OBJECTIVE: Several small, 15-residue peptides that contain portions of the amino acid sequences of both cecropin A and melittin have previously been shown to have broad-spectrum antibacterial activities against aerobic microorganisms, with no undesirable hemolytic properties. It would also be useful to know what effect these hybrid peptides have on anaerobic bacteria. METHODS: The minimum inhibitory concentrations of one hybrid, CA(1--7)M(2--9)NH2, were compared with those of seven other antimicrobial agents against 111 clinical anaerobic strains; Bacteroides fragilis, 24 strains; other Bacteroides fragilis group, 14 strains; other Bacteroides species, 13 strains; Fusobacterium nucleatum, six strains; Clostridium difficile, 22 strains; Clostridium perfringens, 10 strains, Propionibacterium spp., nine strains; and anaerobic cocci, 13 strains. RESULTS: Ninety per cent of strains belonging to the B. fragilis group, fusobacteria, propionibacteria and peptostreptococci were inhibited by 4 mg/L CA(1--7)M(2--9)NH2, and the antimicrobial activity was approximately in the same range as that of chloramphenicol. CONCLUSION: This investigation showed that the antimicrobial spectrum of this cecropin---melittin hybrid also includes anaerobic organisms.
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http://dx.doi.org/10.1111/j.1469-0691.1998.tb00666.x | DOI Listing |
Int J Mol Sci
March 2025
College of Veterinary Medicine, Jilin Agricultural University, Changchun 130012, China.
Porcine reproductive and respiratory syndrome (PRRS) is an infectious disease that can cause reproductive disorders in sows and affect the breathing of piglets, seriously endangering pig breeding worldwide. In this study, NC8 was used as the expression delivery vector of foreign proteins, and a single-chain antibody was designed based on an mAb-PN9cx3 sequence. Three recombinant strains of , namely, NC8/pSIP409-pgsA'-PN9cx3-scFV(E), NC8/pSIP409-pgsA'-PN9cx3-HC(E), and NC8/pSIP409-pgsA'-PN9cx3-LC(E), were successfully constructed.
View Article and Find Full Text PDFHeliyon
February 2025
NYU Pain Research Center, New York University, USA.
Objectives: We evaluated the distribution, epidemiology, and relationships of prophage regions among 500 group genomes.
Methods: Average nucleotide identity (ANI) analysis was carried out to characterize the genome at the species level and phylogenetic analysis was performed to identify the genomic relationship among genomes Prophages in B. fragilis genomes were performed with PHASTEST and pairwise comparison of prophage regions was performed by using Jspecies.
J Crohns Colitis
March 2025
State Key Laboratory of Systems Medicine for Cancer, NHC Key Laboratory of Digestive Diseases, Division of Gastroenterology and Hepatology, Renji Hospital, School of Medicine, Shanghai Jiao Tong University, Shanghai Institute of Digestive Disease, Shanghai Cancer Institute, Shanghai, China.
Background And Aims: Bacteroides fragilis toxin (BFT), produced by enterotoxigenic B. fragilis (ETBF), is crucial for ETBF-induced colitis. This study aims to investigate the impact of BFT-host interactions on N6-methyladenosine (m6A) modification of host mRNA and its underlying mechanisms.
View Article and Find Full Text PDFPediatr Infect Dis J
March 2025
From the Department of Community Health, Faculty of Science and Medicine, University of Fribourg, Fribourg, Switzerland.
There is a critical early window during infancy for establishing the intestinal microbiota. Increasing evidence shows that breast milk (BM) harbors its own distinct microbiota. However, the extent of its contribution to the infant intestinal microbiota remains unclear.
View Article and Find Full Text PDFNan Fang Yi Ke Da Xue Xue Bao
February 2025
College of Animal Science, Anhui Science and Technology University, Fengyang 233100, China.
Objectives: To investigate the therapeutic mechanism of Turcz. (TCT) for antibiotic-associated diarrhea (AAD).
Methods: Network pharmacology, KEGG pathway enrichment analysis and molecular docking were used to identify the shared targets and genes of TCT and AAD, the key signaling pathways and the binding between the active components in TCT and the core protein targets.
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