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1.
BMC Vet Res ; 17(1): 92, 2021 Feb 27.
Article in English | MEDLINE | ID: mdl-33639950

ABSTRACT

BACKGROUND: Between February and April 2016, a slight increase in mortality was observed in a colony consisting of 400 captive Seba's short-tailed bats (Carollia perspicillata). These animals cohabited with other nocturnal animal species in a dome of a private zoo in Switzerland. RESULTS: Gross and histological analysis of two (14.3%) out of the 13 animals submitted for necropsy within this period revealed a necrosuppurative pneumonia, hepatitis, splenitis, enterocolitis, and endometritis, with abundant intralesional colonies of Gram-negative rods. Yersinia (Y.) pseudotuberculosis serotype O:1 and biotype 1 belonging to the sequence type ST90 was isolated from the affected organs in both animals. Following this diagnosis, » of the colony (99 animals) was culled and submitted for gross and histopathological analysis, and a bacterial culture selective for Yersinia spp. of lung, liver, and spleen was performed. From these 99 animals, one gravid female was tested and found to be positive for Y. pseudotuberculosis in the absence of clinical symptoms and histopathological lesions. PCR analysis of altogether three bacterial isolates for virulence factors revealed the presence of the ail gene, and one isolate was also positive for the virF and yadA plasmid genes. CONCLUSIONS: These findings suggest that Carollia perspicillata are susceptible to lethal yersiniosis but do not represent a regular reservoir for Y. pseudotuberculosis. Culling of » of the population was sufficient to limit the spread of this infection among the colony. Moreover, no infections were detected in cohabitant nocturnal animals and caretakers, indicating that the zoonotic risk in this case was low.


Subject(s)
Chiroptera/microbiology , Yersinia pseudotuberculosis Infections/veterinary , Yersinia pseudotuberculosis/isolation & purification , Animals , Animals, Zoo/microbiology , Female , Male , Pregnancy , Serogroup , Switzerland , Yersinia pseudotuberculosis Infections/epidemiology
2.
Mol Phylogenet Evol ; 145: 106705, 2020 04.
Article in English | MEDLINE | ID: mdl-31821880

ABSTRACT

Understanding geographic patterns of interaction between hosts and parasites can provide useful insight into the evolutionary history of the organisms involved. However, poor taxon sampling often hinders meaningful phylogenetic descriptions of groups of parasites. Trypanosome parasites that constitute the Trypanosoma cruzi clade are worldwide distributed infecting several mammalian species, especially bats. Diversity in this clade has been recently expanded by newly discovered species, but the common ancestor and geographical origins of this group of blood parasites are still debated. We present here results based on the molecular characterization of trypanosome isolates obtained from 1493 bats representing 74 species and sampled over 16 countries across four continents. After estimating the appropriate number of hypothetical species in our data set using GMYC models in combination with Poisson Tree Processes (mPTP) and ABGD, the 18S rRNA and gGAPDH genes were used for phylogenetic analyses to infer the major evolutionary relationships in the T. cruzi clade. Then, biogeographical processes influencing the distribution of this cosmopolitan group of parasites was inferred using BioGeoBEARS. Results revealed a large lineages diversity and the presence of trypanosomes in all sampled regions which infected 344 individuals from 31 bat species. We found eight Trypanosoma species, including: five previously known; one subspecies of Trypanosoma livingstonei (Trypanosoma cf. livingstonei); and two undescribed taxa (Trypanosoma sp. 1, Trypanosoma sp. 2), which were found exclusively in bats of the genus Miniopterus from Europe and Africa. The new taxa discovered have both an unexpected position in the global phylogeny of the T. cruzi clade. Trypanosoma sp. 1 is a sister lineage of T. livingstonei which is located at the base of the tree, whereas Trypanosoma sp. 2 is a sister lineage of the Shizotrypanum subclade that contains T. c. cruzi and T. dionisii. Ancestral areas reconstruction provided evidence that trypanosomes of the T. cruzi clade have radiated from Africa through several dispersion events across the world. We discuss the impact of these findings on the biogeography and taxonomy of this important clade of parasites and question the role played by bats, especially those from the genus Miniopterus, on the dispersal of these protozoan parasites between continents.


