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Sent on Saturday, 2010 Apr 10Search kinetoplastids OR kinetoplastid OR Kinetoplastida OR "trypanosoma brucei" OR leishmania OR brucei OR leishmaniasis OR "African trypanosomiasis"
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1. | Rev Salud Publica (Bogota). 2009 Dec;11(6):944-51.[An active search for cases of zoonotic visceral leishmaniasis in indigenous Colombian children and the canine population][Article in Spanish] Romero MH, López MC, Sanchez JA.Departamento de Salud Animal, Facultad de Ciencias Agropecuarias, Universidad de Caldas, Manizales, Colombia. marlyn.romero@ucaldas.edu AbstractOBJECTIVES: Carrying out an active search for cases of canine and human zoonotic visceral leishmaniasis (LVZ) by determining IgG antibodies against Leishmania infantum by indirect immunofluorescence (IFAT) and assessing the risk factors associated with the disease occurring in a Colombian endemic area. METHODS: 580 indigenous children aged less than five and 270 cross-bred dogs from 5 rural areas near the town of Coyaima (Tolima) were evaluated by determining their antibodies using the Colombian Leishmania infantum (infantum) MOHOM/ COL/CLO44B strain as antigen. 527 households in the area were surveyed to assess the risk factors and protective measures being taken. RESULTS: No sero reactivity to Leishmania infantum antigens by IFAT test was observed in the child population. Leishmania infantum antibodies were observed in 68.5 % of the dogs (185/270). The survey found deficiencies in the housing's sanitary conditions. The use of insecticide-impregnated bed-nets was evident in 48 % (130/270) of the dwellings, as were poor knowledge of the disease and a low demand for traditional medical services (41.5 %). CONCLUSIONS: Control measures must be strengthened for interrupting the reservoir-vector-human transmission chain, evaluating health authorities' strategies for promoting protective habits and improving living conditions and the susceptible population's environment. |
PMID: 20379667 [PubMed - in process] | |
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2. | An Pediatr (Barc). 2010 Apr 6. [Epub ahead of print][Visceral chi ldhood leishmaniasis: Diagnosis and treatment. A retrospective review.][Article in Spanish] Prieto Tato LM, La Orden Izquierdo E, Guillén Martín S, Salcedo Lobato E, García Esteban C, García-Bermejo I, Ramos Amador JT.Servicio de Pediatría, Hospital Universitario de Getafe, Getafe, Madrid, España. AbstractINTRODUCTION: Visceral leishmaniasis is endemic in Spain. New diagnostic tools and shorter regimens of treatment are been increasingly being used in children. OBJECTIVES: To analyze the clinical and epidemiological characteristics of cases of visceral leishmaniasis, to evaluate the diagnostic techniques tested and the safety and efficacy of treatments used. METHODS: We retrospectively reviewed the medical records of children diagnosed with visceral leishmaniasis between January 1994 and December 2007 in a tertiary public Hospital in the South of Madrid. The diagnosis of visceral leishmaniasis was based on visualization of Leishmania sp. in bone marrow aspirate or culture or positive PCR analysis of the bone marrow aspirate. RESULTS: Eleven immunocompetent children were identified. Median age was 21 months (range: 4 months - 13 years). Fever was present in all cases, and hepatomegaly and splenomegaly in 10 (91%). Anemia was the most frequent haematological finding (100%). A bone marrow aspirate was obtained in all cases. Leishmania amastigotes were observed in 8 (73%) cases. Leishmania DNA in the bone marrow aspirate was detected in all patients who underwent this procedure. Positive immunofluorescent-antibody test (IFAT) analysis at baseline was observed in 63% of cases tested. The threshold titer for positivity was 1/40. Urinary antigen detection test was positive in 4 out of 6 (67%) children in whom I was performed. Initial treatment consisted of meglumine antimoniate in 3 patients and liposomal amphotericin B (LAB) in 8 (73%) patients. All children had an early clinical response. Only one child treated with LAB relapsed. No severe adverse events were observed with treatment. CONCLUSIONS: Visceral leishmaniasis is still a common disease in our area. Clinical and laboratory findings of visceral leishmaniasis are similar to other Mediterranean area reports. PCR analysis of the bone marrow aspirate was more sensitive than traditional diagnostic techniques. Non-invasive diagnostic techniques may be used as an aid in the diagnosis of visceral leishmaniasis in children. Short course treatment of visceral leishmaniasis with liposomal amphotericin B has been safe and effective. Copyright © 2009 Asociación Española de Pediatría. Published by Elsevier Espana. All rights reserved. |
PMID: 20378427 [PubMed - as supplied by publisher] | |
