TY - JOUR
T1 - Bacterial aggregate size determines phagocytosis efficiency of polymorphonuclear leukocytes
AU - Alhede, Maria
AU - Lorenz, Melanie
AU - Fritz, Blaine Gabriel
AU - Jensen, Peter Østrup
AU - Ring, Hans Christian
AU - Bay, Lene
AU - Bjarnsholt, Thomas
PY - 2020/12
Y1 - 2020/12
N2 - The ability of bacteria to aggregate and form biofilms impairs phagocytosis by polymorphonuclear leukocytes (PMNs). The aim of this study was to examine if the size of aggregates is critical for successful phagocytosis and how bacterial biofilms evade phagocytosis. We investigated the live interaction between PMNs and Pseudomonas aeruginosa, Staphylococcus aureus, Escherichia coli and Staphylococcus epidermidis using confocal scanning laser microscopy. Aggregate size significantly affected phagocytosis outcome and larger aggregates were less likely to be phagocytized. Aggregates of S. epidermidis were also less likely to be phagocytized than equally-sized aggregates of the other three species. We found that only aggregates of approx. 5 μm diameter or smaller were consistently phagocytosed. We demonstrate that planktonic and aggregated cells of all four species significantly reduced the viability of PMNs after 4 h of incubation. Our results indicate that larger bacterial aggregates are less likely to be phagocytosed by PMNs and we propose that, if the aggregates become too large, circulating PMNs may not be able to phagocytose them quickly enough, which may lead to chronic infection.
AB - The ability of bacteria to aggregate and form biofilms impairs phagocytosis by polymorphonuclear leukocytes (PMNs). The aim of this study was to examine if the size of aggregates is critical for successful phagocytosis and how bacterial biofilms evade phagocytosis. We investigated the live interaction between PMNs and Pseudomonas aeruginosa, Staphylococcus aureus, Escherichia coli and Staphylococcus epidermidis using confocal scanning laser microscopy. Aggregate size significantly affected phagocytosis outcome and larger aggregates were less likely to be phagocytized. Aggregates of S. epidermidis were also less likely to be phagocytized than equally-sized aggregates of the other three species. We found that only aggregates of approx. 5 μm diameter or smaller were consistently phagocytosed. We demonstrate that planktonic and aggregated cells of all four species significantly reduced the viability of PMNs after 4 h of incubation. Our results indicate that larger bacterial aggregates are less likely to be phagocytosed by PMNs and we propose that, if the aggregates become too large, circulating PMNs may not be able to phagocytose them quickly enough, which may lead to chronic infection.
KW - Biofilms
KW - Escherichia coli/physiology
KW - Humans
KW - Neutrophils/physiology
KW - Phagocytosis
KW - Pseudomonas aeruginosa/physiology
KW - Skin/microbiology
KW - Staphylococcus aureus/physiology
KW - Staphylococcus epidermidis/physiology
KW - Polymorphonuclear leukocytes (PMNs)
KW - S. epidermidis
KW - Chronic bacterial infection
KW - S. aureus
KW - E. coli
KW - P. aeruginosa
UR - https://www.scopus.com/pages/publications/85090088733
U2 - 10.1007/s00430-020-00691-1
DO - 10.1007/s00430-020-00691-1
M3 - Journal article
C2 - 32880037
SN - 0300-8584
VL - 209
SP - 669
EP - 680
JO - Medical Microbiology and Immunology
JF - Medical Microbiology and Immunology
IS - 6
ER -