[leish-l] Articles found by RefScout 2005/02/25 Newsletter 8/2005 Part I
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This is RefScout-Newsletter 8/2005
Due to more than 100 requests your newsletter has been split. This is part 1.
REQUEST: [ leishmaniasis ]
(81 articles match this request. 1 article matching other requests removed)
PMID: 15725545
TITLE: Participation of Rhipicephalus sanguineus (Acari: Ixodidae) in the
epidemiology of canine visceral leishmaniasis.
AUTHORS: Maria Teresa Zanatta Coutinho, Lilian Lacerda Bueno, Annelise Sterzik,
Ricardo Toshio Fujiwara, Jose Ramiro Botelho, Mario De Maria, Odair Genaro,
Pedro Marcos Linardi
AFFILIATION: Departamento de Parasitologia, Instituto de Ciências Biológicas,
Universidade Federal de Minas Gerais, Caixa Postal 486, Avenida Antônio
Carlos, 6627, Campus UFMG, Belo Horizonte, Minas Gerais, CEP 31270-901,
Brazil.
REFERENCE: Vet Parasitol 2005 Mar 128(1-2):149-55
The vectorial competence of the tick Rhipicephalus sanguineus is
discussed in relation to the epidemiology of canine visceral
leishmaniasis, taking into account its strict association with dogs and
the low indices of natural infection presented by its known vector, the
phlebotomine sand fly Lutzomyia longipalpis. In order to evaluate
natural infection by Leishmania chagasi and the infectivity of these
parasites in the tick, 39 specimens (6 females, 11 males and 22 nymphs)
of R. sanguineus were removed from 21 dogs showing diverse symptoms of
zoonotic visceral leishmaniasis (ZVL). Six ticks (15.4%) gave positive
results for the genus Leishmania using the PCR technique. To determine
the infectivity of the parasites, 36 hamsters were inoculated orally and
peritoneally with macerates of ticks removed from nine dogs symptomatic
for visceral leishmaniasis. After 6 months the hamsters were sacrificed
and necropsied. Serum was removed for IFAT, as well as spleen and liver
fragments to make imprint smears and for PCR. Eight (88.9%) of these
dogs presented ticks that were infective for 14 hamsters (41.2%), 12 (85
.7%) of them infected peritoneally and two (14.3%) orally. PCR revealed
27 smears (40.9%) to be positive, 20 (62.5%) of them infected
peritoneally and seven (20.6%) orally. IFAT showed 14 positive animals (
41.2%). Based on these findings, we suggest that the vectorial capacity
of R. sanguineus for L. chagasi should be evaluated further, opening new
perspectives in the epidemiology of ZVL.
PMID: 15713447
TITLE: Leishmania donovani: identification of novel vaccine candidates using
human reactive sera and cell lines.
AUTHORS: Sunil K Arora, Nirbhai S Pal, S Mujtaba
AFFILIATION: Department of Immunopathology, Postgraduate Institute of Medical
Education and Research, Chandigarh, India.
REFERENCE: Exp Parasitol 2005 Mar 109(3):163-70
Leishmaniasis is a complex of diseases caused by protozoan parasites
belonging to the genus Leishmania. The development of specific
resistance against re-infection after cure suggests that a vaccine
approach is feasible. Various studies in humans and experimental animals
strongly suggest that Th1 type of cell-mediated immune response is
important for protection against the disease. A defined antigen that
could elicit a specific T-cell-mediated immune response in the host
would be an ideal candidate for the vaccine against this parasite. In
order to select a candidate antigen, we established a screening system
to identify the recombinant clone, expressing antigen having T-cell
epitopes from a cDNA library. We screened the library using an
established Leishmania specific cell line (LSCL) from a naive healthy
human subject. The cell line with predominantly CD4(+) cells behaved in
a Leishmania specific manner. Fifty-two immuno-reactive clones were
screened against the LSCL in vitro and we identified three cDNA clones
expressing recombinant antigens that could induce proliferation of these
cells to produce INFgamma. The protective efficacy of one of these
recombinant proteins was investigated in a hamster model of experimental
visceral leishmaniasis and showed protection against a virulent
challenge. The identified antigens might be potential candidates for
vaccine against Leishmania.
