File Download
There are no files associated with this item.
Links for fulltext
(May Require Subscription)
- Publisher Website: 10.1159/000317807
- Scopus: eid_2-s2.0-78649700775
- PMID: 21135563
- WOS: WOS:000292043200007
- Find via
Supplementary
- Citations:
- Appears in Collections:
Article: Bacterial colonization affects the intestinal proteome of preterm pigs susceptible to necrotizing enterocolitis
Title | Bacterial colonization affects the intestinal proteome of preterm pigs susceptible to necrotizing enterocolitis | ||||||
---|---|---|---|---|---|---|---|
Authors | |||||||
Keywords | Germ free Microbial colonization Necrotizing enterocolitis Proteomics Two-dimensional gel electrophoresis | ||||||
Issue Date | 2011 | ||||||
Publisher | S Karger AG. The Journal's web site is located at http://www.karger.com/BON | ||||||
Citation | Neonatology, 2011, v. 99 n. 4, p. 280-288 How to Cite? | ||||||
Abstract | Background: In newborns, colonizing bacteria and enteral nutrition are important for early gut development and immunity. However, in preterm newborns, bacterial colonization, coupled with enteral feeding, can lead to marked intestinal inflammation and disease such as necrotizing enterocolitis (NEC). We hypothesized that the initial bacterial colonization of the gut affects the intestinal proteome independently of enteral feeding. Objective: To identify the intestinal proteins affected by the first colonizing bacteria by comparing the intestinal proteome in formula-fed preterm pigs reared under germ free (GF) or conventional conditions. Methods: Gel-based proteomics of the small intestine to detect proteins that may play a part in the response of the immature intestine to bacterial colonization after birth. Results: Fourteen proteins involved in stress response and detoxification (e.g. heat-shock proteins, peroxiredoxin 1), tissue metabolism and apoptosis (e.g. annexin 2), and some signal transduction pathways were differentially expressed between GF and conventionally reared pigs. Conclusion: The premature intestine is highly responsive to initial bacterial colonization and the specific bacteria-related proteome changes may contribute to the stress response that makes the immature intestine sensitive to the pro-inflammatory effects of enteral feeding. Copyright © 2010 S. Karger AG, Basel. | ||||||
Persistent Identifier | http://hdl.handle.net/10722/133414 | ||||||
ISSN | 2023 Impact Factor: 2.6 2023 SCImago Journal Rankings: 0.874 | ||||||
ISI Accession Number ID |
Funding Information: Research financially supported by the University of Hong Kong and Danish Research Councils. | ||||||
References |
DC Field | Value | Language |
---|---|---|
dc.contributor.author | Jiang, P | en_HK |
dc.contributor.author | Sangild, PT | en_HK |
dc.contributor.author | Siggers, RH | en_HK |
dc.contributor.author | Sit, WH | en_HK |
dc.contributor.author | Lee, CL | en_HK |
dc.contributor.author | Wan, JMF | en_HK |
dc.date.accessioned | 2011-05-11T08:35:45Z | - |
dc.date.available | 2011-05-11T08:35:45Z | - |
dc.date.issued | 2011 | en_HK |
dc.identifier.citation | Neonatology, 2011, v. 99 n. 4, p. 280-288 | en_HK |
dc.identifier.issn | 1661-7800 | en_HK |
dc.identifier.uri | http://hdl.handle.net/10722/133414 | - |
dc.description.abstract | Background: In newborns, colonizing bacteria and enteral nutrition are important for early gut development and immunity. However, in preterm newborns, bacterial colonization, coupled with enteral feeding, can lead to marked intestinal inflammation and disease such as necrotizing enterocolitis (NEC). We hypothesized that the initial bacterial colonization of the gut affects the intestinal proteome independently of enteral feeding. Objective: To identify the intestinal proteins affected by the first colonizing bacteria by comparing the intestinal proteome in formula-fed preterm pigs reared under germ free (GF) or conventional conditions. Methods: Gel-based proteomics of the small intestine to detect proteins that may play a part in the response of the immature intestine to bacterial colonization after birth. Results: Fourteen proteins involved in stress response and detoxification (e.g. heat-shock proteins, peroxiredoxin 1), tissue metabolism and apoptosis (e.g. annexin 2), and some signal transduction pathways were differentially expressed between GF and conventionally reared pigs. Conclusion: The premature intestine is highly responsive to initial bacterial colonization and the specific bacteria-related proteome changes may contribute to the stress response that makes the immature intestine sensitive to the pro-inflammatory effects of enteral feeding. Copyright © 2010 S. Karger AG, Basel. | en_HK |
dc.language | eng | en_US |
dc.publisher | S Karger AG. The Journal's web site is located at http://www.karger.com/BON | en_HK |
dc.relation.ispartof | Neonatology | en_HK |
dc.rights | Neonatology: foetal and neonatal research. Copyright © S Karger AG. | - |
dc.subject | Germ free | en_HK |
dc.subject | Microbial colonization | en_HK |
dc.subject | Necrotizing enterocolitis | en_HK |
dc.subject | Proteomics | en_HK |
dc.subject | Two-dimensional gel electrophoresis | en_HK |
dc.title | Bacterial colonization affects the intestinal proteome of preterm pigs susceptible to necrotizing enterocolitis | en_HK |
dc.type | Article | en_HK |
dc.identifier.openurl | http://library.hku.hk:4550/resserv?sid=HKU:IR&issn=1661-7800&volume=99&issue=4&spage=280&epage=288&date=2010&atitle=Bacterial+colonization+affects+the+intestinal+proteome+of+preterm+pigs+susceptible+to+necrotizing+enterocolitis | - |
dc.identifier.email | Wan, JMF: jmfwan@hku.hk | en_HK |
dc.identifier.authority | Wan, JMF=rp00798 | en_HK |
dc.description.nature | link_to_subscribed_fulltext | - |
dc.identifier.doi | 10.1159/000317807 | en_HK |
dc.identifier.pmid | 21135563 | - |
dc.identifier.scopus | eid_2-s2.0-78649700775 | en_HK |
dc.identifier.hkuros | 184821 | en_US |
dc.relation.references | http://www.scopus.com/mlt/select.url?eid=2-s2.0-78649700775&selection=ref&src=s&origin=recordpage | en_HK |
dc.identifier.volume | 99 | en_HK |
dc.identifier.issue | 4 | en_HK |
dc.identifier.spage | 280 | en_HK |
dc.identifier.epage | 288 | en_HK |
dc.identifier.isi | WOS:000292043200007 | - |
dc.publisher.place | Switzerland | en_HK |
dc.identifier.scopusauthorid | Jiang, P=36147603700 | en_HK |
dc.identifier.scopusauthorid | Sangild, PT=7004115316 | en_HK |
dc.identifier.scopusauthorid | Siggers, RH=14421699900 | en_HK |
dc.identifier.scopusauthorid | Sit, WH=8528923000 | en_HK |
dc.identifier.scopusauthorid | Lee, CL=36600490300 | en_HK |
dc.identifier.scopusauthorid | Wan, JMF=8930305000 | en_HK |
dc.identifier.issnl | 1661-7800 | - |