L. lactis spp. |
Nisin |
Skin infections |
MRSA |
Pros: the wound dressing with nisin can stimulate wound closure and accelerate wound healing of excisional wounds with no adverse effects |
93
|
Lung infections |
P. aeruginosa
|
Pros: nisin can be used to enhance the efficacy of polymyxins in the lung infection treatment by reducing the concentration of polymyxins needed. This may reduce polymyxin toxicity through the administration of significantly lower levels of polymyxin antibiotics |
101 and 195
|
Stomach ulcers |
H. pylori
|
Pros: nisin is a potential antibacterial agent for the treatment of stomach ulcers due to its high resistance to a wide range of pH environments |
101
|
Nisin Z |
Mucosal and bloodstream infections |
C. albicans
|
Pros: nisin Z inhibits the transformation of C. albicans from the blastospore to hyphal form, leading to ultrastructural disturbances |
13
|
Nisin A |
Cancer |
Reduce HNSCC tumorigenesis by inducing preferential apoptosis |
Pros: it can be alternative therapeutic for HNSCC instead of undergoing surgery and chemo- and radiation therapy, which are detrimental to normal cells and tissues and cause further morbidity. It inhibits tumorigenesis in vivo and prolongs survival in vivo
|
196
|
Cons: no preliminary study with an animal model and humans is carried out |
Nisin A (combined with doxorubicin) |
Cancer |
Reduce tumour severity in skin carcinogenesis |
Pros: the combination of nisin A with doxorubicin shows significant increase in treatment effect of cancer as compared to docorubicin alone. This may decrease the doses of doxorubicin and its side effects |
197
|
Cons: no preliminary study with an animal model and humans is carried out |
Nisin F |
Respiratory tract infection |
S. aureus
|
Pros: nisin with concentration at 8192 AU was proved to be safe as no abnormal of trachea, lungs, bronchi and haematology of rats detected |
198
|
Cons: no preliminary study with an animal model and humans is carried out |
Nisin A and Z |
Diarrhoea and inflammation of colon |
C. difficile
|
Pros: both nisin A and Z can inhibit the growth of C. difficile and C. difficile spores were also susceptible to nisin A |
199
|
Cons: there is no in vivo test for the activity of nisin A and Z on C. difficile
|
L. lactis ssp. lactis DPC3147 |
Lacticin 3147 |
Skin and surgical site and prosthetic joint infections |
MRSA and C. acnes
|
Pros: lacticin 3147 improve the antimicrobial efficacy of penicillin G or vancomycin against and reduce the dose of antibiotics needed |
14 and 104
|
Dental carries |
S. mutans
|
Pros: a food grade lacticin 3147 spray dried powder can reduce S. mutans in human saliva up to a 4-log reduction in counts after 20 min |
106
|
L. lactis subsp. lactis A164 and L. lactis subsp. lactis BH5 |
Lacticin A164 and BH5 |
Stomach ulcers |
H. pylori
|
Pros: lacticin A164 and BH5 are potential antibacterial agents for the treatment of stomach ulcers due to its high resistance to a wide range of pH environment |
107
|
S. salivarius K12 |
Salivaricin A2 |
Pneumonia, sinus infection, ear infection, bacteremia and meningtis |
S. pneumoniae
|
Pros: salivaricin A2 has high resistance to heat and a wide range pH environment |
110
|
Cons: no preliminary study with an animal model and humans is carried out |
Salivaricin B |
Scarlet fever, rheumatic fever, pharyngitis, tonsillitis, cellulitis, erysipelas and necrotizing fasciitis |
S. pyogenes
|
Pros: salivaricin B has high resistance to heat and a wide range pH environment |
112
|
Cons: no preliminary study with an animal model and humans is carried out |
Pharyngitis, endocarditis, gastrointestinal tract infection and skin infection |
Corynebacterium spp |
Pros: salivaricin B has high resistance to heat and a wide range pH environment |
112
|
Cons: no preliminary study with an animal model and humans is carried out |
S. salivarius 5M6c |
Salivaricin D |
Empyema and pneumonia |
C. bifermentans
|
Pros: salivaricin D is heat stable and the MIC needed to inhibit C. bifermentans is very low, which is 0.01 nM |