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3. | Joint Bone Spine. 2010 Apr 6. [Epub ahead of print]Visceral leishmaniasis and macrophagic activation syndrome in a patient with rheumatoid arthritis under treatment with adalimumab.Moltó A, Mateo L, Lloveras N, Olivé A, Minguez S.Rheumatology Section, Hospital Universitari Germans Trias I Pujol, Ctra del Canyet s/n, 08916 Badalona, Spain. AbstractBACKGROUND: Visceral leishmaniasis is a protozoan infection usually asymptomatic, but can progress to fatal disease in immunocompromised hosts, especially in HIV patients. Visceral leishmaniasis is rare among patients under immunosuppressive therapies, and even more among patients under anti-TNF-alpha treatment, where only four cases have been described. OBJECTIVE: 1) To describe a patient with rheumatoid arthritis receiving adalimumab who developed fever, pancytopenia, splenomegaly, and extreme hyperferritinemia. 2) To perform a review of the published cases of visceral leishmaniasis and anti-TNF-alpha therapy, and cases of coexisting leishmaniasis and macrophagic activation syndrome by search in PubMed (period 1991-2008). RESULTS: Visceral leishmaniasis was established by bone marrow aspiration, and although there was no histological confirmation, according to HLH-2004 criteria, a secondary macrophagic activation syndrome was established. The patient had a favourable outcome. CONCLUSION: We report herein the fifth case of visceral leishmaniasis in a patient under TNF-alpha therapy, and the first one, to our knowledge, presenting a consequent secondary macrophagic activation syndrome. Copyright © 2010. Published by Elsevier SAS. |
PMID: 20378385 [PubMed - as supplied by publisher] | |
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4. | Parasit Vectors. 2010 Apr 8;3(1):34. [Epub ahead of print]Imported and travelling dogs as carriers of canine vector-borne pathogens in Germany.Menn B, Lorentz S, Naucke TJ.AbstractABSTRACT: BACKGROUND: With the import of pets and pets taken abroad, arthropod-borne diseases have increased in frequency in German veterinary practices. This is reflected by 4,681 dogs that have been either travelled to or relocated from endemic areas to Germany. The case history of these dogs and the laboratory findings have been compared with samples collected from 331 dogs living in an endemic area in Portugal. The various pathogens and the seroprevalences were examined to determine the occurrence of, and thus infection risk, for vector-borne pathogens in popular travel destinations. RESULTS: 4,681 dogs were examined serological for Leishmania infantum, Babesia canis and Ehrlichia canis. Buffy coats were detected for Hepatozoon canis and blood samples were examined for microfilariae via the Knott's test. The samples were sent in from animal welfare organizations or private persons via veterinary clinics. Upon individual requests, dogs were additionally examined serological for Anaplasma phagocytophilum, Borrelia burgdorferi and Rickettsia conorii. Overall B. canis was the most prevalent pathogen detected by antibody titers (23.4%), followed by L. infantum (12.2%) and E. canis (10.1%). Microfilariae were detected in 7.7% and H. canis in 2.7% of the examined dogs. In 332/1862 dogs A. phagocytophilum, in 64/212 B. burgdorferi and in 20/58 R. conorii was detected. Of the 4,681 dogs, in total 4,226 were imported to Germany from endemic areas. Eighty seven dogs joined their owners for a vacation abroad. In comparison to the laboratory data from Germany, we examined 331 dogs from Portugal. The prevalence of antibodies/ pathogens we detected was: 62.8% to R. conorii, 58% to B. canis, 30.5% to A. phagocytophilum, 24.8% to E. canis, 21.1% to H. canis (via PCR), 9.1% to L. infantum and 5.3% to microfilariae. CONCLUSIONS: The examination of 4,681 dogs living in Germany showed pathogens like L. infantum that are non-endemic in Germany. Furthermore, the German data are similar in terms of multiple pathogen infection to the data recorded for dogs from Portugal. Based on these findings the importation of dogs from endemic predominantly Mediterranean regions to Germany as well as travelling with dogs to these regions carries a significant risk of acquiring an infection. Thus we would conclude that pet owners seek advice of the veterinarians prior to importing a dog from an endemic area or travel to such areas. In general, it might be advisable to have a European recording system for translocation of dogs. |
PMID: 20377872 [PubMed - as supplied by publisher] | |
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5. | Parasit Vectors. 2010 Apr 8;3(1):31. [Epub ahead of print]Environmental risk mapping of canine leishmaniasis in France.Chamaille L, Tran A, Meunier A, Bourdoiseau G, Ready P, Dedet JP.AbstractABSTRACT: BACKGROUND: Canine leishmaniasis (CanL) is a zoonotic disease caused by Leishmania infantum, a Trypanosomatid protozoan transmitted by phlebotomine sandflies. Leishmaniasis is endemic in southern France, but the influences of environmental and climatic factors on its maintenance and emergence remain poorly understood. From a retrospective database, including all the studies reporting prevalence or incidence of CanL in France between 1965 and 2007, we performed a spatial analysis in order to i) map the reported cases in France, and ii) produce an environment-based map of the areas at risk for CanL. We performed a Principal Component Analysis (PCA) followed by a Hierarchical Ascendant Classification (HAC) to assess if the locations of CanL could be grouped according to environmental