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SYNOPSIS. Oocysts of Wenyonella baghdadensis sp. n. were found in the feces of 2 of 12 bandicoot rats Nesokia indica Gray & Hardwicke from the Baghdad area. Sporulated oocysts were subspherical to broadly ellipsoidal, 25.4 (18–22) × 20.8 (15–28) μm, with a 2-layered wall, the outer wall being mammillated, without micropyle, micropylar cap, residuum, or polar granule. Sporozoites were ovoid, 11.8 (9–15) × 8.4 (6–10) μm, with Stieda body and residuum. Two sporozoites in each sporocyst were elongate, with granular cytoplasm and a refractile globule, the other 2 were bean-shaped, without granules or refractile globule. Sporulation time equalled 3 days at 22–24 C. Entamoeba coli and Giardia sp. cysts were also found in 3 rats each. 相似文献
3.
Abstract Significantly higher Giardia lamblia trophozoites load in the intestine of infected mice accompanied pronounced influx of suppressor/cytotoxic T cells (Lyt 2.2+ ), T cells (Thy 1.2+ ) and significant reduction in IgA-containing cells in the gut during the establishment and peak phases of infection. The induction of helper/inducer T cells (Lyt 1.1+ ) and significant enhancement of IgA-containing cells in gut resulted in the decline of the trophozoite loads. However, the prior treatment of animals with dexamethasone alone resulted in significant reduction in helper/inducer T cells (Lyt 1.1+ ) and the IgA-containing cells in the gut; the percents of suppressor/cytotoxic T cells (Lyt 2.2+ ) and IgM-containing cells remained unaltered. Although the G. lamblia infection in such animals further significantly increased the influx of suppressor/cytotoxic T cells, the late response of helper/inducer T cells and IgA-containing cells was abrogated during the decline phase of infection. The significant reduction in the trophozoite load — despite immuno-suppressive therapy — appeared to be due to unaltered IgM response in such animals which probably took over the function of IgA in defense against G. lamblia . The data of the investigation thus suggested a role of helper/inducer T cells and antibodies producing cells in gut as important effector cells resulting in the termination of primary G. lamblia infection. 相似文献
4.
Jie Li Peiyuan Wang Aiguo Zhang Ping Zhang Muhamd Alsarakibi Guoqing Li 《The Korean journal of parasitology》2013,51(2):237-241
Giardia lamblia is recognized as one of the most prevalent parasites in dogs. The present study aimed to establish a loop-mediated isothermal amplification (LAMP) assay for rapid and specific detection of G. lamblia from dogs. The fecal samples were collected and prepared for microscopic analysis, and then the genomic DNA was extracted directly from purified cysts. The concentration of DNA samples of G. lamblia were diluted by 10-fold serially ranging from 10-1 to 10-5 ng/µl for LAMP and PCR assays. The LAMP assay allows the amplification to be finished within 60 min under isothermal conditions of 63℃ by employing 6 oligonucleotide primers designed based on G. lamblia elongation factor 1 alpha (EF1α) gene sequence. Our tests showed that the specific amplification products were obtained only with G. lamblia, while no amplification products were detected with DNA of other related protozoans. Sensitivity evaluation indicated that the LAMP assay was sensitive 10 times more than PCR. It is concluded that LAMP is a rapid, highly sensitive and specific DNA amplification technique for detection of G. lamblia, which has implications for effective control and prevention of giardiasis. 相似文献
5.
Richard Atherton Darlene Bhavnani Manuel Calvopi?a Yosselin Vicu?a William Cevallos Joseph Eisenberg 《Memórias do Instituto Oswaldo Cruz》2013,108(4):512-515
The aim of this study was to determine the genetic diversity of
Giardia duodenalis present in a human population living in
a northern Ecuadorian rain forest. All Giardia positive samples
(based on an ELISA assay) were analysed using a semi-nested polymerase chain
reaction-restriction fragment length polymorphism assay that targets the
glutamate dehydrogenase (gdh) gene; those amplified were
subsequently genotyped using NlaIV and RsaI enzymes. The gdh
gene was successfully amplified in 74 of 154 ELISA positive samples; 69 of the
74 samples were subsequently genotyped. Of these 69 samples, 42 (61%) were
classified as assemblage B (26 as BIII and 16 as BIV), 22 (32%) as assemblage A
(3 as AI and 19 as AII) and five (7%) as mixed AII and BIII types. In this study
site we observe similar diversity in genotypes to other regions in Latin
America, though in contrast to some previous studies, we found similar levels of
diarrheal symptoms in those individuals infected with assemblage B compared with
those infected with assemblage A. 相似文献
6.
无义介导的mRNA降解途径(nonsense-mediated mRNA decay,NMD)作为细胞内的一种重要的mRNA质量监控机制,可以降解含有提前终止密码子(premature termination codon,PTC)的异常转录本,从而避免截短蛋白质对细胞的毒害,但其详细的分子机制有待进一步阐释。蓝氏贾第虫(Giardia lamblia)作为一种寄生性单细胞原生动物,进化地位特殊,对其NMD途径的研究有利于阐明基因表达调控的分子和进化机制。本研究通过酵母双杂交及体外pull-down实验分析了贾第虫NMD途径因子上游移码蛋白1(Giardia lamblia up-frameshift 1,GlUPF1)、贾第虫RNA结合蛋白(Giardia lamblia HRP1, GlHRP1)、贾第虫核糖核酸外切酶(Giardia lamblia Ski7p,GlSki7p、Giardia lamblia XRN1,GlXRN1)之间的相互作用关系。结果表明,GlUPF1全长与GlHRP1、GlXRN1(1~500 aa)、GlSki7p间均可发生相互作用。而且GlUPF1的CH结构域和C端结构域分别与GlHRP1、GlXRN1(1~500 aa)、GlSki7p相互作用。说明GlUPF1在贾第虫NMD途径中作为招募平台,在无义mRNA识别和降解过程中发挥重要作用。为此,结合本实验室之前的研究结果,我们提出原生动物贾第虫的NMD途径:在提前终止密码子处SURF(SMG1-UPF1-eRF1-eRF3)复合物形成后,GlUPF1被磷脂酰肌醇3-激酶(suppressor with morphogenetic effect on genitalia 1,SMG1)磷酸化修饰, NMD途径激活,随后GlUPF1与HRP1相互作用,将转录本标记为NMD底物;GlUPF1进而招募下游贾第虫5′-3′核糖核酸降解酶GlXRN1、贾第虫3′-5′ 核糖核酸降解因子GlSki7p,最终降解靶标mRNA。 相似文献
7.
