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Sent on Wednesday, 2009 Apr 29Search kinetoplastids OR kinetoplastid OR Kinetoplastida OR "trypanosoma brucei" OR leishmania OR brucei OR leishmaniasis OR "African trypanosomiasis"
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| PubMed Results |
- 1: Microbes Infect. 2009 Apr;11(4):484-92.
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Population genetics of Leishmania infantum in Israel and the Palestinian Authority through microsatellite analysis.
Institute of Microbiology and Hygiene, Charité Universitätsmedizin Berlin, Berlin, Germany.
Multilocus microsatellite typing (MLMT) was used to investigate the genetic variation among 44 Israeli and Palestinian strains of L. infantum isolated from infected dogs and human cases to determine their population structure and to compare them with strains isolated from different European countries. Most of the Israeli and Palestinian strains had their own individual MLMT profiles; a few shared the same profile. A Bayesian model-based approach and phylogenetic reconstructions based on genetic distances inferred two main populations that were significantly different from the European strains: population A, containing 16 strains from places in the West Bank and 11 strains from central Israel;and population B, containing 7 strains from northern Israel, 9 from central Israel, and one Palestinian strain from the Jenin District.Geographically distributed sub-populations were detected within population B. These results demonstrate similar disease dynamics in Israel and the Palestinian Authority. The re-emergence of VL in the case of population A is more likely owing to increased dog and human contact with sylvatic cycles of parasitic infection rather than to recent introduction from the older foci of northern Israel. The latter scenario could be true for population B found in few foci of Central Israel. (c) 2009 Elsevier Masson SAS. All rights reserved.
PMID: 19399967 [PubMed - in process]
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Related articles
- Population genetics of Leishmania infantum in Israel and the Palestinian Authority through microsatellite analysis.
Microbes Infect. 2009 Feb 11; . Epub 2009 Feb 11.
[Microbes Infect. 2009]
- Identification of geographically distributed sub-populations of Leishmania (Leishmania) major by microsatellite analysis.
BMC Evol Biol. 2008 Jun 24; 8:183. Epub 2008 Jun 24.
[BMC Evol Biol. 2008]
- Genetic polymorphism of Algerian Leishmania infantum strains revealed by multilocus microsatellite analysis.
Microbes Infect. 2008 Oct; 10(12-13):1309-15. Epub 2008 Aug 7.
[Microbes Infect. 2008]
- ReviewSubstance abuse studies and prevention efforts among Arabs in the 1990s in Israel, Jordan and the Palestinian Authority--a literature review.
Addiction. 1999 Feb; 94(2):177-98.
[Addiction. 1999]
- Review[Monitoring of canine leishmaniasis in northern Italy: an update from a scientific network]
Parassitologia. 2004 Jun; 46(1-2):193-7.
[Parassitologia. 2004]
- » See reviews... | » See all...
- Population genetics of Leishmania infantum in Israel and the Palestinian Authority through microsatellite analysis.
-
Population genetics of Leishmania infantum in Israel and the Palestinian Authority through microsatellite analysis.
Institute of Microbiology and Hygiene, Charité Universitätsmedizin Berlin, Berlin, Germany; Al-Quds Nutrition and Health Research Institute, Faculty of Medicine, Al-Quds University, Abu-Deis, The Palestinian Authority.
Multilocus microsatellite typing (MLMT) was used to investigate the genetic variation among 44 Israeli and Palestinian strains of L. infantum isolated from infected dogs and human cases to determine their population structure and to compare them with strains isolated from different European countries. Most of the Israeli and Palestinian strains had their own individual MLMT profiles; a few shared the same profile. A Bayesian model-based approach and phylogenetic reconstructions based on genetic distances inferred two main populations that were significantly different from the European strains: population A, containing 16 strains from places in the West Bank and 11 strains from central Israel; and population B, containing 7 strains from northern Israel, 9 from central Israel, and one Palestinian strain from the Jenin District. Geographically distributed sub-populations were detected within population B. These results demonstrate similar disease dynamics in Israel and the Palestinian Authority. The re-emergence of VL in the case of population A is more likely owing to increased dog and human contact with sylvatic cycles of parasitic infection rather than to recent introduction from the older foci of northern Israel. The latter scenario could be true for population B found in few foci of Central Israel.
