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Corrigendum

Insights into the Antibacterial Mechanism of PEGylated Nano-Bacitracin A Against Streptococcus pneumonia: Both Penicillin-Sensitive and Penicillin-Resistant Strains [Corrigendum]

Pages 2807-2808 | Published online: 29 Jun 2022
This article refers to:
Insights into the antibacterial mechanism of PEGylated nano-bacitracin A against Streptococcus pneumonia: both penicillin-sensitive and penicillin-resistant strains

Hong W, Liu L, Zhang Z, Zhao Y, Zhang D, Liu M. Int J Nanomedicine. 2018;13:6297–6309.

The authors have advised due to an error that occurred inadvertently at the time of figure assembly, on page 6302 is incorrect. The correct is as follows.

Figure 1 The confocal microscope images of S. pneumonia ATCC 49619 (A) and S. pneumonia 16167 (B) stained by LIVE/DEAD after incubation with PEGylated Nano-BA12K, BA solution, and Penicillin G for 0.5, 1, 2, 4, 8, and 12 hours at 37°C.

Abbreviation: BA, bacitracin A.
Figure 1 The confocal microscope images of S. pneumonia ATCC 49619 (A) and S. pneumonia 16167 (B) stained by LIVE/DEAD after incubation with PEGylated Nano-BA12K, BA solution, and Penicillin G for 0.5, 1, 2, 4, 8, and 12 hours at 37°C.

The authors also advised that there are errors in and on page 6306. The correct is as follows.

Figure 7 Cytoplasmic membrane potential variation of S. pneumonia ATCC 49619 (A) and S. pneumonia 16167 (B) treated with PEGylated Nano-BA12K at 1× MICs, as assessed by the release of the membrane potential-sensitive dye disC3-5. The fluorescence intensity was monitored at a λex =622 nm and λem =670 nm as a function of time. Effect of PEGylated Nano-BA12K on the cytoplasmic membrane permeability of S. pneumonia ATCC 49619 (C) and S. pneumonia 16167 (D). PEGylated Nano-BA12K-induced calcein release as a function of time. PEGylated Nano-BA12K was added to PTG/CL SUVs encapsulated with calcein (E). The graphs were derived from average values of three independent trials.

Abbreviations: BA, bacitracin A; CL, caidiolipin; PG, phosphatidylglycerol; MIC, minimal inhibitory concentration; SUV, small unilamellar vesicle.
Figure 7 Cytoplasmic membrane potential variation of S. pneumonia ATCC 49619 (A) and S. pneumonia 16167 (B) treated with PEGylated Nano-BA12K at 1× MICs, as assessed by the release of the membrane potential-sensitive dye disC3-5. The fluorescence intensity was monitored at a λex =622 nm and λem =670 nm as a function of time. Effect of PEGylated Nano-BA12K on the cytoplasmic membrane permeability of S. pneumonia ATCC 49619 (C) and S. pneumonia 16167 (D). PEGylated Nano-BA12K-induced calcein release as a function of time. PEGylated Nano-BA12K was added to PTG/CL SUVs encapsulated with calcein (E). The graphs were derived from average values of three independent trials.

The authors apologize for these errors and advise they do not affect the results and conclusions of the paper.