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This is RefScout-Newsletter 36/2004 for user Jeff32630.






REQUEST: [ leishmaniasis ]

(23 articles match this request)



PMID: 15324405
 

TITLE: Leishmaniasis of the lip in a patient with Down's syndrome.

AUTHORS: C Ferreli, L Atzori, M Zucca, P Pistis, N Aste

AFFILIATION: Dermatology Department, Cagliari University via Ospedale 54-09124,
Cagliari, Italy.

REFERENCE: J Eur Acad Dermatol Venereol 2004 Sep 18(5):599-602

ABSTRACT Cutaneous leishmaniasis is an endemic protozoan infection in 
Sardinia, one of the major islands of the Mediterranean Basin. The main 
causative strain in this country is Leishmania infantum, which rarely 
involves mucocutaneous areas, but has the potential to cause visceral 
leishmaniasis. An atypical leishmaniasis involving the inferior lip of a
 57-year-old female with Down's syndrome was observed at the Dermatology
 Department of Cagliari (italy). The diagnosis was mainly based upon 
histopathological examination, revealing intra- and extra-cellular 
leishmania amastigotes. The leishmania infantum zymodeme MON-111 was 
identified by isoenzymatic characterization. Laboratory investigations 
revealed a normal complete blood count and biochemistry profile, except 
for an inverted CD4/CD8 ratio. Treatment with meglumine antimoniate 60 
mg/kg/day (Glucantime(R)) intramuscularly for 15 days, followed by 
intralesional administration 1 ml weekly for 4 weeks led to complete 
recovery. No relapses were observed at 6-month follow-up. The unusual 
localization is likely to be a reflection of the uncommon site of 
inoculation of the protozoa, transmitted by bites from flying vectors. 
Nevertheless, the presence of Down's syndrome in our patient may have 
contributed to the atypical presentation by traumatic exacerbation of 
the lesion, due to repeated auto-induced microtraumas of the inferior 
lip accompanied by subclinical immunodeficiency. In fact, the specific 
immune response to Leishmania infection depends on a host-cell-mediated 
immune response, reported as defective in Down's syndrome patients. 
Differential diagnosis and early detection of the infection are 
necessary in order to start effective treatment and prevent more serious
 complications.








PMID: 15328080
 

TITLE: Treatment of experimental visceral leishmaniasis with amphotericin B in
stable albumin microspheres.

AUTHORS: J A Sánchez-Brunete, M A Dea, S Rama, F Bolás, J M Alunda, R Raposo,
M T Méndez, S Torrado-Santiago, J J Torrado

AFFILIATION: Facultad de Farmacia, Universidad Complutense, Plaza Ramón y Cajal
s/n, 28040 Madrid, Spain. torrado1 at farm.ucm.es

REFERENCE: Antimicrob Agents Chemother 2004 Sep 48(9):3246-52

Hydrophilic albumin microspheres are proposed as a new delivery system 
for amphotericin B (AMB; AMB microspheres). The acute toxicity of AMB 
microspheres was lower than that of the AMB-deoxycholate (AMB-Doc) 
reference formulation in hamsters. Lethal doses in healthy and infected 
animals were improved at least eight times. Intravenous bolus 
administration of doses of AMB microspheres up to 40 mg/kg of body 
weight did not produce acute symptoms of toxicity. The efficacy of this 
new formulation was tested against Leishmania infantum-infected hamsters
 at doses of 2, 10, 20, and 40 mg/kg. With the 2-mg/kg dose, the 
activity of AMB, as assessed through the parasite load reductions in the
 liver and spleen and the evolution of antibody levels, was also 
improved (P < 0.05) by use of the AMB microsphere system. At the 
higher doses of 10, 20, and 40 mg/kg, reductions in parasite levels of 
more than 99% were achieved in the liver and spleen after the 
administration of AMB microspheres. A pharmacokinetic study was 
performed to study the serum, liver, and spleen AMB concentrations after
 administration of AMB microspheres and the reference formulation. 
Interestingly, a significant accumulation of AMB in the spleen and liver
 was observed after AMB microsphere administration. Our results suggest 
that this new formulation is a promising alternative to the conventional
 AMB-Doc formulation for the treatment of visceral leishmaniasis.




PMID: 15334256
 

TITLE: Improving methods for epidemiological control of canine visceral
leishmaniasis based on a mathematical model. Impact on the incidence of the
canine and human disease.

AUTHORS: Clarisa B Palatnik-De-Sousa, Leopoldina M Batista-De-Melo, Gulnara P
Borja-Cabrera, Marcos Palatnik, Carlile C Lavor

AFFILIATION: Instituto de Microbiologia Prof. Paulo de Góes, Universidade
Federal do Rio de Janeiro, Rio de Janeiro, RJ, 21941-590.

REFERENCE: An Acad Bras Cienc 2004 Sep 76(3):583-93

The mathematical model described by Dye (1996) condemned the 
epidemiological canine visceral leishma-niasis control campaign, 
considering it non-efficient. Using this model, we mathematically 
demonstrate that the control is not efficient, only at low values (rate 
at which latent and infectious dogs are lost by the destruction program
) which match the canine seropositivity observed in the field by the 
immunofluorescency (IF) blood eluates analysis. With higher k values, 
corresponding to IF (k = 0.07) or ELISA ( k = 0.25) results in sera 
samples, the number of infectious dogs declines to a Ro =1 or Ro =0, 
respectively, interrupting the transmission and the advancement of 
epidemics. We also experimentally demonstrate that the dog removal, 
following the results of IF of sera, instead of eluates lead to a 57% (p
 < 0.005) decrease in canine cases and 87.5% (p < 0.005) in 
human cases. Our mathematical and experimental results indicate that the
 control campaign become more efficient by enhancing the sensitivity of 
the diagnostic assay.




PMID: 15334250
 

TITLE: The T-cell anergy induced by Leishmania amazonensis antigens is related
with defective antigen presentation and apoptosis.

AUTHORS: Roberta O Pinheiro, Eduardo F Pinto, Alessandra B Benedito, Ulisses G
Lopes, Bartira Rossi-Bergmann

AFFILIATION: Instituto de Biofísica Carlos Chagas Filho, Universidade Federal
do Rio de Janeiro, Rio de Janeiro, RJ, 21949-900, Brasil.