PMID: 15725531
TITLE: Feline leishmaniasis due to Leishmania (Leishmania) amazonensis in Mato
Grosso do Sul State, Brazil.
AUTHORS: Alda Izabel de Souza, Evânia Marcia Silva Barros, Edna Ishikawa, Iêda
Maria Novaes Ilha, Glaucia Rosely Barbosa Marin, Vânia Lúcia Brandão Nunes
AFFILIATION: Curso de Medicina Veterinária, Centro de Ciências Biológicas,
Agrárias e da Saúde (CCBAS),Universidade para o Desenvolvimento do Estado e
da Região do Pantanal (UNIDERP), rua Alexandre Herculano 1400, 79037-280 Campo
Grande, Mato Grosso do Sul, Brazil.
REFERENCE: Vet Parasitol 2005 Mar 128(1-2):41-5
A case of leishmaniasis in a domestic cat (Felis domesticus) is
described. The animal showed a single, nodular lesion on the nose and
many nodules of different size on the ears and digital regions of all
the paws. Diagnosis was made by microscopic detection of amastigotes in
Giemsa-stained smears from the lesions. By monoclonal antibodies the
aetiological agent was identified as Leishmania (Leishmania) amazonensis
, one of the seven species implicated in human leishmaniasis in Brazil.
The clinical signs in feline leishmaniasis are unspecific and similar to
those observed in other diseases such as cryptococcosis and in
sporotrichosis, commonly found in cats. Leishmaniasis should therefore,
be added to the differential diagnosis by feline veterinary
practitioners and adequate investigations should carried out for dermal
leishmaniasis in the area where the feline infection is detected.
PMID: 15710545
TITLE: Leishmania donovani amastigote components-induced colony-stimulating
factors production.
AUTHORS: P Singal, P P Singh
AFFILIATION: National Institute of Pharmaceutical Education and Research,
Department of Biotechnology, Sector-67, Phase-X, S.A.S. Nagar 160 062, India.
REFERENCE: Parasitol Int 2005 Mar 54(1):9-20
Increased hematopoiesis, driven by colony-stimulating factors (CSFs), is
known to occur in infectious diseases. However, whether Leishmania
donovani component(s) can directly induce the synthesis and secretion of
CSFs is not known. We report that L. donovani amastigote antigens
soluble in culture medium (LDAA; 0.01-10 mg/kg), injected intravenously
in BALB/c mice, induced the production of serum CSFs; maximum induction
(128>16 colonies) occurred at 1 mg/kg. In vitro also, LDAA (0.01-1 mg/
ml) induced mouse peritoneal macrophages (MOs) to elaborate CSFs in the
conditioned medium (CM); 0.1 mg/ml LDAA appeared optimal (68+/-9
colonies). Both in vivo and in vitro, the kinetics of CSF production
were similar with peak response occurring 24 h after stimulation and
return to background levels by 72 h. A predominant approximately 12 kDa
LDAA protein (LDAA-12) also induced CSF production, both in serum and CM
, in a dose-and time-dependent manner. Rabbit anti-LDAA-12 antibody
significantly (p<0.05) reduced both the LDAA-and LDAA-12-induced CSF
production, in vitro. Functionally, the LDAA-12-induced CSFs, both in
the serum and CM, appeared to be similar as they supported the formation
of granulocyte (G), MO (M) and GM colonies, in vitro, in similar
proportion; GM colonies were maximum (>80%). Further, LDAA-12 induced
significantly (p<0.05) high GM-CSF levels both in serum and CM (19+/-
3 and 15+/-2 ng/ml, respectively), as compared to the controls.