PMID: 19397872 [PubMed - as supplied by publisher]
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Related articles
- Population genetics of Leishmania infantum in Israel and the Palestinian Authority through microsatellite analysis.
Microbes Infect. 2009 Apr; 11(4):484-92.
[Microbes Infect. 2009]
- Identification of geographically distributed sub-populations of Leishmania (Leishmania) major by microsatellite analysis.
BMC Evol Biol. 2008 Jun 24; 8:183. Epub 2008 Jun 24.
[BMC Evol Biol. 2008]
- Genetic polymorphism of Algerian Leishmania infantum strains revealed by multilocus microsatellite analysis.
Microbes Infect. 2008 Oct; 10(12-13):1309-15. Epub 2008 Aug 7.
[Microbes Infect. 2008]
- ReviewSubstance abuse studies and prevention efforts among Arabs in the 1990s in Israel, Jordan and the Palestinian Authority--a literature review.
Addiction. 1999 Feb; 94(2):177-98.
[Addiction. 1999]
- Review[Monitoring of canine leishmaniasis in northern Italy: an update from a scientific network]
Parassitologia. 2004 Jun; 46(1-2):193-7.
[Parassitologia. 2004]
- » See reviews... | » See all...
- Population genetics of Leishmania infantum in Israel and the Palestinian Authority through microsatellite analysis.
-
Genetic Admixture in Brazilians Exposed to Infection with Leishmania chagasi.
Interdisciplinary Graduate Program in Molecular and Cellular Biology, University of Iowa; Iowa City, IA 52242.
Summary Visceral leishmaniasis (VL) in northeast Brazil is a disease caused by infection with the protozoan Leishmania chagasi. Infection leads to variable clinical outcomes ranging from asymptomatic infection to potentially fatal disease. Prior studies suggest the genetic background of the host contributes to the development of different outcomes after infection, although it is not known if ancestral background itself influences outcomes. VL is endemic in peri-urban areas around the city of Natal in northeast Brazil. The population of northeast Brazil is a mixture of distinct racial and ethnic groups. We hypothesized that some sub-populations may be more susceptible than others to develop different clinical outcomes after L. chagasi infection. Using microsatellite markers, we examined whether admixture of the population as a whole, or markers likely inherited from a distinct ethnic background, differed between individuals with VL, individuals with an asymptomatic infection, or individuals with no infection. There was no apparent significant difference in overall population admixture proportions among the three clinical phenotype groups. However, one marker on Chr. 22 displayed evidence of excess ancestry from putative ancestral populations among different clinical phenotypes, suggesting this region may contain genes determining the course of L. chagasi infection.
PMID: 19397557 [PubMed - as supplied by publisher]
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- An emerging peri-urban pattern of infection with Leishmania chagasi, the protozoan causing visceral leishmaniasis in northeast Brazil.
Scand J Infect Dis. 2004; 36(6-7):443-9.
[Scand J Infect Dis. 2004]
- Association between the tumor necrosis factor locus and the clinical outcome of Leishmania chagasi infection.
Infect Immun. 2002 Dec; 70(12):6919-25.
[Infect Immun. 2002]
- Genetic predisposition to self-curing infection with the protozoan Leishmania chagasi: a genomewide scan.
J Infect Dis. 2007 Oct 15; 196(8):1261-9. Epub 2007 Sep 13.
[J Infect Dis. 2007]
- ReviewLeishmaniasis: recognition and management with a focus on the immunocompromised patient.
Am J Clin Dermatol. 2002; 3(2):91-105.