REFERENCE: An Acad Bras Cienc 2004 Sep 76(3):519-27

Leishmania amazonensis is the main agent of diffuse cutaneous 
leishmaniasis, a disease associated with anergic immune responses. In 
this study we show that the crude antigen of Leishmania amazonensis (
LaAg) but not L. braziliensis promastigotes (LbAg) contains substances 
that suppress mitogenic and spontaneous proliferative responses of T 
cells. The suppressive substances in LaAg are thermoresistant (100 
masculine C/1h) and partially dependent on protease activity. T cell 
anergy was not due to a decreased production of growth factors as it was
 not reverted by addition of exogenous IL-2, IL-4, IFN-gamma or IL-12. 
LaAg did not inhibit anti-CD3-induced T cell activation, suggesting that
 anergy was due to a defect in antigen presentation. It was also not due
 to cell necrosis, but was accompanied by expressive DNA fragmentation 
in lymph node cells, indicative of apoptosis. Although pre-incubation of
 macrophages with LaAg prevented their capacity to present antigens, 
this effect was not due to apoptosis of the former. These results 
suggest that the T cell anergy found in diffuse leishmaniasis may be the
 result of parasite antigen-driven apoptosis of those cells following 
defective antigen presentation.




PMID: 15322004
 

TITLE: Senescent BALB/c mice are able to develop resistance to Leishmania major
infection.

AUTHORS: Jan Ehrchen, Anca Sindrilaru, Stephan Grabbe, Frank Schönlau,
Christian Schlesiger, Clemens Sorg, Karin Scharffetter-Kochanek, Cord
Sunderkötter

AFFILIATION: Institute of Experimental Dermatology, Department of Dermatology,
University of Münster, Germany.

REFERENCE: Infect Immun 2004 Sep 72(9):5106-14

Aging has been associated with a decline in immunocompetence and 
resistance to infections, partially due to dysregulated NO production by
 macrophages and deficits in mounting Th2 cell responses. We wondered if
 these alterations would reverse the immune response in experimental 
leishmaniasis. Bone-marrow-derived macrophages from 2- and 18-month-old
 (senescent) C57BL/6 or BALB/c mice showed no marked difference in 
leishmanicidal functions. In vivo infections of resistant C57BL/6 mice 
with Leishmania major revealed no difference between senescent and young
 mice. However, among susceptible BALB/c mice, senescent animals showed 
less foot-pad swelling than young mice, and 40 to 60% of them even 
showed healing of ulcers, reduced parasite dissemination, and a Th1 cell
 response. These changes were associated with a spontaneous release of 
interleukin-12 (IL-12) by macrophages from aged but not from young mice
. Since exogenous microbial stimulation can influence immune responses 
during aging, we also infected senescent mice who were raised under 
specific-pathogen-free (SPF) conditions. They showed neither resistance 
nor a Th1 response, but their macrophages still spontaneously released 
IL-12. A microbiological analysis showed that conventionally kept mice, 
but not SPF mice, had experienced infection with murine hepatitis virus
 (MHV), an infection associated with a Th1-like response. We conclude 
that for the reversal of the immune response, senescence is the premier 
requirement but needs to be completed by another mandatory event such as
 microbial stimulation. One of the age-related, but not environment-
related, factors is the spontaneous release of IL-12 by macrophages, 
while confrontation with MHV presents an environment-related difference
, with both having the potential to support a Th1 response.




PMID: 15324473
 

TITLE: Impact of a co-factor on the dynamics of Leishmania donovani infection:
does HIV infection encourage the recurrence of visceral leishmaniasis following
post-kala-azar dermal leishmaniasis?

AUTHORS: A Nandy, M Addy, A K Maji, S K Guha

AFFILIATION: Calcutta School of Tropical Medicine, Chittaranjan Avenue, Calcutta
- 700073, India.

REFERENCE: Ann Trop Med Parasitol 2004 Sep 98(6):651-4




PMID: 15325799
 

TITLE: Dynamics of CD62L/CD45RB CD4(+) and CD8(+) lymphocyte subsets in hepatic
and splenic tissues during murine visceral leishmaniasis.

AUTHORS: Sandra Gomes-Pereira, Olívia Roos Rodrigues, Gabriela Maria
Santos-Gomes

AFFILIATION: Unidade de Leishmanioses, Centro de Malária e Outras Doenças
Tropicais, Instituto de Higiene e Medicina Tropical (IHMT), Universidade Nova
de Lisboa, Rua da Junqueira 96, 1349-008 Lisboa, Portugal.

REFERENCE: Immunol Lett 2004 Aug 95(1):63-70

This study aimed to characterise, for the first time, the dynamics of 
CD4(+) and CD8(+) lymphocyte CD62L/CD45RB subsets, during visceral 
leishmaniasis. Memory/activated status of hepatic and splenic T cells 
was compared in mice strains with "cure" and "non-cure" phenotypes to 
Leishmania infantum infection. In both mice strains, a correlation 
between the dynamics of the memory CD4(+) and CD8(+) T cells (CD62L(low
)/CD45RB(low)) subsets in the liver and the pre-activated phenotype of 
lymphocytes (CD62L(low)/CD45RB(high)) from the spleen was detected 
suggesting that this organ is the source of Leishmania-specific T 
lymphocytes that migrate to the liver, where parasite replication is 
highly active. In the liver, these pre-activated cells become effector T
 lymphocytes, however, a strong regulation of CD8(+) T cell effector 
function was observed, probably preventing hepatic tissue damage. 
Comparing mice strains with "cure" and "non-cure" phenotype, an 
imbalance between "protective" CD45RB(high) and "pathogenic" CD45RB(low
) CD4(+) subsets in B10.D2/n animals might be involved in the evolution 
of a non-healing infection.




PMID: 15294090
 

TITLE: IL-5-Induced Eosinophils Suppress the Growth of Leishmania amazonensis In
Vivo and Kill Promastigotes In Vitro in Response to Either IL-4 or IFN-gamma.

AUTHORS: Yoshiya Watanabe, Emi Hamaguchi-Tsuru, Norihito Morimoto, Youhei
Nishio, Ken-Ichi Yagyu, Yuko Konishi, Mari Tominaga, Jun-Ichi Miyazaki, Masato
Furuya, Akira Tominaga

AFFILIATION: Department of Molecular and Cellular Biology, Kochi Medical School,
Kochi University, Nankoku City, 783-8505, Japan.

