[leish-l] Fwd: Articles found by RefScout 15/06/2005 - 24/2005
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Fri Jun 17 19:56:32 BRT 2005
Date: Wed, 15 Jun 2005 04:37:08
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This is RefScout-Newsletter 24/2005 .
REQUEST: [ leishmaniasis ]
(8 articles match this request)
PMID: 15896700
TITLE: Antiparasitic activity of a triphenyl tin complex against Leishmania
donovani.
AUTHORS: Bikramjit Raychaudhury, Shouvik Banerjee, Shreedhara Gupta, Ran Vir
Singh, Salil C Datta
AFFILIATION: Department of Biological Chemistry, Infectious Diseases Group,
Indian Institute of Chemical Biology, 4 Raja SC Mullick Road, Kolkata 700032,
India.
REFERENCE: Acta Trop 2005 Jul 95(1):1-8
Visceral leishmaniasis is a life-threatening human disease commonly
known as kala-azar. Leishmania donovani is the causative agent of this
parasitic disease transmitted by the sand fly vector to infect hosts.
Triphenyl tin salicylanilide thiosemicarbazone [Ph(3)Sn(OSal.TSCZH)] (
TTST) which is an organometallic complex of triphenyl tin has been
evaluated to explore possibility to develop a potent chemotherapeutic
agent against visceral leishmaniasis. Effect of triphenyl tin complex on
growth inhibition and host-parasite interaction were examined both in
vitro and in vivo. Release of toxic superoxide radical was measured
spectrophotometrically through the formation of blue formazan derived
from reduced nitrobluetetrazolium. To understand mode of action of Ph(3)
Sn(OSal.TSCZH), superoxide dismutase activity was determined
spectrophotometrically by measuring ability of this enzyme to inhibit
pyrogallol autoxidation and also by activity staining of the non-
denaturing polyacrylamide gels after separating superoxide dismutase.
Antileishmanial activity of triphenyl tin complex were found to be
effective both in vitro and in vivo at lower concentrations compared to
the existing toxic drugs available. IC(50) of Ph(3)Sn(OSal.TSCZH) was
calculated as 0.05+/-0.01mg/L. Intracellular survival of the parasite in
host macrophages was inhibited by TTST in a dose dependent manner.
Parasite burden in spleen was reduced to 87% under TTST treatment (10mg/
kg body weight) and under sodium antimony gluconate (20mg/kg body weight
) reduced nearly to 65%. Its action as a chemotherapeutic agent is found
to be mediated through inhibition of superoxide dismutase and
simultaneous release of toxic superoxide radical. We propose that Ph(3)
Sn(OSal.TSCZH) may be considered as a prospective candidate to establish
a better line of therapeutic process against experimental visceral
leishmaniasis.
PMID: 15935321
TITLE: American tegumentary leishmaniasis: A quantitative analysis of Langerhans
cells presents important differences between L. (L.) amazonensis and Viannia
subgenus.
AUTHORS: MarÃlia Brasil Xavier, Fernando Tobias Silveira, Sâmia Demachki,
Márcia Milene Rodrigues Ferreira, José Luiz Martins do Nascimento
AFFILIATION: Departamento de Medicina Comunitária, Universidade do Estado do
Pará, Perebebuà 2623, 66087-670 Belém, Pará, Brazil; Núcleo de Medicina
Tropical, Universidade Federal do Pará, GeneralÃssimo Deodoro 92, 66055-240
Belém, Pará, Brazil.
REFERENCE: Acta Trop 2005 Jul 95(1):67-73
A quantitative study was conducted on the density of Langerhans cells (
LCs) CD1a+ in specimens obtained from patients with American tegumentary
leishmaniasis (ATL) lesions without previous treatment, as well as from
control healthy individuals. LC density was significantly higher among
infected patients when compared to controls and also higher in longer
term ones. Regarding parasite quantities, these were proportionally
inverse and diminished in chronic patients. Localized cutaneous
leishmaniasis (LCL) showed an increase in cell population when compared
to diffuse cutaneous leishmaniasis (DCL). A tendency towards density
increase was observed in LC Leishmania (Leishmania) amazonensis patients
when compared to Leishmania (Viannia) sp. Regarding the delayed
hypersensitivity test (DTH, Montenegro skin test), L. (L.) amazonensis
demonstrated a peculiar behavior because it is a poor cell immune
inducer, presenting - among LCL patients - higher density in negative
Montenegro patients than in positive ones. Negative DTH responses are
usually poor in LC, although this was not evidenced in this study,
possibly due to cell reposition, in order to stimulate immune response.
