390/pathogens5030048openalex-snapshot
Virulence Studies of Different Sequence Types and Geographical Origins of Streptococcus suis Serotype 2 in a Mouse Model of Infection
What points at this work
Incoming claims: where this work appears in other papers’ reference lists and arguments.
inferred← citeshttps://doi.org/10.1002/aro2.37openalex-snapshot
The establishment and application of a one‐step multiplex real‐time polymerase chain reaction assay for the detection of Streptococcus suis, Streptococcus suis serotype 2, and Glaesserella parasuis
inferred← citeshttps://doi.org/10.1002/vetr.3056openalex-snapshot
Risk factors associated with Streptococcus suis cases on pig farms in Spain
inferred← citeshttps://doi.org/10.1007/s12602-021-09887-0openalex-snapshot
Identification and Characterization of a Two-Peptide Class IIb Bacteriocin in Streptococcus pluranimalium Isolated from the Nasal Cavity of a Healthy Pig
inferred← citeshttps://doi.org/10.1016/j.prevetmed.2024.106237openalex-snapshot
The use of oral fluids and sock samples for monitoring key pathogens in pig populations for surveillance purposes
inferred← citeshttps://doi.org/10.1016/j.tvjl.2026.106664openalex-snapshot
Large-scale landscape of porcine respiratory disease complex–associated pathogens in Spanish swine production
inferred← citeshttps://doi.org/10.1016/s2095-3119(21)63644-4openalex-snapshot
Construction of a telomerase-immortalized porcine tracheal epithelial cell model for swine-origin mycoplasma infection
inferred← citeshttps://doi.org/10.1099/mgen.0.001334openalex-snapshot
Streptococcus suis infection on European farms is associated with an altered tonsil microbiome and resistome
inferred← citeshttps://doi.org/10.1128/9781683670131.ch64openalex-snapshot
Immunology ofMycobacterium tuberculosisInfections
inferred← citeshttps://doi.org/10.1128/iai.00366-25openalex-snapshot
Mono- and co-infections of primary porcine respiratory cells with Bordetella bronchiseptica and Streptococcus suis are not affected by the dermonecrotic toxin
inferred← citeshttps://doi.org/10.1186/s12866-020-02071-4openalex-snapshot
Interaction study of Pasteurella multocida with culturable aerobic bacteria isolated from porcine respiratory tracts using coculture in conditioned media
inferred← citeshttps://doi.org/10.1186/s13567-021-00918-wopenalex-snapshot
Review of the speculative role of co-infections in Streptococcus suis-associated diseases in pigs
inferred← citeshttps://doi.org/10.1186/s13567-026-01745-7openalex-snapshot
Lack of significant impact of deoxynivalenol (DON) on both swine dendritic cell activities and systemic infection caused by a virulent Streptococcus suis serotype 2 strain
inferred← citeshttps://doi.org/10.1292/jvms.21-0298openalex-snapshot
Application of mouse model for evaluation of recombinant LpxC and GmhA as novel antigenic vaccine candidates of Glaesserella parasuis serotype 13
inferred← citeshttps://doi.org/10.18174/582380openalex-snapshot
The piglet tonsillar microbiome and Streptococcus suis disease
inferred← citeshttps://doi.org/10.21203/rs.3.rs-2045020/v1openalex-snapshot
Risk factors associated to Streptococcus suis cases in swine farms in Spain
inferred← citeshttps://doi.org/10.21203/rs.3.rs-5042914/v1openalex-snapshot
Development and Application of Fluorescent and Lateral Flow Strip Recombinase-aided Amplification for rapid detection of Glasserella parasuis
inferred← citeshttps://doi.org/10.3390/ani13091511openalex-snapshot
Modeling Co-Infection by Streptococcus suis and Haemophilus parasuis Reveals Influences on Biofilm Formation and Host Response
inferred← citeshttps://doi.org/10.3390/genes15030359openalex-snapshot
Transcriptome Analysis of miRNA and mRNA in Porcine Skeletal Muscle following Glaesserella parasuis Challenge
inferred← citeshttps://doi.org/10.3390/ijms19051307openalex-snapshot
Baicalin Inhibits Haemophilus Parasuis-Induced High-Mobility Group Box 1 Release during Inflammation
inferred← citeshttps://doi.org/10.3390/microorganisms11010160openalex-snapshot
Interaction between Porcine Alveolar Macrophage-Tang Cells and Streptococcus suis Strains of Different Virulence: Phagocytosis and Apoptosis
inferred← citeshttps://doi.org/10.3390/pathogens11070721openalex-snapshot
Temporal Patterns of Phenotypic Antimicrobial Resistance and Coinfecting Pathogens in Glaesserella parasuis Strains Isolated from Diseased Swine in Germany from 2006 to 2021
inferred← citeshttps://doi.org/10.3390/pathogens12040541openalex-snapshot
Role of Metabolic Adaptation of Streptococcus suis to Host Niches in Bacterial Fitness and Virulence
inferred← citeshttps://doi.org/10.3390/pathogens12070866openalex-snapshot
Interactions of Mycoplasma hyopneumoniae and/or Mycoplasma hyorhinis with Streptococcus suis Serotype 2 Using In Vitro Co-Infection Models with Swine Cells
inferred← citeshttps://doi.org/10.3390/vetsci12080750openalex-snapshot
Development and Application of Fluorescent and Lateral Flow Dipstick Recombinase-Aided Amplification for Rapid Detection of Glaesserella parasuis
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