Molecular detection of Pneumocystis in the lungs of cats.


Journal

Medical mycology
ISSN: 1460-2709
Titre abrégé: Med Mycol
Pays: England
ID NLM: 9815835

Informations de publication

Date de publication:
01 Oct 2019
Historique:
received: 04 09 2018
revised: 09 11 2018
accepted: 16 11 2018
pubmed: 20 12 2018
medline: 29 1 2020
entrez: 20 12 2018
Statut: ppublish

Résumé

The genus Pneumocystis comprises potential pathogens that reside normally in the lungs of a wide range of mammals. Although they generally behave as transient or permanent commensals, they can occasionally cause life-threatening pneumonia (Pneumocystis pneumonia; PCP) in immunosuppressed individuals. Several decades ago, the presence of Pneumocystis morphotypes (trophic forms and cysts) was described in the lungs of normal cats and cats with experimentally induced symptomatic PCP (after immunosuppression by corticosteroids); yet to date spontaneous or drug-induced PCP has not been described in the clinical feline literature, despite immunosuppression of cats by long-standing retrovirus infections or after kidney transplantation. In this study, we describe the presence of Pneumocystis DNA in the lungs of normal cats (that died of various unrelated causes; n = 84) using polymerase chain reactions (PCRs) targeting the mitochondrial small and large subunit ribosomal RNA gene (mtSSU rRNA and mtLSU rRNA). The presence of Pneumocystis DNA was confirmed by sequencing in 24/84 (29%) cats, with evidence of two different sequence types (or lineages). Phylogenetically, lineage1 (L1; 19 cats) and lineage 2 (L2; 5 cats) formed separate clades, clustering with Pneumocystis from domestic pigs (L1) and carnivores (L2), respectively. Results of the present study support the notion that cats can be colonized or subclinically infected by Pneumocystis, without histological evidence of damage to the pulmonary parenchyma referable to pneumocystosis. Pneumocystis seems most likely an innocuous pathogen of cats' lungs, but its possible role in the exacerbation of chronic pulmonary disorders or viral/bacterial coinfections should be considered further in a clinical setting.

Identifiants

pubmed: 30566653
pii: 5253597
doi: 10.1093/mmy/myy139
pmc: PMC7107658
doi:

Substances chimiques

DNA, Fungal 0
RNA, Mitochondrial 0
RNA, Ribosomal 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

813-824

Informations de copyright

© The Author(s) 2018. Published by Oxford University Press on behalf of The International Society for Human and Animal Mycology.

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Auteurs

Patrizia Danesi (P)

Istituto Zooprofilattico Sperimentale delle Venezie, Legnaro (PD), Italy.

Michela Corrò (M)

Istituto Zooprofilattico Sperimentale delle Venezie, Legnaro (PD), Italy.

Christian Falcaro (C)

Istituto Zooprofilattico Sperimentale delle Venezie, Legnaro (PD), Italy.

Antonio Carminato (A)

Istituto Zooprofilattico Sperimentale delle Venezie, Legnaro (PD), Italy.

Tommaso Furlanello (T)

Clinica Veterinaria San Marco, Padua, Italy.

Monia Cocchi (M)

Istituto Zooprofilattico Sperimentale delle Venezie, Legnaro (PD), Italy.

Mark B Krockenberger (MB)

Veterinary Pathology Diagnostic Services, Sydney School of Veterinary Science, University of Sydney, Sydney, New South Wales, Australia.

Wieland Meyer (W)

Molecular Mycology Research Laboratory, Centre for Infectious Diseases and Microbiology, Faculty of Medicine and Health, Westmead Clinical School, Marie Bashir Institute for Emerging Infectious Diseases and Biosecurity, University of Sydney, Westmead Hospital, Westmead Institute for Medical Research, Sydney, Australia.

Gioia Capelli (G)

Istituto Zooprofilattico Sperimentale delle Venezie, Legnaro (PD), Italy.

Richard Malik (R)

Centre for Veterinary Education, B22, University of Sydney, Sydney, New South Wales, Australia.

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Classifications MeSH