109
|
Cons: no preliminary study with an animal model and humans is carried out |
Infections in immunocompromised humans |
Ln. lactis
|
Pros: salivaricin D is heat stable and the MIC needed to inhibit Ln. lactis is low, which is 0.1 nM |
109
|
Cons: no preliminary study with an animal model and humans is carried out |
Pneumonia, sinus infection, ear infection, bacteremia and meningtis |
S. pneumoniae
|
Pros: salivaricin D is heat stable and the MIC needed to inhibit S. pneumoniae is very low, which is around 0.03–0.06 nM |
109
|
Cons: no preliminary study with an animal model and humans is carried out |
Scarlet fever, rheumatic fever, pharyngitis, tonsillitis, cellulitis, erysipelas and necrotizing fasciitis |
S. pyogenes
|
Pros: salivaricin D is heat stable |
109
|
Cons: no preliminary study with an animal model and humans is carried out |
B. subtilis 168 |
Subtilosin A |
Urinary tract infection |
E. faecalis
|
Pros: subtilosin A exert inhibitory effect against E. faecalis with MIC of 3.125 mg L−1
|
109
|
Cons: no preliminary study with an animal model and humans is carried out. Besides that, no information about characterization of the bacteriocin is available |
Periodontitis and tooth loss |
P. gingivalis
|
Pros: subtilosin A exert inhibitory effect against P. gingivalis with MIC of 3.125–6.25 mg L−1
|
109
|
Cons: no preliminary study with an animal model and humans is carried out. Besides that, no information about characterization of the bacteriocin is available |
Pneumonia, urinary tract infection, skin infections and meningitis |
K. pneumoniae
|
Pros: subtilosin A exert inhibitory effect against K. pneumoniae with MIC of 1.25–25 mg L−1
|
120
|
Cons: no preliminary study with an animal model and humans is carried out. Besides that, no information about characterization of the bacteriocin is available |
Methylmalonic aciduria in immunocompromised patients |
K. rhizophila
|
Pros: subtilosin A exert inhibitory effect against K. rhizophila with MIC of 1.25 mg L−1
|
121
|
Cons: no preliminary study with an animal model and humans is carried out. Besides that, no information about characterization of the bacteriocin is available |
Gastrointestinal infection, meningitis, urinary tract infection, skin infection and respiratory infection |
E. aerogenes or K. aerogenes
|
Pros: subtilosin A exert inhibitory effect against K. aerogenes with MIC of 1.25 mg L−1
|
109
|
Cons: no preliminary study with an animal model and humans is carried out. Besides that, no information about characterization of the bacteriocin is available |
Scarlet fever, rheumatic fever, pharyngitis, tonsillitis, cellulitis, erysipelas and necrotizing fasciitis |
S. pyogenes
|
Pros: subtilosin A exert inhibitory effect against S. pyogenes with MIC of 1.25 mg L−1
|
109
|
Cons: no preliminary study with an animal model and humans is carried out. Besides that, no information about characterization of the bacteriocin is available |
Shigellosis |
S. sonnei
|
Pros: subtilosin A exert inhibitory effect against S. sonnei with MIC of 1.25 mg L−1
|
123
|
Cons: no preliminary study with an animal model and humans is carried out. Besides that, no information about characterization of the bacteriocin is available |
Pneumonia, urinary tract infections and bacteremia |
P. aeruginosa
|
Pros: subtilosin A exerts inhibitory effect against P. aeruginosa with MIC of 50 mg L−1
|
124
|
Cons: no preliminary study with an animal model and humans is carried out. Besides that, no information about characterization of the bacteriocin is available |
Dental plaque formation |
S. gordonii
|
Pros: subtilosin A exerts inhibitory effect against S. gordonii with MIC of 83.25 mg L−1
|
109
|
Cons: no preliminary study with an animal model and humans is carried out. Besides that, no information about characterization of the bacteriocin is available |
Bacillus sp. strain HIL Y-85, 54728 |
Mersacidin |
Abscesses, furuncle, bloodstream infection and pneumonia |
