Paracoccidioides brasiliensis pancreatic destruction in Calomys callosusexperimentally infected
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The wild rodent Calomys callosus is notably resistant to Trypanosoma cruzi infection. In order to better characterize this animal model for experimental infections, we inoculated C. callosus intraperitoneally with Paracoccidioides brasiliensis, a thermally dimorphic fungus that causes a chronic disease with severe granuloma formation in the mouse and humans. The dissemination of P. brasiliensis cells through the lungs, liver, pancreas, and spleen was assessed by histological analysis.
The animals were susceptible to infection and showed a granulomatous reaction. C. callosus presented peritonitis characterized by the presence of exudates containing a large number of yeast cells. Extensive accumulation of yeast cells with intense destruction of the parenchyma was observed in the pancreas, which reduced the glucose levels of infected animals. These lesions were regressive in the liver, spleen, and lungs until complete recovery. The role of estrogen during C. callosus infection with P. brasiliensis was addressed by infecting ovariectomized animals. It was observed a reduced inflammatory response as well as reduced extension of tissue damage. Removal of ovaries reestablished the normal glucose levels during infection.
Taken together, the results presented here reveal the pancreas as being an important organ for the persistence of P. brasiliensis during infection of C. callosus and that estrogen plays an important role in the susceptibility of the animals to this pathogen.
KeywordsEstrogen Yeast Cell Infected Animal Granuloma Formation Trypanosoma Cruzi
Calomys callosus (Rodentia-Cricetidae), a wild rodent, exists near farm residences in savannas and cattle breeding areas. It has been adapted to be bred in captivity under controlled laboratory conditions and values for reproductive parameters, such as age at reproduction, pregnancy time, number of litters, male/female ratio, growth curve, and some external anatomical values have also been determined [1, 2]. Laboratory inbred strain was obtained for experimental purpose [3, 4]. This rodent has been described as a reservoir of Trypanosoma cruzi, the causative agent of Chagas disease and of the hantaviroses, zoonoses caused by the Bunyaviridae family [5, 6].
C. callosus naturally and experimentally infected with T. cruzi presents high parasitaemia values during the presumable first days of infection, which progressively decreases until becoming negative a few weeks later showing regression of the lesions within a few days . The infection is accompanied by inflammation of both myocardium and skeletal muscle characterized initially by an infiltrate containing macrophages, fibroblasts and small numbers of lymphocytes. Although the mechanism underlying the resistance of C. callosus to T. cruzi infection is not totally understood, its ability to control and avoid tissue lesions might be a key factor involved in its resistance to pathogens [5, 6, 8, 9]. Nevertheless, when C. callosus was experimentally infected with Toxoplama gondii, they were highly susceptible and all animals died on the acute phase of the infection .
Paracoccidioides brasiliensis is a thermally dimorphic fungus that causes a chronic disease with severe granuloma formation widely spread in Latin America . Different P. brasiliensis strains have been evaluated in the mouse model of infection showing notably differences in the susceptibility pattern [12, 13]. Because of the unique response of C. callosus to different pathogens they may be useful as an animal model for the development of experimental infections by P. brasiliensis. A recent work showed that C. callosus succumbs to the P. brasiliensis strain 18 infection, presenting evidence of inflammatory reaction in several organs and specific humoral response to P. brasiliensis antigens . Natural infection of C. callosus with P. brasiliensis has not yet been reported even though they reside in endemic areas of Paracoccidioidomycosis (PCM). The mechanisms underlining the protective immune response for PCM seems to involve estrogen, because women tend to be more resistant to the infection, added to the fact that estrogen avoids the transition from conidia to yeast, the infective form of infection [11, 15].
A P. brasiliensis strain isolated from a patient in the Brazilian savannas (PB01) was shown to be more virulent than the strain 18 . This study was designed to analyze the infection of C. callosus with PB01 strain by investigating the inflammatory lesions in several organs as well as to investigate the role of estrogen in the susceptibility of the animals. In order to evaluate whether estrogen affects the C. callosus susceptibility, the ovaries were removed because they are the main source of estrogen.
In this report we present data supporting the susceptibility of C. callosus to infection with PB01 strain, which is resolved after 90 days in the liver, lungs, and spleen, but viable fungi remained during all studied time in the pancreas. We also demonstrate that the persistence of the fungus in the pancreas alters glucose levels. Evidence is shown about the involvement of estrogen in the inflammatory response.
