Literature DB >> 10691092

Influence of the genetic background on the pattern of lesions developed by resistant and susceptible mice infected with Paracoccidioides brasiliensis.

C F Xidieh1, H L Lenzi, V L Calich, E Burger.   

Abstract

To compare the sequential evolution of lesions developed by resistant (A/Sn) and susceptible (B10.A) mice to Paracoccidioides brasiliensis infection we inoculated a virulent isolate of the fungus and collected the pancreas/peripancreatic omentum monthly (from 1 to 6 months) post infection. After fixation, tissue sections were stained by conventional methods for light microscopy to investigate the cellular composition, the extracellular matrix (ECM) patterns and the morphology of the yeasts in the lesions. In both strains, the fungal lesions were localized mostly in the omentum; a few lesions in the pancreatic parenchyma were observed, mostly in B10.A mice. In both strains, macrophages and plasmocytes were the predominant cells in all lesions, followed by neutrophils (PMN) and macrophages transformed into giant and epithelioid cells. Remarkable differences were observed between resistant and susceptible mice, specially related to the ECM structure of the granulomatous lesions. In A/Sn mice, from the 1st month on, the coexistence of two types of lesions was observed: one type showed a well-defined encapsulated nodule, constituted mainly of type I collagen. Neutrophils were abundant in areas of massive fungal destruction and few viable yeasts were observed. The other type showed residual characteristics, with sparse collagen deposits and presence of xantomatous-like macrophages, containing degenerated fungi. Such residual lesions predominated after the 2nd month and were the only type observed from the 4th month on, indicating the control of the infection. In B10.A mice, on the contrary, only one type of lesion was observed, showing less tendency to encapsulation and the formation of multiple small granulomatous foci, individualized by reticular type III collagen fibers. There were many plasmocytes in the periphery and large numbers of budding yeasts, with no evidence of fungal destruction. In the course of the infection the lesions progressively increased in number and size. Altogether, the comparative histopathological analysis demonstrates the influence of the genetic pattern of the host on the lesions developed by resistant and susceptible mice to P. brasiliensis infection.

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Year:  1999        PMID: 10691092     DOI: 10.1007/s004300050103

Source DB:  PubMed          Journal:  Med Microbiol Immunol        ISSN: 0300-8584            Impact factor:   3.402


  10 in total

1.  Intercellular adhesion molecule-1 is required for the early formation of granulomas and participates in the resistance of mice to the infection with the fungus Paracoccidioides brasiliensis.

Authors:  Ana P Moreira; Ana P Campanelli; Karen A Cavassani; Janeusa T Souto; Beatriz R Ferreira; Roberto Martinez; Marcos A Rossi; João S Silva
Journal:  Am J Pathol       Date:  2006-10       Impact factor: 4.307

2.  Paracoccidioidomycosis: reduction in fungal load and abrogation of delayed-type hypersensitivity anergy in susceptible inbred mice submitted to therapy with trimethoprim-sulfamethoxazole.

Authors:  Renata Scavone; Eva Burger
Journal:  Med Microbiol Immunol       Date:  2003-06-28       Impact factor: 3.402

3.  Matrix metalloproteinases with gelatinolytic activity induced by Paracoccidioides brasiliensis infection.

Authors:  Angela Satie Nishikaku; Luciana Cristina Ribeiro; Raphael Fagnani Sanchez Molina; Bernardo Paulo Albe; Cláudia da Silva Cunha; Eva Burger
Journal:  Int J Exp Pathol       Date:  2009-10       Impact factor: 1.925

4.  B cell-deficient mice display enhanced susceptibility to Paracoccidioides brasiliensis Infection.

Authors:  F S M Tristão; L A Panagio; F A Rocha; K A Cavassani; A P Moreira; M A Rossi; J S Silva
Journal:  Mycopathologia       Date:  2013-06-14       Impact factor: 2.574

5.  Nitric oxide participation in granulomatous response induced by Paracoccidioides brasiliensis infection in mice.

Authors:  Angela Satie Nishikaku; Raphael Fagnani Sanchez Molina; Luciana Cristina Ribeiro; Renata Scavone; Bernardo Paulo Albe; Cláudia Silva Cunha; Eva Burger
Journal:  Med Microbiol Immunol       Date:  2009-04-10       Impact factor: 3.402

6.  Structural and topographic dynamics of pulmonary histopathology and local cytokine profiles in Paracoccidioides brasiliensis conidia-infected mice.

Authors:  Damaris Lopera; Tonny W Naranjo; Oswaldo G Cruz; Angela Restrepo; Luz Elena Cano; Henrique Leonel Lenzi
Journal:  PLoS Negl Trop Dis       Date:  2011-07-12

7.  Low-level laser therapy to the mouse femur enhances the fungicidal response of neutrophils against Paracoccidioides brasiliensis.

Authors:  Eva Burger; Ana Carolina S C Mendes; Giulia M A C Bani; Maísa R P L Brigagão; Gérsika B Santos; Luiz Cosme C Malaquias; Jorge Kleber Chavasco; Liana M Verinaud; Zoilo P de Camargo; Michael R Hamblin; Felipe F Sperandio
Journal:  PLoS Negl Trop Dis       Date:  2015-02-12

Review 8.  Regulatory T cells in paracoccidioidomycosis.

Authors:  Vera L G Calich; Ronei L Mamoni; Flávio V Loures
Journal:  Virulence       Date:  2018-08-01       Impact factor: 5.882

Review 9.  Paracoccidioidomycosis: Current Perspectives from Brazil.

Authors:  Rinaldo Poncio Mendes; Ricardo de Souza Cavalcante; Sílvio Alencar Marques; Mariângela Esther Alencar Marques; James Venturini; Tatiane Fernanda Sylvestre; Anamaria Mello Miranda Paniago; Ana Carla Pereira; Julhiany de Fátima da Silva; Alexandre Todorovic Fabro; Sandra de Moraes Gimenes Bosco; Eduardo Bagagli; Rosane Christine Hahn; Adriele Dandara Levorato
Journal:  Open Microbiol J       Date:  2017-10-31

10.  Resistance to P. brasiliensis Experimental Infection of Inbred Mice Is Associated with an Efficient Neutrophil Mobilization and Activation by Mediators of Inflammation.

Authors:  Felipe Fornias Sperandio; Gisele Pesquero Fernandes; Ana Carolina Silvério Cerqueira Mendes; Giulia Maria de Alencar Castro Bani; Vera Lucia Garcia Calich; Eva Burger
Journal:  Mediators Inflamm       Date:  2015-12-24       Impact factor: 4.711

  10 in total

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