Such results confirm the important role of LC in ATL, while suggesting
that L. (L.) amazonensis may be a good model for LC studies as APC in
ATL, due to its spectral immunological and clinical behavior.
PMID: 15941439
TITLE: Post-kala-azar dermal leishmaniasis with visceral leishmaniasis: a rare
presentation.
AUTHORS: Arpana Rijal, Sudha Agrawal, Arun Agarwalla, Anshoo Agrawal, Suman
Rijal
AFFILIATION: From the Department of Dermatology, Pathology and Medicine, B. P.
Koirala Institute of Health Sciences, Dharan, Nepal.
REFERENCE: Int J Dermatol 2005 Jun 44(6):494-6
PMID: 15941427
TITLE: Short Communication: Palestinian infantile visceral leishmaniasis caused
by a genetic variant of Leishmania infantum belonging to a new zymodeme.
AUTHORS: Khaldoun A Bader, Lionel F Schnur, Abedelmajeed Nasereddin, Francine
Pratlong, Jean-Pierre Dedet, Loay Shaheen, Obaida Yousef, Charles L Greenblatt
AFFILIATION: Department of Parasitology, Hebrew University-Hadassah Medical
School, Jerusalem, Israel.
REFERENCE: Trop Med Int Health 2005 Jun 10(6):618-20
Summary The parasites causing a Palestinian case of infantile visceral
leishmaniasis (IVL) and those from four dogs from the Jenin District
were identified serologically, biochemically and molecular biologically
as Leishmania infantum, showing dogs act as a reservoir. The strain from
the human case was distinct because of its unique 200-bp kDNA-
polymerase chain reaction (PCR) component in its restriction fragment
length polymorphism (RFLP) profile after digestion with the endonuclease
RsaI, and by the electrophoretic mobility of its malate dehydrogenase (
MDH(140)), designating it the reference strain of a new zymodeme of L.
infantum, MON-281.
PMID: 15949184
TITLE: Evaluation of a dot-immunoblot assay for detecting leishmanial antigen in
naturally infected Phlebotomus argentipes (Diptera: Psychodidae).
AUTHORS: V Kumar, S Bimal, S Kesari, A J Kumar, A K Bagchi, M A Akbar, K
Kishore, S K Bhattacharya, P Das
AFFILIATION: Rajendra Memorial Research Institute of Medical Sciences, Indian
Council of Medical Research, Agamkuan, Patna - 800 007, Bihar, India.
REFERENCE: Ann Trop Med Parasitol 2005 Jun 99(4):371-6
A simple and highly reproducible dot-immunoblot assay was developed to
detect leishmanial antigen in Phlebotomus argentipes that were naturally
infected with Leishmania donovani. The test was sensitive to as little
as 10 ng of antigenic protein (equivalent to the gut content of one
laboratory-infected sandfly) and also appeared to be specific, in that
it gave a positive result with some P. argentipes (the primary vector of
L. donovani in India) and L. donovani but not with P. papatasi or other
pathogens.When used to investigate a large number of sandflies
collected from two areas of the Indian state of Bihar where visceral
leishmaniasis is endemic, the assay appeared sufficiently sensitive and
specific to detect the naturally infected insects. The simplicity,
reproducibility, high sensitivity and high specificity of the assay
should make it useful for field studies, particularly in determining the
prevalence of sandfly infection, the local level of transmission, and
the impact of vector-control programmes.
PMID: 15848791
TITLE: Altered platelet aggregation and coagulation disorders related to
clinical findings in 30 dogs naturally infected by Leishmania infantum.
