Interference with homologous immunity and faecal egg excretion in Schistosoma infections in mice concurrently infected with Trypanosoma brucei and Schistosoma mansoni

The effects of the blood protozoan, Trypanosoma brucei, was assessed on the homologous immunity to Schistosoma mansoni infection and the distribution of S. mansoni eggs in the tissues and faeces of dually infected mice. The trypanosome infection reduced the homologous protection induced by a primary S. mansoni infection against a challenge infection and the faecal excretion of eggs during the primary schistosome infection. The findings are discussed in relation to the immunosuppressive action of Trypanosoma infection.     

Effect of vitamins on Trichinella spiralis Owen, 1835 infection in mice

The effects of vitamins A, B complex, E, and ADE on the body weight, eosinophilia, intensity of infection and distribution of T. spiralis larvae were studied in mice. The greatest loss of weight followed after the application of vitamins B complex and E. An increased eosinophilia appeared in the majority of infected mice since day 7 p.i., reaching the maximum on day 21 p.i. In mice receiving vitamins B complex, A, and ADE, the increased eosinophilia was observed still on day 60 p.i. The highest levels of eosinophilia occurred after the application of vitamins B complex and E, which was directly proportional to the intensity of infection. The lowest intensity of infection was recorded in mice receiving vitamin A. Though there were great differences between individual mice, the greatest number of larvae were localized in the diaphragm and left masseter.     

An experimental transmission of porcine strains of Blastocystis sp. in the laboratory mice and gerbils.

Outbred laboratory mice were successfully infected with porcine strains of Blastocystis sp. using faecal stages as well as stages from fresh or passaged cultures. In contrast, inbred BALB/c mice and gerbils were only rarely infected and the intensity of their infection was mostly negligible. Blastocystis sp. was never observed inside the host cells. These results indicate a low host specificity of Blastocystis sp. as well as different sensitivity of investigated hosts to Blastocystis sp. infection.     

Experimental infection of immunocompetent and immunodeficient mice with Encephalitozoon cuniculi

An experimental infection with the microsporidian Encephalitozoon cuniculi Levaditi, Nicolau et Schoen, 1923 was studied using a model of immunocompetent BALB/c mice and immunodeficient SCID mice. The course of infection after intraperitoneal inoculation of E. cuniculi spores was evaluated using the presence of spores in peritoneal macrophages as a criterion. First significant decrease in the proportion of infected cells was recorded on day 9 post infection (p.i.) in BALB/c mice. From day 14 p.i. no spores were observed in macrophages from BALB/c mice, while the number of infected macrophages from SCID mice increased until the death of the mice. The natural killer (NK) cell activity of mouse splenocytes was compared with the production of interferon gamma (IFN-gamma) by these cells. While in BALB/c mice NK activity peaked on days 9 and 14 p.i., in SCID mice the marked increase of NK activity was recorded close before death of mice, on day 21 p.i. in correlation with the production of IFN-gamma. Production of specific antibodies was demonstrated from day 9 p.i. in sera from BALB/c mice. It is concluded that intraperitoneal infection of SCID mice with spores of E. cuniculi results in the marked increase in the number of peritoneal exudate cells and in the percentage of infected cells close before death of mice. Neither high activity of NK cells nor increased production of IFN-gamma are sufficient for the recovery of SCID mice from an E. cuniculi infection.     

Rheumatoid factor-like IgM in Plasmodium berghei (Apicomplexa: Haemosporida) infections of BALB/c mice

Groups of female BALB/c mice infected by intravenous injection with 50 erythrocytes containing Plasmodium berghei Vincke et Lips, 1948 were sacrificed on days 3 through 12 after infection. Rheumatoid factor-like IgM (RF-IgM) and parasite-specific IgG levels were determined by enzyme-linked immunosorbent assay in serum specimens and in culture medium removed from spleen cell cultures established at sacrifice. All four mouse IgG subisotypes were recognized by RF-IgM molecules induced by Plasmodium berghei infection, and in this regard, the parasite-induced RF-IgM response resembled that induced by lipopolysaccharide polyclonal activation. Plasmodium berghei infection resulted in a biphasic RF-IgM response, with infected animals demonstrating significantly increased levels of RF-IgM early in the infection and significantly decreased levels late in the infection, compared to uninfected control mice. The decreased levels of RF-IgM observed late in infection correlated with increasing parasitaemia levels, and were primarily due to a decrease in RF-IgM specific for mouse IgG2a. Late infection levels of RF-IgM specific for IgGI, IgG2b, and IgG3 were not significantly different from those of control animals.     

