Intestinal peptide transporter PepT1 is over-expressed during acute cryptosporidiosis in suckling rats as a result of both malnutrition and experimental parasite infection

被引:32
作者
Barbot, L [1 ]
Windsor, E
Rome, S
Tricottet, V
Reynès, M
Topouchian, A
Huneau, JF
Gobert, JG
Tomé, D
Kapel, N
机构
[1] Univ Paris 05, Fac Sci Pharmaceut & Biol, Lab Biol Anim & Parasitaire, F-75006 Paris, France
[2] Grp Hosp Pitie Salpetriere, Serv Coprol Fonctionnelle, Div Vincent de Paul, F-75013 Paris, France
[3] Inst Natl Agron Paris Grignon, UMR 914 Physiol Nutr & Comportement Alimentaire, F-75005 Paris, France
[4] Univ Paris 05, Fac Sci Pharmaceut & Biol, Serv Commun Imagerie Cellulaire & Mol, F-75006 Paris, France
[5] Ctr Hosp Paul Brosse, Anat Pathol Lab, F-94804 Villejuif, France
关键词
D O I
10.1007/s00436-002-0776-3
中图分类号
R38 [医学寄生虫学]; Q [生物科学];
学科分类号
07 ; 0710 ; 09 ; 100103 ;
摘要
Cryplosporidium parvum infection induces amino acid malnutrition leading to growth retardation in children. Owing to the nutritional efficiency of peptides compared to free amino acids and the resistance of the di-tripeptide transporter PepT1 to mucosal injury, we analyzed the intestinal expression of PepT1 during experimental acute cryptosporidiosis in suckling rats from day 4 to day 50. PepT1 mRNA levels were increased at the peak of infection (day 10) all along the small intestine and normalized after spontaneous clearance of the parasite (day 21). Immunolocalization of PepT1 showed that its expression was maintained in the brush border membrane of enterocytes in infected rats from day 4 to day 50 all along the small intestine. Our results suggest a transcriptional up-regulation during acute cryptosporidiosis in response to both C. parvum-induced malnutrition and parasite implantation. As no treatment is available, a semi-elemental diet should be considered part of the treatment of cryptosporidiosis.
引用
收藏
页码:364 / 370
页数:7
相关论文
共 39 条
[1]  
Adibi S. A., 1981, PHYSL GASTROINTESTIN, P1073
[2]  
ADIBI SA, 1974, GASTROENTEROLOGY, V67, P586
[3]   Cryptosporidiosis in northeastern Brazilian children: Association with increased diarrhea morbidity [J].
Agnew, DG ;
Lima, AAM ;
Newman, RD ;
Wuhib, T ;
Moore, RD ;
Guerrant, RL ;
Sears, CL .
JOURNAL OF INFECTIOUS DISEASES, 1998, 177 (03) :754-760
[4]   VILLOUS ATROPHY, CRYPT HYPERPLASIA, CELLULAR INFILTRATION, AND IMPAIRED GLUCOSE-NA ABSORPTION IN ENTERIC CRYPTOSPORIDIOSIS OF PIGS [J].
ARGENZIO, RA ;
LIACOS, JA ;
LEVY, ML ;
MEUTEN, DJ ;
LECCE, JG ;
POWELL, DW .
GASTROENTEROLOGY, 1990, 98 (05) :1129-1140
[5]   PepT1-mediated epithelial transport of dipeptides and cephalexin is enhanced by luminal leptin in the small intestine [J].
Buyse, M ;
Berlioz, F ;
Guilmeau, S ;
Tsocas, A ;
Voisin, T ;
Péranzi, G ;
Merlin, D ;
Laburthe, M ;
Lewin, MJM ;
Rozé, C ;
Bado, A .
JOURNAL OF CLINICAL INVESTIGATION, 2001, 108 (10) :1483-1494
[6]   Cryptosporidium parvum infection in suckling rats:: Impairment of mucosal permeability and Na+-glucose cotransport [J].
Capet, C ;
Kapel, N ;
Huneau, JF ;
Magne, D ;
Laikuen, R ;
Tricottet, V ;
Benhamou, Y ;
Tomé, D ;
Gobert, JG .
EXPERIMENTAL PARASITOLOGY, 1999, 91 (02) :119-125
[7]  
Checkley W, 1998, AM J EPIDEMIOL, V148, P497, DOI 10.1093/oxfordjournals.aje.a009675
[8]  
Checkley W, 1997, AM J EPIDEMIOL, V145, P156, DOI 10.1093/oxfordjournals.aje.a009086
[9]   EXPRESSION OF AMINO-ACID AND PEPTIDE-TRANSPORT SYSTEMS IN RAT SMALL-INTESTINE [J].
CHEESEMAN, CI .
AMERICAN JOURNAL OF PHYSIOLOGY, 1986, 251 (05) :G636-G641
[10]   SINGLE-STEP METHOD OF RNA ISOLATION BY ACID GUANIDINIUM THIOCYANATE PHENOL CHLOROFORM EXTRACTION [J].
CHOMCZYNSKI, P ;
SACCHI, N .
ANALYTICAL BIOCHEMISTRY, 1987, 162 (01) :156-159