TY - JOUR
T1 - Bacteriophage therapy
T2 - A revitalized therapy against bacterial infectious diseases
AU - Matsuzaki, Shigenobu
AU - Rashel, Mohammad
AU - Uchiyama, Jumpei
AU - Sakurai, Shingo
AU - Ujihara, Takako
AU - Kuroda, Masayuki
AU - Ikeuchi, Masahiko
AU - Tani, Toshikazu
AU - Fujieda, Mikiya
AU - Wakiguchi, Hiroshi
AU - Imai, Shosuke
N1 - Funding Information:
Acknowledgments This work was supported in part by the Grant-in-Aid for Scientific Research from the Japanese Ministry of Education, Science, Sports, and Culture [16659265 (S.M.), 16659278 (M.F.)]; by a research grant from the Japan Science and Technology Agency (S.M.); by the President Research Fund of Kochi Medical School Hospital (S.I.); and by a Special Research Grant for Green Science from Kochi University, Japan (S.I.).
PY - 2005/10
Y1 - 2005/10
N2 - Bacteriophage (phage) therapy involves using phages or their products as bioagents for the treatment or prophylaxis of bacterial infectious diseases. Much evidence in support of the effectiveness of phage therapy against bacterial infectious diseases has accumulated since 1980 from animal model studies conducted in Western countries. Reports indicate that appropriate administration of living phages can be used to treat lethal infectious diseases caused by gram-negative bacteria, such as Escherichia coli, Pseudomonas aeruginosa, Acinetobacter baumannii, Klebsiella pneumoniae, Vibrio vulnificus, and Salmonella spp., and gram-positive bacteria, such as Enterococcus faecium and Staphylococcus aureus. The phage display system and genetically modified nonreplicating phages are also effective for treatment of Helicobacter pylori and P. aeruginosa, respectively. In addition to phage particles per se, purified phage-encoded peptidoglycan hydrolase (lysin) is also reported to be effective for the treatment of bacterial infectious diseases caused by gram-positive bacteria such as Streptococcus pyogenes, S. pneumoniae, Bacillus anthracis, and group B streptococci. All phage lysins that have been studied to date exhibit immediate and strong bacteriolytic activity when applied exogenously. Furthermore, phage-coded inhibitors of peptidoglycan synthesis (protein antibiotics), search methods for novel antibacterial agents using phage genome informatics, and vaccines utilizing phages or their products are being developed. Phage therapy will compensate for unavoidable complications of chemotherapy such as the appearance of multidrug resistance or substituted microbism.
AB - Bacteriophage (phage) therapy involves using phages or their products as bioagents for the treatment or prophylaxis of bacterial infectious diseases. Much evidence in support of the effectiveness of phage therapy against bacterial infectious diseases has accumulated since 1980 from animal model studies conducted in Western countries. Reports indicate that appropriate administration of living phages can be used to treat lethal infectious diseases caused by gram-negative bacteria, such as Escherichia coli, Pseudomonas aeruginosa, Acinetobacter baumannii, Klebsiella pneumoniae, Vibrio vulnificus, and Salmonella spp., and gram-positive bacteria, such as Enterococcus faecium and Staphylococcus aureus. The phage display system and genetically modified nonreplicating phages are also effective for treatment of Helicobacter pylori and P. aeruginosa, respectively. In addition to phage particles per se, purified phage-encoded peptidoglycan hydrolase (lysin) is also reported to be effective for the treatment of bacterial infectious diseases caused by gram-positive bacteria such as Streptococcus pyogenes, S. pneumoniae, Bacillus anthracis, and group B streptococci. All phage lysins that have been studied to date exhibit immediate and strong bacteriolytic activity when applied exogenously. Furthermore, phage-coded inhibitors of peptidoglycan synthesis (protein antibiotics), search methods for novel antibacterial agents using phage genome informatics, and vaccines utilizing phages or their products are being developed. Phage therapy will compensate for unavoidable complications of chemotherapy such as the appearance of multidrug resistance or substituted microbism.
KW - Genetic modification
KW - Lysin
KW - Multidrug-resistant bacteria
KW - Phage therapy
KW - Protein antibiotics
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U2 - 10.1007/s10156-005-0408-9
DO - 10.1007/s10156-005-0408-9
M3 - Review article
C2 - 16258815
AN - SCOPUS:27644460427
SN - 1341-321X
VL - 11
SP - 211
EP - 219
JO - Journal of Infection and Chemotherapy
JF - Journal of Infection and Chemotherapy
IS - 5
ER -