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1.
Caryospora duszynskii Upton, Current et Barnard, 1984 was successfully transmitted to snakes of the genus Elaphe by feeding them previously infected mice. Fifty thousand oocysts were orally administered to two mouse strains, BALB/c and Crl:CD-1(ICR)BR, which were subsequently fed to captive-born coccidia-free Elaphe guttata (L.) in two respective independent experiments. Both E. guttata expelled C. duszynskii oocysts in their faeces, beginning on day 18 and 26 post infection (p.i.) and shed oocysts continuously through the end of the experiment, day 230 and 135 p.i., respectively. There were no parasitic stages or lesions in mice, as revealed by histological examination. Experiments proved that rodents serve as paratenic hosts for C. duszynskii. In summary we discuss the life-cycle strategies of Caryospora spp. in reptiles and present three general modes of their development.  相似文献   

2.
Four lambs 4 months old were inoculated with Cryptosporidium andersoni oocysts (bovine isolate) in a dose of 5 x 10(6) per animal followed later by 1 x 10(7) oocysts per animal. No animal shed Cryptosporidium oocysts during 56 days post infection, no lamb showed clinical symptoms of cryptosporidiosis and no macroscopic changes were detected in the abomasum immediately after autopsy. Histological examinations did not demonstrate the occurrence of Cryptosporidium in the abomasum and other selected organs.  相似文献   

3.
The pre–penetration and post–penetration stages of infection by Cladosporium allii–cepae on onion foliage was examined on inoculated plants kept at 15° C and 80–90% r.h. The pathogen entered the leaf usually through stomata but occasionally by penetrating the cuticle. Invasion of the palisade and mesophyll tissues led to the formation of a leaf cavity after 7 days and after 30 days the pathogen sporulated on the leaf surface.  相似文献   

4.
Experimental infections of 7-28-day-old chickens with Cryptosporidium oocysts isolated from spontaneously infected chickens demonstrated that the endogenous development of this parasite takes place simultaneously in the organs of digestive, respiratory and excretory systems and in bursa of Fabricius. It was demonstrated for the first time that the oocysts of Cryptosporidium are shed through the respiratory tract into the beak cavity. A novel rapid and simple method has been developed for the detection of oocysts. Its principle is the rinsing of the beak cavity. This method enabled to isolate the oocysts from experimentally infected chickens and immediately use them in the dose of 6 X 10(5) for peroral infection of a 37-day-old chicken. The prepatent period was 8 days, patent period 12 days. On days 4-7 after the first detection of Cryptosporidium oocysts in chicken excrements, the oocysts were detected also by the method of beak cavity rinsing. This indicates that the oocysts released from the respiratory tract are infective. This fact is important from the epizootological viewpoint in relation with possible spreading of Cryptosporidium infections in chicken farms.  相似文献   

5.
ABSTRACT Barley has two flowering types, chasmogamous (open-flowering) and cleistogamous (closed-flowering). We examined the effect of the timing of Fusarium graminearum infection on Fusarium head blight (FHB) and mycotoxin accumulation in barley cultivars with different flowering types using greenhouse experiments. In the first experiment, 13 cultivars were spray inoculated at two different developmental stages, and the severity of FHB was evaluated. The effect of the timing of infection differed among cultivars. Cleistogamous cultivars were resistant at anthesis but susceptible at 10 days after anthesis, whereas chasmogamous cultivars were already susceptible at anthesis. In the second experiment, five cultivars were inoculated at three different developmental stages and the concentrations of deoxynivalenol (DON) and nivalenol (NIV) in mature grain were analyzed. Cleistogamous cultivars accumulated more mycotoxins (DON and NIV) when inoculated 10 or 20 days after anthesis than when inoculated at anthesis, whereas chasmogamous cultivars accumulated more mycotoxins when inoculated at anthesis. Thus, the most critical time for F. graminearum infection and mycotoxin accumulation in barley differs with cultivar, and likely is associated with the flowering type. Late infection, even without accompanied FHB symptoms, was also significant in terms of the risk of mycotoxin contamination.  相似文献   