Neutralizing (100%) goat anti-mouse tumour necrosis factor-alpha (TNF-
alpha) immunoglobulin G did not affect the LDAA-12-induced CSF
production by MOs, indicating it to be TNF-alpha-independent. LDAA-12
induced de novo CSF production, as MOs co-treated with LDAA-12 and
cycloheximide (50 mug/ml) did not elaborate CSFs. The CSF-inducing
capability of LDAA-12 appeared to be heat (70 C; 1 h)-labile, destroyed
by proteases (pronase E and trypsin) and was unaffected by sodium
periodate treatment. In LDAA-12-treated mice, the splenic and femur
colony forming unit-GM counts showed a maximum of 2.2- and 1.9-fold
increase, respectively, as compared to the controls. These data are the
first to directly demonstrate that L. donovani amastigote components can
induce the production of CSFs that may play important role(s) in the
pathogenesis of visceral leishmaniasis.
PMID: 15710520
TITLE: The susceptibility of domestic cats (Felis catus) to experimental
infection with Leishmania braziliensis.
AUTHORS: L Simões-Mattos, M R F Mattos, M J Teixeira, J W Oliveira-Lima, C M L
Bevilaqua, R C Prata-Júnior, C M Holanda, F C M Rondon, K M S Bastos, Z C B
Coêlho, I C B Coêlho, A Barral, M M L Pompeu
AFFILIATION: Faculdade de Veterinária (FAVET), Programa de Pós-Graduação em
Ciências Veterinárias (PPGCV), Universidade Estadual do Ceará (UECE),
Ceará, CEP 60.740-000, Brazil.
REFERENCE: Vet Parasitol 2005 Feb 127(3-4):199-208
Over the last few years, several cases of feline leishmaniasis (FL) with
cutaneous and visceral forms have been reported around the world.
Nonetheless, the real susceptibility of cats to infection with
Leishmania spp. and the outcome of leishmaniasis in these animals are
poorly understood. Experimental studies on feline models will contribute
to the knowledge of natural FL. Thus, in order to determine the
susceptibility of domestic cats (Felis catus) to experimental infection
with Leishmania braziliensis, 13 stray cats were infected with 10(7)
promastigotes by the intradermal route in the ear and nose
simultaneously and followed up for 72 weeks. Soon after infection, the
earliest indication of a lesion was a papule on the ear at 2 weeks post-
infection (w.p.i.). The emergence of satellite papules around the
primary lesion was observed about 4 w.p.i. Two weeks later these papules
coalesced and formed a huge and irregular nodule. Thereafter, there was
lesion dissemination to the external and marginal surface of the
ipsilateral ear, and later to the contralateral ear. At 10 w.p.i., some
nodules became ulcerated. Nose lesions presented a similar evolution. At
both sites, the largest lesion sizes occurred at 10 w.p.i. and started
to decrease 15 days later. Ear and nose nodules healed at 32 and 40 w.p.
i., respectively. Specific L. braziliensis IgG antibody titers (optical
density>/=0.01 as positive result) were detected as early as 2 w.p.i. (0
.09+/-0.02) in only three animals (23%), and all cats had positive
titers at 20 w.p.i. (0.34+/-0.06). Only three animals (38%) continued to
show positive serology at 72 w.p.i. (0.08+/-0.02). Up to that time,
none of the cats had lesion recurrence. In a feline model of cutaneous
leishmaniasis, it seems that there is no correlation between active
lesions and positive serology. The implications of these data are
discussed.
PMID: 15710523
TITLE: Clinical and serological aspects of visceral leishmaniasis in Northeast
Brazilian dogs naturally infected with Leishmania chagasi.
AUTHORS: M A O Almeida, E E V Jesus, M L B Sousa-Atta, L C Alves, M E A Berne, A
M Atta
AFFILIATION: Escola de Medicina Veterinária, Universidade Federal da Bahia,
Salvador, Bahia, Brazil.