Serum protein profile of mice during infection with single and repeated doses of Hymenolepis nana eggs

Significant alterations in serum protein of mice following Hymenolepis nana infection were observed. These changes were recorded as decrease in albumin, increase in gamma globulin and a temporary rise in alpha-1, alpha-2 and beta globulins. The decrease in albumin and increase in gamma globulin occurred as early as on 1st day after infection. The alpha-1 and alpha-2 globulins did not show definite profile during infection. The beta globulin predominantly increased till the day 20 post infection and thereafter generally decreased. Repeated infection did not enhance any further alterations in serum protein. There was no significant correlation between infection dose levels and serum protein changes.     

Susceptibility of IFN-gamma or IL-12 knock-out and SCID mice to infection with two microsporidian species, Encephalitozoon cuniculi and E. intestinalis

Susceptibility of three strains of immunodeficient mice to two related microsporidian species Encephalitozoon cuniculi Levaditi, Nicolau et Schoen, 1923 and Encephalitozoon intestinalis (Cali, Kotler et Orenstein, 1993) was compared. While both, severe combined immunodeficient (SCID) and interferon-gamma knock-out (IFN-gamma KO) mice, succumbed to either intraperitoneal (i.p.) or peroral (p.o.) (natural) infection with both parasites, only i.p. infection with E. cuniculi killed interleukin-12 knock-out (IL-12 KO) mice. IFN-gamma KO mice died earlier than SCID mice. Adoptive transfer of naive splenocytes from IFN-gamma KO mice did not protect the SCID mice from a lethal infection with either of the Encephalitozoon species. However, reconstituted mice survived significantly longer (P<0.05), thus indicating the role of IFN-gamma produced by host NK cells in the development of mechanisms of anti-microsporidial protective immunity. Non-lethal outcome of the infection always correlated with the increase in CD8+ T lymphocyte subpopulation. Both E. intestinalis-infected IFN-gamma KO and IL-12 KO mice produced comparable levels of specific antibodies, suggesting that antibodies did not protect IFN-gamma KO mice from lethal infection.     

Cytokine response to infection with the microsporidian, Encephalitozoon cuniculi.

The production of three cytokines, interferon gamma (IFN-gamma), interleukin 10 (IL-10) and interleukin 12 (IL-12), was measured after intraperitoneal infection of immunocompetent Balb/c mice and immunodeficient SCID mice with the microsporidian, Encephalitozoon cuniculi Levaditi, Nicolau et Schoen, 1923. High levels of IFN-gamma were detected in ex vivo cultures of peritoneal exudate cells (PEC) of Balb/c mice, a lower, but earlier IFN-gamma response was observed in PEC from SCID mice. The early IL-10 response was detected in ex vivo cultures of splenocytes from Balb/c but not from SCID mice, explaining a delay in the IFN-gamma response in Balb/c mice. IL-12 was detected in PEC cultures from SCID mice, indicating an alternative pathway of IFN-gamma production by NK cells stimulated by IL-12 derived from macrophages.     

The dynamics of eosinophilia in concurrent infections with Trichinella spiralis Owen, 1835 and Toxascaris leonina Linstow, 1909

The concurrent infection with larvae of Trichinella spiralis and eggs of Toxascaris leonina was studied under various conditions using 75 male white mice. The changes in content of eosinophilic leucocytes in the blood, as well as the total number and distribution of larvae of both parasites in different body tissues were demonstrated. The primary infection with Toxascaris leonina caused an increase in the number of eosinophilic leucocytes from day 4 p.i., whereas the infection with Trichinella spiralis larvae induced an increase only from day 7 p.i. An antagonism was observed between the two parasite species: the primary infection with T. leonina led to a decrease in the total number of muscle larvae of T. spiralis, and, vice versa, the primary infection with T. spiralis suppressed the development of T. leonina.     

Mouse (Mus musculus) as intermediate host of Sarcocystis sp. from the goshawk (Accipiter gentilis)

Sporocysts from the goshawk (Accipiter gentilis) were experimentally transferred to the mouse (Mus musculus). It was found that the goshawk is the host of one of the sarcosporidians inducing muscle sarcocystosis in mice. Thin-walled, sporulated oocysts expelled by the goshawk measured 16.5-19.0 X 12.0-13.0 micron. Those which measured 12.0-13.5 X 8.2-9.0 micron were widely elliptical, with rounded poles. No asexual reproduction of parasites was detected in the viscera of mice. The cysts started to appear in skeletal muscles on day 20 after oral infection with 10,000 or 100,000 sporocysts per mouse. The cysts measuring 15-630 X 18-65 micron contained widely oval metrocytes (2.8-4.3 X 1.5-2.8 micron) or banana-shaped cystozoites (6.0-8.0 X 2.0-3.8 micron). Three months after infection the cysts were found also in the tongue of mice. No morphological differences were observed between the oocysts-sporocysts from owls (Tyto alba and Asio otus) and goshawk, not even between the muscle cysts of these sarcosporidians in mice. The possibility of passaging the species Sarcocystis dispersa from the long-eared owl through the digestive tract of goshawk is discussed.     

