TY  - JOUR
  - Rea, MC,Alemayehu, D,Casey, PG,O'Connor, PM,Lawlor, PG,Walsh, M,Shanahan, F,Kiely, B,Ross, RP,Hill, C
  - 2014
  - February
  - Microbiology-SGM
  - Bioavailability of the anti-clostridial bacteriocin thuricin CD in gastrointestinal tract
  - Validated
  - Altmetric: 1 ()
  - DIFFICILE INFECTION INTESTINAL MICROBIOTA NARROW-SPECTRUM SPORE-FORMERS EPIDEMIOLOGY NISIN
  - 160
  - 439
  - 445
  - Thuricin CD is a two component narrow spectrum bacteriocin comprising two peptides with targeted activity against Clostridium difficile. This study examined the bioavailability of thuricin with a view to developing it as an effective antimicrobial against intestinal infection. One of the peptides, Trn-beta, was found to be degraded by the gastric enzymes pepsin and a-chymotrypsin both in vitro and in vivo, whereas Trn-alpha was resistant to digestion by these enzymes and hence was detected in the intestinal porcine digesta following oral ingestion by pigs. In order to determine if spores of the producing organism Bacillus thuringiensis DPC 6431 could be used to deliver the bacteriocin to the gut, spores were fed to 30 mice (approx. 10(8)-2x10(8) per animal) and their germination, growth and production of thuricin in the gastrointestinal tract (GIT) of the animals was monitored. Almost 99% of the spores delivered to the GIT were excreted in the first 24 h and neither Trn-alpha nor Trn-beta was detected in the gut or faecal samples of the test mice, indicating that ingestion of B. thuringiensis spores may not be a suitable vehicle for the delivery of thuricin CD. When thuricin CD was delivered rectally to mice (n=40) and C. difficile shedding monitored at 1, 6, 12 and 24 h post-treatment, there was a >95% (>1.5 log units) reduction of C. difficile 027 in the colon contents of infected mice (n=10) 1 h post-treatment compared with the control group (n=10; P<0.001). Furthermore, 6 h post-treatment there was a further 1.5 log reduction in C. difficile numbers (n=10) relative to the control group (n=10; P<0.05). These results would suggest that rectal administration of thuricin may be a promising mode of delivery of thuricin CD to the colon.
  - 10.1099/mic.0.068767-0
DA  - 2014/02
ER  - 

@article{V279269364,
   = {Rea,  MC and Alemayehu,  D and Casey,  PG and O'Connor,  PM and Lawlor,  PG and Walsh,  M and Shanahan,  F and Kiely,  B and Ross,  RP and Hill,  C },
   = {2014},
   = {February},
   = {Microbiology-SGM},
   = {Bioavailability of the anti-clostridial bacteriocin thuricin CD in gastrointestinal tract},
   = {Validated},
   = {Altmetric: 1 ()},
   = {DIFFICILE INFECTION INTESTINAL MICROBIOTA NARROW-SPECTRUM SPORE-FORMERS EPIDEMIOLOGY NISIN},
   = {160},
  pages = {439--445},
   = {{Thuricin CD is a two component narrow spectrum bacteriocin comprising two peptides with targeted activity against Clostridium difficile. This study examined the bioavailability of thuricin with a view to developing it as an effective antimicrobial against intestinal infection. One of the peptides, Trn-beta, was found to be degraded by the gastric enzymes pepsin and a-chymotrypsin both in vitro and in vivo, whereas Trn-alpha was resistant to digestion by these enzymes and hence was detected in the intestinal porcine digesta following oral ingestion by pigs. In order to determine if spores of the producing organism Bacillus thuringiensis DPC 6431 could be used to deliver the bacteriocin to the gut, spores were fed to 30 mice (approx. 10(8)-2x10(8) per animal) and their germination, growth and production of thuricin in the gastrointestinal tract (GIT) of the animals was monitored. Almost 99% of the spores delivered to the GIT were excreted in the first 24 h and neither Trn-alpha nor Trn-beta was detected in the gut or faecal samples of the test mice, indicating that ingestion of B. thuringiensis spores may not be a suitable vehicle for the delivery of thuricin CD. When thuricin CD was delivered rectally to mice (n=40) and C. difficile shedding monitored at 1, 6, 12 and 24 h post-treatment, there was a >95% (>1.5 log units) reduction of C. difficile 027 in the colon contents of infected mice (n=10) 1 h post-treatment compared with the control group (n=10; P<0.001). Furthermore, 6 h post-treatment there was a further 1.5 log reduction in C. difficile numbers (n=10) relative to the control group (n=10; P<0.05). These results would suggest that rectal administration of thuricin may be a promising mode of delivery of thuricin CD to the colon.}},
   = {10.1099/mic.0.068767-0},
  source = {IRIS}
}