Fungal suspensions and growth conditions
Paracoccidioides brasiliensis, strain 01 was provided by the Mycology collection of Research Center for Tropical Pathology – Federal University of Goiás. The yeast forms were grown on solid Fava Netto agar medium at 37°C. After 7 days, the yeast cells were harvested, washed in sterile saline, and adjusted to 108 cells/mL based on haemocytometer counts. Viability, determined by the fluorescein and ethidium bromide staining methods, was always higher than 85% .
Adult female C. callosus (8–12 weeks) were used throughout this study. The animals were bred in the Animal Facilities of the University of São Paulo and Research Center for Tropical Pathology – Federal University of Goiás. The animals were handled and maintained under strict ethical conditions according to the international recommendations for animal welfare (NIH Publication n° 23, 1985) and the Ethical Committee for human and animal sciences of Federal University of Goiás (012/1999).
In order to evaluate the blood leukocyte and glucose levels of C. callosus infected with P. brasiliensis, the animals were i.p. injected followed by macroscopic and microscopic evaluations done at days 7, 15, 30, 45, 60, and 75 post infection (three to four animals were analyzed per group at each time point of infection). The organs showing macroscopic lesions were selected for further analysis. Control groups consisted of three animals per time point inoculated with sterile saline.
To determine the role of estrogen during P. brasiliensis infection, an additional C. callosus group (seventy animals) was subdivided into two sets: one being bilaterally ovarectomized (31 animals) and the other sham-operated (39 animals). Forty days after surgery, all animals were inoculated in the peritoneum with 1 × 106 viable infective forms of P. brasiliensis. An additional control group consisting of non-operated and non-infected animals (5 animals per time point) received only saline injection.
On days 15, 45, 60, and 75 of infection, two to three animals from each group were sacrificed, grossly inspected, and fragments of mesentery, liver, spleen, pancreas, and lungs were collected and fixed in 10% formaldehyde. Representative sections from each organ were embedded in paraffin, processed and stained with haematoxilin-eosin (HE). Quantification of the lesion extensions was determined using a computer-aided densitometric software (OPTIMAS Bioscan Inc. WA, USA). For each organ, five slides with tissue sections were entirely evaluated. The number and area of the granulomas were determined, and the extent of tissue section occupied by the lesion was calculated by dividing the area occupied with lesions by the total area of the organ.
Leukocyte counts and glucose levels
Blood samples for leukocyte counts or glucose determinations were withdrawn from the retro-orbital plexus. Leucocytes were counted in a haemocytometer and the results were reported as number of leukocytes per mL of blood. Serum glucose levels were determined by the method of Trinder  and reported as mg/dL.
PB01 infection in Calomys callosus
Effect of P. brasiliensis infection on glucose blood levels of C. callosus
Effect of ovariectomy on P. brasiliensis infection of C. callosus
Discussion and conclusion
Several species of wild animals are known to harbor many types of infectious agents. The induced infections usually are silent, most likely due to efficient immunologic mechanisms of resistance resulting from years of co-evolution of hosts and pathogens. In nature, armadillos (Dasypus noveminctus) were found infected with P. brasiliensis in endemic area [20, 21]. C. callosus and human beings in endemic area of paracoccidioidomycosis constitute one example in which pathogenic fungus and a regional well established rodent are living in a close environmental relationship. However, there are no reports describing C. callosus infected with P. brasiliensis in nature. The lack of such information can be alternatively ascribed either to a complete resistance of C. callosus to the fungus or to an efficient immune resistance developed by the host. The later hypothesis is however the most probable in face of the demonstration in this present report and by others , that this rodent can be experimentally infected with P. brasiliensis.
