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Sent on Thursday, 2010 May 13Search kinetoplastids OR kinetoplastid OR Kinetoplastida OR "trypanosoma brucei" OR leishmania OR brucei OR leishmaniasis OR "African trypanosomiasis"
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| 1. | Vet Res Commun. 2010 May 13. [Epub ahead of print]Monoclonal gammopathy associated with multiple myeloma and visceral leishmaniasis in the dog: A comparison of two cases.Antognoni MT, Birettoni F, Miglio A, Lalli P, Porciello F, Mangili Pecci V.Department of Pathology, Diagnostic and Veterinary Clinic, University of Perugia, Perugia, Italy, mariateresa.antognoni@unipg.it. AbstractThe term monoclonal gammopathy (MG) suggests the presence of clonal immunoglobulins in blood serum that are recognized as narrow spikes in the beta and/or gamma region of the electrophoretic pattern of serum. In the dog, MG is rare and is associated with a heterogeneous group of diseases that include multiple myeloma (the most common source of MG) as well as infectious and chronic inflammatory diseases such as Leishmaniasis. In this paper, two cases of MG are described: the first case is associated with multiple myeloma of monoclonal component type IgA/lambda, with the latter rare in dogs, and the second case involves MG that developed 3 years after an initial diagnosis of Leishmaniasis. |
| PMID: 20461463 [PubMed - as supplied by publisher] | |
| 2. | J Cell Sci. 2010 May 11. [Epub ahead of print]ADF/cofilin-driven actin dynamics in early events of Leishmania cell division.Tammana TV, Sahasrabuddhe AA, Bajpai VK, Gupta CM.AbstractADF/cofilin is an actin-dynamics-regulating protein that is required for several actin-based cellular processes such as cell motility and cytokinesis. A homologue of this protein has recently been identified in the protozoan parasite Leishmania, which has been shown to be essentially required in flagellum assembly and cell motility. However, the role of this protein in cytokinesis remains largely unknown. We show here that deletion of the gene encoding ADF/cofilin in these organisms results in several aberrations in the process of cell division. These aberrations include delay in basal body and kinetoplast separation, cleavage furrow progression and flagellar pocket division. In addition to these changes, the intracellular trafficking and actin dynamics are also adversely affected. All these abnormalities are, however, reversed by episomal complementation. Together, these results indicate that actin dynamics regulates early events in Leishmania cell division. |
| PMID: 20460437 [PubMed - as supplied by publisher] | |
| 3. | J Helminthol. 2010 May 12:1-12. [Epub ahead of print]Resistance and resilience of traditionally managed West African Dwarf goats from the savanna zone of northern Nigeria to naturally acquired trypanosome and gastrointestinal nematode infections.Behnke JM, Chiejina SN, Musongong GA, Nnadi PA, Ngongeh LA, Abonyi FO, Fakae BB.School of Biology, University of Nottingham, University Park, Nottingham NG7 2RD, UK. AbstractA survey was conducted of gastrointestinal nematode infections and trypanosomosis in Nigerian West African Dwarf (WAD) goats from the savanna region of the country. Animals were screened at two markets, Gboko and Akpagher, from the beginning of April until the end of September, coinciding with the end of the dry season and the first 5 months of the wet season. Of 1054 goats that were examined, 80.5% carried gastrointestinal (GI) nematodes belonging to the genera Haemonchus (61.0%), Oesophagostomum (21.0%) and Trichostrongylus (17.9%). Faecal egg counts (FEC) increased very slowly but significantly from April to maximum levels in September, and varied marginally between the two market sources. The majority of goats (68.8 and 70.1% at the two markets) had low FEC not exceeding 50 eggs/g (epg). FEC did not differ significantly between the sexes or between age classes. Packed cell volume (PCV) also declined significantly with month of the study, but was affected by host sex (a significant month x sex interaction) being generally higher in male animals throughout the period. There was a highly significant negative correlation between log10(FEC+1) and PCV, when all other factors had been taken into account. Body