Luisa H. M. Miranda

Dr. Luisa H. M. Miranda

orcid

Research Focus & Metrics

Academic Career Length

18Years (2009-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

View All Publications
13 June 2018 in Scientific Reports
Verified
Journal Article
Open access
PDF file
ESElaine Waite de Souza
Elaine Waite de Souza
CBCintia de Moraes Borba
Cintia de Moraes Borba
Sandro PereiraSandro Pereira
Sandro Pereira
IGIsabella Dib Ferreira Gremião
Isabella Dib Ferreira Gremião
ILIngeborg Maria Langohr
Ingeborg Maria Langohr
RMRodrigo Caldas Menezes
Rodrigo Caldas Menezes
Zoonotic sporotrichosis caused by the fungus Sporothrix brasiliensis is usually severe in cats. This study investigated the associations between clinical features, fungal load, coinfections, histological skin changes, and response to itraconazole in cats with sporotrichosis caused by S. brasiliensis. Fifty-two cats with skin lesions and a definitive diagnosis of sporotrichosis were treated with itraconazole for a maximum period of 36 weeks. The animals were submitted to clinical examination and two subsequent collections of samples from the same skin lesion for fungal diagnosis and histopathology, as well as serology for feline immunodeficiency (FIV) and leukaemia (FeLV) viruses. Thirty-seven (71%) cats were clinically cured. Nasal mucosa lesions and respiratory signs were associated with treatment failure. Cats coinfected with FIV/FeLV (n = 12) had a lower neutrophil count in the lesion. A high fungal load in skin lesions was linked to young age and treatment failure, as well as to a longer time of wound healing, poorly formed granulomas and fewer neutrophils, macrophages and lymphocytes in these lesions. These results indicate that itraconazole is effective, but nasal mucosal involvement, respiratory signs and high fungal loads in skin lesions are predictors of treatment failure that will assist in the development of better treatment protocols for cats.

1 July 2013 in Comparative Immunology, Microbiology and Infectious Diseases
Verified
Journal Article
Closed access
LMLuisa H. M. Miranda
Luisa H. M. Miranda
FCFátima Conceição-Silva
Fátima Conceição-Silva
LQLeonardo Quintella
Leonardo Quintella
BKBianca P. Kuraiem
Bianca P. Kuraiem
Sandro PereiraSandro Pereira
Sandro Pereira
TSTânia M.P. Schubach
Tânia M.P. Schubach

6 January 2021 in Journal of Fungi
Verified
Journal Article
Open access
PDF file
Patrizia DanesiPatrizia Danesi
Patrizia Danesi
CFCHRISTIAN FALCARO
CHRISTIAN FALCARO
LSLaura J. Schmertmann
Laura J. Schmertmann
LMLuisa H. M. Miranda
Luisa H. M. Miranda
MKMark Krockenberger
Mark Krockenberger
RMRichard Malik
Richard Malik
Cryptococcosis is typically a sporadic disease that affects a broad range of animal species globally. Disease is a consequence of infection with members of the Cryptococcus neoformans or Cryptococcus gattii species complexes. Although cryptococcosis in many domestic animals has been relatively well-characterized, free-living wildlife animal species are often neglected in the literature outside of occasional case reports. This review summarizes the clinical presentation, pathological findings and potential underlying causes of cryptococcosis in various other animals, including terrestrial wildlife species and marine mammals. The evaluation of the available literature supports the hypothesis that anatomy (particularly of the respiratory tract), behavior and environmental exposures of animals play vital roles in the outcome of host–pathogen–environment interactions resulting in different clinical scenarios. Key examples range from koalas, which exhibit primarily C. gattii species complex disease presumably due to their behavior and environmental exposure to eucalypts, to cetaceans, which show predominantly pulmonary lesions due to their unique respiratory anatomy. Understanding the factors at play in each clinical scenario is a powerful investigative tool, as wildlife species may act as disease sentinels.