REFERENCE: Vet Parasitol 2005 Feb 127(3-4):227-32
Human visceral leishmaniasis is endemic in the northeast of Brazil,
where the domestic dog is an important parasite reservoir in the
infectious cycle of Leishmania chagasi. In this study, we evaluated the
clinical signs of canine visceral leishmaniasis (CVL), serum protein
profile and the antileishmanial IgG antibody production in 86 dogs
living in northeast endemic areas of leishmaniasis. Thirty dogs from a
leishmaniasis-free area were used as a control group. The major clinical
signs of CVL seen were emaciation and skin ulcers (80%), followed by
onychogryphosis and conjunctivitis (73%). Depilation was observed in 60
% of animals while lymphadenomegaly, splenomegaly, liver enlargement or
kidney involvement was less frequent (</=20%). VL seropositive dogs
presented with serum hyperproteinemia, hypoalbuminemia,
hypergammaglobulinemia and decreased albumin/globulin ratio. A lower
sensitivity and higher specificity was observed for promastigote
indirect fluorescent antibody test (IFAT) (83 and 100%, respectively)
compared with enzyme-linked immunosorbent assay (ELISA) (94 and 90%),
which uses a crude extract of Leishmania. There was a positive
correlation between IFAT and ELISA titers of antileishmanial IgG
antibodies (Spearman test, P<0.05), which was augmented in CVL dogs.
This study found that the determination of serum protein, A/G ratio and
the use of two different leishmanial serological tests like IFAT and
ELISA are essential in CVL screening.
PMID: 15703426
TITLE: Case records of the Massachusetts General Hospital. Weekly
clinicopathological exercises. Case 4-2005. A 35-year-old man with nasal
congestion, swelling, and pain.
AUTHORS: Peter F Weller, Marlene L Durand, Ben Z Pilch
AFFILIATION: Division of Infectious Diseases, Beth Israel Deaconess Medical
Center, Boston, USA.
REFERENCE: N Engl J Med 2005 Feb 352(6):609-15
PMID: 15712551
TITLE: Mastoid abscess caused by Nocardia in a child with visceral
leishmaniasis.
AUTHORS: Pratima Gupta, Saurabh Varshney, Biswaroop Chaterjee, R K Saxena
AFFILIATION: Department of Microbiology, Himalayan Institute of Medical
Sciences, Jollygrant, Dehradun (UA) 248140, India.
REFERENCE: Trop Doct 2005 Jan 35(1):45-6
PMID: 15626463
TITLE: Immunoglobulin G and E responses in various stages of canine
leishmaniosis.
AUTHORS: Laura Iniesta, Montserrat Gállego, Montserrat Portús
AFFILIATION: Laboratori de Parasitologia, Facultat de Farmà cia, Universitat de
Barcelona, Avda. Diagonal s/n, Barcelona, E-08028, Spain.
REFERENCE: Vet Immunol Immunopathol 2005 Jan 103(1-2):77-81
Pathogenesis in visceral leishmaniosis is associated with depressed
cellular immunity and a significant rise of antileishmanial antibodies.
We assessed the relative levels of immunoglobulin E anti-Leishmania
infantum, together with those of IgG, IgG1 and IgG2, using the enzyme-
linked immunosorbent assay (ELISA) test, in non-infected and infected
dogs with or without symptoms, and their association with symptoms to
differentiate the stages of the infection. The expression of all
immunoglobulins (IgG, IgG1, IgG2 and IgE) was higher in symptomatic dogs
than in all other categories. IgG and IgG2 expression was higher in the
infected asymptomatic group than in the non-infected group, whereas
IgG1 and IgE expression was only higher in symptomatic animals. This
correlation between the expression of IgG1 and IgE and the pathology of
leishmaniosis points to their potential role as markers of the active
disease.
PMID: 15717090
TITLE: [American cutaneous leishmaniasis: phlebotomine transmission area in the
Municipality of Uberlandia, MG.]
AUTHORS: Jureth Couto Lemos, Samuel do Carmo Lima
AFFILIATION: Escola Técnica de Saúde, Universidade Federal de Uberlândia,
Uberlândia, MG.
REFERENCE: Rev Soc Bras Med Trop 2005 Jan-Feb 38(1):22-6
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