Soro-conversão e avaliação das alterações renais em cães infectados por Leishmania (Infantum) chagasi

This study investigated the sero-conversion period in which dogs from endemic areas test positive for visceral leishmaniasis (VL) as well as the early post-infection period in which renal alterations are observed. Dogs that were initially negative for Canine Visceral Leishmaniasis (CVL) were clinically evaluated every three months by serological, parasitological and biochemical tests until sero-conversion was confirmed, and six months later a subsequent evaluation was performed. Samples of kidney tissues were processed and stained with Hematoxylin and Eosin (H&E), Periodic Acid Schiff (PAS) and Masson’s trichrome stain and lesions were classified based on the WHO criteria. Of the 40 dogs that initially tested negative for VL, 25 (62.5%) exhibited positive serological tests during the study period. Of these 25 dogs, 15 (60%) tested positive within three months, five (20%) tested positive within six months and five (20%) tested positive within nine months. The dogs exhibited antibody titers between 1:40 and 1:80 and 72% of the dogs exhibited clinical symptoms. The Leishmania antigen was present in the kidneys of recently infected dogs. We found higher levels of total protein and globulin as well as lower levels of albumin in the infected dogs when compared to the control dogs. Additionally, infected dogs presented levels of urea and creatinine that were higher than those of the uninfected dogs. Glomerulonephritis was detected in some of the dogs examined in this study. These data suggest that in Teresina, the sero-conversion for VL occurs quickly and showed that the infected dogs presented abnormal serum proteins, as well as structural and functional alterations in the kidneys during the early post-infection period.Este estudo investigou o período em que o cão torna-se positivo para leishmaniose visceral (VL) em área endêmica e as alterações renais no período recente pós-infecção. Cães negativos para VL foram avaliados clinicamente a cada três meses por testes sorológicos, parasitológicos e bioquímicos até a soro-conversão e seis meses após. Foram colhidos tecido renal de seis cães, submetidos a processamento de rotina e corados com HE, PAS e Masson e as lesões foram classificadas com base nos critérios da OMS. Dos 40 cães nagativos para VL, 25 (62,5%) apresentaram sorologia positiva durante o estudo. Desses, 15 (60%) tornaram-se positiva nos primeiros três meses, cinco (20%) tornaram-se positivas dentro de seis meses e cinco (20%) tornaram-se positivas dentro de nove meses. Os cães apresentavam títulos de anticorpos entre 1:40 e 1:80, e 72% mostraram sinais clínicos. Antígeno de Leishmania estava presente no rim. Foram encontrados níveis mais elevados de proteína total e globulina, e menores níveis de albumina em cães infectados quando comparados aos controles. Além disso, os cães infectados apresentaram níveis de uréia e creatinina maior do que os cães controles. Glomerulonefrite foi observada em cinco cães. Os resultados sugerem que em Teresina a soro-conversão para VL ocorre rapidamente e os cães apresentam proteínas séricas anormais e alterações na estrutura e função dos rins em um período recente pós-infecção

The performance of serological tests for Leishmania infantum infection screening in dogs depends on the prevalence of the disease

Dogs are considered the main reservoir of Leishmania infantum. This protozoan causes visceral leishmaniasis (VL), an uncontrolled urban zoonosis in Brazil. Serological tests and polymerase chain reaction (PCR) on peripheral blood were performed to identify infected dogs in scenarios of higher and lower prevalence of the disease (Teresina and Vitória). One-hundred infected and 57 non-infected animals from Teresina and 100 non-infected animals from Vitória were studied. Animal selection was not dependent on previous serology. The sensitivity (Teresina) and specificity (Teresina and Vitória) were as follows: indirect antibody fluorescence (IFAT) cut-off of 1:40 (IFAT 1:40): 96%, 18%, and 76%; IFAT 1:80: 90%, 33%, and 93%; direct agglutination test (DAT): 96%, 33%, and 98%; fast agglutination screening test (FAST): 93%, 68%, and 100%; immunochromatographic assay with a recombinant rK39 antigen (rK39): 88%, 74%, and 98%; enzyme linked immunosorbent assay (ELISA): 91%, 79%, and 98%; rapid dual-path platform test (TR DPP®): 98%, 60%, and 98%; and blood PCR: 29%, 93%, and 97%, respectively. In the high transmission area, none of the tests adequately discriminated L. infantum-infected from non-infected dogs. However, in the high transmission city, the area under the receiver operating characteristic (ROC) curve of FAST, DAT, ICrK39, ELISA and TR DPP® was high

Histopathological evaluation of the intestine of jabutis (Chelonoidis carbonarius e Chelonoidis denticulatus) reared in captivity and parasitized by helminths (Chapiniella variabilis and Atractis thapari)