Elizabeth Lara-Reyes Israel A. Quijano-Hernndez Roger I. Rodríguez-Vivas Javier Del ngel-Caraza Jos Simn Martínez-Castaeda 《Biomédica : revista del Instituto Nacional de Salud》2021,41(4):756
Introduction:
Endoparasites and ectoparasites in dogs are of global distribution. The close relationship between dogs and man implies a risk for the transmission of zoonotic parasites. Therefore, it is necessary to determine the parasites hosted by dogs in specific areas and the factors associated with their presence.Objectives:
To identify and to estimate the prevalence of endoparasites and ectoparasites in domiciled dogs in the Metropolitan area of Toluca, México, and the prevalence of D. caninum in fleas of the genus Ctenocephalides spp.Materials and methods:
We collected samples from 402 domiciled dogs in four reference hospitals in the area in Toluca. We diagnosed endoparasites using direct smear, flotation, and sedimentation techniques and we performed the taxonomic identification of ectoparasites. Finally, the molecular diagnosis of D. caninum in fleas was made using the polymerase chain reaction technique (PCR).Results:
A total of 37.2% of dogs were positive for endoparasites; the genera or species identified were Toxocara spp., Giardia spp., Ancylostoma spp., Cystoisospora spp., D. caninum, Taenia spp., and Trichuris vulpis; the prevalence of ectoparasites was 13.13%. We identified fleas of the species Ctenocephalides felis, Ctenocephalides canis; only one animal was parasitized with Rhipicephalus sanguineus and another one with Trichodectes canis; the prevalence of D. caninum in fleas was 9.5%.Conclusion:
The prevalence of endoparasites was 37.2% while that of ectoparasites was 13.1%; this is the first analysis of endoparasites and ectoparasites conducted in the same population of dogs in México together with the molecular diagnosis of D. caninum in fleas. 相似文献8.
Campanati L Bré MH Levilliers N de Souza W 《Biology of the cell / under the auspices of the European Cell Biology Organization》1999,91(7):499-506
By means of immunofluorescence, immunoelectron microscopy and immunoblotting, we show that polyglycylation, a posttranslational modification of tubulin widely spread among eukaryotes, is present in the diplomonad, Giardia lamblia, a putative ancestral cell possessing a highly developed microtubular cytoskeleton. This modification was recently discovered in the ciliated protist, Paramecium, and was not found in the Euglenozoa, a lineage considered as ancient. We used two monoclonal antibodies (mAbs), TAP 952 and AXO 49, specifically recognizing mono- and polyglycylated tubulin isoforms, to detect this modification in Giardia extracts and to localize it in the different classes of microtubules within the cell. The alpha- and beta-tubulin subunits were recognized by the two mAbs, indicating that both tubulin subunits are glycylated, in agreement with lately reported mass spectrometry results. Noticeably, Giardia tubulin was much more reactive with AXO 49 than with TAP 952. In situ, AXO 49 intensely labeled the microtubules present in the four pairs of flagella and the median body, and lightly decorated the microtubules from the adhesive disc. In contrast, TAP 952 intensely labeled only the microtubules of the median body. The results indicate a differential expression of glycylated isoforms within various microtubular structures of Giardia lamblia. They also suggest that the complete set of enzymes required for polyglycylation is expressed in very divergent eukaryotes. 相似文献
9.
A protein with a relative molecular mass of 31 kDa was specifically extracted by EGTA from a detergent-insoluble fraction of Giardia lamblia. N-terminal sequencing showed this protein to be identical to alpha 1-giardin, a component of the ventral disc which, based on its predicted amino acid sequence, has been classified as annexin XIX. Purified alpha 1-giardin associated with multilamellar phosphatidyl serine-containing vesicles in a Ca(2+)-dependent manner, confirming that it is a functional annexin. Molecular modelling of the amino acid sequence of the giardial annexin into the X-ray structure of annexin V suggests that the Ca(2+)-binding sites, which, as in other annexins, are all located on the convex surface of the molecule, are of the low-affinity type III. 相似文献
10.
Centrin in Giardia lamblia - ultrastructural localization 总被引:2,自引:0,他引:2
Giardia lamblia is a multiflagellar parasite and one of the earliest diverging eukaryotic cells. It possesses a complex cytoskeleton based on different groups of microtubular structures - a ventral adhesive disc, four pairs of flagella, a median body and funis. Centrin is an important member of the EF-hand family of calcium-binding proteins, and it is known to show calcium-sensitive contractile behaviour. In the present study, we performed an ultrastructural localization of centrin in G. lamblia using several monoclonal antibodies to centrin. Microtubular structures such as the basal bodies, all the flagella axonemes, the adhesive disc, funis, and the median bodies presented positive labelling to centrin. In addition, the dense rods also demonstrated positive labelling. These results show that centrin is located in key positions related to microtubules. The role of centrin in these dynamic regions is discussed. 相似文献