Humoral intestinal immunity against Encephalitozoon cuniculi (Microsporidia) infection in mice

Three strains of mice, BALB/c, IL-12 knock-out (KO) and INF-gamma knock-out, were chosen as an experimental model for the study of intestinal immunity induction against Encephalitozoon cuniculi Levaditi, Nicolau et Schoen, 1923 infection. Mice were infected perorally with 10(7) spores and re-infected with the same dose 70 days after the first infection. The anti-E. cuniculi IgA, IgG and IgM responses in sera and extracts of stool samples were determined by ELISA. Results have shown specific antibody production in the sera and intestinal secretions of all three strains of mice induced orally by E. ciniculi spores. BALB/c mice developed a stronger humoral immune response than IL-12 KO mice. The lowest antibody response developed in INF-gamma KO mice that succumbed to the infection within 28 days post infection.     

Influence of thymic preparations on the result of experimental infection with Taenia crassiceps (Zeder, 1800) in ICR mice

Thymalin (Thymarin) and T-activin--thymic preparations of polypeptidic character--were used for influencing the parasitic infection in a model system mouse--Taenia crassiceps. A single subcutaneous application of 100 micrograms of Thymalin per mouse at the day of infection resulted in a decrease (by 54.9%) in the number of cysticerci in peritoneal cavity of experimental mice compared with the controls. Administration of Thymalin with T. crassiceps larval homogenate at various intervals before and after infection resulted in a statistically significant increase of the level of specific antibodies in the serum of infected mice, this increase, however, did not correlate with the corresponding protective effect. Immunosuppressant azathioprine, injected subcutaneously from 7th to 3rd day preceding infection at a dose of 100 micrograms resulted in a significant increase in the number of T. crassiceps larvae in the peritoneal cavity of experimental mice compared with the controls (by 48.7%). T-activin, injected subcutaneously to mice, immunosuppressed by azathioprine, led to a restoration of resistance of mice to T. crassiceps infection. Subcutaneous application of T-activin alone had a significant protective effect (decrease in cysticerci number by 53.7% in comparison with the controls). Correlation of the level of specific antibodies in the serum of infected mice, value of spleen index and number of T. crassiceps cysticerci in peritoneal cavity of mice was not detected.     

Spontaneous infection of white laboratory mice with Emmonsia crescens Emmons et Jellison, 1960 under natural conditions

Fifty white laboratory mice were planted in a microbiotope in which adiaspiromycosis has been detected in 52 Microtus arvalis during the last 10 years. Four of the white mice became infected with adiaspiromycosis. Serological tests revealed the infection in two mice exposed for 3 months. After 4 months' exposure, another two mice were found to be infected and the positive serological results were confirmed by microscopical examination which revealed adiaspores in their lungs. The infection was thus detected by serological methods sooner than by microscopical examination.     

Two ways of experimental infection of Ixodes ricinus ticks (Acari: Ixodidae) with spirochetes of Borrelia burgdorferi sensu lato complex

A previously reported procedure for the introduction of Borrelia spirochetes into tick larvae by immersion in a suspension of spirochetes was tested on Ixodes ricinus (L.) ticks and three of the most medically important European Borrelia genomic species, B. burgdorferi sensu stricto, B. garinii and B. afzelii. The procedure was compared with "classical" infection of nymphs by feeding on infected mice. Both methods yielded comparable results (infection rate 44-65%) with the exception of B. afzelii, which produced better results using the immersion method (44%) compared with feeding on infected mice (16%). Nymphs infected by the immersion method at the larval stage were able to transmit the infection to na?ve mice as shown by serology and PCR detection of spirochetal DNA in organs. The immersion method is faster than feeding on infected mice and provides more reproducible conditions for infection. It can be exploited for studies on both pathogen transmission and Borrelia-vector interactions.     