AUTHORS: P Ciaramella, A Pelagalli, L Cortese, M E Pero, M Corona, P Lombardi, L
Avallone, A Persechino
AFFILIATION: Department of Veterinary Clinical Science, Section of Internal
Medicine, University of Naples, Federico II, Via Delpino 1, 80137 Napoli,
Italy. paociara at unina.it
REFERENCE: Vet J 2005 May 169(3):465-7
PMID: 15813687
TITLE: [Clinical cases in Medical Mycology. Case No. 14]
AUTHORS: Ricardo Negroni, Alicia Arechavala, Gabriela López Daneri
AFFILIATION: Hospital de Infecciosas Francisco Javier Muñiz, Buenos Aires,
Argentina. micologÃa at fmed.uba.ar
REFERENCE: Rev Iberoam Micol 2005 Mar 22(1):60-1
PMID: 15945169
TITLE: Prospective study among cutaneous leishmaniasis cases in Tripoli Central
Hospital, Tripoli, Libya.
AUTHORS: A A El Buni, H Edwebi, A L Ben Darif
AFFILIATION: Medical Microbiology and Parasitology Department, Faculty of
Medicine, Al-Arab Medical University, Benghazi, Libya.
REFERENCE: Arch Inst Pasteur Tunis 1997 Jan-Apr 74(1-2):3-4
One hundred and nine cases of cutaneous leishmaniasis were referred to
Dermatology unit, Tripoli Central Hospital from 24 localities in north-
west Libya during the period from September to December 1994. Clinically
most of the lesions were multiple and distributed on the uncovered
parts of the body, and the size ranged from 1 to 5 cm. In diameter. The
prevalence of infection was 65.3% among age groups 1-30 year old.
Patients responded well to the treatment with sodium stibagluconate.
REQUEST: [ leishmania ]
(11 articles match this request. 4 articles matching other requests removed)
PMID: 15950742
TITLE: Adjuvant effect of Taenia crassiceps glycans against leishmanial antigens
in mice infected with Leishmania mexicana.
AUTHORS: Senarath Dissanayake, Allen Shahin, Abdul Majeed Ameen
AFFILIATION: Department of Microbiology, Faculty of Medicine, United Arab
Emirates University, PO Box 17666, Al Ain, United Arab Emirates.
REFERENCE: Mol Immunol 2005 Aug 42(12):1495-502
Complex glycans derived from lipid, nucleic acid and protein free
extracts of Taenia crassiceps metacestode larvae were found to have
adjuvant effect against Leishmania mexicana antigens in BALB/c mice
experimentally infected with L. mexicana. A single intraperitoneal or
subcutaneous injection of Taenia glycans altered the Th-1/Th-2 balance
in experimentally infected mice as determined by Western blot analysis
of IgG 1 and IgG 2a antibodies to L. mexicana antigens. Leishmania
antigens which were immunogenic in Taenia glycan vaccinated mice were
different from those of non-vaccinated mice. Vaccination induced
leishmania antigen specific IFN-gamma expression in vitro culture by
spleen cells from Taenia glycan vaccinated-leishmania infected mice and
not from mock vaccinated-leishmania infected BALB/c mice. We conclude
that T. crassiceps glycans have immunoadjuvant effects against
leishmania and may be developed as adjuvants in anti-leishmania vaccines.
PMID: 15939291
TITLE: Development of an inducible protein expression system based on the
protozoan host Leishmania tarentolae.
AUTHORS: Susanna Kushnir, Klaus Gase, Reinhard Breitling, Kirill Alexandrov
AFFILIATION: Department of Physical Biochemistry, Max-Planck-Institute for
Molecular Physiology, Otto-Hahn-Strasse 11, 44227 Dortmund, Germany.
REFERENCE: Protein Expr Purif 2005 Jul 42(1):37-46
Production of functional eukaryotic proteins in recombinant form is a
bottle-neck in various post-genomic applications and in life science in
general. At least partially this is due to the problems associated with
the use of endogenous RNA polymerase II for high-level transcription of
heterologous genes in eukaryotic expression systems. To circumvent these
problems we developed a new inducible protein expression system based
on the protozoan host Leishmania tarentolae (Trypanosomatidae). We have
created a strain of L. tarentolae constitutively co-expressing T7 RNA
polymerase and tetracycline repressor. This strain could be stably
transformed with the heterologous target gene under control of the T7
promoter/TET operator assembly, which can initiate transcription upon
addition of tetracycline to the culture medium. Using this system, we
demonstrated that enhanced green fluorescent protein (EGFP) could be
overexpressed to a level of ca. 1% of total cellular protein. The
developed system was tested for its ability to inducibly co-express
multiple genes. Using two copies of the egfp gene integrated at two
different genomic sites, we could obtain expression levels reaching 4%
of total cellular protein. Further possible improvements and
applications of the developed system are discussed.