The granuloma formation in PCM varies in humans and experimental animals according to several factors such as inoculum, route of infection, host susceptibility, and resistance. Previously, it was shown that using a virulent P. brasiliensis 18 strain, C. callosus presented a destructive granuloma formation and disease progression . However, that work failed to show the lesion and granuloma formation in several other important organs. The present work demonstrated for the first time that these animals showed a different inflammatory response at the inoculation area (peritoneum and pancreas) compared to disseminated areas (liver and lungs). The granulomatous reaction organized in C. callosus infected with P. brasiliensis in the spleen, liver, and lungs, was characterized by an inflammatory cell infiltrate rich in epithelioid cells scattered over the lesions, in contrast to the organized granulomas observed in the mouse model of infection . The number of viable fungi diminished quickly in spleen, liver and lungs during the infection until complete disappearance after 60 days of observation. The disagreement between our findings and a recently published data  could be attributed to several important factors such as host susceptibility characteristics as a consequence of different C. callosus genetic backgrounds, ours being isogenic strains ; animal housing conditions; and P. brasiliensis strain virulence differences due to a distinct P. brasiliensis isolate (PB01), and laboratory culture collection maintenance procedures. Our results are consistent with the pattern of experimental infection of C. callosus with T. cruzi, where all the infected animals survived but had positive parasitological tests, until the end of the experiments. The lesions induced by this parasite were characterized by severe inflammation in the myocardium and skeletal muscle, which gradually subsided becoming absent or residual on the 64th day of infection [1, 6, 9, 22]. Thus, with two distinct infection agents, P. brasiliensis and T. cruzi, C. callosus, although able to acquire experimental infections, became cured or without detectable tissue lesions as the time elapsed.
Despite the fact that lungs, liver, and lymph nodes showed no detectable lesions in the chronic phase of infection, C. callosus developed persistent pancreatic infection. This observation may be due to the local peritoneal involvement, as a consequence of the inoculation site. Similarly, macroscopical observations revealed that the minor omentum was the most affected tissue by the infection, which is colocalized with the pancreas. These findings prompted us to address the question whether the fungi growth alters the endocrine homeostasis of C. callosus. As the infection with P. brasiliensis destroys the pancreas, one would expect alterations on glucose serum levels affecting the survival of the animals but, surprisingly, in our experiments C. callosus had a long term surviving curve (more than 250 days after the infection, Fig. 2). This hypothesis was confirmed by our results as C. callosus infected with P. brasiliensis showed a significant reduction of glucose levels as infection progressed (Fig. 3 and 5). Taken together, these data infer that the infection progression develops differently in accordance to the anatomical site, reinforcing that the pancreas could present an adequate environment for the fungi development.
As seen in several infectious disease models, P. brasiliensis infection also induces leukocytosis. The leukocytes blood levels were higher during the infection as compared with the non-infected animals (Fig. 4A, day 0). C. callosus presented two distinct leukocytosis peaks flanked by periods of normal blood cell counts. It is interesting to note that when lymphocytes and monocytes blood levels were higher, the granulomatous reaction unexpectedly presented polymorphonuclear cells (PMC) and mononuclear cells (MNC). An interesting observation was the presence of eosinophils seen in the granulomas and in the blood of infected animals at the early stages, a fact that is not present during infection in the mouse model [4, 13]. The presence of eosinophils in the analyzed organs, except the pancreas, correlated positively with parasite clearance. A diverse picture of granulomas was however observed coinciding with the second peak of leukocytosis: high monocyte blood cells counts and predominance of macrophages in the granuloma cell infiltrates. The persistence of the leukocytosis until 105 and 120 days of infection could be ascribed to higher colonization of the pancreas by the fungi, in view of the fact that at the correspondent time the lesions in the others organs had attained complete recovery.
Paracoccidioidomycosis incidence in humans appears to be higher in men than in women [11, 15]. This difference being attributed either to inhibition of the conversion of mycelium into yeast forms of growth provoked by estrogen or by non-specific host resistance to the fungus . The analysis of mechanisms underlying estrous cycle and host resistance to P. brasiliensis has been reported . Sano et al,  showed that even using three different inoculation routes, the clearance of the yeast cells in mice, was influenced by the estrogen presence. All female mice presented lower bacterial burden in the blood, peritoneal cavity, and lungs when compared with males. In order to verify if such gender-determined resistance also occurs in C. callosus we investigated the effect of the estrogen using ovariectomized animals to eliminate the source of estrogen. The lesions found in sham-operated and ovariectomized animals were equally occupied by large numbers of the fungi. Despite having the same amount of fungi, the sham-operated group presented a more vigorous liver inflammatory response. We also showed that ovariectomized infected C. callosus presented more organized granulomatous lesions with fewer pancreatic lesions. Thus the inflammatory response to P. brasiliensis was directly affected by the absence of the estrogen which could be one of the aspects contributing to the susceptibly of the disease.