6.
Faecal samples of 56 common house crows (Corvus splendens Vieillot) were collected from the Petaling Jaya and Kelang districts of Selangor, peninsular Malaysia, and examined for coccidia. Intestinal tracts of 8 of the above crows wee histologically examined under light microscopy to determine the site of coccidial infection and the endogenous stages present. Fifty three (94.6%) crows had coccidial oocysts morphologically conforming to only one species of Isospora in their faeces at the time they were examined. The sporulated oocysts were found to be Isospora corviae (Ray et al. 1952) which has been emended to I. corvi. These oocysts are redescribed in greater detail. Corvus splendens is a new host record for I. corvi. Coccidial infection was observed in all the intestinal tracts and generally confined to the anterior two thirds of the intestine. The parasites occurred within intestinal epithelial cells, located usually above the host cell nucleus. Developmental stages of both the asexual and sexual phases were found in the epithelium, and are deemed to be the endogenous stages of I. corvi on the basis of the oocysts recovered from the same crows used for histological study. These stages are described here for the first time. The prevalence of I. corvi, its relationship with the host C. splendens, and its probable transmission from C. macrorhynchus are discussed.  相似文献   

7.
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.  相似文献   

8.
Reports on demodicid mites of the old world species of deer are reviewed and Demodex kutzeri sp. n. (= D. cervi sensu Kutzer and Grünberg 1972; part.) described in all stages of the life cycle. The occurrence of D. kutzeri on two host species, Cervus elaphus L., 1758 and C. nippon pseudaxis Eydoux et Souleyet, 1841 is reported and discussed as a rare phenomenon in the genus Demodex.  相似文献   

9.
10.
Saliva-activated transmission (SAT) of Borrelia burgdorferi sensu stricto was demonstrated using real-time PCR and salivary gland extract (SGE) from partially fed Ixodes ricinus ticks. C3H/HeN mice were injected intradermally with 1.5 x 10(3) spirochetes mixed with 40 microg of SGE per mouse. The control group was inoculated with the same dose of spirochetes without SGE. The accelerating effect of SGE on spirochete proliferation was demonstrated on day 1 post infection, when a 4.2-fold increase in spirochetes was found in the skin and a 10-fold increase in the blood, compared with control mice. The data represent the first direct evidence of a SAT effect of I. ricinus SGE on infection with the Lyme disease agent B. burgdorferi.  相似文献   

11.
The effect of microclimate variables on development ofClonostachys rosea and biocontrol ofBotrytis cinerea was investigated on rose leaves and crop residues. C.rosea established and sporulated abundantly on inoculated leaflets incubated for 7–35 days at 10°, 20° and 30°C and then placed on paraquat—chloramphenical agar (PCA) for 15 days at 20°C. On leaflets kept at 10°C, the sporulation after incubation on PCA increased from 60% to 93% on samples taken 7 to 21 days after inoculation, but decreased to 45% on material sampled after 35 days. A similar pattern was observed on leaves incubated at either 20° or 30°C. The sporulation ofC. rosea on leaf disks on PCA was not affected when the onset of high humidity occurred 0, 4, 8, 12 or 16 h after inoculation. However, sporulation was reduced to 54–58% on leaflets kept for 20–24 h under dry conditions after inoculation and before being placed on PCA. The fungus sporulated on 68–74% of the surface of leaf disks kept for up to 24 h at high humidity after inoculation, but decreased to 40–51% if the high humidity period before transferral to PCA was prolonged to 36–48 h. The growth ofC. rosea on leaflets was reduced at low inoculum concentrations (103 and 104 conidia/ml) because of competition with indigenous microorganisms, but at higher concentrations (105 and 106 conidia/ml) the indigenous fungi were inhibited. Regardless of the time of application ofC. rosea in relation toB. cinerea, the pathogen’s sporulation was reduced by more than 99%. The antagonist was able to parasitize hyphae and conidiophores ofB. cinerea in the leaf residues. AsC. rosea exhibited flexibility in association with rose leaves under a wide range of microclimatic conditions, and in reducingB. cinerea sporulation on rose leaves and residues, it can be expected to suppress the pathogen effectively in rose production systems.  相似文献   