PMID: 15925459
TITLE: Intragenomic spliced leader RNA array analysis of kinetoplastids reveals
unexpected transcribed region diversity in Trypanosoma cruzi.
AUTHORS: Sean Thomas, Scott J Westenberger, David A Campbell, Nancy R Sturm
AFFILIATION: Molecular Biology Institute, University of California, Los Angeles,
CA, USA; Department of Microbiology Immunology and Molecular Genetics, David
Geffen School of Medicine, University of California, Los Angeles, CA, USA.
REFERENCE: Gene 2005 Jun 352():100-8
The spliced leader RNA gene (SL RNA) repeat is present in large
multicopy arrays and has been used as a marker for the diversity of
kinetoplastid protozoans. Intra-array variation could affect conclusions
made using a randomly isolated repeat as a marker. We examined the
Leishmania major (Friedlin) and Trypanosoma cruzi (CL Brener) genome
projects for SL RNA repeat sequences in order to assess their
homogeneity and the possible effects of sequence variation on taxonomic
interpretation. Of the dozens of distinct sequence classes examined, no
single copy would bias clustering analyses with regard to other closely
related species or isolates. Six dimorphic sites within the T. cruzi
transcribed region were found to be linked and are predicted to yield a
heterogeneous SL RNA population. The variation that exists among the
repeats paints a picture of the broad mechanisms of array maintenance
and evolution where site-specific mutations in a single repeat may be
spread throughout the array and recombined with existing repeats to
create new sequence classes, all occurring under selective pressure to
maintain or increase the fitness of the cell line in which these events
occur.
PMID: 15947206
TITLE: Eukaryotic UDP-Galactopyranose Mutase (GLF Gene) in Microbial and
Metazoal Pathogens.
AUTHORS: Stephen M Beverley, Katherine L Owens, Melissa Showalter, Cara L
Griffith, Tamara L Doering, Victoria C Jones, Michael R McNeil
AFFILIATION: Department of Molecular Microbiology, Washington University Medical
School, 660 S. Euclid Ave., St. Louis, MO 63110. beverley at borcim.wustl.edu.
REFERENCE: Eukaryot Cell 2005 Jun 4(6):1147-54
Galactofuranose (Gal(f)) is a novel sugar absent in mammals but present
in a variety of pathogenic microbes, often within glycoconjugates that
play critical roles in cell surface formation and the infectious cycle.
In prokaryotes, Gal(f) is synthesized as the nucleotide sugar UDP-Gal(f
) by UDP-galactopyranose mutase (UGM) (gene GLF). Here we used a
combinatorial bioinformatics screen to identify a family of candidate
eukaryotic GLFs that had previously escaped detection. GLFs from three
pathogens, two protozoa (Leishmania major and Trypanosoma cruzi) and one
fungus (Cryptococcus neoformans), had UGM activity when expressed in
Escherichia coli and assayed in vivo and/or in vitro. Eukaryotic GLFs
are closely related to each other but distantly related to prokaryotic
GLFs, showing limited conservation of core residues around the substrate
-binding site and flavin adenine dinucleotide binding domain. Several
eukaryotes not previously investigated for Gal(f) synthesis also showed
strong GLF homologs with conservation of key residues. These included
other fungi, the alga Chlamydomonas and the algal phleovirus Feldmannia
irregularis, parasitic nematodes (Brugia, Onchocerca, and Strongyloides
) and Caenorhabditis elegans, and the urochordates Halocynthia and
Cionia. The C. elegans open reading frame was shown to encode UGM
activity. The GLF phylogenetic distribution suggests that Gal(f)
synthesis may occur more broadly in eukaryotes than previously supposed
. Overall, GLF/Gal(f) synthesis in eukaryotes appears to occur with a
disjunct distribution and often in pathogenic species, similar to what
is seen in prokaryotes. Thus, UGM inhibition may provide an attractive
drug target in those eukaryotes where Gal(f) plays critical roles in
cellular viability and virulence.
PMID: 15886061
TITLE: Substrate preferences and glucose uptake in glibenclamide-resistant
Leishmania parasites.