MRSA |
Pros: mersacidin is heat stable. Elevated interleukin-1β and tumour necrosis factor-α titres were not found in mice treated with mersacidin, but found in untreated mice. Besides that, differences in the cytokine profiles were not induced by mersacidin |
200
|
Cons: no study on site of action (epithelium versus blood) of mersacidin and its application on humans is carried out |
Pneumonia, sinus infection, ear infection, bacteremia and meningtis |
S. pneumoniae
|
Pros: mersacidin is heat stable. It can be used to enhance the inhibition effect of antibiotics such as penicillin and ampicillin on S. pneumoniae and reduce the dosage of antibiotics |
128
|
Cons: no study on site of action (epithelium versus blood) of mersacidin and its application on humans is carried out |
Pneumonia and meningitis |
M. luteus
|
Pros: mersacidin is heat stable and produces antibacterial activity earlier than nisin and subtilin. It can be used to enhance the inhibition effect of antibiotics such as penicillin and ampicillin on M. luteus and reduce the dosage of antibiotics |
125 and 129
|
Cons: no study on site of action (epithelium versus blood) of mersacidin and its application on humans is carried out |
Infections of abdomen, skin, bloodstream and urinary tract |
E. faecium and E. faecalis
|
Pros: mersacidin is heat stable. It can be used to enhance the inhibition effect of antibiotics such as ampicillin on E. faecium and E. faecalis and reduce the dosage of antibiotics |
130
|
Cons: no study on site of action (epithelium versus blood) of mersacidin and its application on humans is carried out |
L. lactis MG1614 |
Enterocin A |
Listeriosis |
L. monocytogenes
|
Pros: enterocin A is thermostable, proteinaceous, resistant to catalase and does not produce hemolysin |
132 and 133
|
Cons: the inhibition effect of enterocin A on L. monocytogenes is not obvious. It can be enhanced by the combination use of thyme essential oils and enterocin A |
Infection of bladder |
E. coli
|
Pros: enterocin A is thermostable, proteinaceous, resistant to catalase and does not produce hemolysin |
132 and 133
|
Cons: the inhibition effect of enterocin A on E. coli is not obvious. It can be enhanced by the combination use of thyme essential oils and enterocin A |
E. hirae LD3 |
Enterocin LD3 |
Pneumonia and meningitis |
M. luteus
|
Pros: enterocin LD3 is thermostable up to 121 °C (at 15 psi pressure) and high resistance to acidic environment with range pH 2–6 |
56 and 134
|
Cons: no preliminary study with an animal model and humans is carried out. Besides that, no information about characterization of the bacteriocin is available |
E. faecalis
|
Enterocin AS-48 |
Diarrhoea and infections of respiration tract and wounds |
B. cereus
|
Pros: the viable cell count of B. cereus decreases rapidly with adding of 20–35 μg mL−1 enterocin. Enterocin AS-48 also increase the heat sensitivity of endospores in which the inactivation of endospores can be achieved at 90 °C and 95 °C for 1 min |
49
|
E. hirae 20C |
Enterocin E20C |
Gastroenteritis, bacteremia and enteric fever |
S. enterica
|
Pros: enterocin E20C is not only can be used alone in the treatment of gastroenteritis, bacteremia and enteric fever, but also has synergistic interaction with antibiotics such as ampicillin, penicillin, ceftriaxone, and ciprofloxacin against a ciprofloxacin- and penicillin-resistant strain of S. enterica. It was proved to reduce the MIC needed by ampicillin, penicillin, ceftriaxone, and ciprofloxacin to inhibit S. enterica, which were decreased 6.9, 13.1, 6.4 and 12.8 folds, respectively |
55
|
S. epidermidis
|
Epidermin |
Infections of respiratory tract, skin and surgical site |
S. aureus
|
Pros: epidermin has high resistance to heat and a wide range pH environment |
137
|
Cons: no preliminary study of the inhibition effect of epidermin on S. aureus with an animal model and humans is carried out |
Pneumonia, sinus infection, ear infection, bacteremia and meningtis |
S. pneumoniae
|
