Aspergillus Fumigatus In the Mesenteric Lymph Nodes and Intestinal Mucosa of Cattle

1969 ◽  
Vol 125 (4) ◽  
pp. xiii-xiv ◽  
Author(s):  
N.J.L. Gilmour ◽  
K.W. Angus
2002 ◽  
Vol 70 (12) ◽  
pp. 6788-6797 ◽  
Author(s):  
Susan M. Paulin ◽  
Patricia R. Watson ◽  
Annette R. Benmore ◽  
Mark P. Stevens ◽  
Philip W. Jones ◽  
...  

ABSTRACT Host and bacterial factors that determine whether Salmonella serotypes remain restricted to the gastrointestinal tract or penetrate beyond the mucosa and cause systemic disease remain largely undefined. Here, factors influencing Salmonella host specificity in calves were assessed by characterizing the pathogenesis of different serotypes. Salmonella enterica serotype Dublin was highly virulent intravenously, whereas S. enterica serotype Choleraesuis was moderately virulent. Both serotypes were virulent in calves infected orally. In contrast, S. enterica serotypes Gallinarum and Abortusovis were avirulent by either route. Serotypes Dublin, Gallinarum, and Abortusovis colonized the intestinal tract 24 h after oral inoculation, yet only serotype Dublin was consistently recovered from systemic tissues. Serotypes Dublin and Gallinarum invaded bovine intestines in greater numbers and induced greater enteropathogenic responses than serotypes Choleraesuis and Abortusovis. However, only serotype Dublin was able to persist within the intestinal mucosa, and use of a novel cannulation model demonstrated that serotype Dublin was able to pass through the mesenteric lymph nodes in greater numbers than serotype Gallinarum. Together, these results suggest that initial interactions with the intestinal mucosa do not correlate with host specificity, although persistence within tissues and translocation via efferent lymphatics appear to be crucial for the induction of bovine salmonellosis.


1984 ◽  
Vol 87 (3) ◽  
pp. 606-614 ◽  
Author(s):  
C. Matuchansky ◽  
R. Colin ◽  
J. Hemet ◽  
G. Touchard ◽  
P. Babin ◽  
...  

2004 ◽  
Vol 78 (1) ◽  
pp. 17-24 ◽  
Author(s):  
A. Cywińska ◽  
K. Czumińska ◽  
A. Schollenberger

AbstractHost responses to primary infections withHeligmosomoides polygyruswere studied in fast responding FVB mice (H-2q). Pathological changes in the intestinal mucosa, mesenteric lymph nodes and spleen were examined. Features of the fast response were typical: low effectiveness of infection and limiting of parasite survival and egg production, with worm expulsion occurring about 60 days post-infection. The intestinal inflammatory response involved infiltration by different cells into the intestinal mucosa and granulomata formation. As is typical for intestinal nematode infection enteropathy, decreased villus:crypt ratio and hyperplasia of goblet and Paneth cells were also present. Reactions of the intestinal mucosa, mesenteric lymph nodes and spleen increased over time post-infection and after worm expulsion. Enteropathy may help worm expulsion by creating an unfavourable environment forH. polygyrus. The implications of these findings and the potential role of intestinal intraepithelial lymphocytes in the pathogenesis of generated lesions are discussed.


1984 ◽  
Vol 18 (3) ◽  
pp. 252-257 ◽  
Author(s):  
J. W. M. A. Mullink ◽  
F. H. M. Morsink

The numbers of IgA-producing cells in intestinal mucosa, mesenteric lymph nodes, lungs and bronchial lymph nodes were scored in rats and mice. A statistically significant difference in the scores existed between germ-free and SPF mice and between gnotobiotic and SPF rats. In a group of SPF rats a statistically significant difference in the scores was demonstrated in relation to several bacterial and viral agents.


2006 ◽  
Vol 203 (3) ◽  
pp. 497-500 ◽  
Author(s):  
Andrew J. Macpherson ◽  
Karen Smith

The surface of the intestinal mucosa is constantly assaulted by food antigens and enormous numbers of commensal microbes and their products, which are sampled by dendritic cells (DCs). Recent work shows that the mesenteric lymph nodes (MLNs) are the key site for tolerance induction to food proteins and that they also act as a firewall to prevent live commensal intestinal bacteria from penetrating the systemic immune system.


2001 ◽  
Vol 120 (5) ◽  
pp. A183-A183
Author(s):  
H KOBAYASHI ◽  
H NAGATA ◽  
S MIURA ◽  
T AZUMA ◽  
H SUZUKI ◽  
...  

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