El estudio tuvo como objetivo identificar y describir lesiones intestinales ocasionadas por helmintos en jabutis (Chelonoidis carbonarius y Chelonoidis denticulatus) criados en cautiverio en el Parque Zoobotánico de Teresina, estado de Piauí, Brasil. La evaluación parasitológica de 142 de estas tortugas reveló que todas estaban parasitados por helmintos (ascarídeos y estrongilideos), que fueron identificados como Atractis thapari y Chapiniella variabilis por medio de microscopio de luz y microscopio electrónico. Los 12 animales más parasitados (seis de cada especie) fueron eutanasiados y muestras de intestino delgado y grueso fueron evaluadas por histopatología. Macroscópicamente, todos los intestinos, tanto delgado como grueso, presentaban hiperemia. Microscópicamente, en el intestino delgado se observó hiperemia (12/12), hiperplasia difusa de células caliciformes (8/12) y edema de submucosa (1/12). En el intestino grueso se observó hiperemia, variando entre discreta a intensa (12/12) y enteritis transmural granulomatosa focalmente extensa e intensa (1/12).The aim of this study was to identify and describe intestinal lesions caused by helminths in red-footed tortoise (Chelonoidis carbonarius) and yellow-footed tortoise (Chelonoidis denticulatus) reared in captivity in the Zoo and Botanical Park of Teresina, Piauí State, Brazil. The parasitological evaluation of 142 of these tortoises revealed that all were parasitized by helminths (ascarids and strongyles), which were identified as Atractis thapari and Chapiniella variabilis by light and electron microscopy. The 12 most parasitized tortoises (six per species) were euthanized, and samples of small and large intestine were evaluated by histopathology. Macroscopically, all small and large intestines had hyperaemia. Microscopically, hyperaemia (12/12), diffuse goblet cell hyperplasia (8/12) and submucosa oedema (1/12) were observed in the small intestine. Hyperaemia was observed in the large intestine, varying from discrete to intense (12/12) and focally extensive and severe transmural granulomatous enteritis (1/12)

Leishmania (infantum) chagasi in canine urinary sediment

Canine visceral leishmaniasis (CVL) is difficult to diagnosis, mainly due to the presence of asymptomatic animals, the diversity of clinical symptoms and the difficulty in obtaining diagnostic evidence of high sensitivity and specificity. The purpose of this study was to diagnose CVL in urinary sediment of 70 dogs of different breeds, sexes and ages from the veterinary hospital of the Federal University of Piauí and Zoonosis Control Center of Teresina, Brazil. The serological tests were TR DPP® for CVL and enzyme-linked immunosorbent assay (ELISA) for CVL, parasitological exams of bone marrow and lymph nodes and urine sediment cultures. Leishmania was detected in the bone marrow and/or lymph node of 61.0% of the animals (43/70), and urine sediment culture was positive in 9.30% (4/43) of these animals. In the serological exams, 70.0% (49/70) were reactive using the DPP and 78.2% (55/70) were reactive using ELISA. The goal of this study was to diagnose the presence of L. (infantum) chagasi in a culture of urinary sediment

Serological tests fail to discriminate dogs with visceral leishmaniasis that transmit Leishmania infantum to the vector Lutzomyia longipalpis

Abstract INTRODUCTION The control of reservoirs for Leishmania infantum -induced zoonotic visceral leishmaniasis requires the identification of dogs posing a population risk. Here, we assessed the performance of several assays to identify Lutzomyia longipalpis infectious dogs. METHODS We evaluated 99 dogs that were positive for visceral leishmaniasis based on parasite identification. Serological analyses were performed using an enzyme-linked immunosorbent assay, immunofluorescence antibody tests in 1:40 and 1:80 dilutions, rapid dual path platform tests, immunochromatographic assay with a recombinant rK39 antigen, fast agglutination screening tests, and direct agglutination tests. We also performed PCR to analyze peripheral blood and xenodiagnosis. RESULTS Forty-six dogs infected at least one L. longipalpis specimen. Although the serological test sensitivities were above 85% for detecting L. longipalpis infectious dogs, none showed a satisfactory performance, as both specificity (0.06 to 13%) and the area under the receiver operating characteristic curve (45 to 53%) were low. The PCR results were also weak, with a sensitivity of 30%, specificity of 72%, and an area under the receiver operating characteristic curve of 51%. The infected L. longipalpis proportion was higher among asymptomatic dogs than symptomatic dogs. Among the symptomatic dogs, those with ulceration-free skin diseases were more infectious, with an odds ratio of 9.3 (confidence interval of 1.10 - 428.5). The larger the number of insects fed, the greater the detected infectiousness. CONCLUSIONS Our study supports the imperative to develop novel technologies for identifying the infectious dogs that transmit L. infantum for the benefit of public health