Compartment-specific antioxidative defense in Arabidopsis against virulent and avirulent Pseudomonas syringae

The accumulation of reactive oxygen species (ROS) during biotic stress is either part of a hypersensitive response of the plant or induced directly by the pathogen. Antioxidants such as ascorbate and glutathione counteract the accumulation of ROS and are part of the defense reaction. The aim of the present study was to investigate the compartment-specific importance of ascorbate and glutathione during a virulent and avirulent Pseudomonas syringae infection in Arabidopsis thaliana. Peroxisomes were found to be the hotspot for glutathione accumulation reaching 452% and 258% of control levels 24 h postinoculation during the virulent and avirulent infection, respectively. An accumulation of ascorbate could also be observed in vacuoles during Pseudomonas syringae infection, whereas glutathione remained absent in this cell compartment. Neither glutathione nor ascorbate accumulated in the apoplast during pathogen infection demonstrating an only negligible role of these antioxidants in the apoplast during pathogen infection. Compartment-specific changes followed a recently proposed stress model with an increase of ascorbate and glutathione in most cell compartments at the early stages of infection and a strong drop at the later stage of infection when a strong accumulation of ROS and symptoms occurred in the leaves. This study highlights the importance of certain cell compartments and antioxidants in general for the protection of pathogen-induced ROS accumulation.     

Attenuation of Schistosoma mansoni cercarial infectivity to albino mice by methanol extract of some plant species

This study elucidates the activity of certain plants’ methanol extract: Anagallis arvensis, Solanum nigrum (green fruits), Chenopodium ambrosioides, Calendula officinalis and Sesbania sesban, on the infectivity of S. mansoni cercariae to albino mice. Then, some parasitological parameters, e.g. the worm load/mouse, number of ova/g tissue in liver and intestine and the developmental stages of ova in the small intestinal wall (Oogram) of infected mice were determined. In addition, certain biochemical parameters of serum from infected mice (total protein, albumin, the activities of AlT, AsT, AcP and AkP enzymes) were, also, recorded.The results showed that exposure of S. mansoni cercariae for 30 min to the tested plants’ methanol extract before mice infection has a higher suppressive effect on their infectivity to albino mice then those exposed to this extract during mice infection. The number of worms recovered/infected mouse and the number of ova/g tissue from liver and intestine of mice groups infected with cercariae exposed to the tested plants’ methanol extract either pre- or during mice infection were less than those of infected control groups (e.g. the reduction rates of worm load/mouse and number of ova/g tissue in the intestine were 46.1% and 76.8%, respectively, for mice infected with cercariae exposed to 5 ppm of A. arvensis during mice infection).The results, also, indicated that exposing S. mansoni cercariae to methanol extract of the experimental plants either pre- or during mice infection reduced the activities of the enzymes AlT, AsT, AcP and AkP that were elevated in mice infected with untreated cercariae, meanwhile, the concentrations of total protein and albumin were increased in the serum of mice infected with these treated cercariae in comparison with those of mice group infected with untreated cercariae.     

Susceptibility of some species of rodents to rickettsiae.

The present study was designed to test the susceptibility of free-living rodents, viz Apodemus flavicollis, Microtus arvalis, Clethrionomys glareolus, Mus musculus, and outbred white mice from Dobrá Voda farm, CSFR, to Coxiella burnetii, rickettsiae of the spotted fever group (Rickettsia sibirica, R. conorii, R. slovaca and R. akari) and rickettsiae of typhus group (R. typhi and R. prowazekii) by various routes of administration. The highest levels of antibodies to C. burnetii were found in A. flavicollis and M. arvalis inoculated intraperitoneally and intracerebrally. Antibodies to C. burnetii exerted peak levels between days 13 and 16 in contrast to white mice which showed maximum levels on day 28. When 10(0.5) and 10(0.05) EID50/0.25 ml of C. burnetii was administered intraperitoneally to A. flavicollis, M. arvalis and white mice, the agent was detected only in organs of wild animals. In addition to spleen, the bone marrow appeared as a predilective tissue for the detection of this agent. R. akari at a dose of 10(4.5) EID50/0.25 ml caused overt illness and death in rodents. Antibody levels to R. sibirica and R. conorii were dependent on dosage, route of inoculation and duration of infection, but were not dependent on animal species. Antibodies to R. slovaca and R. akari were dependent on dosage, infection duration and animal species but were not dependent on the route of infection. For R. conorii, R. sibirica and R. slovaca a sharp increase of antibody levels with high titres on days 4-6 and peak levels about day 11 post intraperitoneal infection was characteristic. Antibody level to R. akari increased up to day 21. Spotted fever group rickettsiae in rodents inoculated intraperitoneally were observed in various organs, particularly in tunica vaginalis and spleen at days 2-8 post infection. R. typhi at a dose of 10(4.3) EID50/0.25 ml inoculated intracerebrally or intraperitoneally killed white mice and inoculated intraperitoneally killed C. glareolus and M. musculus. The antibody response of white mice to intraperitoneal, subcutaneous or intranasal inoculation of this rickettsia was low and no antibody was detected following peroral administration. M. musculus did not develop antibodies after intracerebral, intranasal, subcutaneous or peroral inoculation of R. typhi. The target organs for this rickettsia were the spleen and tunica vaginalis. R. prowazekii inoculated intraperitoneally into white mice at a dose of 10(6.5) EID50/0.25 ml and at a dose of 10(4.5) EID50 into C. glareolus was fatal for these rodents.(ABSTRACT TRUNCATED AT 400 WORDS)     

