Severe clinical presentation of visceral leishmaniasis in naturally infected dogs with disruption of the splenic white pulp

Autor: Floriano G Leal Junior, Joselli Santos Silva, Washington Luis Conrado dosSantos, Luiz Antonio Rodrigues de Freitas, Isadora dos Santos Lima, José P Moura-Neto, Daniela Farias Larangeira, Patrício An Souza, Valter dos Anjos Almeida, Deborah Bittencourt Mothé Fraga
Jazyk: angličtina
Rok vydání: 2014
Předmět:
Male
Pathology
lcsh:Medicine
Protozoology
chemistry.chemical_compound
Dog Diseases
Leishmania infantum
lcsh:Science
Leishmaniasis
Leishmania
Multidisciplinary
biology
Zoonotic Diseases
medicine.anatomical_structure
Lymphatic system
Infectious Diseases
Veterinary Diseases
Medicine
Leishmaniasis
Visceral

Female
Veterinary Pathology
Research Article
Neglected Tropical Diseases
Veterinary Medicine
medicine.medical_specialty
Anemia
Immunology
Spleen
Enzyme-Linked Immunosorbent Assay
Immunopathology
Real-Time Polymerase Chain Reaction
Microbiology
Veterinary Immunology
Dogs
medicine
Parasitic Diseases
Animals
Biology
Creatinine
business.industry
lcsh:R
Albumin
DNA
Protozoan

biology.organism_classification
medicine.disease
Veterinary Parasitology
Visceral leishmaniasis
chemistry
Parastic Protozoans
Veterinary Science
lcsh:Q
business
Biomarkers
Zdroj: PLoS ONE, Vol 9, Iss 2, p e87742 (2014)
PLoS ONE
ISSN: 1932-6203
Popis: In this work, we investigated the association between the disruption of splenic lymphoid tissue and the severity of visceral leishmaniasis in dogs. Clinical and laboratory data from 206 dogs were reviewed. Spleen sections collected during the euthanasia of these animals were analyzed, and the splenic lymphoid tissue samples were classified as well organized (spleen type 1), slightly disorganized (spleen type 2), or moderately to extensively disorganized (spleen type 3). Of 199 dogs with evidence of Leishmania infection, 54 (27%) had spleen type 1, 99 (50%) had spleen type 2, and 46 (23%) had spleen type 3. The number of clinical signs associated with visceral leishmaniasis was significantly higher in the animals with evidence of Leishmania infection and spleen type 2 or 3 than in the animals with spleen type 1. Alopecia, anemia, dehydration, dermatitis, lymphadenopathy, and onychogryphosis were all more frequent among animals with evidence of Leishmania infection and spleen type 3 than among the dogs with evidence of Leishmania infection and spleen type 1. The association between the severity of canine visceral leishmaniasis and the disorganization of the splenic lymphoid tissue was even more evident in the group of animals with positive spleen culture. Conjunctivitis and ulceration were also more common in the animals with spleen type 3 than in the animals with spleen type 1. The serum levels (median, interquartile range) of albumin (1.8, 1.4–2.3 g/dL) and creatinine (0.7, 0.4–0.8 mg/dL) were significantly lower and the serum levels of aspartate aminotransferase were significantly higher (57, 39–95 U) in animals with spleen type 3 than in animals with spleen type 1 (2.8, 2.4–3.4 g/dL; 0.9, 0.7–1.2 mg/dL and 23, 20–32 U, respectively). Our data confirm the hypothesis that disruption of the splenic lymphoid tissue is associated with a more severe clinical presentation of canine visceral leishmaniasis.
Databáze: OpenAIRE