12.
Development of Clonostachys rosea in rose leaves and petals and control of Botrytis cinerea by the agent were investigated. C. rosea germinated, established endophytic growth, and sporulated abundantly whether the tissues were mature, senescent or dead when inoculated. Germination incidence was moderate on mature and senescent leaves (47% and 35%) and petals (31% and 43%), and high (>98%) on dead tissues. Sporulation of C. rosea in tissues inoculated when mature, senescent or dead averaged 41%, 61%, and 75% in leaves, and 48%, 87% and 53% in petals. When leaves were wounded with needles before inoculation, germination of C. rosea increased from 45–56% to 90–92%, but sporulation became high (>75%) regardless of wounds. When leaves were inoculated with C. rosea at 0–24h after wounding and subsequently with B. cinerea, germination of the pathogen was reduced by 25–41% and sporulation by 99%. A humid period prior to inoculation of senescent or dead leaves promoted communities of indigenous fungi, reduced sporulation of C. rosea and B. cinerea, and, in dead leaves, increased control of the pathogen associated with C. rosea. Applied at high density, isolates of indigenous Penicillium sp. and Alternaria alternata from rose interacted with C. rosea and reduced control of the pathogen by 16% and 21%, respectively. In conclusion, C. rosea markedly suppressed sporulation of B. cinerea in rose leaves and petals regardless of developmental stage, minor wounds, and natural densities of microflora. This versatility should allow C. rosea to effectively control inoculum production of B. cinerea in rose production systems.  相似文献   

13.
Two experimental trials were performed to elucidate the role of rodents in the life cycle of Hepatozoon species using snakes as intermediate hosts. In one trial, two ball pythons, Python regius Shaw, 1802 were force fed livers of laboratory mice previously inoculated with sporocysts of Hepatozoon ayorgbor Sloboda, Kamler, Bulantová, Votypka et Modry, 2007. Transmission was successful in these experimentally infected snakes as evidenced by the appearance of intraerythrocytic gamonts, which persisted until the end of trial, 12 months after inoculation. Developmental stages of haemogregarines were not observed in histological sections from mice. In another experimental trial, a presence of haemogregarine DNA in mice inoculated with H. ayorgbor was demonstrated by PCR in the liver, lungs and spleen.  相似文献   

14.
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)  相似文献   

15.
In a controlled environment (15/10°C) (day/night) container experiment on winter wheat (cv. Avalon), eyespot incidence (percentage of plants affected) and number of leaf sheaths penetrated after 6 weeks increased with inoculum concentration (102−106 conidia mL−1) of Oculimacula yallundae (OY) or Oculimacula acuformis (OA), but there was no difference between the two species. In an outdoor container experiment, seedlings inoculated with OY 2 weeks after sowing had a greater incidence of eyespot than those inoculated with OA, when assessed 7 weeks after inoculation. Seedlings inoculated with OA at 10 or 20 weeks after sowing developed more severe eyespot by maturity than those inoculated with OY. In an experiment at 15/10°C with seedlings inoculated with OY + OA 2 weeks after sowing, more leaf sheaths were penetrated by OY (3·0 per plant) than OA (2·3 per plant) 6 weeks after inoculation. Field experiments with winter wheat consistently showed leaf sheath production, leaf sheath death, and number of leaf sheaths infected or penetrated by OA or OY were related linearly to thermal time (°C days) after sowing. Depending on cultivar, season and sample, a new leaf sheath was produced in 116–216°C days; a leaf sheath died in 221–350°C days; and infection of a new leaf sheath occurred in 129–389°C days. The mean number of living leaf sheaths infected differed between samples, cultivars and seasons for both OY and OA. Regression analysis of the 1985/86 data suggested that OY progressed more rapidly than OA through the leaf sheaths, and that both the pathogens progressed more rapidly than the rate of leaf sheath death, but more slowly than the rate at which leaf sheaths were produced. It also suggested that OA progressed more slowly than the rate at which leaf sheaths died in 1987/88, but OY did not.  相似文献   

16.
In a gnotobiotic piglet infected with 50.10(6) oocysts of Cryptosporidium parvum, developmental stages of the parasite were found in the duodenum, anterior jejunum and middle jejunum on the first day post infection (1 DPI). During the studies of the ultrastructure, trophozoites and meronts of C. parvum were encountered in the microvillous zone of enterocytes, and the outer membrane of parasites was a continuation of the membrane of microvilli. Unusual was the attachment of C. parvum trophozoite on the opening of a goblet cell, as well as a meront localized in the cytoplasm in the enterocyte of anterior jejunum. These findings show that C. parvum is very adaptive and capable of developing in a still undescribed location.  相似文献   