Although, in ovariectomized animals the lesions in liver, spleen, and lungs rapidly evolved to the reorganization of the organ structures, the fungus progressively colonized the pancreas. The process of pancreas colonization was gradual, occurring in both ovariectomized and sham-operated animals (Fig. 7A). Therefore, it can be suggested that C. callosus is capable of sequestering the yeast forms of P. brasiliensis in the pancreas allowing their reproduction, without dissemination. The mechanisms underlying such fungus tropism to a particular organ deserve further investigation.
Estrogen hormones positively affect the synthesis and release of insulin by pancreatic cells . The extensive colonization of the pancreas by fungi was expected to disturb the functions controlled by this organ. Indeed sham-operated C. callosus presented along the infection reduction of glucose blood levels, when compared with the non-infected sham-operated animals. The decrease in glucose levels was not observed in ovariectomized and infected animals, supporting the protective effect exerted by the absence of the estrogen during infection.
In this study, it was observed: a) The experimental infection of C. callosus by P. brasiliensis is different from the other animal models since the organized granulomatous lesions are more diffuse and gradually diminished, b) In C. callosus the pancreas were persistently infected, c) The function of the pancreas was affected by the infection of C. callosus, and d) The presence of estrogen directly affected the pancreas function of infected animals. The results presented here show a predisposition of the P. brasiliensis to grow in the pancreas of C. callosus.
Supported by grant from Conselho Nacional de Pesquisa – CNPq-Brasil N° 471348/2004-0.
- 1.Mello DA, Valin E, Teixeira ML: Alguns aspectos do comportamento de cepas silvestres de Trypanosoma cruzi em camundongos e Calomys callosus (Rodentia). Rev Saúde Pública S. Paulo. 1979, 13: 314-322.Google Scholar
- 2.Hodara VL, Kajon AE, Quintans C, Montoro L, Merani MS: Parametros metricos y reproductivos de Calomys musculinus (Thomas, 1913) y Calomys callidus (Thomas, 1916) (RODENTIA, CRICETIDAE). Revista del Museo Argentino de Ciencia Naturales e Instituto Nacional de Las Ciencias Naturales. 1984, 3: 453-459.Google Scholar
- 4.Silva LS, Santa Ana-Limongi LC, Kipnis A, Junqueira-Kipnis AP: Perfil de migração celular agudo induzido pela presença de corpo estranho em Calomys callosus. Ciência Animal Brasileira. 2008, 9 (2): 462-469.Google Scholar
- 5.Ribeiro RD: New reservoirs of Trypanosoma cruzi. Rev Bras Biol. 1973, 33:Google Scholar
- 7.Magalhães-Santos IF, Souza MM, Lima CSC, Andrade SG: Infection of Calomys callosus (Rodentia Cricetidae) with Strains of Different Trypanosoma cruzi Biodermes: Pathogenicity, Histotropism, and Fibrosis Induction. Mem Inst Oswaldo Cruz. 2004, 99: 407-413. 10.1590/S0074-02762004000400011.PubMedCrossRefGoogle Scholar
- 12.Arruda C, Valente-Ferreira RC, Pina A, Kashino SS, Fazioli RA, Vaz CA, Franco MF, Keller AC, Calich VL: Dual role of interleukin-4 (IL-4) in pulmonary: endogenous IL-4 can induce protection or exacerbation of disease depending on the host genetic pattern. Infect Immun. 2004, 72 (7): 3932-40. 10.1128/IAI.72.7.3932-3940.2004.PubMedCentralPubMedCrossRefGoogle Scholar
- 16.Carrero LL, Niño-Vega G, Teixeira MM, Carvalho MJ, Soares CM, Pereira M, Jesuino RS, McEwen JG, Mendoza L, Taylor JW, Felipe MS, San-Blas G: New Paracoccidioides brasiliensis isolate reveals unexpected genomic variability in this human pathogen. Fungal Genet Biol. 2008, 45 (5): 605-12. 10.1016/j.fgb.2008.02.002.PubMedCrossRefGoogle Scholar
- 20.Naïf D, Ferreira LCL, Barret TV, Naiff MF, Arias JR: Paracoccidioidomicose enzoótica em tatus (Dasypus noveminctus) no Estado do Pará. Ver per Rev. 1986, 28 (1): 19-27.Google Scholar
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