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Streptococcus agalactiae glyceraldehyde-3-phosphate dehydrogenase (GAPDH) elicits multiple cytokines from human cells and has a minor effect on bacterial persistence in the murine female reproductive tract
- Source :
- Virulence, Vol 12, Iss 1, Pp 3015-3027 (2021), Virulence, article-version (VoR) Version of Record
- Publication Year :
- 2021
- Publisher :
- Taylor & Francis, 2021.
-
Abstract
- Streptococcus agalactiae glyceraldehyde 3-phosphate dehydrogenase (GAPDH), encoded by gapC, is a glycolytic enzyme that is associated with virulence and immune-mediated protection. However, the role of GAPDH in cellular cytokine responses to S. agalactiae, bacterial phagocytosis and colonization of the female reproductive tract, a central host niche, is unknown. We expressed and studied purified recombinant GAPDH (rGAPDH) of S. agalactiae in cytokine elicitation assays with human monocyte-derived macrophage, epithelial cell, and polymorphonuclear leukocyte (PMN) co-culture infection models. We also generated a S. agalactiae mutant that over-expresses GAPDH (oeGAPDH) from gapC using a constitutively active promoter, and analysed the mutant in murine macrophage antibiotic protection assays and in virulence assays in vivo, using a colonization model that is based on experimental infection of the reproductive tract in female mice. Human cell co-cultures produced interleukin (IL)-1β, IL-6, macrophage inflammatory protein (MIP)-1, tumour necrosis factor (TNF)-α and IL-10 within 24 h of exposure to rGAPDH. PMNs were required for several of these cytokine responses. However, over-expression of GAPDH in S. agalactiae did not significantly affect measures of phagocytic uptake compared to an empty vector control. In contrast, oeGAPDH-S. agalactiae showed a small but statistically significant attenuation for persistence in the reproductive tract of female mice during the chronic phase of infection (10-28 days post-inoculation), relative to the vector control. We conclude that S. agalactiae GAPDH elicits production of multiple cytokines from human cells, and over-expression of GAPDH renders the bacterium more susceptible to host clearance in the female reproductive tract. One-sentence summary: This study shows Streptococcus agalactiae glyceraldehyde 3-phosphate dehydrogenase, an enzyme that functions in glycolysis, gluconeogenesis and virulence, modifies phagocytosis outcomes, including cytokine synthesis, and effects bacterial persistence in the female reproductive tract.
- Subjects :
- Microbiology (medical)
host-microbe interaction
Phagocytosis
medicine.medical_treatment
Immunology
Virulence
Infectious and parasitic diseases
RC109-216
medicine.disease_cause
Microbiology
Mice
stomatognathic system
medicine
cytokine
Animals
Humans
Immunologic Factors
Macrophage inflammatory protein
Glyceraldehyde 3-phosphate dehydrogenase
glyceraldehyde-3-phosphate dehydrogenase
Innate immune system
biology
pathogenesis
Glyceraldehyde-3-Phosphate Dehydrogenases
Infectious Diseases
Cytokine
Streptococcus agalactiae
biology.protein
innate immune response
Cytokines
Parasitology
Tumor necrosis factor alpha
Female
streptococcus agalactiae
Research Article
Research Paper
Subjects
Details
- Database :
- OpenAIRE
- Journal :
- Virulence, Vol 12, Iss 1, Pp 3015-3027 (2021), Virulence, article-version (VoR) Version of Record
- Accession number :
- edsair.doi.dedup.....bc5f1a7c02dd8746e3e552e248b5a515
- Full Text :
- https://doi.org/10.6084/m9.figshare.16802467.v2