TY - JOUR
T1 - Dormant cells of Staphylococcus aureus are resuscitated by spent culture supernatant
AU - Pascoe, Ben
AU - Dams, Lucy
AU - Wilkinson, Tom S.
AU - Harris, Llinos G.
AU - Bodger, Owen
AU - Mack, Dietrich
AU - Davies, Angharad P.
PY - 2014/2
Y1 - 2014/2
N2 - We describe the first in vitro model of dormancy in Staphylococcus aureus, showing that cells are generated which can be resuscitated by addition of spent medium supernatant taken from cultures of the same organism. Over 30 days, culturable counts in dormant cultures of S. aureus SH1000 fell from 10(6)-10(7) cfu/ml to <10 cfu/ml as measured by the Most Probable Number method in liquid culture, while total counts as determined by microscopy, and supported by data from RT-qPCR, remained around 10(6)-10(7) cells/ml. Supplementing cultures with 25-50% spent medium resulted in a >600-fold increase in bacterial growth. Resuscitation was a specific effect, greatly reduced by boiling or addition of trypsin to the spent supernatant. Supernatant also effected a reduction in lag phase of dormant cultures. SEM demonstrated the presence of small coccoid cells in dormant cultures. The results are similar to those seen with resuscitation promoting factors (Rpfs) in actinobacteria. This is the first time resuscitation has been demonstrated in Staphylococcus aureus, which is an important human pathogen. A better understanding of control and reactivation of dormant cells could lead to major improvements in managing staphylococcal infections; resuscitation could be an important step in restoring susceptibility to antibiotic treatment.
AB - We describe the first in vitro model of dormancy in Staphylococcus aureus, showing that cells are generated which can be resuscitated by addition of spent medium supernatant taken from cultures of the same organism. Over 30 days, culturable counts in dormant cultures of S. aureus SH1000 fell from 10(6)-10(7) cfu/ml to <10 cfu/ml as measured by the Most Probable Number method in liquid culture, while total counts as determined by microscopy, and supported by data from RT-qPCR, remained around 10(6)-10(7) cells/ml. Supplementing cultures with 25-50% spent medium resulted in a >600-fold increase in bacterial growth. Resuscitation was a specific effect, greatly reduced by boiling or addition of trypsin to the spent supernatant. Supernatant also effected a reduction in lag phase of dormant cultures. SEM demonstrated the presence of small coccoid cells in dormant cultures. The results are similar to those seen with resuscitation promoting factors (Rpfs) in actinobacteria. This is the first time resuscitation has been demonstrated in Staphylococcus aureus, which is an important human pathogen. A better understanding of control and reactivation of dormant cells could lead to major improvements in managing staphylococcal infections; resuscitation could be an important step in restoring susceptibility to antibiotic treatment.
KW - Anti-Bacterial Agents
KW - Bacteriological Techniques
KW - Cold Temperature
KW - Colony Count, Microbial
KW - Culture Media, Conditioned
KW - Microscopy, Electron, Scanning
KW - Staphylococcus aureus
KW - Time Factors
KW - Trypsin
UR - http://dx.doi.org/10.1371/journal.pone.0085998
UR - http://dx.doi.org/10.1371/journal.pone.0085998
U2 - 10.1371/journal.pone.0085998
DO - 10.1371/journal.pone.0085998
M3 - Article
C2 - 24523858
SN - 1932-6203
VL - 9
SP - e85998
JO - PLoS ONE
JF - PLoS ONE
IS - 2
ER -