Pros: epidermin has high resistance to heat and a wide range pH environment |
137
|
Cons: no preliminary study of the inhibition effect of epidermin on S. pneumoniae with an animal model and humans is carried out |
Scarlet fever, rheumatic fever, pharyngitis, tonsillitis, cellulitis, erysipelas and necrotizing fasciitis |
S. pyogenes
|
Pros: epidermin has high resistance to heat and a wide range pH environment. Besides that, it can reduce the dose of penicillin |
138
|
Cons: no preliminary study of the inhibition effect of epidermin on S. pyogenes with an animal model and humans is carried out |
Infections of urinary tract, wound and soft tissue |
S. faecalis
|
Pros: epidermin has high resistance to heat and a wide range pH environment |
139
|
Cons: no preliminary study of the inhibition effect of epidermin on S. faecalis with an animal model and humans is carried out |
Endocarditis, cerebrospinal fluid shunt infection in an infant, mediastinitis and spontaneous bacterial peritonitis |
C. xerosis
|
Pros: epidermin has high resistance to heat and a wide range pH environment |
137
|
Cons: no preliminary study of the inhibition effect of epidermin on C. xerosis with an animal model and humans is carried out |
Pneumonia and meningitis |
M. luteus
|
Pros: epidermin has high resistance to heat and a wide range pH environment |
140
|
Cons: no preliminary study of the inhibition effect of epidermin on M. luteus with an animal model and humans is carried out |
Infection of brain, liver, breast, and lung abscesses |
P. anaerobicus
|
Pros: epidermin has high resistance to heat and a wide range of pH environment |
138
|
Cons: no preliminary study of the inhibition effect of epidermin on P. anaerobicus with an animal model and humans is carried out |
Acnes |
P. acnes
|
Pros: epidermin has high resistance to heat and a wide range of pH environment |
138
|
Cons: no preliminary study of the inhibition effect of epidermin on P. acnes with an animal model and humans is carried out |
S. gallinarum
|
Gallidermin |
Infections of respiratory tract, skin and surgical site |
S. aureus
|
Pros: gallidermin inhibits not only the growth of S. aureus in a dose-dependent manner but also efficiently prevents biofilm formation. Besides that, it displayed no cytotoxic effects on fibroblasts and hemolyzed less than 1% of human RBCs, and did not induce reactive oxygen species production or cell aggregation in whole blood |
89 and 137
|
Prosthetic valve endocarditis (PVE) infections and intracardiac abscesses |
S. epidermidis
|
Pros: gallidermin inhibits not only the growth of S. epidermidis in a dose-dependent manner but also efficiently prevents biofilm formation. Besides that, it displayed no cytotoxic effects on fibroblasts and hemolyzed less than 1% of human RBCs, and did not induce reactive oxygen species production or cell aggregation in whole blood |
89 and 137
|
Osteoarticular infections |
S. simulans
|
Pros: gallidermin can be used to enhance the inhibition effect of antibiotics on S. simulans and reduce the dosage of antibiotics. Besides that, it displayed no cytotoxic effects on fibroblasts and hemolyzed less than 1% of human RBCs, and did not induce reactive oxygen species production or cell aggregation in whole blood |
89 and 141
|
Pneumonia, sinus infection, ear infection, bacteremia and meningtis |
S. pneumoniae
|
Pros: gallidermin can be used to enhance the inhibition effect of antibiotics on S. pneumoniae and reduce the dosage of antibiotics. Besides that, it displayed no cytotoxic effects on fibroblasts and hemolyzed less than 1% of human RBCs, and did not induce reactive oxygen species production or cell aggregation in whole blood |
89 and 137
|
Scarlet fever, rheumatic fever, pharyngitis, tonsillitis, cellulitis, erysipelas and necrotizing fasciitis |
S. pyogenes
|
Pros: gallidermin can be used to enhance the inhibition effect of antibiotics on S. pyogenes and reduce the dosage of antibiotics. Besides that, it displayed no cytotoxic effects on fibroblasts and hemolyzed less than 1% of human RBCs, and did not induce reactive oxygen species production or cell aggregation in whole blood |
