Fluoroscence in situ hybridization of chicken intestinal samples with bacterial rRNA targeted oligonucleotide probes

Research output: Chapter in Book/Report/Conference proceedingArticle in proceedingsResearch

Standard

Fluoroscence in situ hybridization of chicken intestinal samples with bacterial rRNA targeted oligonucleotide probes. / Olsen, Katja Nyholm; Francesch, M.; Christensen, Henrik.

Ikke angivet. ed. / I. Romboli; D. Flock; A. Franchini. World's Poultry Science Association, 2006. (World's Poultry Science Journal; No. Suppl.).

Research output: Chapter in Book/Report/Conference proceedingArticle in proceedingsResearch

Harvard

Olsen, KN, Francesch, M & Christensen, H 2006, Fluoroscence in situ hybridization of chicken intestinal samples with bacterial rRNA targeted oligonucleotide probes. in I Romboli, D Flock & A Franchini (eds), Ikke angivet. World's Poultry Science Association, World's Poultry Science Journal, no. Suppl., European Poultry Conference, Verona, Italy, 10/09/2006.

APA

Olsen, K. N., Francesch, M., & Christensen, H. (2006). Fluoroscence in situ hybridization of chicken intestinal samples with bacterial rRNA targeted oligonucleotide probes. In I. Romboli, D. Flock, & A. Franchini (Eds.), Ikke angivet World's Poultry Science Association. World's Poultry Science Journal No. Suppl.

Vancouver

Olsen KN, Francesch M, Christensen H. Fluoroscence in situ hybridization of chicken intestinal samples with bacterial rRNA targeted oligonucleotide probes. In Romboli I, Flock D, Franchini A, editors, Ikke angivet. World's Poultry Science Association. 2006. (World's Poultry Science Journal; No. Suppl.).

Author

Olsen, Katja Nyholm ; Francesch, M. ; Christensen, Henrik. / Fluoroscence in situ hybridization of chicken intestinal samples with bacterial rRNA targeted oligonucleotide probes. Ikke angivet. editor / I. Romboli ; D. Flock ; A. Franchini. World's Poultry Science Association, 2006. (World's Poultry Science Journal; No. Suppl.).

Bibtex

@inproceedings{ee110af0a1c011ddb6ae000ea68e967b,
title = "Fluoroscence in situ hybridization of chicken intestinal samples with bacterial rRNA targeted oligonucleotide probes",
abstract = "The objective was to develop a fast and accurate molecular method for the quantification of the intestinal flora in chickens by rRNA fluorescence in situ hybridization (FISH). Seven weeks old conventionally reared Lohmann hens were used to set up the method. To sample ileal intestinal content, the distal part from Meckels diverticulum to the ileo-caecal junction was removed. Fixation was performed in ethanol and phosphate buffered saline. After washing by centrifugation, the sample was resuspended in pre-heated hybridization buffer with oligonucleotide probe labelled with Cy3 (10ng/µl). The cells were hybridized for 24-72h, centrifuged, washed with pre-heated hybridization buffer, centrifuged and resuspended in Millipore quality water before filtration onto a 0.22 µm black polycarbonate filter. The probes used in this study were, LGC354A, LGC354B, LGC354C, Strc493, Bacto1080, Sal3, Chis150, EUB338, Probe D and Non-EUB338 according to previous publications. Cultures of 38 bacterial strains representing type strains within the genera Bacillus, Listeria, Campylobacter, Bacteroides, Clostridium, Enterococcus, Streptococcus, Escherichia, Salmonella and Lactobacillus were used for optimization of hybridization conditions on slides. Signal was obtained from all 38 reference strains with probe EUB338 and not from the non-sense probe Non-EUB338. In most cases, signal was obtained from the expected target sequence. In the samples from the seven weeks old Lohman hens, 3-7 ×108 bacterial cells per g of sample were counted by the EUB338 probe. Three weeks old male broiler Ross 308 chickens were used to investigate the bacterial composition of the intestine. The birds received a wheat-barley diet. Counts with the EUB338 probe were 1.97x108(std 1.45x108) The means of counts obtained with probes targeting the rRNA of genera Lactobacillus, Bacillus, Enterococcus-Streptococcus, Enterobacteriaceae, Salmonella, Clostridium and Bacteriodes were around 1 ×108 bacterial cells per g of gut material. As for the EUB338 probe, huge variations were observed between the six different samples analysed even though each sample was obtained from a pool of six chickens allocated in the same cage. The technique will be used to investigate the effect of antimicrobials, feed additive, rearing conditions and Salmonella - and Campylobacter status on the bacterial composition of the chicken intestine.",
author = "Olsen, {Katja Nyholm} and M. Francesch and Henrik Christensen",
year = "2006",
language = "English",
series = "World's Poultry Science Journal",
number = "Suppl.",
editor = "I. Romboli and D. Flock and A. Franchini",
booktitle = "Ikke angivet",
publisher = "World's Poultry Science Association",
note = "null ; Conference date: 10-09-2006 Through 14-09-2006",

}

RIS

TY - GEN

T1 - Fluoroscence in situ hybridization of chicken intestinal samples with bacterial rRNA targeted oligonucleotide probes

AU - Olsen, Katja Nyholm

AU - Francesch, M.