condition scores (BCS) also declined with month of the study, but there was a marked difference between the two sexes, with male animals generally showing a greater stability of BCS across the months compared with females. Trypanosome infections were found in only 4% of the goats and only during the rainy season. Most infections (92.86%) were caused by Trypanosoma brucei alone although T. vivax and T. congolense were occasionally detected. Overall, the majority of goats sampled each month maintained generally good body condition (BCS 3.0-5.0), normal or slightly reduced PCV, even when concurrently infected with trypanosomes and GI nematodes. However, four concurrently infected goats showed signs of overt anaemia during periods of peak infection, during the late rainy season, with marked reductions in PCV ( < 15%). Two of the infected goats were also in poor body condition with BCS of < 2.0. There was no evidence of additive or synergistic pathogenic effects of the two parasites. These results are discussed in the context of the unexpectedly strong resistance and resilience of the savanna WAD ecotype to its native strains of GI nematode and trypanosome parasites. |
| PMID: 20459880 [PubMed - as supplied by publisher] | |
| 4. | Parasitology. 2010 May 12:1-7. [Epub ahead of print]Spatial analysis of Leishman ia donovani exposure in humans and domestic animals in a recent kala azar focus in Nepal.Khanal B, Picado A, Bhattarai NR, VAN DER Auwera G, DAS ML, Ostyn B, Davies CR, Boelaert M, Dujardin JC, Rijal S.B.P. Koirala Institute of Health Sciences, Dharan, Nepal. AbstractSUMMARYVisceral leishmaniasis (VL) is a major public health problem in the Indian subcontinent where the Leishmania donovani transmission cycle is described as anthroponotic. However, the role of animals (in particular domestic animals) in the persistence and expansion of VL is still a matter of debate. We combined Direct Agglutination Test (DAT) results in humans and domestic animals with Geographic Information System technology (i.e. extraction maps and scan statistic) to evaluate the exposure to L. donovani on these 2 populations in a recent VL focus in Nepal. A Poisson regression model was used to assess the risk of infection in humans associated with, among other factors, the proportion of DAT-positive animals in the proximities of the household. The serological results showed that both humans and domestic animals were exposed to L. donovani. DAT-positive animals and humans were spatially clustered. The presence of serologically positive goats (IRR=9.71), past VL cases (IRR=2.62) and the proximity to a forest island dividing the study area (IRR=3.67) increased the risk of being DAT-positive in humans. Even if they are not a reservoir, domestic animals, and specially goats, may play a role in the distribution of L. donovani, in particular in this new VL focus. |
| PMID: 20459877 [PubMed - as supplied by publisher] | |
| 5. | BMC Infect Dis. 2010 May 11;10(1):112. [Epub ahead of print]T cells, adhesion molecules and modulation of apoptosis in visceral leishmaniasis glomerulonephritis.Costa FA, Prianti MG, Silva TC, Silva SM, Guerra JL, Goto H.AbstractABSTRACT: BACKGROUND: Immune complex deposition is the accepted mechanism of pathogenesis of VL glomerulopathy however other immune elements may participate. Further in the present study, no difference was seen between immunoglobulin and C3b deposit intensity in glomeruli between infected and non-infected dogs thus T cells, adhesion molecules and parameters of proliferation and apoptosis were analysed in dogs with naturally acquired VL from an endemic area. The dog is the most important domestic reservoir of the protozoa Leishmania (L.) chagasi that causes visceral leishmaniasis (VL). The similarity of VL manifestation in humans and dogs renders the study of canine VL nephropathy of interest with regard to human pathology. METHODS: From 55 dogs with VL and 8 control non-infected dogs from an endemic area, kidney samples were analyzed by immunohistochemistry for immunoglobulin and C3b deposits, staining for CD4+ and CD8+ T cells, ICAM-1, P-selectin and quantified using morphometry. Besides proliferation marker Ki-67, apoptosis markers M30 and TUNEL staining, and related cytokines TNF-alfa, IL-1alfa were searched and