REFERENCE: DNA Cell Biol 2004 Jul 23(7):412-8

In IL-5 transgenic mice (C3H/HeN-TgN(IL-5)-Imeg), in which 50% of 
peripheral blood leukocytes are eosinophils, the development of 
infection by Leishmania amazonensis was clearly suppressed. To determine
 mechanistically how this protozoan parasite is killed, we performed in 
vitro killing experiments. Either IL-4 or IFN-gamma effectively 
stimulated eosinophils to kill Leishmania amazonensis promastigotes, and
 most of the killing was inhibited by catalase but not by the NO 
inhibitor L-N5-(1-iminoethyl)-ornithine, suggesting that hydrogen 
peroxide is responsible for the killing of L. amazonensis by eosinophils
. There was no significant degranulation of eosinophils in the culture, 
because eosinophil peroxidase was not detected in culture supernatants 
when L. amazonensis promastigotes were killed by activated eosinophils. 
Such resistance was also observed in BALB/c mice, which are highly 
susceptible to L. amazonensis. Expression plasmids for IL-4, IL-5, and 
IFN-gamma were transferred into muscle by electroporation in vivo 
starting 1 week before infection. Expression plasmid for IL-5 was most 
effective in slowing the development of infection among three expression
 plasmids. Expression plasmid for IL-4 was slightly effective and that 
for IFN-gamma had no effect on the progress of disease. These results 
suggest that IL-5 gene transfer into muscle by electroporation is useful
 as a supplementary protection method against L. amazonensis infection.








PMID: 15184505
 

TITLE: Low dose Leishmania major promotes a transient T helper cell type 2
response that is down-regulated by interferon gamma-producing CD8+ T cells.

AUTHORS: Jude E Uzonna, Karen L Joyce, Phillip Scott

AFFILIATION: Department of Pathobiology, School of Veterinary Medicine,
University of Pennsylvania, 3800 Spruce Street, Philadelphia 19104, USA.

REFERENCE: J Exp Med 2004 Jun 199(11):1559-66

An unresolved issue in the field of T helper (Th) cell development 
relates to the findings that low doses of antigen promote Th2 cell 
development in vitro, whereas several classic in vivo studies suggest 
the opposite. Here we resolve this paradox by studying the early immune 
response in mice after infection with different doses of Leishmania 
major. We found that low parasite doses induced a Th2 response in C57BL/
6 (B6) mice, whereas high doses induced a Th1 response. However, the Th2
 response in low dose-infected mice was transient and the animals healed
. The appearance of a Th1 response after low dose infection was 
dependent upon the concomitant activation of interferon gamma-producing 
CD8+ T cells. In the absence of CD8+ T cells, the Th2 response was 
maintained. However, either neutralization of interleukin (IL)-4 or 
administration of IL-12 promoted a Th1 response after low dose infection
 of CD8-deficient mice, indicating that the required role for CD8+ T 
cells was limited to modulation of CD4+ T cell responses. Thus, the 
discrepant results seen between in vivo and in vitro studies on the 
effects of antigen dose on Th cell differentiation may depend upon 
whether CD8+ T cells participate in the immune response.




PMID: 15189464
 

TITLE: Evaluation of a urinary antigen-based latex agglutination test in the
diagnosis of kala-azar in eastern Nepal.

AUTHORS: S Rijal, M Boelaert, S Regmi, B M S Karki, D Jacquet, R Singh, M L
Chance, F Chappuis, M Hommel, P Desjeux, P Van der Stuyft, D Le Ray, S Koirala

AFFILIATION: B.P. Koirala Institute of Health Sciences, Dharan, Nepal.
sumanrijal2 at yahoo.com

REFERENCE: Trop Med Int Health 2004 Jun 9(6):724-9

BACKGROUND: We evaluated the diagnostic accuracy as well as the 
reproducibility of the urine latex agglutination test 'KAtex' in the 
diagnosis of kala-azar in patients recruited at a tertiary care centre 
in Dharan, Nepal, between November 2000 and January 2002. METHODS: All 
patients presenting with fever of 2 weeks or more and splenomegaly were 
consecutively enrolled. Bone marrow and--if negative--spleen aspirates 
were examined for Leishmania donovani. Serum and urine samples were 
taken in duplicate for the Direct Agglutination Test (DAT) and KAtex. 
The reference laboratory determined sensitivity and specificity of KAtex
. Reproducibility between both laboratories was assessed. RESULTS: KAtex
 was performed on urine from 155 parasitologically confirmed kala-azar 
and 77 non-kala-azar cases (parasitology and DAT-negative). KAtex showed
 a sensitivity of 47.7% (74/155, 95% CI: 39.7-55.9) and a specificity of
 98.7% (76/77, 95% CI: 93.0-100.0). Reproducibility of KAtex showed a 
kappa of 0.684 (P < 0.001, n = 232). CONCLUSION: KAtex evaluation 
showed high specificity, low sensitivity and moderate reproducibility. A
 urine test for kala-azar could become a real breakthrough in kala-azar 
management if its reproducibility and sensitivity could be further 
improved.




PMID: 15266752
 

TITLE: Nectar and honeydew feeding of Phlebotomus papatasi in a focus of
Leishmania major in Neot Hakikar oasis.

AUTHORS: Günter Müller, Yosef Schlein

AFFILIATION: Department of Parasitology, The Kuvin Center for Study of
Infectious and Tropical Diseases, The Hebrew University- Hadassah Medical
School, Box 12272, Jerusalem 91120, Israel.

REFERENCE: J Vector Ecol 2004 Jun 29(1):154-8

Feeding of Phlebotomus papatasi Scopoli on nectar and honeydew was 
investigated in Neot Hakikar, an oasis in the southern Jordan Valley. 
Sand flies were caught with miniature light traps in cleared areas with 
large Tamarix nilotica Bunge bushes, in colonies of the sandrat 
Psammomys obesus Cretzschmar. Fly series were trapped and compared 
according to the condition of T. nilotica bushes: with flowers, soiled 
with honeydew excreted by cicadas, or without flowers. Near flowering 
bushes the catch was five times greater (7.9: 1.6 flies/trap) and the 
proportion of sugar-positive flies was also much greater (49.9:17.3%) 
than near bushes without flowers. The catch was three times greater (6.6
:2.2 flies/trap) near cicada- infested than near uninfested bushes. 
Color markers within the gut, obtained from infested or uninfested 
bushes that had been sprayed with food dye, indicated feeding of 33.2% 
and 4.5% of these series, respectively. Sand flies were strongly 
attracted to flowers of T. nilotica. In similar trap series, those 
baited with flowering branches caught 231 flies, whereas with baits of 
honeydew- soiled branches, control regular branches or wet filter paper
, the catch ranged between 11 to 15 flies. This study is the first 
evidence of nectar feeding by sand flies in the field and it indicates 
that nectar may be an important and an attractive source of sugar.




