Antimicrobial and antibiofilm activity of LL-37 and its truncated variants against Burkholderia pseudomallei.
Kanthawong. Sakawrat S; Bolscher. Jan G M JG; Veerman. Enno C I EC; van Marle. Jan J; de Soet. Hans J J HJ; Nazmi. Kamran K; Wongratanacheewin. Surasakdi S; Taweechaisupapong. Suwimol S
Key Findings
- LL-31 (missing the last six amino acids of LL-37) showed the strongest killing effect against B. pseudomallei
- 20 µM LL-31 killed the bacteria in about 2 hours by breaking their cell membranes
- LL-31 was more effective than the antibiotic ceftazidime against bacteria growing in biofilm
Practical Outcomes
- While LL-31 looks promising as a new antimicrobial, it’s still early‑stage lab work and not ready for personal use. Biohackers should view this as a signal that peptide‑based antibiotics are being explored, but any real‑world application would require safety testing, dosing studies, and regulatory approval before it could be used safely.
Summary
Researchers found that a shortened version of the natural peptide LL-37, called LL-31, can quickly kill the dangerous bacteria Burkholderia pseudomallei, even when the bacteria form protective biofilms, and it works better than a common antibiotic in lab tests.
Abstract
The Gram-negative bacterium Burkholderia pseudomallei is the aetiological agent of melioidosis, which is an endemic disease in tropical areas of Southeast Asia and Northern Australia. Burkholderia pseudomallei has intrinsic resistance to a number of commonly used antibiotics and has also been reported to develop a biofilm. Resistance to killing by antimicrobial agents is one of the hallmarks of bacteria grown in biofilm. The aim of this study was to determine the antimicrobial activity and mechanisms of action of LL-37 and its truncated variants against B. pseudomallei both in planktonic and biofilm form, as LL-37 is an antimicrobial peptide that possessed strong killing activity against several pathogens. Antimicrobial assays revealed that LL-31, a truncated variant of LL-37 lacking the six C-terminus residues, exhibited the strongest killing effect. Time-kill experiments showed that 20 μM LL-31 can reach the bactericidal endpoint within 2h. Freeze-fracture electron microscopy of bacterial cells demonstrated that these peptides disrupt the membrane and cause leakage of intracellular molecules leading to cell death. Moreover, LL-31 also possessed stronger bactericidal activity than ceftazidime against B. pseudomallei grown in biofilm. Thus, LL-31 should be considered as a potent antimicrobial agent against B. pseudomallei both in planktonic and biofilm form.
Study Information
pubmed
2011
2011-10-17T00:00:00.000Z
10.1016/j.ijantimicag.2011.09.010
75
30