89 and 137
|
Infections of urinary tract, wound and soft tissue |
S. faecalis
|
Pros: gallidermin can be used to enhance the inhibition effect of antibiotics on S. faecalis and reduce the dosage of antibiotics. Besides that, it displayed no cytotoxic effects on fibroblasts and hemolyzed less than 1% of human RBCs, and did not induce reactive oxygen species production or cell aggregation in whole blood |
89 and 137
|
Endocarditis, cerebrospinal fluid shunt infection in an infant, mediastinitis and spontaneous bacterial peritonitis |
C. xerosis
|
Pros: gallidermin can be used to enhance the inhibition effect of antibiotics on C. xerosis and reduce the dosage of antibiotics. Besides that, it displayed no cytotoxic effects on fibroblasts and hemolyzed less than 1% of human RBCs, and did not induce reactive oxygen species production or cell aggregation in whole blood |
89 and 137
|
Pneumonia and meningitis |
M. luteus
|
Pros: gallidermin can be used to enhance the inhibition effect of antibiotics on M. luteus and reduce the dosage of antibiotics. Besides that, it displayed no cytotoxic effects on fibroblasts and hemolyzed less than 1% of human RBCs, and did not induce reactive oxygen species production or cell aggregation in whole blood |
89 and 137
|
Infection of brain, liver, breast, and lung abscesses |
P. anaerobicus
|
Pros: gallidermin can be used to enhance the inhibition effect of antibiotics on P. anaerobicus and reduce the dosage of antibiotics. Besides that, it displayed no cytotoxic effects on fibroblasts and hemolyzed less than 1% of human RBCs, and did not induce reactive oxygen species production or cell aggregation in whole blood |
89 and 137
|
Acnes |
P. acnes
|
Pros: gallidermin can be used to enhance the inhibition effect of antibiotics on P. acnes and reduce the dosage of antibiotics. Besides that, it displayed no cytotoxic effects on fibroblasts and hemolyzed less than 1% of human RBCs, and did not induce reactive oxygen species production or cell aggregation in whole blood |
89 and 137
|
L. fermentum GA715 |
Fermencin SA715 |
Pneumonia, urinary tract infections and bacteremia |
P. aeruginosa
|
Pros: fermencin SA715 possesses high thermal and pH stability |
28
|
Cons: no preliminary study of the inhibition effect of fermencin SA715 on P. aeruginosa with an animal model and humans is carried out |
Pneumonia and meningitis |
M. luteus
|
Pros: fermencin SA715 possesses high thermal and pH stability |
28
|
Cons: no preliminary study of the inhibition effect of fermencin SA715 on M. luteus with an animal model and humans is carried out |
Infection of bladder |
E. coli
|
Pros: fermencin SA715 possesses high thermal and pH stability |
28
|
Cons: no preliminary study of the inhibition effect of fermencin SA715 on E. coli with an animal model and humans is carried out |
Infections of respiratory tract, skin and surgical site |
S. aureus
|
Pros: fermencin SA715 possesses high thermal and pH stability |
28
|
Cons: no preliminary study of the inhibition effect of fermencin SA715 on S. aureus with an animal model and humans is carried out |
Pharyngitis, endocarditis, gastrointestinal tract infection and skin infection |
Corynebacterium spp |
Pros: fermencin SA715 possesses high thermal and pH stability |
28
|
Cons: no preliminary study of the inhibition effect of fermencin SA715 on Corynebacterium spp with an animal model and humans is carried out |
L. fermentum SD11 |
Fermencin SD11 |
Dental carries and gingivitis |
S. mutans, S. sobrinus, A. actinomycetemcomitans, F. nucleatum, P. gingivalis and C. albicans
|
Pros: fermencin SD11 is stable at acidic environment and may be used an alternative approach for promoting oral health or prevention of oral diseases |
144 and 146
|
Cons: no preliminary study of the inhibition effect of fermencin SD11 with an animal model and humans is carried out |