PMID: 15243162
 

TITLE: Immune response to Leishmania infection.

AUTHORS: Amit Awasthi, Ram Kumar Mathur, Bhaskar Saha

AFFILIATION: National Center for Cell Science, Ganeshkhind, Pune, India.
amitawasthi at nccs.res.in

REFERENCE: Indian J Med Res 2004 Jun 119(6):238-58

Antileishmanial immune response is shown to be host genotype dependent 
so that some inbred strains of mouse are susceptible while others are 
resistant. The resistance is conferred by T-helper type-1 (Th1) cells 
while the susceptibility is conferred by Th2 cells. Th1 cells secrete IL
-2 and IFN-gamma but Th2 cells secrete IL-4, IL-5 and IL-10. It has been
 shown that IFN-gamma activates macrophages to express iNOS2, the enzyme
 catalyzing the formation of nitric oxide. Nitric oxide kills the 
intracellular amastigotes. In contrast, Th2 immune response limits the 
action of Th1 functions via IL-10 and IL-4, which deactivate macrophages
 helping intracellular parasite growth and disease progression. Being a 
parasite, Leishmania ensures its own survival by modulating host immune 
system either by inducing immunosuppression or by promoting pro-
parasitic host functions. A detailed knowledge of this host-parasite 
interaction would help in designing prophylactic and therapeutic 
strategies against this infection.




PMID: 15135863
 

TITLE: Rapid detection of Leishmania infantum infection in dogs: comparative
study using an immunochromatographic dipstick rk39 test and direct
agglutination.

AUTHORS: M Mohebali, M Taran, Z Zarei

AFFILIATION: School of Public Health, Institute of Public Health Research,
Tehran University of Medical Sciences, P.O. Box 6446, Tehran 14155, Iran.
mmohebali at hotmail.com

REFERENCE: Vet Parasitol 2004 May 121(3-4):239-45

A rapid, sensitive and specific tool for detection of Leishmania 
infantum infection in dogs, would be highly desirable, because it would 
allow control interventions in endemic areas of Zoonotic visceral 
leishmaniosis (ZVL). In this study, we compared an immunochromatographic
 dipstick test with direct agglutination test (DAT) for detecting L. 
infantum infections in dogs from areas of ZVL endemic in Iran. The 
validity of the dipstick rk39 (Cypress Diagnostic Company, Belgium) for 
canine visceral leishmaniosis (CVL) was compared with a standard direct 
agglutination test on 116 clinically suspected dogs and 152 healthy 
controls from endemic areas of Ardabil and East Azerbaijan provinces, 
north-western of Iran for 1 year. A sensitivity of 70.9% and specificity
 of 84.9% were found at a 1:320 cut off titer when DAT confirmed cases 
were compared with healthy control. As the dipstick rk39 test is rapid, 
noninvasive and does not require much expertise or elaborate equipment, 
it can be used for screening and diagnosis of canine visceral 
leishmaniosis in remote endemic areas.




PMID: 15330071
 

TITLE: [Lutzomyia whitmani periurbanization in a focus of cutaneous
leishmaniasis in the State of Maranhão, Brazil]

AUTHORS: Francisco Santos Leonardo, José Manuel Macário Rebêlo

AFFILIATION: Distrito Sanitário de Codó da Fundação Nacional de Saúde, São
Luís, MA, Brasil.

REFERENCE: Rev Soc Bras Med Trop 2004 May-Jun 37(3):282-4

An entomological survey was performed in the periurban area of the 
municipality of Dom Pedro in the state of Maranhão in 2000, in order to
 estimate the abundance of Lutzomyia longipalpis, due to the occurrence 
of one suspect death caused by kala azar. However, it was surprisingly 
verified that 82.4% (2,440 specimens) from the total of 2,961 sand flies
 captured in the peridomicile were Lutzomyia whitmani. This association 
has indicated a new pattern for cutaneous leishmaniasis transmission (
urban), as has been observed with regard to kala azar in the northeast 
of Brazil.




PMID: 15329037
 

TITLE: Amphotericin B lipid complex: in visceral leishmaniasis.

AUTHORS: David R Goldsmith, Caroline M Perry

AFFILIATION: Adis International Limited, Auckland, New Zealand.

REFERENCE: Drugs 2004  64(17):1905-11

black triangle Amphotericin B lipid complex is a lipid formulation of 
amphotericin B, an antifungal drug with activity against Leishmania spp
. Amphotericin B lipid complex appears to enhance uptake of amphotericin
 B by infected macrophages in patients with visceral leishmaniasis (VL
). black triangle In randomised, open-label, dose-ranging studies, short
-course treatment with once-daily amphotericin B lipid complex (5-15 mg/
kg total cumulative dose over 5 days), administered by intravenous 
infusion, produced high rates of apparent (day 19) [93-100%] and 
definitive (6 months) [79-100%] cures in Indian patients with antimonial
-resistant VL. black triangle Amphotericin B lipid complex appeared to 
be as effective as liposomal amphotericin B or the conventional 
deoxycholate formulation in a randomised, open-label study conducted in 
India in a mixed population of patients with previously untreated or 
antimonial-resistant VL. black triangle In patients with HIV infection 
and VL, amphotericin B lipid complex 3 mg/kg/day for 5 or 10 days 
appeared to be as effective as meglumine antimonate 20 mg/kg/day for 28 
days in a small randomised pilot study in southern Europe. black 
triangle Amphotericin B lipid complex was generally well tolerated in 
patients with VL. Infusion-related reactions were the most common 
adverse events associated with amphotericin B lipid complex.




PMID: 15323268
 

TITLE: Fine-needle aspiration cytology in the diagnosis of cutaneous
leishmaniasis.

