Seven- to eight-week-old rabbits were infected with Eimeria intestinalis Cheissin, 1948, a highly immunogenic coccidium, or Eimeria flavescens Marotel et Guilhon, 1941, which is weakly immunogenic. Immune response was investigated at 7, 14 and 21 days post inoculation (DPI). The level of serum immunoglobulins, lymphocyte proliferation stimulated by parasite antigens and weight of mesenteric lymph nodes (MLN) showed similar dynamics in rabbits inoculated with both coccidia species. The amount of serum IgG and IgM, but not IgA, was increased from 14 DPI. The lymphocytes from MLN of infected animals significantly reacted to stimulation with parasite antigen 14 and 21 DPI and MLN were enlarged at 14 DPI. Thus, both parasite species elicited immune response characterized by these parameters in a similar manner despite of their different immunogenicity. The only apparent difference in the responses was in the percentage of CD8+ lymphocytes in the specific site of parasite development (the last third of the small intestine in E. intestinalis, caecum in E. flavescens), which increased in rabbits infected with E. intestinalis but not with E. flavescens. This parameter reflects the status of local immunity and hence the results suggest that the local reaction plays an important role in induction of protective immunity to coccidia in rabbits.
To investigate into the relationship between two Rubisco activase (RCA) isoforms and photosynthetic rate, a set of enzyme-linked immunosorbent assay (ELISA) were developed for accurate quantification of two RCA polypeptides based on two specific monoclonal antibodies against different RCA isoforms. The results showed that content of RCA small isoform (RCAS) was 5-fold more than that of RCA large isoform (RCAL) content in all leaves and the RCAL/RCAS ratio reached maximum in the leaf with the highest photosynthetic rate. Although the difference in two RCA polypeptides accumulation in leaves was caused by different transcript level of two isoforms, the decrease of RCAL/RCAS ratio during leaf aging was not attributed to transcriptional regulation. The leaves with higher photosynthetic capacity exhibited higher RCAL/RCAS ratio and the decrease in photosynthetic rate and Rubisco activation state highly correlated with the decline of RCAL/RCAS ratio during leaf aging. Our results suggest that there is a posttranscriptional mechanism regulating the RCAL/RCAS ratio, which may play as a regulator modulating photosynthetic capacity during leaf aging in rice plant. and D. Wang ... [et al.].
Intact chloroplasts were isolated from dark-senescing primary barley (Hordeum vulgare L.) leaves in order to study selective ribulose-1,5-bisphosphate carboxylase/oxygenase (RuBPCO) degradation by the stromal and membrane fractions. RuBPCO specific degradation was estimated and characterised applying sensitive avidin-biotin ELISA method with non-modified or oxidatively modified biotinylated RuBPCO (BR) as substrates. Distinct proteolytic activities were detected. They differed in ATP and divalent metal ion dependence, protease inhibitory profile, and dynamics in the time-course of dark-induced senescence. The results supported involvement of ATP- and metal ion-dependent serine type proteolytic activity against non-modified BR early in induced senescence and appearance of ATP-independent activity at later stage. Active oxygen-modified BR was degraded by ATP-independent serine-type protease probably containing essential SH-groups and requiring divalent metal ions. and L. Simova-Stoilova, K. Demirevska-Kepova, Z. Stoyanova.
The variations in antibody responses (total IgG and IgGl, IgG2a, IgG2b, and IgG2c subclasses) were studied in two groups of rats infected with metacercariae of the trematode Fasciola hepatica L. Animals of group 1 were 4 weeks old, and rats of group 2 were 13 weeks old. All IgG subclasses increased during the course of infection except IgG2c, which decreased. The younger rats reached more marked responses than the older, at least during the period of this trial. IgGl and IgG2a antibodies reached the highest levels, and among these two, IgG2a response was slightly superior to IgGl,