TY - JOUR
T1 - The role of bacterial size, shape and surface in macrophage engulfment of uropathogenic E. coli cells
AU - Peterson, Elizabeth
AU - Söderström, Bill
AU - Prins, Nienke
AU - Le, Giang H.B.
AU - Hartley-Tassell, Lauren E.
AU - Evenhuis, Chris
AU - Grønnemose, Rasmus Birkholm
AU - Andersen, Thomas Emil
AU - Møller-Jensen, Jakob
AU - Iosifidis, Gregory
AU - Duggin, Iain G.
AU - Saunders, Bernadette
AU - Harry, Elizabeth J.
AU - Bottomley, Amy L.
PY - 2024/9
Y1 - 2024/9
N2 - Uropathogenic Escherichia coli (UPEC) can undergo extensive filamentation in the host during acute urinary tract infections (UTIs). It has been hypothesised that this morphological plasticity allows bacteria to avoid host immune responses such as macrophage engulfment. However, it is still unclear what properties of filaments are important in macrophage-bacteria interactions. The aim of this work was to investigate the contribution of bacterial biophysical parameters, such as cell size and shape, and physiological parameters, such as cell surface and the environment, to macrophage engulfment efficiency. Viable, reversible filaments of known lengths and volumes were produced in the UPEC strain UTI89 using a variety of methods, including exposure to cell-wall targeting antibiotics, genetic manipulation and isolation from an in vitro human bladder cell model. Quantification of the engulfment ability of macrophages using gentamicin-protection assays and fluorescence microscopy demonstrated that the ability of filaments to avoid macrophage engulfment is dependent on a combination of size (length and volume), shape, cell surface and external environmental factors. UTI89 filamentation and macrophage engulfment efficiency was also found to occur independently of the SOS-inducible filamentation genes, sulA and ymfM in both in vivo and in vitro models of infection. Compared to filaments formed via antibiotic inhibition of division, the infection-derived filaments were preferentially targeted by macrophages. With several strains of UPEC now resistant to current antibiotics, our work identifies the importance of bacterial physiological and morphological states during infection.
AB - Uropathogenic Escherichia coli (UPEC) can undergo extensive filamentation in the host during acute urinary tract infections (UTIs). It has been hypothesised that this morphological plasticity allows bacteria to avoid host immune responses such as macrophage engulfment. However, it is still unclear what properties of filaments are important in macrophage-bacteria interactions. The aim of this work was to investigate the contribution of bacterial biophysical parameters, such as cell size and shape, and physiological parameters, such as cell surface and the environment, to macrophage engulfment efficiency. Viable, reversible filaments of known lengths and volumes were produced in the UPEC strain UTI89 using a variety of methods, including exposure to cell-wall targeting antibiotics, genetic manipulation and isolation from an in vitro human bladder cell model. Quantification of the engulfment ability of macrophages using gentamicin-protection assays and fluorescence microscopy demonstrated that the ability of filaments to avoid macrophage engulfment is dependent on a combination of size (length and volume), shape, cell surface and external environmental factors. UTI89 filamentation and macrophage engulfment efficiency was also found to occur independently of the SOS-inducible filamentation genes, sulA and ymfM in both in vivo and in vitro models of infection. Compared to filaments formed via antibiotic inhibition of division, the infection-derived filaments were preferentially targeted by macrophages. With several strains of UPEC now resistant to current antibiotics, our work identifies the importance of bacterial physiological and morphological states during infection.
KW - Animals
KW - Escherichia coli Infections/microbiology
KW - Humans
KW - Macrophages/microbiology
KW - Mice
KW - Phagocytosis
KW - Urinary Tract Infections/microbiology
KW - Uropathogenic Escherichia coli
U2 - 10.1371/journal.ppat.1012458
DO - 10.1371/journal.ppat.1012458
M3 - Journal article
C2 - 39241059
AN - SCOPUS:85203309913
SN - 1553-7366
VL - 20
JO - PLOS Pathogens
JF - PLOS Pathogens
IS - 9
M1 - e1012458
ER -