Subject(s)
Chiroptera/parasitology , Trypanosoma cruzi/classification , Africa , Animals , Bayes Theorem , Biological Evolution , Europe , Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)/classification , Glyceraldehyde-3-Phosphate Dehydrogenase (Phosphorylating)/genetics , Phylogeny , RNA, Ribosomal, 18S/classification , RNA, Ribosomal, 18S/genetics , Trypanosoma cruzi/isolation & purification
3.
Mol Biochem Parasitol ; 84(2): 215-27, 1997 Feb.
Article in English | MEDLINE | ID: mdl-9084041

ABSTRACT

The deduced amino acid sequence of Leishmania major sw3 cDNA reveals the presence of characteristic histone H1 amino acid motifs. However, the open reading frame is of an unusually small size for histone H1 (105 amino acids) because it lacks the coding potential for the central hydrophobic globular domain of linker histones present in other eukaryotes. Here, we provide biochemical evidence that the SW3 protein is indeed a L. major nuclear histone H1, and that it is differentially expressed during the life cycle of the parasite. Due to its high lysine content, the SW3 protein can be purified to a high degree from L. major nuclear lysates with 5% perchloric acid, a histone H1 preparative method. Using an anti-SW3 antibody, this protein is detected as a 17 kDa or as a 17/19 kDa doublet in the nuclear subfraction in different L. major strains. The nuclear localization of the SW3 protein is further supported by immunofluorescence studies. During in vitro promastigote growth, both the sw3 cytoplasmic mRNA and its protein progressively accumulate within parasites from early log phase to stationary phase. Within amastigotes, the high level of H1 expression is maintained but decreases when amastigotes differentiate into promastigotes. Together, these observations suggest that the different levels of this histone H1 protein could influence the varying degrees of chromatin condensation during the life-cycle of the parasite, and provide us with tools to study this mechanism.


Subject(s)
Histones/genetics , Leishmania major/growth & development , Leishmania major/genetics , Amino Acid Sequence , Animals , Cell Nucleus/metabolism , DNA, Complementary/genetics , DNA, Protozoan/genetics , Gene Expression Regulation, Developmental , Genes, Protozoan , Histones/isolation & purification , Histones/metabolism , Leishmania major/metabolism , Molecular Sequence Data , RNA, Messenger/genetics , RNA, Messenger/metabolism , RNA, Protozoan/genetics , RNA, Protozoan/metabolism
6.
Gene ; 122(2): 297-304, 1992 Dec 15.
Article in English | MEDLINE | ID: mdl-1487144

ABSTRACT

Developmentally regulated mechanisms involving alternative RNA splicing and/or polyadenylation, as well as transcription termination, are implicated in controlling the levels of secreted mu (mu s), membrane mu (mu m) and delta immunoglobulin (Ig) heavy chain mRNAs during B cell differentiation (mu gene encodes the mu heavy chain). Using expression vectors constructed with genomic DNA segments composed of the mu m polyadenylation signal region, we analyzed poly(A) site utilization and termination of transcription in stably transfected myeloma cells and in murine fibroblast L cells. We found that the gene segment containing the mu m poly(A) signals, along with 536 bp of downstream flanking sequence, acted as a transcription terminator in both myeloma cells and L cell fibroblasts. Neither a 141-bp DNA fragment (which directed efficient polyadenylation at the mu m site), nor the 536-bp flanking nucleotide sequence alone, were sufficient to obtain a similar regulation. This shows that the mu m poly(A) region plays a central role in controlling developmentally regulated transcription termination by blocking downstream delta gene expression. Because this gene segment exhibited the same RNA processing and termination activities in fibroblasts, it appears that these processes are not tissue-specific.


Subject(s)
Genes, Immunoglobulin , Immunoglobulin mu-Chains/genetics , Poly A , Terminator Regions, Genetic , Alternative Splicing , Animals , Base Sequence , Blotting, Northern , Gene Expression Regulation , Genetic Vectors , Humans , L Cells , Mice , Molecular Sequence Data , Tumor Cells, Cultured
8.
Biochem Biophys Res Commun ; 178(1): 8-15, 1991 Jul 15.
Article in English | MEDLINE | ID: mdl-1648916

ABSTRACT

Structural definition of the receptors for neurotropic and angiogenic modulators such as fibroblast growth factors and related polypeptides will yield insight into the mechanisms that control early development, embryogenesis, organogenesis, wound repair and neovessel formation. We isolated 3 murine cDNAs encoding different binding domains of these receptors (flg). Comparison of these ectoplasmic portions showed that two of the forms corresponded to previously described murine molecules whereas the third one had a different ectoplasmic portion generated by specific changes in two regions. Interestingly, expression of this third form seems to be restricted in its tissue distribution. Such modifications could influence the ligand specificity of the different receptors and/or their binding affinity.


Subject(s)
DNA/genetics , Receptors, Cell Surface/genetics , Amino Acid Sequence , Animals , Antisense Elements (Genetics) , Base Sequence , Cell Line , DNA/isolation & purification , Fibroblast Growth Factors/metabolism , Filaggrin Proteins , Humans , L Cells/metabolism , Mice , Molecular Sequence Data , Oligonucleotide Probes , Receptors, Fibroblast Growth Factor , Ribonuclease, Pancreatic , Sequence Homology, Nucleic Acid , Transcription, Genetic
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