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Macrophage polarization during Streptococcus agalactiae infection is isolate specific

INTRODUCTION: Streptococcus agalactiae (Group B Streptococcus, GBS), a Gram-positive commensal in healthy adults, remains a major cause of neonatal infections, usually manifesting as sepsis, meningitis, or pneumonia. Intrapartum antibiotic prophylaxis has greatly reduced the incidence of early-onset...

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Autores principales: Janžič, Larisa, Repas, Jernej, Pavlin, Mojca, Zemljić-Jokhadar, Špela, Ihan, Alojz, Kopitar, Andreja Nataša
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192866/
https://www.ncbi.nlm.nih.gov/pubmed/37213504
http://dx.doi.org/10.3389/fmicb.2023.1186087
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author Janžič, Larisa
Repas, Jernej
Pavlin, Mojca
Zemljić-Jokhadar, Špela
Ihan, Alojz
Kopitar, Andreja Nataša
author_facet Janžič, Larisa
Repas, Jernej
Pavlin, Mojca
Zemljić-Jokhadar, Špela
Ihan, Alojz
Kopitar, Andreja Nataša
author_sort Janžič, Larisa
collection PubMed
description INTRODUCTION: Streptococcus agalactiae (Group B Streptococcus, GBS), a Gram-positive commensal in healthy adults, remains a major cause of neonatal infections, usually manifesting as sepsis, meningitis, or pneumonia. Intrapartum antibiotic prophylaxis has greatly reduced the incidence of early-onset disease. However, given the lack of effective measures to prevent the risk of late-onset disease and invasive infections in immunocompromised individuals, more studies investigating the GBS-associated pathogenesis and the interplay between bacteria and host immune system are needed. METHODS: Here, we examined the impact of 12 previously genotyped GBS isolates belonging to different serotypes and sequence types on the immune response of THP-1 macrophages. RESULTS: Flow cytometry analysis showed isolate-specific differences in phagocytic uptake, ranging from 10% for isolates of serotype Ib, which possess the virulence factor protein β, to over 70% for isolates of serotype III. Different isolates also induced differential expression of co-stimulatory molecules and scavenger receptors with colonizing isolates inducing higher expression levels of CD80 and CD86 compared to invasive isolates. In addition, real-time measurements of metabolism revealed that macrophages enhanced both glycolysis and mitochondrial respiration after GBS infection, with isolates of serotype III being the most potent activators of glycolysis and glycolytic ATP production. Macrophages also showed differential resistance to GBS-mediated cell cytotoxicity as measured by LDH release and real-time microscopy. The differences were evident both between serotypes and between isolates obtained from different specimens (colonizing or invasive isolates) demonstrating the higher cytotoxicity of vaginal compared with blood isolates. CONCLUSIONS: Thus, the data suggest that GBS isolates differ in their potential to become invasive or remain colonizing. In addition, colonizing isolates appear to be more cytotoxic, whereas invasive isolates appear to exploit macrophages to their advantage, avoiding the immune recognition and antibiotics.
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spelling pubmed-101928662023-05-19 Macrophage polarization during Streptococcus agalactiae infection is isolate specific Janžič, Larisa Repas, Jernej Pavlin, Mojca Zemljić-Jokhadar, Špela Ihan, Alojz Kopitar, Andreja Nataša Front Microbiol Microbiology INTRODUCTION: Streptococcus agalactiae (Group B Streptococcus, GBS), a Gram-positive commensal in healthy adults, remains a major cause of neonatal infections, usually manifesting as sepsis, meningitis, or pneumonia. Intrapartum antibiotic prophylaxis has greatly reduced the incidence of early-onset disease. However, given the lack of effective measures to prevent the risk of late-onset disease and invasive infections in immunocompromised individuals, more studies investigating the GBS-associated pathogenesis and the interplay between bacteria and host immune system are needed. METHODS: Here, we examined the impact of 12 previously genotyped GBS isolates belonging to different serotypes and sequence types on the immune response of THP-1 macrophages. RESULTS: Flow cytometry analysis showed isolate-specific differences in phagocytic uptake, ranging from 10% for isolates of serotype Ib, which possess the virulence factor protein β, to over 70% for isolates of serotype III. Different isolates also induced differential expression of co-stimulatory molecules and scavenger receptors with colonizing isolates inducing higher expression levels of CD80 and CD86 compared to invasive isolates. In addition, real-time measurements of metabolism revealed that macrophages enhanced both glycolysis and mitochondrial respiration after GBS infection, with isolates of serotype III being the most potent activators of glycolysis and glycolytic ATP production. Macrophages also showed differential resistance to GBS-mediated cell cytotoxicity as measured by LDH release and real-time microscopy. The differences were evident both between serotypes and between isolates obtained from different specimens (colonizing or invasive isolates) demonstrating the higher cytotoxicity of vaginal compared with blood isolates. CONCLUSIONS: Thus, the data suggest that GBS isolates differ in their potential to become invasive or remain colonizing. In addition, colonizing isolates appear to be more cytotoxic, whereas invasive isolates appear to exploit macrophages to their advantage, avoiding the immune recognition and antibiotics. Frontiers Media S.A. 2023-05-04 /pmc/articles/PMC10192866/ /pubmed/37213504 http://dx.doi.org/10.3389/fmicb.2023.1186087 Text en Copyright © 2023 Janžič, Repas, Pavlin, Zemljić-Jokhadar, Ihan and Kopitar. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Microbiology
Janžič, Larisa
Repas, Jernej
Pavlin, Mojca
Zemljić-Jokhadar, Špela
Ihan, Alojz
Kopitar, Andreja Nataša
Macrophage polarization during Streptococcus agalactiae infection is isolate specific
title Macrophage polarization during Streptococcus agalactiae infection is isolate specific
title_full Macrophage polarization during Streptococcus agalactiae infection is isolate specific
title_fullStr Macrophage polarization during Streptococcus agalactiae infection is isolate specific
title_full_unstemmed Macrophage polarization during Streptococcus agalactiae infection is isolate specific
title_short Macrophage polarization during Streptococcus agalactiae infection is isolate specific
title_sort macrophage polarization during streptococcus agalactiae infection is isolate specific
topic Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10192866/
https://www.ncbi.nlm.nih.gov/pubmed/37213504
http://dx.doi.org/10.3389/fmicb.2023.1186087
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