I. Gohin et al., ANALYSIS OF THE IMMUNE-RESPONSE IN SHEEP EFFERENT LYMPH DURING SALMONELLA-ABORTUSOVIS INFECTION, Veterinary immunology and immunopathology, 60(1-2), 1997, pp. 111-130
The efferent lymph duct of the ovine prescapular lymph node was cannul
ated, and Salmonella abortusovis (SAG), a specific pathogen for sheep
inducing abortion and mortality of newborn lambs, was inoculated by th
e subcutaneous route in this lymph node drained area, While the presca
pular lymph node draining the inoculation site represented an efficien
t barrier for the vaccinal SAO Rv6 strain spreading, SAO 15/5 virulent
bacteria were steadily detected in efferent lymph of infected sheep.
The inoculation of the virulent strain of SAO induced a greater increa
se of the cell output than did the attenuated vaccinal strain, but pro
portions of blast cells appearing in the efferent lymph were similar i
n both cases. Flow cytometry analysis showed that B and T cell outputs
were both increased during SAO infections, but while T cell subset pr
oportions slightly decreased, B cell percentages significantly rose, a
nd, at the peak response, almost all of the lymphoblast cells were act
ivated B cells. Typical antibody profiles characteristic of a primary
immune response were observed, and antibody titres were greater in the
efferent lymph of animals inoculated with the virulent strain of SAG.
Many of the cytokine mRNAs we investigated were steadily detected by
RT-PCR in efferent lymph cells of control sheep, but frequencies of de
tection of IL-2, IFN gamma, IL-1 beta and TNF alpha mRNAs were augment
ed in efferent lymph cells following inoculation of both SAO virulent
or vaccinal strains. IL-10 and IL-8 mRNAs could only be detected after
a SAO inoculation, while detection of IL-4 mRNAs was increased only i
n efferent lymph cells from SAO virulent strain-infected sheep. The ef
ferent lymph cannulation technique thus appeared a very powerful way t
o study the in vivo development of the immune response to SAG, in its
natural host, the sheep. (C) 1997 Elsevier Science B.V.