Impact of Phosphorylcholine Expression on the Adherence and Invasion of <i>Streptococcus pyogenes</i> to Epithelial Cells

Phosphorylcholine (PC) is a structural component of various pathogens and is involved in bacterial adhesion via the platelet-activating factor receptor (PAF-R). In this study, we investigated how PC expression affects cell adhesion and invasion of <i>Streptococcus pyogenes</i> (<i>...

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Main Authors: Hiroyuki Iuchi, Junichiro Ohori, Hisahiro Matsuzaki, Takeshi Tokushige, Sakiko Toge, Masaru Yamashita
Format: Article
Language:English
Published: MDPI AG 2022-02-01
Series:Microorganisms
Subjects:
Online Access:https://www.mdpi.com/2076-2607/10/3/527
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author Hiroyuki Iuchi
Junichiro Ohori
Hisahiro Matsuzaki
Takeshi Tokushige
Sakiko Toge
Masaru Yamashita
author_facet Hiroyuki Iuchi
Junichiro Ohori
Hisahiro Matsuzaki
Takeshi Tokushige
Sakiko Toge
Masaru Yamashita
author_sort Hiroyuki Iuchi
collection DOAJ
description Phosphorylcholine (PC) is a structural component of various pathogens and is involved in bacterial adhesion via the platelet-activating factor receptor (PAF-R). In this study, we investigated how PC expression affects cell adhesion and invasion of <i>Streptococcus pyogenes</i> (<i>S. pyogenes</i>). Eight clinical strains of <i>S. pyogenes</i> were cultured, and PC expression was measured using fluorescence-activated cell sorting. Bacterial adherence and invasion were examined using Detroit 562 cells. An anti-PC-specific monoclonal antibody (TEPC-15) was used to inhibit bacterial PC, and a PAF-R antagonist (ABT-491) was used to inhibit cellular PAF-R. The <i>emm</i> gene was amplified by the polymerase chain reaction with the standard primers. The level of PC expressed on the <i>S. pyogenes</i> surfaces differed in each strain and differed even in the same <i>emm</i> genotype. Adherence assay experiments showed a significant negative correlation between TEPC-15 and ABT-491 inhibitory effects and PC expression in <i>S. pyogenes</i>. Similarly, intracellular invasion assay experiments showed a significant negative correlation between TEPC-15 and ABT-491 inhibitory effects and PC expression in <i>S. pyogenes</i>. This study suggests that <i>S. pyogenes</i> is involved in cell adhesion and invasion by PC.
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spelling doaj.art-1cb91e7e735645f7a34829ddc2c597602023-11-30T21:35:32ZengMDPI AGMicroorganisms2076-26072022-02-0110352710.3390/microorganisms10030527Impact of Phosphorylcholine Expression on the Adherence and Invasion of <i>Streptococcus pyogenes</i> to Epithelial CellsHiroyuki Iuchi0Junichiro Ohori1Hisahiro Matsuzaki2Takeshi Tokushige3Sakiko Toge4Masaru Yamashita5Department of Otolaryngology, Head and Neck Surgery, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8520, JapanDepartment of Otolaryngology, Head and Neck Surgery, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8520, JapanDepartment of Otolaryngology, Head and Neck Surgery, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8520, JapanDepartment of Otolaryngology, Head and Neck Surgery, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8520, JapanDepartment of Otolaryngology, Head and Neck Surgery, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8520, JapanDepartment of Otolaryngology, Head and Neck Surgery, Kagoshima University Graduate School of Medical and Dental Sciences, Kagoshima 890-8520, JapanPhosphorylcholine (PC) is a structural component of various pathogens and is involved in bacterial adhesion via the platelet-activating factor receptor (PAF-R). In this study, we investigated how PC expression affects cell adhesion and invasion of <i>Streptococcus pyogenes</i> (<i>S. pyogenes</i>). Eight clinical strains of <i>S. pyogenes</i> were cultured, and PC expression was measured using fluorescence-activated cell sorting. Bacterial adherence and invasion were examined using Detroit 562 cells. An anti-PC-specific monoclonal antibody (TEPC-15) was used to inhibit bacterial PC, and a PAF-R antagonist (ABT-491) was used to inhibit cellular PAF-R. The <i>emm</i> gene was amplified by the polymerase chain reaction with the standard primers. The level of PC expressed on the <i>S. pyogenes</i> surfaces differed in each strain and differed even in the same <i>emm</i> genotype. Adherence assay experiments showed a significant negative correlation between TEPC-15 and ABT-491 inhibitory effects and PC expression in <i>S. pyogenes</i>. Similarly, intracellular invasion assay experiments showed a significant negative correlation between TEPC-15 and ABT-491 inhibitory effects and PC expression in <i>S. pyogenes</i>. This study suggests that <i>S. pyogenes</i> is involved in cell adhesion and invasion by PC.https://www.mdpi.com/2076-2607/10/3/527phosphorylcholine<i>Streptococcus pyogenes</i>PAF-R<i>emm</i> genotype
spellingShingle Hiroyuki Iuchi
Junichiro Ohori
Hisahiro Matsuzaki
Takeshi Tokushige
Sakiko Toge
Masaru Yamashita
Impact of Phosphorylcholine Expression on the Adherence and Invasion of <i>Streptococcus pyogenes</i> to Epithelial Cells
Microorganisms
phosphorylcholine
<i>Streptococcus pyogenes</i>
PAF-R
<i>emm</i> genotype
title Impact of Phosphorylcholine Expression on the Adherence and Invasion of <i>Streptococcus pyogenes</i> to Epithelial Cells
title_full Impact of Phosphorylcholine Expression on the Adherence and Invasion of <i>Streptococcus pyogenes</i> to Epithelial Cells
title_fullStr Impact of Phosphorylcholine Expression on the Adherence and Invasion of <i>Streptococcus pyogenes</i> to Epithelial Cells
title_full_unstemmed Impact of Phosphorylcholine Expression on the Adherence and Invasion of <i>Streptococcus pyogenes</i> to Epithelial Cells
title_short Impact of Phosphorylcholine Expression on the Adherence and Invasion of <i>Streptococcus pyogenes</i> to Epithelial Cells
title_sort impact of phosphorylcholine expression on the adherence and invasion of i streptococcus pyogenes i to epithelial cells
topic phosphorylcholine
<i>Streptococcus pyogenes</i>
PAF-R
<i>emm</i> genotype
url https://www.mdpi.com/2076-2607/10/3/527
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