Interactions of the Skin Pathogen Haemophilus ducreyi With the Human Host

The obligate human pathogen Haemophilus ducreyi causes both cutaneous ulcers in children and sexually transmitted genital ulcers (chancroid) in adults. Pathogenesis is dependent on avoiding phagocytosis and exploiting the suppurative granuloma-like niche, which contains a myriad of innate immune cel...

Full description

Bibliographic Details
Main Authors: Julie A. Brothwell, Brad Griesenauer, Li Chen, Stanley M. Spinola
Format: Article
Language:English
Published: Frontiers Media S.A. 2021-02-01
Series:Frontiers in Immunology
Subjects:
Online Access:https://www.frontiersin.org/articles/10.3389/fimmu.2020.615402/full
id doaj-3bc1cda844b145ba91a1e99ec72bfedd
record_format Article
spelling doaj-3bc1cda844b145ba91a1e99ec72bfedd2021-02-03T05:01:48ZengFrontiers Media S.A.Frontiers in Immunology1664-32242021-02-011110.3389/fimmu.2020.615402615402Interactions of the Skin Pathogen Haemophilus ducreyi With the Human HostJulie A. Brothwell0Brad Griesenauer1Li Chen2Stanley M. Spinola3Stanley M. Spinola4Stanley M. Spinola5Department of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN, United StatesDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN, United StatesDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, United StatesDepartment of Microbiology and Immunology, Indiana University School of Medicine, Indianapolis, IN, United StatesDepartment of Medicine, Indiana University School of Medicine, Indianapolis, IN, United StatesDepartment of Pathology and Laboratory Medicine, Indiana University School of Medicine, Indianapolis, IN, United StatesThe obligate human pathogen Haemophilus ducreyi causes both cutaneous ulcers in children and sexually transmitted genital ulcers (chancroid) in adults. Pathogenesis is dependent on avoiding phagocytosis and exploiting the suppurative granuloma-like niche, which contains a myriad of innate immune cells and memory T cells. Despite this immune infiltrate, long-lived immune protection does not develop against repeated H. ducreyi infections—even with the same strain. Most of what we know about infectious skin diseases comes from naturally occurring infections and/or animal models; however, for H. ducreyi, this information comes from an experimental model of infection in human volunteers that was developed nearly three decades ago. The model mirrors the progression of natural disease and serves as a valuable tool to determine the composition of the immune cell infiltrate early in disease and to identify host and bacterial factors that are required for the establishment of infection and disease progression. Most recently, holistic investigation of the experimentally infected skin microenvironment using multiple “omics” techniques has revealed that non-canonical bacterial virulence factors, such as genes involved in central metabolism, may be relevant to disease progression. Thus, the immune system not only defends the host against H. ducreyi, but also dictates the nutrient availability for the invading bacteria, which must adapt their gene expression to exploit the inflammatory metabolic niche. These findings have broadened our view of the host-pathogen interaction network from considering only classical, effector-based virulence paradigms to include adaptations to the metabolic environment. How both host and bacterial factors interact to determine infection outcome is a current focus in the field. Here, we review what we have learned from experimental H. ducreyi infection about host-pathogen interactions, make comparisons to what is known for other skin pathogens, and discuss how novel technologies will deepen our understanding of this infection.https://www.frontiersin.org/articles/10.3389/fimmu.2020.615402/fullHaemophilus ducreyiinteractomemetabolomeskinimmune response
collection DOAJ
language English
format Article
sources DOAJ
author Julie A. Brothwell
Brad Griesenauer
Li Chen
Stanley M. Spinola
Stanley M. Spinola
Stanley M. Spinola
spellingShingle Julie A. Brothwell
Brad Griesenauer
Li Chen
Stanley M. Spinola
Stanley M. Spinola
Stanley M. Spinola
Interactions of the Skin Pathogen Haemophilus ducreyi With the Human Host
Frontiers in Immunology
Haemophilus ducreyi
interactome
metabolome
skin
immune response
author_facet Julie A. Brothwell
Brad Griesenauer
Li Chen
Stanley M. Spinola
Stanley M. Spinola
Stanley M. Spinola
author_sort Julie A. Brothwell
title Interactions of the Skin Pathogen Haemophilus ducreyi With the Human Host
title_short Interactions of the Skin Pathogen Haemophilus ducreyi With the Human Host
title_full Interactions of the Skin Pathogen Haemophilus ducreyi With the Human Host
title_fullStr Interactions of the Skin Pathogen Haemophilus ducreyi With the Human Host
title_full_unstemmed Interactions of the Skin Pathogen Haemophilus ducreyi With the Human Host
title_sort interactions of the skin pathogen haemophilus ducreyi with the human host
publisher Frontiers Media S.A.
series Frontiers in Immunology
issn 1664-3224
publishDate 2021-02-01
description The obligate human pathogen Haemophilus ducreyi causes both cutaneous ulcers in children and sexually transmitted genital ulcers (chancroid) in adults. Pathogenesis is dependent on avoiding phagocytosis and exploiting the suppurative granuloma-like niche, which contains a myriad of innate immune cells and memory T cells. Despite this immune infiltrate, long-lived immune protection does not develop against repeated H. ducreyi infections—even with the same strain. Most of what we know about infectious skin diseases comes from naturally occurring infections and/or animal models; however, for H. ducreyi, this information comes from an experimental model of infection in human volunteers that was developed nearly three decades ago. The model mirrors the progression of natural disease and serves as a valuable tool to determine the composition of the immune cell infiltrate early in disease and to identify host and bacterial factors that are required for the establishment of infection and disease progression. Most recently, holistic investigation of the experimentally infected skin microenvironment using multiple “omics” techniques has revealed that non-canonical bacterial virulence factors, such as genes involved in central metabolism, may be relevant to disease progression. Thus, the immune system not only defends the host against H. ducreyi, but also dictates the nutrient availability for the invading bacteria, which must adapt their gene expression to exploit the inflammatory metabolic niche. These findings have broadened our view of the host-pathogen interaction network from considering only classical, effector-based virulence paradigms to include adaptations to the metabolic environment. How both host and bacterial factors interact to determine infection outcome is a current focus in the field. Here, we review what we have learned from experimental H. ducreyi infection about host-pathogen interactions, make comparisons to what is known for other skin pathogens, and discuss how novel technologies will deepen our understanding of this infection.
topic Haemophilus ducreyi
interactome
metabolome
skin
immune response
url https://www.frontiersin.org/articles/10.3389/fimmu.2020.615402/full
work_keys_str_mv AT julieabrothwell interactionsoftheskinpathogenhaemophilusducreyiwiththehumanhost
AT bradgriesenauer interactionsoftheskinpathogenhaemophilusducreyiwiththehumanhost
AT lichen interactionsoftheskinpathogenhaemophilusducreyiwiththehumanhost
AT stanleymspinola interactionsoftheskinpathogenhaemophilusducreyiwiththehumanhost
AT stanleymspinola interactionsoftheskinpathogenhaemophilusducreyiwiththehumanhost
AT stanleymspinola interactionsoftheskinpathogenhaemophilusducreyiwiththehumanhost
_version_ 1724289368566267904