Immune response of the long-tailed field mouse (Apodemus sylvaticus) to tick-borne encephalitis virus infection.

The immune response following infection with a virulent strain of Central European encephalitis (CEE) virus in a natural host, long-tailed field mouse (Apodemus sylvaticus L.) and white laboratory-bread ICR mouse, was compared. Viraemia was demonstrated in ICR mice after intraperitoneal infection with a dose of 10(5) LD50/0.5 ml. The virus titres were high in the spleen and, particularly, in the brain. In A. sylvaticus the virus was detected in the blood and spleen, but not in the brain. CEE virus multiplied in peritoneal macrophages from ICR mice, but not from A. sylvaticus. The infection induced a strong interferon response in both hosts. The natural killer (NK) cell activity increase was twice as high in A. sylvaticus compared to ICR mice. The neutralization antibodies appeared sooner in A. sylvaticus and reached higher titres in the early phases of infection.     

Studies on the control of zucchini yellow mosaic virus in courgettes by mild strain protection

Mild-strain cross protection was used in field trials at Wellesbourne and in Jersey in attempts to protect courgette plants against severe strains of zucchini yellow mosaic virus. Test plants were sap inoculated with the mild strain and then challenged by an aphid-transmitted severe strain after different periods. Approximately 14 days of incubation were required following mild-strain inoculation to provide protection against subsequent infection by severe strains. No protection occurred if severe strains were introduced 2 days (48 h) after mild-strain inoculation and protection was intermediate if the severe-strain challenge occurred after 7–8 days. Some breakdown in protection occurred in the later stages of the trial at Wellesbourne, but not in Jersey. This loss of protection may be associated with high inoculum pressures.     

The influence of <Emphasis Type="Italic">Aphanomyces cochlioides</Emphasis> on selected physiological processes in sugar beet leaves and yield parameters

Alterations in some physiological processes in source leaves of sugar beet—such as chlorophyll and carbohydrate concentrations, stomatal conductance, rate of net photosynthesis and transpiration, and activity of the photosynthetic apparatus during root interaction with Aphanomyces cochlioides, were investigated. The influence of time of infection on plant health, yield quality and quantity was also examined. Plants were infected at different times of their growth period: on the sowing day and 4 or 8 weeks after sowing. A variation treatment, with non-pelleted seeds infected on the sowing day, was also analyzed. The experiment showed that development of disease symptoms depends on the time of infection and seed protection. A significant root yield decrease was observed in case of late infection, as compared to the yield of plants infected on the sowing day. The fresh weight of leaves was significantly increased where there was late infection. The infected plants showed a lower content of K⁺, Na⁺ and α-amino-N than did the controls. Infection by A. cochlioides induced chlorophyll degradation mostly in older leaves with the occurrence of natural senescence processes. Chlorophyll fluorescence parameters indicated that the photosynthetic apparatus of younger leaves was more sensitive to pathogen infection, when compared to older ones. The photochemical efficiency of photosystem II was reduced in young leaves mainly due to disturbance of the water-splitting system. In plants grown from non-pelleted seeds a strong impairment of PSII was observed only in those leaves which developed during early pathogen infection. In young leaves of plants infected in the fourth week after sowing, inhibition of the rate of net photosynthesis was correlated with the increase in intercellular CO₂ concentration, indicating some disturbance in the carbon assimilation phase. In mature leaves of late infected plants the reduction of photosynthesis net rate was associated with a decrease of stomatal conductance and an increase of diffusion resistance to CO₂ and H₂O, which was also the cause of the transpiration rate inhibition. When the leaves developed during early infection, an increase of specific leaf weight and accumulation of carbohydrates was observed. In mature leaves of non-protected plants infected on the sowing day, the recovery of all physiological processes was observed together with a diminution of disease symptoms.