[Am J Clin Dermatol. 2002]
- ReviewAnimal models for vaccine studies for visceral leishmaniasis.
Indian J Med Res. 2006 Mar; 123(3):439-54.
[Indian J Med Res. 2006]
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- An emerging peri-urban pattern of infection with Leishmania chagasi, the protozoan causing visceral leishmaniasis in northeast Brazil.
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The FIP-1 like polyadenylation factor in trypanosomes and the structural basis for its interaction with CPSF30.
INGEBI-CONICET, Vta. de Obligado 2490, 2P, CP 1428, 1428 Buenos Aires, Argentina.
In trypanosomes transcription is polycistronic and individual mRNAs are generated by a trans-splicing/polyadenylation coupled reaction. We identified a divergent trypanosome FIP1-like, a factor required for mRNA 3' end formation from yeasts to human. Here we showed that it is a nuclear protein with a speckled distribution essential for trypanosome viability. A strong interaction was found between TcFIP1-like and TcCPSF30, a component of the polyadenylation complex. We determined the specific amino acids in each protein involved in the interaction. Significant differences were found between the trypanosome interaction surface and its human counterpart. Although CPSF30/FIP1 interaction is known in other organisms, this is the first report mapping the interaction surface at the amino acid level.
PMID: 19338765 [PubMed - indexed for MEDLINE]
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- tbCPSF30 depletion by RNA interference disrupts polycistronic RNA processing in Trypanosoma brucei.
J Biol Chem. 2003 Jul 18; 278(29):26870-8. Epub 2003 May 13.
[J Biol Chem. 2003]
- The interaction between two Arabidopsis polyadenylation factor subunits involves an evolutionarily-conserved motif and has implications for the assembly and function of the polyadenylation complex.
Protein Pept Lett. 2008; 15(1):76-88.
[Protein Pept Lett. 2008]
- A serendipitous discovery that in situ proteolysis is essential for the crystallization of yeast CPSF-100 (Ydh1p).
Acta Crystallogr Sect F Struct Biol Cryst Commun. 2006 Oct 1; 62(Pt 10):1041-5. Epub 2006 Sep 30.
[Acta Crystallogr Sect F Struct Biol Cryst Commun. 2006]
- ReviewFormation of the 3' end of histone mRNA: getting closer to the end.
Gene. 2007 Jul 15; 396(2):373-90. Epub 2007 May 4.
[Gene. 2007]
- ReviewA history of poly A sequences: from formation to factors to function.
Prog Nucleic Acid Res Mol Biol. 2002; 71:285-389.
[Prog Nucleic Acid Res Mol Biol. 2002]
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- tbCPSF30 depletion by RNA interference disrupts polycistronic RNA processing in Trypanosoma brucei.
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Trypanosomatid EST: a neglected information resource regarding flagellated protozoa?
Laboratório de Epidemiologia Molecular de Doenças Infecciosas, Instituto Oswaldo Cruz-Fiocruz, Rio de Janeiro, RJ, Brasil. abrandao@fiocruz.br
PMID: 18949338 [PubMed - indexed for MEDLINE]
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- Analysis of expressed sequence tags from Trypanosoma cruzi amastigotes.
Mem Inst Oswaldo Cruz. 2005 Jul; 100(4):385-9. Epub 2005 Aug 17.
[Mem Inst Oswaldo Cruz. 2005]
- Generation and analysis of expressed sequence tags from Trypanosoma cruzi trypomastigote and amastigote cDNA libraries.
Mol Biochem Parasitol. 2004 Aug; 136(2):221-5.
[Mol Biochem Parasitol. 2004]
- Construction of a normalized cDNA library for the Trypanosoma cruzi genome project.
J Eukaryot Microbiol. 1999 Sep-Oct; 46(5):542-4.
[J Eukaryot Microbiol. 1999]
- ReviewParasite genome initiatives.