AUTHORS: Masoom Kassi, Iqbal Tareen, Anwar Qazi, Pashtoon Murtaza Kasi

AFFILIATION: Bolan Medical College Complex Hospital, Quetta, Pakistan.
masoomkassi at yahoo.com

REFERENCE: Ann Saudi Med 2004 Mar-Apr 24(2):93-7

BACKGROUND: In areas of endemicity without sufficient laboratory 
infrastructure, cutaneous leishmaniasis (CL) is often diagnosed on the 
basis of clinical characteristics, but parasitologic confirmation is 
essential to exclude erroneous diagnoses. We compared fine-needle 
aspiration cytology (FNAC) with the conventional method of excisional 
biopsy to assess the efficacy, utility and accuracy of FNAC for the 
diagnosis of CL. MATERIALS AND METHODS: In a consecutive series of 100 
patients referred for a suspected CL lesion during June 2001 to May 2002
, FNAC and 'excisional biopsy followed by histopathology' were done 
using hematoxylin and eosin (H&E) stain for both procedures. RESULTS
: The study group included 40 males and 60 females, ranging in age from 
1 to 70 with a mean age of 28.4 years. In more than 60% of cases, the 
lesions were on the face. By histopathological examination, 86 of 100 
patients were positive for CL; while FNAC showed 77 cases as positive 
for CL. Taking histopathology as a standard diagnostic procedure, FNAC 
showed a remarkably high sensitivity (89%) and specificity (100%). The 
positive and negative predictive values were 100% and 60%, respectively
. CONCLUSION: FNAC is easier, less painful and more cost effective than 
the conventional 'scraping method/biopsy followed by histopathology'. 
The high sensitivity and specificity eliminate the need for other time 
consuming and invasive procedures. Limitations include poor sampling and
 poor yield.








PMID: 15323269
 

TITLE: A new epidemic focus of zoonotic cutaneous leishmaniasis in central
Iran.

AUTHORS: Mohammad Reza Yaghoobi-Ershadi, Reza Jafari, Ahmad Ali Hanafi-Bojd

AFFILIATION: School of Public Health and Institute of Public Health Research,
Tehran University of Medical Sciences, Tehran, Iran. Rezatr12 at yahoo.com

REFERENCE: Ann Saudi Med 2004 Mar-Apr 24(2):98-101

BACKGROUND: Reports from the health center of Yazd province of 
increasing cutaneous leishmaniasis (CL) cases led us to carry out an 
epidemiological study using standard techniques in Ardakan County, 
central Iran, during 2001. PATIENTS AND METHODS: Data was collected on 
the prevalence of scars and ulcers over a period of 14 months among 621 
households in three villages around Ardakan County. Smears were prepared
 by scraping the edges of the ulcers. We collected the same data on all 
school children aged 7 to 11 years old in the area. To determine the 
reservoir host of the disease, rodents and dogs were caught and examined
. Sandflies were collected biweekly from indoor and outdoor locations in
 the study area, and then identified. Parasites isolated from human and 
rodents were characterized by RAPD-PCR technique. RESULTS: The 
prevalence of scars and ulcers were 30.4% and 24.6%, respectively, in 
3024 individuals in the three villages. Individuals 10 to 14 years of 
age were the most highly infected age group, with a rate of 28.4%. Males
 and females were equally infected. Examination of 892 students in 
primary schools showed a rate of 22.9% for scars and 23.7% for ulcers. 
Meriones libycus (42.2%) and Rhombomys opimus (57.8%) were present 
around the villages. Both were infected with Leishmania. Three of 19 M. 
libycus (15.7%) and 3 out of 26 R. opimus (11.5%) had positive results. 
The active season of sandflies was late April to late November. 
Phlebotomus papatasi and Sergentomyia sintoni were the dominant species 
indoors and outdoors. Natural leptomonad infection was found in P. 
caucasicus and S. sintoni from gerbil and Jird burrows. CONCLUSION: 
Based on this survey, there is an epidemic of zoonotic CL in the area, 
with Leishmania major as the agent, M. libycus and R. opimus as the 
reservoir hosts, and most probably Phlebotomus papatasi as the vector 
because about 77% of indoor sandflies were of this species.




PMID: 15334262
 

TITLE: [Clinical and epidemiological aspects of visceral leishmaniasis in
children up to 15 years of age in Alagoas, Brasil]

AUTHORS: Célia Maria Silva Pedrosa, Eliana Maria Mauricio da Rocha

AFFILIATION: Departamento de Clínica Médica, Centro de Ciências da Saúde,
Universidade Federal de Alagoas, Maceió, AL.

REFERENCE: Rev Soc Bras Med Trop 2004 Jul-Aug 37(4):300-4

In order to investigate epidemiological and clinical characteristics of 
visceral leishmaniasis in children up to 15 years old, a prospective 
study was carried out in Alagoas, Brasil from 1981 to 1995. Of the 530 
diagnosed cases, predominantly from the rural area of Alagoas State, 58
% were male and 42% female, being 55.3% children under 5 years old. The 
most frequently observed clinical manifestations were: 
hepatosplenomegaly, fever and parlor. The average size of the liver and 
the spleen of patients with shorter time of disease (<30 days) were 
smaller than those presenting sickness for a extended time (> 360 days
). No matter the length of disease there was reduction of the liver and 
the spleen after treatment. However, the reduction of the spleen was 
higher in those patients with less time of sickness. With relation to 
liver that diference was not observed.




PMID: 15334263
 

TITLE: [Visceral leishmaniasis among Indians of the State of Roraima, Brazil:
clinical and epidemiologic aspects of the cases observed from 1989 to 1993]

AUTHORS: Jorge Augusto O Guerra, Marcus Luíz B Barros, Nelson Ferreira Fé,
Marcus Vinitius F Guerra, Eloy Castellon, Marcilene Gomes Paes, Italo A
Sherlock

REFERENCE: Rev Soc Bras Med Trop 2004 Jul-Aug 37(4):305-11

A description of the epidemiological profile of visceral leishmaniasis 
among Indians in the State of Roraima, Brazil, was based on the clinical
 characteristics of human and dog disease, ecological aspects of the 
area where the cases occurred and entomologic investigations performed 
from 1989 to 1993. The 82 human cases were reported in six out of eight 
Counties that existed then in the state; there was a 69.5% predominance 
of male cases among those registered and a greater (52.4%) occurrence of
 the disease in children from zero to ten years old. The rate of natural
 infection was 10.3% out of 3,773 dogs examined in 74 different 
locations. Lutzomyia longipalpis was found in 31 areas with greater 
prevalence of the disease. The human and animal cases as well as the 
vectors were concentrated in areas where mountains and arable soil 
predominate, typical locations for the occurrence of American visceral 
leishmaniasis.




PMID: 15332732
 

TITLE: Seroepidemiological study of visceral leishmaniasis among humans and
animal reservoirs in Bushehr province, Islamic Republic of Iran.

AUTHORS: M Mohebali, Y Hamzavi, G H Edrissian, A Forouzani

AFFILIATION: School of Public Health and Institute of Public Health Research,
Teheran University of Medical Sciences, Teheran, Islamic Republic of Iran.

