Staphylococcus aureus infections represent a great concern due to their versatility and involvement in different types of diseases. The shortage of available clinical options, especially to treat multiresistant strains, makes the discovery of new effective compounds essential. Here we describe the activity of the previously described cell division inhibitor C109 against methicillin-sensitive and-resistant S. aureus strains. Antibiofilm activity was assessed using microtiter plates, confocal microscopy, and in an in vitro biofilm wound model. The ability of C109 to block FtsZ GTPase activity and polymerization was tested in vitro. Altogether, the results show that the FtsZ inhibitor C109 has activity against a wide range of S. aureus strains and support its use as an antistaphylococcal compound.

Antistaphylococcal activity of the ftsz inhibitor c109 / Trespidi, G.; Scoffone, V. C.; Barbieri, G.; Marchesini, F.; Abualsha'Ar, A.; Coenye, T.; Ungaro, F.; Makarov, V.; Migliavacca, R.; De Rossi, E.; Buroni, S.. - In: PATHOGENS. - ISSN 2076-0817. - 10:7(2021), p. 886. [10.3390/pathogens10070886]

Antistaphylococcal activity of the ftsz inhibitor c109

Ungaro F.;
2021

Abstract

Staphylococcus aureus infections represent a great concern due to their versatility and involvement in different types of diseases. The shortage of available clinical options, especially to treat multiresistant strains, makes the discovery of new effective compounds essential. Here we describe the activity of the previously described cell division inhibitor C109 against methicillin-sensitive and-resistant S. aureus strains. Antibiofilm activity was assessed using microtiter plates, confocal microscopy, and in an in vitro biofilm wound model. The ability of C109 to block FtsZ GTPase activity and polymerization was tested in vitro. Altogether, the results show that the FtsZ inhibitor C109 has activity against a wide range of S. aureus strains and support its use as an antistaphylococcal compound.
2021
Antistaphylococcal activity of the ftsz inhibitor c109 / Trespidi, G.; Scoffone, V. C.; Barbieri, G.; Marchesini, F.; Abualsha'Ar, A.; Coenye, T.; Ungaro, F.; Makarov, V.; Migliavacca, R.; De Rossi, E.; Buroni, S.. - In: PATHOGENS. - ISSN 2076-0817. - 10:7(2021), p. 886. [10.3390/pathogens10070886]
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Utilizza questo identificativo per citare o creare un link a questo documento: https://hdl.handle.net/11588/877413
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