variables related to climate, forest cover, and human and dog densities. For each group, the potential distribution of CanL in France was mapped using a species niche modelling approach (Maxent model). RESULTS: Results revealed the existence of two spatial groups of CanL cases. The first group is located in the Cevennes region (southern Massif Central), at altitudes of 200-1000 m above sea level, characterized by relatively low winter temperatures (1.9degrees C average), 1042 mm average annual rainfall and much forest cover. The second group is located on the Mediterranean coastal plain, characterized by higher temperatures, lower rainfall and less forest cover. These two groups may correspond to the environments favoured by the two sandfly vectors in France, Phlebotomus ariasi and Phlebotomus perniciosus respectively. Our niche modelling of these two eco-epidemiological patterns was based on environmental variables and led to the first risk map for CanL in France. CONCLUSION: Results show how an ecological approach can help to improve our understanding of the spatial distribution of CanL in France. |
PMID: 20377867 [PubMed - as supplied by publisher] | |
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6. | Parasit Vectors. 2010 Apr 8;3(1):27. [Epub ahead of print]Canine babesiosis in northern Portugal and molecular characterization of vector-borne co-infections.Cardoso L, Yisaschar-Mekuzas Y, Rodrigues FT, Costa A, Machado J, Diz-Lopes D, Baneth G.AbstractABSTRACT: BACKGROUND: Protozoa and bacteria transmitted by arthropods, including ticks and phlebotomine sand flies, may cause a wide range of canine vector-borne diseases. Dogs can be simultaneously or sequentially infected with multiple pathogens. Canine babesiosis caused by Babesia canis canis and Babesia canis vogeli is known to occur in Portugal. This study assessed, by means of blood smear examination, PCR and DNA nucleotide sequencing, the presence of Babesia spp. and co-infecting agents Leishmania, Anaplasma/Ehrlichia and Hepatozoon in 45 dogs from northern Portugal clinically suspected of babesiosis. RESULTS: Forty-four dogs (98%) had infection with B. canis canis and one with B. canis vogeli. Co-infections were detected in nine animals (20%). Eight dogs were found infected with two vector-borne agents: six with B. canis canis and Leishmania infantum; one with B. canis canis and Ehrlichia canis; and one with B. canis canis and Hepatozoon canis. Another dog was infected with three vector-borne pathogens: B. canis vogeli, E. canis and L. infantum. Overall, L. infantum was found in seven (16%), E. canis in two (4%), and H. canis in one (2%) out of the 45 dogs with babesiosis. Almost 90% of the 45 cases of canine babesiosis were diagnosed in the colder months of October (18%), November (27%), December (20%), February (13%) and March (9%). Co-infections were detected in February, March, April, May, October and November. Twenty-two (50%) out of 44 dogs infected with B. canis were found infested by ticks including Dermacentor spp., Ixodes spp. and Rhipicephalus sanguineus. Mortality (9%) included two co-infected dogs that died spontaneously and two with single infections that were euthanized. CONCLUSIONS: Babesia canis canis is the main etiological agent of canine babesiosis in northern Portugal. A higher sensitivity of Babesia spp. detection was obtained with PCR assays, compared to the observation of blood smears. Twenty percent of the dogs were co-infected with L. infantum, E. canis or H. canis. Furthermore, this is the first molecular identification of H. canis in dogs from northern Portugal. |
PMID: 20377861 [PubMed - as supplied by publisher] | |
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7. | Expert Rev Anti Infect Ther. 2010 Apr;8(4):419-33.Current diagnosis and treatment of cutaneous and mucocutaneous leishmaniasis.Goto H, Lindoso JA.Laboratório de Soroepidemiologia do Instituto de Medicina Tropical da Universidade de São Paulo, Avenida Dr. Enéas de Carvalho Aguiar, Prédio II, São Paulo, SP, Brazil. hgoto@usp.br AbstractTegumentary leishmaniasis, comprising the cutaneous and mucocutaneous forms, is caused by at least 13 dermotropic species of protozoa of the genus Leishmania, most of which are prevalent in the New World. Although diseases in the Old and New Worlds share similar characteristics, the ultimate manifestations and severity are quite different, with more severe forms associated with mucosal lesions observed in the New World. For the diagnosis and treatment of leishmaniasis, differences based on clinical features, usefulness/sensitivity of diagnostic methods and therapeutic responses are mainly emphasized. We present a critical review of the diagnostic methods, their contribution and the necessity for their improvement/development, particularly in molecular diagnosis aimed at detection and species identification, as well as serodiagnosis. In addition to a review of the drugs currently utilized, we describe differences in their effectiveness in Old and New World leishmaniasis. HIV/Leishmania coinfection is also presented in the context of diagnosis and treatment. |
PMID: 20377337 [PubMed - in process] | |
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