REFERENCE: East Mediterr Health J 2001 Nov 7(6):912-7

Using direct agglutination tests, a survey of visceral leishmaniasis was
 carried out among children and adults from 13 villages and from nomadic
 tribes in Bushehr province during 1998-99. Of the 1496 plasma samples, 
the overall seropositive rate (titres > or = 1:3200) was 3.4%. Almost 
all cases (94.1%) were in children under 10 years old. Eighteen patients
 were diagnosed with kala azar; fever and splenomegaly were the 
predominant signs and symptoms. Parasitology and serology examinations 
of local animals identified dogs and jackals infected with Leishmania 
infantum. Suggestions for control of visceral leishmaniasis in this area
 are to eliminate stray dogs, identify cases among humans and suspected 
leashed dogs, and treat infected individuals.




PMID: 15332749
 

TITLE: Post kala azar dermal leishmaniasis in Sudan.

AUTHORS: Y M Kordofani, Y T Nour, A M El-Hassan, M H Shalayel

AFFILIATION: Department of Dermatology, College of Medicine, University of Juba,
Juba, Sudan.

REFERENCE: East Mediterr Health J 2001 Nov 7(6):1061-4

Post kala azar dermal leishmaniasis (PKDL) is a condition that develops 
after treatment of kala azar. We report on 42 patients with suspected 
PKDL, 40% of whom were children. Diagnosis was made though investigation
 of family history of kala azar, clinical examination and the use of 
laboratory investigations, such as skin smear, skin biopsy, bone marrow 
aspiration and the leishmanin skin test. Regarding the lesions, 24 
patients (57%) had papular lesions, 10 (24%) had hypopigmented 
maculopapular lesions and 8 (19%) had nodular lesions. The lesions of 
PKDL may be confused with other dermatological diseases and therefore it
 is important that clinicians and pathologists collaborate in diagnosing
 such cases.




********************************************************************************************************************

 The following references are revised files and are brought to you in accordance
to license agreement with the NLM.

********************************************************************************************************************


PMID: 11334675
 

TITLE: Association analysis of HLA-class II and class III gene polymorphisms in
the susceptibility to mediterranean visceral leishmaniasis.

AUTHORS: A Meddeb-Garnaoui, S Gritli, S Garbouj, M Ben Fadhel, R El Kares, L
Mansour, B Kaabi, L Chouchane, A Ben Salah, K Dellagi

AFFILIATION: Laboratory of Immunology, Institut Pasteur de Tunis,
Tunis-Belvédère, Tunisia. amel.garnaoui at pasteur.rns.tn

REFERENCE: Hum Immunol 2001 May 62(5):509-17

HLA-DRB1, -DQB1, TNFalpha, TNFbeta, HSP70-2 and HSP70-hom genetic 
polymorphisms were analyzed in 156 unrelated patients who developed 
mediterranean visceral leishmaniasis (MVL) due to Leishmania infantum, 
and 154 unrelated healthy controls, who have got asymptomatic infection 
with this parasite and were selected on the basis of a positive 
leishmanin skin test (LST). A significantly reduced frequency of HLA-DR2
 was observed among MVL patients (16.1%), compared with controls (26.3
%) (relative risk = 0.54; p = 0.04). HLA-DR2/DR13 as well as HLA-DQB1*
0201/- genotype frequencies were significantly lower in patients vs 
controls (relapse rate = 0.17 and 0.46, respectively; p < 0.05). 
However, using Bonferroni correction, none of these associations 
remained significant. No association was found, between either the -308 
base pair TNFalpha gene polymorphism or the NcoI polymorphism in the 
first intron of the TNFbeta gene and susceptibility to MVL. Analysis of 
PstI and NcoI polymorphisms in the coding region of HSP70-2 and HSP70-
hom genes, respectively, revealed a significantly higher frequency of 
homozygotes for the HSP70-2/PstI negative allele, among patients (21.8
%) vs controls (12.6%) (relapse rate = 1.94; p = 0.04). Again, this 
result was not significant after using Bonferroni correction. These 
results do not support association between susceptibility to MVL and the
 MHC class II and class III loci analyzed in this study.




PMID: 11161745
 

TITLE: Speciation and population structure in the morphospecies Lutzomyia
longipalpis (Lutz & Neiva) as derived from the mitochondrial ND4 gene.

AUTHORS: S I Soto, T Lehmann, E D Rowton, I D Vélez B, C H Porter

AFFILIATION: PECET, Universidad de Antioquia, Apartado 1226, Medellín,
Colombia.

REFERENCE: Mol Phylogenet Evol 2001 Jan 18(1):84-93

Recent studies have suggested that the phlebotomine sand fly Lutzomyia 
longipalpis (Diptera: Psychodidae), the principal vector of visceral 
leishmaniasis in the Neotropics, may consist of several allopatric 
sibling species. Phylogenetic and population genetic analyses of 
nucleotide variation in a 618-bp fragment of the mitochondrial ND4 gene 
were carried out on specimens of Lu. longipalpis from several locations 
in Central and South America. The analyses were concordant with previous
 findings, indicating that certain allopatric populations of Lu. 
longipalpis have become sufficiently differentiated as to represent 
sibling species. Phylogenetic analyses revealed deep genetic divisions 
between four clades represented by specimens from northern South America
, Brazil, Central America, and an isolated Colombian population. Strong 
differentiation also was observed between certain populations within the
 first two clades. Partitioning of genetic diversity within and between 
Central American populations did not show the presence of more than one 
species in the region. However, distance, even within the 70-km range of
 the Honduran collection sites, was found to have a remarkably strong 
effect on gene flow. The highly subdivided population structure may be 
due to the patchiness of their distribution. F(ST) values comparing a 
Guatemalan population with several Honduran populations revealed a level
 of differentiation associated with a negligible rate of gene flow.




REQUEST: [ leishmania ]

(21 articles match this request. 11 articles matching other requests removed)



PMID: 15149284
 

TITLE: Transketolase from Leishmania mexicana has a dual subcellular
localization.

AUTHORS: Nicola J Veitch, Dante A Maugeri, Juan Jose Cazzulo, Ylva Lindqvist,
Michael P Barrett

AFFILIATION: Division of Infection and Immunity, Institute of Biomedical and
Life Sciences, Joseph Black Building, University of Glasgow, Glasgow G12 8QQ,
Scotland, UK.