quantified. RESULTS: We observed similar IgG, IgM and IgA and C3b deposit intensity in dogs with VL and non-infected control dogs. However we detected the Leishmania antigen in cells in glomeruli in 54, CD4+ T cells in the glomeruli of 44, and CD8+ T cells in 17 of a total of 55 dogs with VL. Leishmania antigen was absent and T cells were absent/scarse in eight non-infected control dogs. CD 4+ T cells predominate in proliferative patterns of glomerulonephritis, however the presence of CD4+ and CD8+ T cells were not different in intensity in different patterns of glomerulonephritis. The expression of ICAM-1 and P-selectin was significantly greater in the glomeruli of infected dogs than in control dogs. In all patterns of glomerulonephritis the expression of ICAM -1 ranged from minimum to moderately severe and P-selectin from absent to severe. In the control animals the expression of these molecules ranged from absent to medium intensity. It was not observed any correlation between severity of the disease and these markers. There was a correlation between the number of Leishmania antigen positive cells and CD4+ T cells, and between the number of CD4+ T cells and CD8+ T cells. In dogs presenting different histopathological patterns of glomerulonephritis, parameters of proliferation and apoptosis were studied. Ki-67, a proliferative marker, was not detected locally, but fewer apoptotic cells and lower TNF- expression were seen in infected animals than in non-infected controls. CONCLUSION: Immunopathogenic mechanisms of VL glomerulonephritis are complex and data in the present study suggest no clear participation of immunoglobulin and C3b deposits in these dogs but the possible migration of CD4+ T cells into the glomeruli, participation of adhesion molecules, and diminished apoptosis of cells contributing to determine the proliferative pattern of glomerulonephritis in VL. |
| PMID: 20459816 [PubMed - as supplied by publisher] | |
| 6. | Microb Cell Fact. 2010 May 10;9(1):29. [Epub ahead of print]A highly efficient pipeline for protein expression in Leishmania tarentolae using infrared fluorescence protein as marker.Dortay H, Mueller-Roeber B.AbstractABSTRACT: BACKGROUND: Leishmania tarentolae, a unicellular eukaryotic protozoan, has been established as a novel host for recombinant protein production in recent years. Current protocols for protein expression in Leishmania are, however, time consuming and require extensive lab work in order to identify well-expressing cell lines. Here we established an alternative protein expression work-flow that employs recently engineered infrared fluorescence protein (IFP) as a suitable and easy-to-handle reporter protein for recombinant protein expression in Leishmania. As model proteins we tested three proteins from the plant Arabidopsis thaliana, including a NAC and a type-B ARR transcription factor. RESULTS: IFP and IFP fusion proteins were expressed in Leishmania and rapidly detected in cells by deconvolution microscopy and in culture by infrared imaging of 96-well microtiter plates using small cell culture volumes (2uL - 100uL). Motility, shape and growth of Leishmania cells were not impaired by intracellular accumulation of IFP. In-cell detection of IFP and IFP fusion proteins was straightforward already at the beginning of the expression pipeline and thus allowed early pre-selection of well-expressing Leishmania clones. Furthermore, IFP fusion proteins retained infrared fluorescence after electrophoresis in denaturing SDS-polyacrylamide gels, allowing direct in-gel detection without the need to disassemble cast protein gels. Thus, parameters for scaling up protein production and streamlining purification routes can be easily optimized when employing IFP as reporter. CONCLUSIONS: Using IFP as biosensor we devised a protocol for rapid and convenient protein expression in Leishmania tarentolae. Our expression pipeline is superior to previously established methods in that it significantly reduces the hands-on-time and work load required for identifying well-expressing clones, refining protein production parameters and establishing purification protocols. The facile in-cell and in-gel detection tools built on IFP make Leishmania amenable for high-throughput expression of proteins from plant and animal sources. |
