Comprehensive study of the intestinal stage of listeriosis in a rat ligated ileal loop system

被引:98
作者
Pron, B
Boumaila, C
Jaubert, F
Sarnacki, S
Monnet, JP
Berche, P
Gaillard, JL
机构
[1] Fac Necker Enfants Malad, Microbiol Lab, INSERM, U411, F-75730 Paris 15, France
[2] Fac Necker Enfants Malad, Pathol Lab, F-75730 Paris 15, France
[3] Fac Necker Enfants Malad, Unite Chirurg Expt, F-75730 Paris 15, France
关键词
D O I
10.1128/IAI.66.2.747-755.1998
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
The intestinal stage of listeriosis was studied in a rat ligated ileal loop system. Listeria monocytogenes translocated to deep organs,vith similar efficiencies after inoculation of loops with or without Peyer's patches. Bacterial seeding of deep organs was demonstrated as early as 15 min after inoculation, It was dose dependent and nonspecific, as the Delta inlAB, the Delta hly, and the Delta actA L. monocytogenes mutants and the nonpathogenic species, Listeria innocua, translocated similarly to wild-type L, monocytogenes strains, The levels of uptake of listeriae by Peyer's patches and villous intestine were similar and low, 50 to 250 CFU per cm(2) of tissue. No listeria cells crossing the epithelial sheet of Peyer's patches and villous intestine were observed by transmission electron microscopy, The lack of significant interaction of listeriae and the follicle-associated epithelium of Peyer's patches was confirmed by scanning electron microscopy. The follicular tissue of Peyer's patches was a preferential site of Listeria replication. With all doses tested, the rate of bacterial growth was 10 to 20 times higher in Peyer's patches than in villous intestine, At early stages of Peyer's patch infection, listeriae were observed inside mononuclear cells of the dome area. Listeriae then disseminated throughout the follicular tissue except for the germinal center. The virulence determinants hly and, to a lesser extent, actA, but not inlAB, were required for the completion of this process, This study suggests that Peyer's patches are preferential sites for replication rather than for entry of L. monocytogenes, due to the presence of highly permissive mononuclear cells whose nature remains to be defined.
引用
收藏
页码:747 / 755
页数:9
相关论文
共 38 条
[21]   A MICROBIOLOGICAL, HISTOPATHOLOGICAL AND IMMUNOHISTOLOGICAL STUDY OF THE INTRAGASTRIC INOCULATION OF LISTERIA-MONOCYTOGENES IN MICE [J].
MARCO, AJ ;
PRATS, N ;
RAMOS, JA ;
BRIONES, V ;
BLANCO, M ;
DOMINGUEZ, L ;
DOMINGO, M .
JOURNAL OF COMPARATIVE PATHOLOGY, 1992, 107 (01) :1-9
[22]   INTRACELLULAR AND CELL-TO-CELL SPREAD OF LISTERIA-MONOCYTOGENES INVOLVES INTERACTION WITH F-ACTIN IN THE ENTEROCYTE-LIKE CELL-LINE CACO-2 [J].
MOUNIER, J ;
RYTER, A ;
COQUISRONDON, M ;
SANSONETTI, PJ .
INFECTION AND IMMUNITY, 1990, 58 (04) :1048-1058
[23]  
Neutra M R, 1992, Trends Cell Biol, V2, P134, DOI 10.1016/0962-8924(92)90099-9
[24]   HOST-RESISTANCE TO AN INTRAGASTRIC INFECTION WITH LISTERIA-MONOCYTOGENES IN MICE DEPENDS ON CELLULAR-IMMUNITY AND INTESTINAL BACTERIAL-FLORA [J].
OKAMOTO, M ;
NAKANE, A ;
MINAGAWA, T .
INFECTION AND IMMUNITY, 1994, 62 (08) :3080-3085
[25]   ACUTE-INFLAMMATION CAUSES EPITHELIAL INVASION AND MUCOSAL DESTRUCTION IN EXPERIMENTAL SHIGELLOSIS [J].
PERDOMO, OJJ ;
CAVAILLON, JM ;
HUERRE, M ;
OHAYON, H ;
GOUNON, P ;
SANSONETTI, PJ .
JOURNAL OF EXPERIMENTAL MEDICINE, 1994, 180 (04) :1307-1319
[26]   CYTOPATHOGENIC EFFECTS IN ENTEROCYTE-LIKE CACO-2 CELLS DIFFERENTIATE VIRULENT FROM AVIRULENT LISTERIA STRAINS [J].
PINE, L ;
KATHARIOU, S ;
QUINN, F ;
GEORGE, V ;
WENGER, JD ;
WEAVER, RE .
JOURNAL OF CLINICAL MICROBIOLOGY, 1991, 29 (05) :990-996
[27]  
PINE L, 1990, LAB INVEST, V26, P694
[28]   MOLECULAR DETERMINANTS OF LISTERIA-MONOCYTOGENES PATHOGENESIS [J].
PORTNOY, DA ;
CHAKRABORTY, T ;
GOEBEL, W ;
COSSART, P .
INFECTION AND IMMUNITY, 1992, 60 (04) :1263-1267
[29]  
RACZ P, 1972, LAB INVEST, V26, P694
[30]   HEMOLYSIN IS REQUIRED FOR EXTRAINTESTINAL DISSEMINATION OF LISTERIA-MONOCYTOGENES IN INTRAGASTRICALLY INOCULATED MICE [J].
ROLL, JT ;
CZUPRYNSKI, CJ .
INFECTION AND IMMUNITY, 1990, 58 (09) :3147-3150