REFERENCE: Biochem J 2004 Sep 382(Pt 2):759-67

Transketolase has been characterized in Leishmania mexicana. A gene 
encoding this enzyme was identified and cloned. The gene was expressed 
in Escherichia coli and the protein was purified and characterized. An 
apparent K(m) of 2.75 mM for ribose 5-phosphate was determined. X-ray 
crystallography was used to determine the three-dimensional structure of
 the enzyme to a resolution of 2.2 A (1 A identical with 0.1 nm). The C-
terminus of the protein contains a type-1 peroxisome-targeting signal, 
suggestive of a possible glycosomal subcellular localization. 
Subcellular localization experiments performed with promastigote forms 
of the parasite revealed that the protein was predominantly cytosolic, 
although a significant component of the total activity was associated 
with the glycosomes. Transketolase is thus the first enzyme of the 
nonoxidative branch of the pentose phosphate pathway whose presence has 
been demonstrated in a peroxisome-like organelle.








PMID: 15325312
 

TITLE: Isolation of Leishmania glycosomes by a rapid method.

AUTHORS: Bikramjit Raychaudhury, Shreedhara Gupta, Shouvik Banerjee, Banasri
Das, Salil C Datta

AFFILIATION: Infectious Diseases Group, Department of Biological Chemistry,
Indian Institute of Chemical Biology, Kolkata 700 032, India.

REFERENCE: Anal Biochem 2004 Sep 332(2):404-8




PMID: 15325040
 

TITLE: Sero-epidemiological survey of Neospora caninum infection in dogs in
north-eastern Italy.

AUTHORS: Gioia Capelli, Stefano Nardelli, Antonio Frangipane di Regalbono,
Antonio Scala, Mario Pietrobelli

AFFILIATION: Dipartimento di Scienze Sperimentali Veterinarie, University of
Padua, Italy.

REFERENCE: Vet Parasitol 2004 Sep 123(3-4):143-8

Risk factors associated with Neospora caninum seroprevalence in north-
eastern Italy in healthy dogs were assessed. Antibodies to N. caninum 
were found in 10.9% of 707 kennel and owned dogs by a commercial 
competitive ELISA (VMRD((R)) Inc.). All dogs were negative for 
Leishmania infantum by indirect fluorescent antibody test indicating no 
cross reactivity or association between the two protozoa in this area. 
Seroprevalence association with breed and age of dogs and other factors 
are discussed.




PMID: 15322192
 

TITLE: Inhibition of lipopolysaccharide-induced macrophage IL-12 production by
Leishmania mexicana amastigotes: the role of cysteine peptidases and the
NF-kappaB signaling pathway.

AUTHORS: Pamela Cameron, Adrienne McGachy, Mary Anderson, Andrew Paul, Graham H
Coombs, Jeremy C Mottram, James Alexander, Robin Plevin

AFFILIATION: Department of Immunology, Strathclyde Institute for Biomedical
Sciences, University of Strathclyde, Glasgow, United Kingdom.

REFERENCE: J Immunol 2004 Sep 173(5):3297-304

Infection with lesion-derived Leishmania mexicana amastigotes inhibited 
LPS-induced IL-12 production by mouse bone marrow-derived macrophages. 
This effect was associated with expression of cysteine peptidase B (CPB
) because amastigotes of CPB deletion mutants had limited ability to 
inhibit IL-12 production, whereas preincubation of cells with a CPB 
inhibitor, cathepsin inhibitor IV, was able to suppress the effect of 
wild-type amastigotes. Infection with wild-type amastigotes resulted in 
a time-dependent proteolytic degradation of IkappaBalpha and IkappaBbeta
 and the related protein NF-kappaB. This effect did not occur with 
amastigotes of CPB deletion mutants or wild-type promastigotes, which do
 not express detectable CPB. NF-kappaB DNA binding was also inhibited by
 amastigote infection, although nuclear translocation of cleaved 
fragments of p65 NF-kappaB was still observed. Cysteine peptidase 
inhibitors prevented IkappaBalpha, IkappaBbeta, and NF-kappaB 
degradation induced by amastigotes, and recombinant CPB2.8, an 
amastigote-specific isoenzyme of CPB, was shown to degrade GST-
IkappaBalpha in vitro. LPS-mediated IkappaBalpha and IkappaBbeta 
degradation was not affected by these inhibitors, confirming that the 
site of degradation of IkappaBalpha, IkappaBbeta, and NF-kappaB by the 
amastigotes was not receptor-driven, proteosomal-mediated cleavage. 
Infection of bone marrow macrophages with amastigotes resulted in 
cleavage of JNK and ERK, but not p38 MAPK, whereas preincubation with a 
cysteine peptidase inhibitor prevented degradation of these proteins, 
but did not result in enhanced protein kinase activation. Collectively, 
our results suggest that the amastigote-specific cysteine peptidases of 
L. mexicana are central to the ability of the parasite to modulate 
signaling via NF-kappaB and consequently inhibit IL-12 production.




PMID: 15328135
 

TITLE: Combination Therapy Using Sodium Antimony Gluconate in
Stearylamine-Bearing Liposomes against Established and Chronic Leishmania
donovani Infection in BALB/c Mice.

AUTHORS: Swati Pal, Rajesh Ravindran, Nahid Ali

AFFILIATION: Indian Institute of Chemical Biology, 4 Raja S.C. Mullick Rd.,
Calcutta 700032, India. nali at iicb.res.in

REFERENCE: Antimicrob Agents Chemother 2004 Sep 48(9):3591-3

In this work we report the activity seen with combination therapy using 
sodium antimony gluconate in liposomes composed of egg phosphatidyl 
choline and stearylamine for elimination of Leishmania donovani 
parasites from the liver and spleen of BALB/c mice with established and 
chronic infections.




PMID: 15314146
 

TITLE: Modulation of the Leishmania donovani peroxin 5 quaternary structure by
peroxisomal targeting signal 1 ligands.

AUTHORS: Kleber P Madrid, Gregory De Crescenzo, Shengwu Wang, Armando Jardim

AFFILIATION: Institute of Parasitology, McGill University, Montreal, Quebec,
Canada.

REFERENCE: Mol Cell Biol 2004 Sep 24(17):7331-44

The import of proteins containing the peroxisomal targeting signal 1 (
PTS1) into the Leishmania glycosome is dependent on the docking of the 
PTS1-loaded LdPEX5 cytosolic receptor with LdPEX14 on the glycosome 
surface. Here we show that, in the absence of PTS1, LdPEX5 is a tetramer
 that is stabilized by two distinct interaction domains; the first is a 
coiled-coil motif encompassing residues 277 to 310, whereas the second 
domain is localized to residues 1 to 202. By using microcalorimetry, 
surface plasmon resonance, and size exclusion chromatography techniques
, we show that PTS1 peptide binding to LdPEX5 tetramers promotes their 
dissociation into dimeric structures, which are stabilized by a coiled-
coil interaction. Moreover, we demonstrated that the resulting LdPEX5-
PTS1 complex is remarkably stable and exhibits extremely slow 
dissociation kinetics. However, binding of LdPEX14 to LdPEX5 modulates 
the LdPEX5-PTS1 affinity as it decreases the thermodynamic dissociation 
constant for this latter complex by 10-fold. These changes in the 
oligomeric state of LdPEX5 and in its affinity for PTS1 ligand upon 
LdPEX14 binding may explain how, under physiological conditions, LdPEX5 
can function to deliver and unload its cargo to the protein 
translocation machinery on the glycosomal membrane.