| PMID: 20459748 [PubMed - as supplied by publisher] | |
| 7. | BMC Microbiol. 2010 May 7;10(1):136. [Epub ahead of print]The Leishmania amazonensis TRF (TTAGGG repeat binding factor) homologue binds and co-localizes with telomeres.da Silva MS, Perez AM, da Silveira RD, de Moraes CE, Siqueira-Neto JL, Freitas-Junior LH, Cano MI.AbstractABSTRACT: BACKGROUND: Telomeres are specialized structures at the end of the chromosomes, essential for maintaining genome stability and cell viability. The importance of telomeric proteins for telomere maintenance has increased our interest in the identification of homologues within the genus Leishmania. The mammalian TRF1 and TRF2 proteins, for example, bind double-stranded telomeres via a Myb-like DNA-binding domain and are involved with telomere length regulation and chromosome end protection. In addition, TRF2 can modulate the activity of several enzymes and influence the conformation of telomeric DNA. In this work, we identified and characterized a Leishmania protein (LaTRF) homologous to both mammalian TRF1 and TRF2. RESULTS: LaTRF was cloned using a PCR-based strategy. ClustalW and bl2seq sequence analysis showed that LaTRF shared sequence identity with the Trypanosoma brucei TRF (TbTRF) protein and had the same degree of sequence similarities with the dimerization (TRFH) and the canonical DNA-binding Myb-like domains of both mammalian TRFs. LaTRF was predicted to be an 82.5 kDa protein, indicating that it is double the size of the trypanosome TRF homologues. Western blotting and indirect immunofluorescence combined with fluorescence in situ hybridization showed that LaTRF, similarly to hTRF2, is a nuclear protein that also associates with parasite telomeres. Native and full length LaTRF and a mutant bearing the putative Myb-like domain expressed in bacteria bound double-stranded telomeric DNA in vitro. Chromatin immunoprecipitation showed that LaTRF interacted specifically with telomeres in vivo. CONCLUSION: The nuclear localization of LaTRF, its association and co-localization with parasite telomeres and its high identity with TbTRF protein, support the hypothesis that LaTRF is a Leishmania telomeric protein. |
| PMID: 20459667 [PubMed - as supplied by publisher] | |
| 8. | Transfusion. 2009 Nov;49(11):2352-8.Estimation of sensitivity and specificity of several Trypanosoma cruzi antibody assays in blood donors in Argentina.Remesar MC, Gamba C, Colaianni IF, Puppo M, Sartor PA, Murphy EL, Neilands TB, Ridolfi MA, Leguizamón MS, Kuperman S, Del Pozo AE.Hospital de Pediatría Prof. Dr. Juan P. Garrahan, Ciudad Autónoma de Buenos Aires, Buenos Aires, Argentina. mremesar@garrahan.gov.ar AbstractBACKGROUND: The absence of a gold standard test for Trypanosoma cruzi antibodies represents a problem not only for the evaluation of screening tests, but also for appropriate blood donor counseling. The aim of this study was to estimate the sensitivity and specificity of multiple blood donor screening tests for T. cruzi antibodies in Argentina. STUDY DESIGN AND METHODS: From June 2006 to March 2007 a sample of 1455 blood donors was recruited from two blood banks in Chaco province, an area of Argentina with highly endemic T. cruzi infection. Samples were tested by three epimastigote lysate enzyme immunoassays (EIAs), one recombinant antigen EIA, two indirect hemagglutination assay (IHA) tests, a particle agglutination assay (PA), and a research trans-sialidase inhibition assay (TIA). Sensitivity and specificity were estimated using latent class analysis (LCA). RESULTS: LCA estimated the consensus prevalence of T. cruzi infection at 24.5%. Interassay correlation was higher among the four EIA tests and TIA compared to IHA tests. Assay sensitivities varied from 96 to 99.7 for different EIAs, 91% for TIA, 84% for PA, and 66 to 74% for IHA tests. Relative to the LCA, assay specificities were from 96% to almost 100%. CONCLUSION: Based on the comparison of several tests in a large population from an endemic area for T. cruzi infection, our data showed an adequate sensitivity for EIA tests in contrast to PA and IHA assays. The latter tests should no longer be used for blood donor screening. |
| PMID: 19903291 [PubMed - indexed for MEDLINE] | |
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