-
Je něco špatně v tomto záznamu ?
Preliminary insights into the impact of dietary starch on the ciliate, Neobalantidium coli, in captive chimpanzees
K. Schovancová, K. Pomajbíková, P. Procházka, D. Modrý, P. Bolechová, KJ. Petrželková,
Jazyk angličtina Země Spojené státy americké
Typ dokumentu časopisecké články, práce podpořená grantem
NLK
Directory of Open Access Journals
od 2006
Free Medical Journals
od 2006
Public Library of Science (PLoS)
od 2006
PubMed Central
od 2006
Europe PubMed Central
od 2006
ProQuest Central
od 2006-12-01
Open Access Digital Library
od 2006-10-01
Open Access Digital Library
od 2006-01-01
Open Access Digital Library
od 2006-01-01
Medline Complete (EBSCOhost)
od 2008-01-01
Nursing & Allied Health Database (ProQuest)
od 2006-12-01
Health & Medicine (ProQuest)
od 2006-12-01
Public Health Database (ProQuest)
od 2006-12-01
ROAD: Directory of Open Access Scholarly Resources
od 2006
- MeSH
- Ciliophora metabolismus MeSH
- dietní sacharidy aplikace a dávkování MeSH
- Pan troglodytes * MeSH
- škrob aplikace a dávkování MeSH
- zvířata MeSH
- Check Tag
- ženské pohlaví MeSH
- zvířata MeSH
- Publikační typ
- časopisecké články MeSH
- práce podpořená grantem MeSH
Infections caused by the intestinal ciliate Neobalantidium coli are asymptomatic in most hosts. In humans and captive African great apes clinical infections occasionally occur, manifested mainly by dysentery; however, factors responsible for development of clinical balantidiasis have not been fully clarified. We studied the effect of dietary starch on the intensities of infection by N. coli in two groups of captive chimpanzees. Adult chimpanzees infected by N. coli from the Hodonín Zoo and from the Brno Zoo, Czech Republic, were fed with a high starch diet (HSD) (average 14.7% of starch) for 14 days, followed by a five-day transition period and subsequently with a period of low starch diet (LoSD) (average 0.1% of starch) for another 14 days. We collected fecal samples during the last seven days of HSD and LoSD and fixed them in 10% formalin. We quantified trophozoites of N. coli using the FLOTAC method. The numbers of N. coli trophozoites were higher during the HSD (mean ± SD: 49.0 ± 134.7) than during the LoSD (3.5 ± 6.8). A generalized linear mixed-effects model revealed significantly lower numbers of the N. coli trophozoites in the feces during the LoSD period in comparison to the HSD period (treatment contrast LoSD vs. HSD: 2.7 ± 0.06 (SE), z = 47.7; p<0.001). We conclude that our data provide a first indication that starch-rich diet might be responsible for high intensities of infection of N. coli in captive individuals and might predispose them for clinically manifested balantidiasis. We discuss the potential nutritional modifications to host diets that can be implemented in part to control N. coli infections.
Citace poskytuje Crossref.org
- 000
- 00000naa a2200000 a 4500
- 001
- bmc14074466
- 003
- CZ-PrNML
- 005
- 20141006122237.0
- 007
- ta
- 008
- 141006s2013 xxu f 000 0|eng||
- 009
- AR
- 024 7_
- $a 10.1371/journal.pone.0081374 $2 doi
- 035 __
- $a (PubMed)24282589
- 040 __
- $a ABA008 $b cze $d ABA008 $e AACR2
- 041 0_
- $a eng
- 044 __
- $a xxu
- 100 1_
- $a Schovancová, Kateřina $u Institute of Botany and Zoology, Masaryk University, Brno, Czech Republic.
- 245 10
- $a Preliminary insights into the impact of dietary starch on the ciliate, Neobalantidium coli, in captive chimpanzees / $c K. Schovancová, K. Pomajbíková, P. Procházka, D. Modrý, P. Bolechová, KJ. Petrželková,
- 520 9_
- $a Infections caused by the intestinal ciliate Neobalantidium coli are asymptomatic in most hosts. In humans and captive African great apes clinical infections occasionally occur, manifested mainly by dysentery; however, factors responsible for development of clinical balantidiasis have not been fully clarified. We studied the effect of dietary starch on the intensities of infection by N. coli in two groups of captive chimpanzees. Adult chimpanzees infected by N. coli from the Hodonín Zoo and from the Brno Zoo, Czech Republic, were fed with a high starch diet (HSD) (average 14.7% of starch) for 14 days, followed by a five-day transition period and subsequently with a period of low starch diet (LoSD) (average 0.1% of starch) for another 14 days. We collected fecal samples during the last seven days of HSD and LoSD and fixed them in 10% formalin. We quantified trophozoites of N. coli using the FLOTAC method. The numbers of N. coli trophozoites were higher during the HSD (mean ± SD: 49.0 ± 134.7) than during the LoSD (3.5 ± 6.8). A generalized linear mixed-effects model revealed significantly lower numbers of the N. coli trophozoites in the feces during the LoSD period in comparison to the HSD period (treatment contrast LoSD vs. HSD: 2.7 ± 0.06 (SE), z = 47.7; p<0.001). We conclude that our data provide a first indication that starch-rich diet might be responsible for high intensities of infection of N. coli in captive individuals and might predispose them for clinically manifested balantidiasis. We discuss the potential nutritional modifications to host diets that can be implemented in part to control N. coli infections.
- 650 _2
- $a zvířata $7 D000818
- 650 _2
- $a Ciliophora $x metabolismus $7 D016798
- 650 _2
- $a dietní sacharidy $x aplikace a dávkování $7 D004040
- 650 _2
- $a ženské pohlaví $7 D005260
- 650 12
- $a Pan troglodytes $7 D002679
- 650 _2
- $a škrob $x aplikace a dávkování $7 D013213
- 655 _2
- $a časopisecké články $7 D016428
- 655 _2
- $a práce podpořená grantem $7 D013485
- 700 1_
- $a Pomajbíková, Kateřina
- 700 1_
- $a Procházka, Petr
- 700 1_
- $a Modrý, David
- 700 1_
- $a Bolechová, Petra
- 700 1_
- $a Petrželková, Klára J
- 773 0_
- $w MED00180950 $t PloS one $x 1932-6203 $g Roč. 8, č. 11 (2013), s. e81374
- 856 41
- $u https://pubmed.ncbi.nlm.nih.gov/24282589 $y Pubmed
- 910 __
- $a ABA008 $b sig $c sign $y a $z 0
- 990 __
- $a 20141006 $b ABA008
- 991 __
- $a 20141006122714 $b ABA008
- 999 __
- $a ok $b bmc $g 1042349 $s 873378
- BAS __
- $a 3
- BAS __
- $a PreBMC
- BMC __
- $a 2013 $b 8 $c 11 $d e81374 $i 1932-6203 $m PLoS One $n PLoS One $x MED00180950
- LZP __
- $a Pubmed-20141006