TABLE 3.
Sources and effects of AMPs.
| Name of AMPs | Amino acid sequence | Net charge | 3D structure | Source | Effects on biofilm | Disadvantages | References |
| Japonicin-2LF | FIVPSIFLLK KAFCIALKKC | 4 | Helix | Frog skin secretion | Eradicates the methicillin-resistant S. aureus biofilm matrix as well as kills all the sessile bacteria | Futile against P. aeruginosa biofilms. The anti-biofilm activity concealed by the changes in LPS contents and cell wall structure of microorganisms | Yuan et al., 2019 |
| Dermaseptin-PT9 | GLWSKIKDAAKT AGKAALGFVNEMV | 2 | Helix | Frog skin secretion | Inhibits the biofilm formation of S. aureus, MRSA, and E. coli | More potent activity against Gram-negative bacteria | Li et al., 2019 |
| Phylloseptin-PTa | FLSLIPAA ISAVSALANHF | 2 | Helix | Frog skin secretion | More potent against S. aureus biofilm | Anti-biofilm activity changed by the hydrophobicity, charges and α-helicity of the peptides | Liu et al., 2017 |
| Moronecidin-like | FFRNLWKGAK AAFRAGHAAWRA | 6 | Unknown | Seahorse | Inhibits surface attachment of S. aureus biofilm | More effectual against Gram-positive bacteria than Gram-negative bacteria The outer membrane proteins of Gram-negative bacteria may hinder translocation of AMPs through the outer membrane |
Mohammadi et al., 2018 |
| Mastoporan | LNLKALL AVAKKIL | 4 | Helix | European hornet venom | Suppresses biofilm formation by S. aureus and P. aeruginosa | Release histamine from mammalian mast cells may lead to an immune response | Chen et al., 2018 |
| Melittin | GIGAVLKVLTTG LPALISWIKRKRQQ | 6 | Helix | Honeybee venom | Induce disintegration of the MDR P. aeruginosa and degrades the biofilm | The toxicity of melittin on normal cells is a disadvantage for clinical applications (in case of third-degree burn patients, all three layers of skin are destroyed, so cytotoxicity of melittin hardly limits its applications) | Khozani et al., 2019 |
| NA-CATH | KRFKKFFKKLKNSV KKRAKKFFKKPKVIGVTFPF | 15 | Helix | Chinese cobra (Naja atra) | Prevent biofilm formation of Burkholderia thailandensis | The small size of the peptide restricts its large-scale synthesis |
Blower et al., 2015 de Barros et al., 2019 |
| Defensin ZmD32 |
RTCQSQSHRFRGPCLRRS NCANVCRTEGFPGG RCRGFRRRCFCTTHC | 12 | Combine Helix and Beta structure | Corn, Zea mays | Active against Candida albicans biofilms | Anti-biofilm activity of many defensins lost in the presence of salt | Kerenga et al., 2019 |
| Capsicumicine | RSCQQQIQQ AQQLSSCQQYLKQ | – | Unknown | Red pepper, Capsicum bacattum | Prevents the establishment of S. epidermidis biofilm by matrix anti-assembly (MAA) mechanism | NS | Von Borowski et al., 2020 |
| Rhesus theta defensin-1 | GFCRCLCRRGVCRCICTR | 5 | Beta | Monkey leukocytes | Active against established C. albicans biofilms | Most of the host defense peptides exhibit undesirable pro-inflammatory properties and low bioavailability | Basso et al., 2019 |
NS, not specified.