17.
以棉蚜Aphis gossypii Glover饲养日本通草蛉Chrysoperla nippoensis(Okamoto)作为对照,用一种半固体人工饲料连续饲养10代日本通草蛉,对日本通草蛉各生长阶段的生长和发育指标进行观测。结果显示,用人工饲料饲养的日本通草蛉的幼虫历期为13~15d,蛹期为8d,较对照组的7d和6d分别延长6~8d和2d;用棉蚜饲养的对照组日本通草蛉幼虫累计存活率为94%,成虫获得率为87%,而人工饲料饲养连续10代的幼虫累计存活率为81%~89%,成虫获得率69%~79%。取食人工饲料的日本通草蛉成虫,在产卵前期、产卵量、产卵期及寿命方面与对照组存在显著的差异,人工饲料组草蛉的产卵前期为5.07~5.22d,而对照组草蛉的产卵前期为4.12d,人工饲料组草蛉的产卵量为190~390粒,对照组的单雌产卵量为667.2粒,人工饲料组草蛉的寿命为36~38d,对照组成虫寿命52d。以上结果表明,这种半固体人工饲料可以满足日本通草蛉幼虫生长发育基本需要,可用于日本通草蛉的室内继代饲养,但需要进一步优化配方。  相似文献   

18.
It was confirmed, after experimental infection of 24 weaned pigs with different doses (200,000 and 4 mil.) of Eimeria debliecki oocysts that the developmental cycle of E. debliecki occurs in the anterior jejunum and after a high dose of oocysts also in the duodenum and anterior parts of the middle jejunum. Pathological changes characterized by a light atrophy of the villi, scarcely dispersed minute erosions of the epithelium in upper parts of the mucosa and an inflammatory response in the propria of the anterior jejunum were found in the area of the largest occurrence of developmental stages of E. debliecki (from 50 cm to 100 cm from the pylorus). An inflammatory infiltrate in the propria of the anterior jejunum from 3 DPI to 5 DPI contained a conspicuously large number of plasma cells with Russell bodies. Cellular changes were detected only in enterocytes with developmental stages of E. debliecki. Changes of the microvillous zone were observed in infected enterocytes; dilated mitochondria, free ribosomes and an increased number of residual bodies were found in the cytoplasm of enterocytes. The degree of the cellular changes of enterocytes was dependent on the maturity of the developmental stage of E. debliecki. Based on pathological changes observed by the use of light and electron microscopy, the coccidium E. debliecki is considered to be pathogenic for weaned pigs in spite it does not provoke a clinical infection.  相似文献   

19.
The effects of different levels of inoculum of Aspergillus carbonarius and time of inoculation on berry infection and the development of aspergillus bunch rot on grapevines (cv. Sultana) were studied under field conditions. Inflorescences at full bloom were inoculated with aqueous spore suspensions of A. carbonarius containing 0 or 1 × 106 spores mL−1 in 2004/05 and 0, 1 × 102 or 1 × 105 spores mL−1 in 2005/06. In both years, the incidence of infection in inoculated berries was significantly higher than in uninoculated berries. Incidence of infection in berries from veraison until harvest was higher than at earlier stages of bunch development (berry set to berries that were still hard and green). Inoculation of bunches at veraison did not significantly increase A. carbonarius infection prior to harvest, at harvest, 6 days after harvest or when berries were over-ripe. Bunches inoculated at harvest did not significantly increase infection 6 days after harvest or when berries were over-ripe. Aspergillus carbonarius was isolated more frequently from the pedicel end (53·1%) than from the middle section (37·5%) and distal end (35·0%) of berries that were inoculated with 105 spores mL−1.  相似文献   

20.
The wood mouse (Apodemus sylvaticus) has been used as an indicator species to assess, both in the field and the laboratory, the effects of carbophenothion and, in the laboratory, the effects of chlorfenvinphos as seed dressings on winter wheat. Wood mice were fed in the laboratory with wheat treated with carbophenothion and chlorfenvinphos and the effects on esterase levels were determined for periods of up to 7 days and on returning the mice to untreated wheat. The significant inhibition of plasma acetylcholinesterase and cholinesterase and brain and liver nitrophenyl acetate esterase during the 6-month period after carbophenothion-treated grain was drilled was found to reflect the carbophenothion residue in the gut contents of the mice. The degree of esterase inhibition differentiated mice trapped on the field from those caught in adjacent woodland. Inhibition of the plasma, brain, and liver esterases in wood mice fed wheat treated with the recommended rate of carbophenothion confirmed that the continued esterase inhibition obtained in the field-trapped mice during the field trial was due to chronic pesticide exposure. The pattern of esterase inhibition in the wood mice reflected the persistence of the two organophosphorus pesticides.  相似文献   

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