7 August 2018 in Journal of Fungi
Verified
Journal Article
Open access
PDF file
LMLuisa H. M. Miranda
Luisa H. M. Miranda
JSJéssica Nunes Silva
Jéssica Nunes Silva
IGIsabella Dib Ferreira Gremiao
Isabella Dib Ferreira Gremiao
RMRodrigo Caldas Menezes
Rodrigo Caldas Menezes
RARodrigo Almeida-Paes
Rodrigo Almeida-Paes
Sandro PereiraSandro Pereira
Sandro Pereira
Skin lesions in feline sporotrichosis usually present a high fungal burden, making cats an important source of infection. This study evaluated the fungal burden and isolation in skin lesions of feline sporotrichosis during treatment with itraconazole (ITZ), combined with or without potassium iodide (KI). Treatment-naïve cats with culture-confirmed sporotrichosis and presenting skin ulcers were treated for up to 40 weeks with oral ITZ alone (n = 74) or combined with KI (n = 56). These cats were submitted to monthly sampling of the same lesion for mycological culture and cytopathology until healing of lesion or up to twelve weeks. The fungal burden was expressed as the mean yeast cell count in three microscopic fields from imprint smears. The fungal burden before treatment was significantly higher in cats in which the lesion persisted and in cases of treatment failure when using ITZ alone. After twelve weeks, the median fungal burden decreased to zero in both treatment protocols, suggesting a potential decrease in the risk of transmission of Sporothrix spp. from cats. These findings encourage the early treatment of feline sporotrichosis as a control measure. Moreover, the fungal burden in feline sporotrichosis lesions can be a prognostic indicator and a parameter for choosing appropriate therapeutic regimen.

30 November 2018 in PLOS ONE
Verified
Journal Article
Open access
PDF file
LMLuisa H. M. Miranda
Luisa H. M. Miranda
MMMarina Meli
Marina Meli
FCFátima Conceição-Silva
Fátima Conceição-Silva
MNMarilisa Novacco
Marilisa Novacco
RMRodrigo Caldas Menezes
Rodrigo Caldas Menezes
Regina Hofmann-LehmannRegina Hofmann-Lehmann
Regina Hofmann-Lehmann
Feline sporotrichosis due to Sporothrix brasiliensis is frequently severe and often correlated to zoonotic transmission. Feline Immunodeficiency Virus (FIV) and Feline Leukemia Virus (FeLV) cause immunodeficiency in cats; no association has been identified with critical cases of sporotrichosis. Moreover, the cytokine profile in Sporothrix-infected cats and a potential impact of retrovirus co-infections on their immunity is unknown. This study assessed immunological parameters in cats with sporotrichosis with and without FIV or FeLV co-infection. FeLV infection was detected by antigen ELISA and by provirus PCR. FIV infection was investigated through ELISA and Western blot. Cytokine transcription (IFN-γ, IL-4, IL-5, IL-6, IL-10, IL-12, TNF-α) was quantified using RT-qPCR and lymphocyte subpopulations (CD4, CD8, CD5 and CD21) were assessed by flow cytometry. Thirty cats with sporotrichosis were recruited to the study, including three FIV-positive and five FeLV-positive (progressive infection) cats. One cat with regressive FeLV infection was excluded from statistics. In comparison to retrovirus-negative cats, FIV-positive cats and FeLV-positive cats had higher IL-10 levels, FeLV-positive cats had lower IL-4 levels and FIV-positive cats had lower IL-12 levels and a lower CD4+/CD8+ ratio. Remarkably, all cats with poor general condition were FeLV (progressive infection) or FIV-positive, but the retrovirus status was not associated with the sporotrichosis treatment length or outcome. The immunological changes and the more severe clinical presentation observed in cats with retrovirus co-infections encourage future prospective studies that address the impact of these changes on prognostic determinants of feline sporotrichosis and the development of new therapy strategies that control disease spread.

10 April 2009 in Mycopathologia
Verified
Journal Article
Closed access
PDF file
LMLuisa H. M. Miranda
Luisa H. M. Miranda
LQLeonardo Quintella
Leonardo Quintella
ISI. B. dos Santos
I. B. dos Santos
RMRodrigo Caldas Menezes
Rodrigo Caldas Menezes
FFF. B. Figueiredo
F. B. Figueiredo
TST. M. P. Schubach
T. M. P. Schubach