AUTHORS: Nestor Luis Uzcategui, Katherine Figarella, Natacha Camacho, Alicia
Ponte-Sucre
AFFILIATION: Laboratorio de FisiologÃa Molecular, Instituto de Medicina
Experimental, Facultad de Medicina, Universidad Central de Venezuela, Caracas,
Venezuela.
REFERENCE: Comp Biochem Physiol C Toxicol Pharmacol 2005 Mar-Apr
140(3-4):395-402
Several drug-resistant mammalian cell types exhibit increased glycolytic
rates, preferential synthesis of ATP through oxidative phosphorylation
, and altered glucose transport. Herein we analyzed the influence of
parasite growth phase on energy substrate uptake and use in a Leishmania
strain [NR(Gr)] selected for resistance against glibenclamide.
Glibenclamide is an ABC-transporter blocker which modulates the function
of glucose transporters in some mammalian cells. Our results
demonstrate for the first time that compared to glibenclamide-sensitive
Leishmania, exponential phase glibenclamide-resistant parasites exhibit
decreased use of glucose as energy substrate, decreased glucose uptake
and decreased glucose transporter expression. However, compared to
glibenclamide-sensitive cells, stationary phase resistant parasites
display an increased use of amino acids as energy substrate and an
increased activity of the enzymes hexokinase, phosphoglucose isomerase,
and especially NAD(+)-linked glutamate dehydrogenase. These results
suggest that drug resistance in Leishmania involves a metabolic
adaptation that promotes a stage dependent modulation of energy
substrate uptake and use as a physiological response to the challenge
imposed by drug pressure.
PMID: 15941064
TITLE: [Risk factors of leishmanin-skin test positivity in transmission of
Leishmania infantum in the center of Tunisia]
AUTHORS: A Ben Salah, N Ben Alaya Bouafif, S Chlif, A Gharbi, N Bel Haj Hamida,
A Zaatour, K Dellagi
AFFILIATION: Institut Pasteur de Tunis, 13 Place Pasteur-BP 74, 1002 Tunis
Belvédère, Tunisie.
REFERENCE: Arch Inst Pasteur Tunis 2003 80(1-4):17-27
This work aims to estimate prevalence and evaluate risk factors of
leishmanin-skin test positivity. A cross-sectional leishmanin skin test
study was carried out on a sample of 3190 healthy volunteers living in
the gouvernorates of Kairouan and Kasserine. Age standardized prevalence
of leishmanin-skin test positivity was 45.9% (CI95% = [43.9-47.9])
confirming the hyper endemicity of this region. The rate of leishmanin-
skin test positivity ranged from 75.9% (CI95% = [71.9-79.5]) in Zaghdoud
(Kairouan) to 6.5% (CI95% = [3.7-11.01) in Abdeladhim (Kasserine).
There is no significant difference between men and women suggesting a
similar exposure to infection. In the districts of Zaghdoud, Sidi Amor,
El Hajeb and chbika, age specific rates showed a rapid increasing
positive prevalence with age reaching a proportion exceeding 80% after
the age of 15 years. However, the age specific prevalence from other
delegations showed a progressive increasing trend with age, with a low
rate for younger children and a plateau of 75% after 45 years.
Multivariate analysis of leishmanin-skin test positivity risk factors
showed that only district and age are determinants of this infection.
PMID: 15941068
TITLE: [Importance of morphological study of amastigote forms to differentiate
Leishmania infantum and Leishmania major species]
AUTHORS: K Aoun, M K Chahed, M Mokni, Z Harrat, A Bouratbine
AFFILIATION: Laboratoire de parasitologie clinique, Institut pasteur de Tunis,
BP 74, 1002 Tunis Belvédère, Tunisie.
REFERENCE: Arch Inst Pasteur Tunis 2003 80(1-4):53-6
The microscopic study of the dermal smears of 62 cases of cutaneous
leishmaniose, 27 infected by Leishmania (L.) infantum and 35 by L. major
, showed that the amastigotes of L. infantum are meaningfully smaller (p
< 0.001). This criteria is a simple pary alternative to distinguish
these 2 species which have completely different epidemiology, recovery
delay and prophylactic dispositions.
REQUEST: [ sand fly ]
(1 article matches this request. 1 article matching other requests removed)
REQUEST: [ sandfly ]
(1 article matches this request. 1 article matching other requests removed)
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