Int J Parasitol. 2001 May 1; 31(5-6):532-6.
[Int J Parasitol. 2001]
- Review[Genetic network controlling cell differentiation in Dictyostelium]
Tanpakushitsu Kakusan Koso. 2005 Dec; 50(16 Suppl):2219-24.
[Tanpakushitsu Kakusan Koso. 2005]
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- Analysis of expressed sequence tags from Trypanosoma cruzi amastigotes.
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Ecological control of Triatoma dimidiata (Latreille, 1811): five years after a Costa Rican pilot project.
Laboratorio de Zoonosis, Escuela de Medicina Veterinaria, Facultad de Ciencias de Salud, Universidad Nacional, Campus Benjamín Nuñes, Heredia, Costa Rica. rodrigozeledon@ice.co.cr
An ecological pilot project for the control of Triatoma dimidiata allowed a new evaluation four and five years after environmental modifications in the peridomestic areas of 20 households. It was verified that the two groups of houses, 10 case-houses and 10 control-houses, were free of insects after those periods of time. In the first group, the owners started a chicken coop in the backyard and a colony of bugs was found there without infesting the house. In the second group, the inhabitants of one house once again facilitated the conditions for the bugs to thrive in the same store room, reaffirming that man-made ecotopes facilitates colonization. This ecological control method was revealed to be reliable and sustainable and it is recommended to be applied to those situations where the vectors of Chagas disease can colonize houses and are frequent in wild ecotopes.
PMID: 18949337 [PubMed - indexed for MEDLINE]
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- Environmental management for the control of Triatoma dimidiata (Latreille, 1811), (Hemiptera: Reduviidae) in Costa Rica: a pilot project.
Mem Inst Oswaldo Cruz. 2006 Jun; 101(4):379-86.
[Mem Inst Oswaldo Cruz. 2006]
- A survey on Triatoma dimidiata in an urban area of the province of Heredia, Costa Rica.
Mem Inst Oswaldo Cruz. 2005 Oct; 100(6):507-12. Epub 2005 Nov 8.
[Mem Inst Oswaldo Cruz. 2005]
- Evidence of colonization of man-made ecotopes by Triatoma dimidiata (Latreille, 1811) in Costa Rica.
Mem Inst Oswaldo Cruz. 2001 Jul; 96(5):659-60.
[Mem Inst Oswaldo Cruz. 2001]
- Chagas' disease: risk factors for house infestation by Triatoma dimidiata, the major vector of Trypanosoma cruzi in Costa Rica.
Am J Epidemiol. 1991 Apr 1; 133(7):740-7.
[Am J Epidemiol. 1991]
- ReviewTriatoma dimidiata (Latreille, 1811): a review of its diversity across its geographic range and the relationship among populations.
Infect Genet Evol. 2007 Mar; 7(2):343-52. Epub 2006 Nov 13.
[Infect Genet Evol. 2007]
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- Environmental management for the control of Triatoma dimidiata (Latreille, 1811), (Hemiptera: Reduviidae) in Costa Rica: a pilot project.
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Trypanosoma cruzi: a stage-specific calpain-like protein is induced after various kinds of stress.
Instituto Carlos Chagas-Fiocruz, Curitiba, PR, Brasil.
Calpains are calcium-dependent cysteine proteinases found in all living organisms and are involved in diverse cellular processes. Calpain-like proteins have been reported after in silico analysis of the Tritryps genome and are believed to play important roles in cell functions of trypanosomatids. We describe the characterization of a member of this family, which is differentially expressed during the life-cycle of Trypanosoma cruzi.
PMID: 18949332 [PubMed - indexed for MEDLINE]
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Exp Parasitol. 2007 Sep; 117(1):99-105. Epub 2007 Mar 27.
[Exp Parasitol. 2007]
- TcRRMs and Tcp28 genes are intercalated and differentially expressed in Trypanosoma cruzi life cycle.