AU - Christensen, Henrik

N1 - Conference code: 12

PY - 2006

Y1 - 2006

N2 - The objective was to develop a fast and accurate molecular method for the quantification of the intestinal flora in chickens by rRNA fluorescence in situ hybridization (FISH). Seven weeks old conventionally reared Lohmann hens were used to set up the method. To sample ileal intestinal content, the distal part from Meckels diverticulum to the ileo-caecal junction was removed. Fixation was performed in ethanol and phosphate buffered saline. After washing by centrifugation, the sample was resuspended in pre-heated hybridization buffer with oligonucleotide probe labelled with Cy3 (10ng/µl). The cells were hybridized for 24-72h, centrifuged, washed with pre-heated hybridization buffer, centrifuged and resuspended in Millipore quality water before filtration onto a 0.22 µm black polycarbonate filter. The probes used in this study were, LGC354A, LGC354B, LGC354C, Strc493, Bacto1080, Sal3, Chis150, EUB338, Probe D and Non-EUB338 according to previous publications. Cultures of 38 bacterial strains representing type strains within the genera Bacillus, Listeria, Campylobacter, Bacteroides, Clostridium, Enterococcus, Streptococcus, Escherichia, Salmonella and Lactobacillus were used for optimization of hybridization conditions on slides. Signal was obtained from all 38 reference strains with probe EUB338 and not from the non-sense probe Non-EUB338. In most cases, signal was obtained from the expected target sequence. In the samples from the seven weeks old Lohman hens, 3-7 ×108 bacterial cells per g of sample were counted by the EUB338 probe. Three weeks old male broiler Ross 308 chickens were used to investigate the bacterial composition of the intestine. The birds received a wheat-barley diet. Counts with the EUB338 probe were 1.97x108(std 1.45x108) The means of counts obtained with probes targeting the rRNA of genera Lactobacillus, Bacillus, Enterococcus-Streptococcus, Enterobacteriaceae, Salmonella, Clostridium and Bacteriodes were around 1 ×108 bacterial cells per g of gut material. As for the EUB338 probe, huge variations were observed between the six different samples analysed even though each sample was obtained from a pool of six chickens allocated in the same cage. The technique will be used to investigate the effect of antimicrobials, feed additive, rearing conditions and Salmonella - and Campylobacter status on the bacterial composition of the chicken intestine.

AB - The objective was to develop a fast and accurate molecular method for the quantification of the intestinal flora in chickens by rRNA fluorescence in situ hybridization (FISH). Seven weeks old conventionally reared Lohmann hens were used to set up the method. To sample ileal intestinal content, the distal part from Meckels diverticulum to the ileo-caecal junction was removed. Fixation was performed in ethanol and phosphate buffered saline. After washing by centrifugation, the sample was resuspended in pre-heated hybridization buffer with oligonucleotide probe labelled with Cy3 (10ng/µl). The cells were hybridized for 24-72h, centrifuged, washed with pre-heated hybridization buffer, centrifuged and resuspended in Millipore quality water before filtration onto a 0.22 µm black polycarbonate filter. The probes used in this study were, LGC354A, LGC354B, LGC354C, Strc493, Bacto1080, Sal3, Chis150, EUB338, Probe D and Non-EUB338 according to previous publications. Cultures of 38 bacterial strains representing type strains within the genera Bacillus, Listeria, Campylobacter, Bacteroides, Clostridium, Enterococcus, Streptococcus, Escherichia, Salmonella and Lactobacillus were used for optimization of hybridization conditions on slides. Signal was obtained from all 38 reference strains with probe EUB338 and not from the non-sense probe Non-EUB338. In most cases, signal was obtained from the expected target sequence. In the samples from the seven weeks old Lohman hens, 3-7 ×108 bacterial cells per g of sample were counted by the EUB338 probe. Three weeks old male broiler Ross 308 chickens were used to investigate the bacterial composition of the intestine. The birds received a wheat-barley diet. Counts with the EUB338 probe were 1.97x108(std 1.45x108) The means of counts obtained with probes targeting the rRNA of genera Lactobacillus, Bacillus, Enterococcus-Streptococcus, Enterobacteriaceae, Salmonella, Clostridium and Bacteriodes were around 1 ×108 bacterial cells per g of gut material. As for the EUB338 probe, huge variations were observed between the six different samples analysed even though each sample was obtained from a pool of six chickens allocated in the same cage. The technique will be used to investigate the effect of antimicrobials, feed additive, rearing conditions and Salmonella - and Campylobacter status on the bacterial composition of the chicken intestine.

M3 - Article in proceedings

T3 - World's Poultry Science Journal

BT - Ikke angivet

A2 - Romboli, I.

A2 - Flock, D.

A2 - Franchini, A.

PB - World's Poultry Science Association

Y2 - 10 September 2006 through 14 September 2006

ER -

ID: 8027558