PMID: 15322011
 

TITLE: Chemokine gene expression in toll-like receptor-competent and -deficient
mice infected with Leishmania major.

AUTHORS: Simone Antoniazi, Helen P Price, Pascale Kropf, Marina A Freudenberg,
Chris Galanos, Deborah F Smith, Ingrid Müller

AFFILIATION: Imperial College London, Faculty of Medicine, Department of
Immunology, Norfolk Place, London W2 1PG, United Kingdom.

REFERENCE: Infect Immun 2004 Sep 72(9):5168-74

We studied the expression of a subset of chemokines, including RANTES/
CCL5, MIP-1alpha/CCL3, IP-10/CXCL10, and MCP-1/CCL2, in Toll-like 
receptor (TLR)-competent and -deficient mice after infection with 
Leishmania major. Chemokine expression at the site of infection (the 
footpad), in the draining lymph nodes and in the spleens of infected 
animals was determined by using two different methods of analysis. The 
results indicate that L. major infection causes overall upregulation of 
RANTES/CCL5, MIP-1alpha/CCL3, IP-10/CXCL10, and MCP-1/CCL2 in the 
footpads and lymph nodes, while expression of these chemokines is 
constitutive in the spleens of TLR4-competent mice (C57BL/10ScSn) and 
TLR4-deficient mice (C57BL10/ScN). Different patterns of expression were
 detected depending on the time postinfection, but there was little 
variation in the expression of these four chemokines in the presence or 
absence of TLR4.




PMID: 15220340
 

TITLE: Leishmania major LmACR2 Is a Pentavalent Antimony Reductase That Confers
Sensitivity to the Drug Pentostam.

AUTHORS: Yao Zhou, Nadine Messier, Marc Ouellette, Barry P Rosen, Rita
Mukhopadhyay

AFFILIATION: Department of Biochemistry and Molecular Biology, Wayne State
University School of Medicine, Detroit, Michigan 48201 and Centre de Recherche
en Infectiologie and Département de Microbiologie, Faculté de Médecine,
Université Laval, Quebec G1V 4G2, Canada.

REFERENCE: J Biol Chem 2004 Sep 279(36):37445-51

Arsenicals and antimonials are first line drugs for the treatment of 
trypanosomal and leishmanial diseases. To create the active form of the 
drug, Sb(V) must be reduced to Sb(III). Because arsenic and antimony are
 related metalloids, and arsenical resistant Leishmania strains are 
frequently cross-resistant to antimonials, we considered the possibility
 that Sb(V) is reduced by a leishmanial As(V) reductase. The sequence 
for the arsenate reductase of Saccharomyces cerevisiae, ScAcr2p, was 
used to clone the gene for a homologue, LmACR2, from Leishmania major. 
LmACR2 was able to complement the arsenate-sensitive phenotype of an 
arsC deletion strain of Escherichia coli or an ScACR2 deletion strain of
 Saccharomyces cerevisiae. Transfection of Leishmania infantum with 
LmACR2 augmented Pentostam sensitivity in intracellular amastigotes. 
LmACR2 was purified and shown to reduce both As(V) and Sb(V). This is 
the first report of an enzyme that confers Pentostam sensitivity in 
intracellular amastigotes of Leishmania. We propose that LmACR2 is 
responsible for reduction of the pentavalent antimony in Pentostam to 
the active trivalent form of the drug in Leishmania.




PMID: 15213342
 

TITLE: Visceral leishmaniasis in a patient with Wegener's granulomatosis.

AUTHORS: S Sollima, M Corbellino, R Piolini, S Calattini, S Imparato, S
Antinori

REFERENCE: Rheumatology (Oxford) 2004 Jul 43(7):935-7




********************************************************************************************************************

 The following references are revised files and are brought to you in accordance
to license agreement with the NLM.

********************************************************************************************************************


PMID: 9707568
 

TITLE: Cloning of Leishmania nucleoside transporter genes by rescue of a
transport-deficient mutant.

AUTHORS: G Vasudevan, N S Carter, M E Drew, S M Beverley, M A Sanchez, A
Seyfang, B Ullman, S M Landfear

AFFILIATION: Department of Molecular Microbiology and Immunology, Oregon Health
Sciences University, Portland, OR 97201, USA.

REFERENCE: Proc Natl Acad Sci U S A 1998 Aug 95(17):9873-8

All parasitic protozoa studied to date are incapable of purine 
biosynthesis and must therefore salvage purine nucleobases or 
nucleosides from their hosts. This salvage process is initiated by 
purine transporters on the parasite cell surface. We have used a mutant 
line (TUBA5) of Leishmania donovani that is deficient in adenosine/
pyrimidine nucleoside transport activity (LdNT1) to clone genes encoding
 these nucleoside transporters by functional rescue. Two such genes, 
LdNT1.1 and LdNT1.2, have been sequenced and shown to encode deduced 
polypeptides with significant sequence identity to the human 
facilitative nucleoside transporter hENT1. Hydrophobicity analysis of 
the LdNT1.1 and LdNT1.2 proteins predicted 11 transmembrane domains. 
Transfection of the adenosine/pyrimidine nucleoside transport-deficient 
TUBA5 parasites with vectors containing the LdNT1.1 and LdNT1.2 genes 
confers sensitivity to the cytotoxic adenosine analog tubercidin and 
concurrently restores the ability of this mutant line to take up [3H]
adenosine and [3H]uridine. Moreover, expression of the LdNT1.2 ORF in 
Xenopus oocytes significantly increases their ability to take up [3H]
adenosine, confirming that this single protein is sufficient to mediate 
nucleoside transport. These results establish genetically and 
biochemically that both LdNT1 genes encode functional adenosine/
pyrimidine nucleoside transporters.




REQUEST: [ sand fly ]

(1 article matches this request. 1 article matching other requests removed)



REQUEST: [ sandfly ]

(0 articles match this request)














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