Biochem Biophys Res Commun. 2004 Sep 24; 322(3):985-92.
[Biochem Biophys Res Commun. 2004]
- Exploring the FL-160-CRP gene family through sequence variability of the complement regulatory protein (CRP) expressed by the trypomastigote stage of Trypanosoma cruzi.
Infect Genet Evol. 2008 May; 8(3):258-66. Epub 2008 Jan 16.
[Infect Genet Evol. 2008]
- ReviewStage-specific gene expression during Trypanosoma cruzi metacyclogenesis.
Genet Mol Res. 2003 Mar 31; 2(1):159-68. Epub 2003 Mar 31.
[Genet Mol Res. 2003]
- ReviewThe life cycle of Trypanosoma cruzi revisited.
Int J Parasitol. 2001 May 1; 31(5-6):472-81.
[Int J Parasitol. 2001]
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- Trypanosoma cruzi: molecular characterization of an RNA binding protein differentially expressed in the parasite life cycle.
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Trypanosoma cruzi: blood parasitism kinetics and their correlation with heart parasitism intensity during long-term infection of Beagle dogs.
Departamento de Ciências Biológicas, Instituto de Ciências Exatas e Biológicas, Campus Universitário, Universidade Federal de Ouro Preto, MG, Brasil. vanjamv@iceb.ufop.br
The goals of the present study were to evaluate the kinetics of blood parasitism by examination of fresh blood, blood culture (BC) and PCR assays and their correlation with heart parasitism during two years of infection in Beagle dogs inoculated with the Be-78, Y and ABC Trypanosoma cruzi strains. Our results showed that the parasite or its kDNA is easily detected during the acute phase in all infected animals. On the other hand, a reduced number of positive tests were verified during the chronic phase of the infection. The frequency of positive tests was correlated with T. cruzi strain. The percentage of positive BC and blood PCR performed in samples from animals inoculated with Be-78 and ABC strains were similar and significantly larger in relation to animals infected with the Y strain.Comparison of the positivity of PCR tests performed using blood and heart tissue samples obtained two years after infection showed two different patterns associated with the inoculated T. cruzi strain: (1) high PCR positivity for both blood and tissue was observed in animals infected with Be-78 or ABC strains; (2) lower and higher PCR positivity for the blood and tissue, respectively, was detected in animals infected with Y strains. These data suggest that the sensitivity of BC and blood PCR was T. cruzi strain dependent and, in contrast, the heart tissue PCR revealed higher sensitivity regardless of the parasite stock.
PMID: 18949320 [PubMed - indexed for MEDLINE]
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Mem Inst Oswaldo Cruz. 2007 May; 102(2):141-7.
[Mem Inst Oswaldo Cruz. 2007]
- Chronic Chagas' disease in rhesus monkeys (Macaca mulatta): evaluation of parasitemia, serology, electrocardiography, echocardiography, and radiology.
Am J Trop Med Hyg. 2003 Jun; 68(6):683-91.
[Am J Trop Med Hyg. 2003]
- Blood culture and polymerase chain reaction for the diagnosis of the chronic phase of human infection with Trypanosoma cruzi.
Parasitol Res. 2002 Oct; 88(10):894-900. Epub 2002 Jun 15.
[Parasitol Res. 2002]
- Comparison of Trypanosoma cruzi infection in dogs inoculated with blood or metacyclic trypomastigotes of Berenice-62 and Berenice-78 strains via intraperitoneal and conjunctival routes.
Rev Soc Bras Med Trop. 2002 Jul-Aug; 35(4):339-45.
[Rev Soc Bras Med Trop. 2002]
- A study of experimental reinfection by Trypanosoma cruzi in dogs.
Am J Trop Med Hyg. 2001 Dec; 65(6):958-65.
[Am J Trop Med Hyg. 2001]
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- Trypanosoma cruzi high infectivity in vitro is related to cardiac lesions during long-term infection in Beagle dogs.
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