TABLE 2.
Pathogens exploiting the ECM for invasion.
Pathogen | ECM molecule(s) bound | Infection strategy |
S. aureus | Laminin, collagen I, IV, VI, elastin, FN Singh et al., 2012 | Tissue invasion and infection |
Candida albicans | Laminin, collagen I, IV, FN Singh et al., 2012 | Tissue attachment and enrichment |
HPV-11 | Laminin 5 Culp et al., 2006 | Exploits interaction of α6-integrin with laminin 5 for keratinocyte invasion |
HPV-16 | HSPG, laminin 5, heparan sulfate Sapp and Bienkowska-Haba, 2009; DiGiuseppe et al., 2017 | Used for attachment to BM, interstitial matrix or cell membranes prior to infection, brings virus in close vicinity of target cell that interacts with matrix |
Polyomavirus | Laminin 5, collagen IV at BM Singh et al., 2012 | Large T-antigen on virus binds to BM proteins |
Merkel cell polyomavirus | Sulfated GAGs i.e., heparan sulfate; Matrosovich et al., 2013; Becker et al., 2019 | Binding used to attach to sialic acid receptors on fibroblasts for cell invasion |
HSV family | HSPG on cell surface Hadigal et al., 2020 | Used for initial attachment before invasion |
Coronavirus | HSPG Lang et al., 2011; Milewska et al., 2014; Owczarek et al., 2018 | Enrichment of viruses around cells to enhance infection |
The list shown is not exhaustive. S. aureus, Staphylococcus aureus; FN, fibronectin; HPV, human papillomavirus; HSV, herpes simplex virus; HSPG, heparan sulfate proteoglycan; GAG, galactosaminoglycan/glycosaminoglycan; BM, basement membrane.