An improved high-performance liquid chromatography (HPLC) method for detection of variations in the hydroxyproline content of tissue homogenates from Paracoccidioides brasiliensis-infected mice
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Detection of Modified Forms of Cytosine Using Sensitive Immunohistochemistry
Published on: August 16, 2016
Magnus Ake Gidlund1, Raphael Fagnani Sanchez Molina2, Eva Burger2
1Department of Immunology, Institute of Biomedical Sciences (ICB), University of São Paulo (USP), São Paulo, SP, Brazil.
Background:
Paracoccidioidomycosis (PCM) is a severe granulomatous disease. The hallmark of this mycosis is fibrin degradation and granuloma formation as a result of a wound-healing process in the context of excessive inflammation. Therefore, as the content of collagen can be assessed by the methodology described in this manuscript, we propose that the content of hydroxyproline (HYP) be employed as a new and efficient measurement of granulomatous lesions developed. To estimate the level of HYP the major byproduct of the degradation process, we hypothesized that this simple and efficient technique could serve as a marker of disease severity.
Methods:
Five B10.A female mice were infected with P. brasiliensis and, after 15 days, the omentum was removed, subjected to histopathological analysis or processed (i.e. deproteinized and derivatized), and further analyzed on a reverse phase HPLC using a C-18 column. The omentum of five uninfected controls was also collected and similarly analyzed.
Results:
Infected mice showed numerous, disseminated paracoccidioidomycotic lesions, as well as marked collagen deposits, as observed in histopathologic analysis, and high levels of HYP. Normal uninfected mice showed no granulomas, little or no deposits of collagen fibers, and very low levels of HYP, as evaluated by HPLC. Our results show that the disease intensity as evaluated number and the morphology of the granulomatous lesions were correlated to the HYP levels using small tissue samples from the omentum, the main target organ of P. brasiliensis.
Conclusions:
Here we propose an alternative methodology to follow disease evolution and, to some extent, fungal load in experimental P. brasiliensis infection and suggest its usefulness to other diseases with pronounced fibrin degradation.
Insights
Hydroxyproline (HYP) levels effectively measure granulomatous lesions in paracoccidioidomycosis (PCM). This method correlates HYP concentration with disease severity, offering a new tool for monitoring fungal infections.
Area of Science:
- Mycology
- Immunology
- Biochemistry
Background:
- Paracoccidioidomycosis (PCM) is a severe granulomatous fungal disease characterized by fibrin degradation and excessive inflammation.
- The wound-healing process in PCM involves granuloma formation, with collagen content potentially reflecting disease progression.
Purpose of the Study:
- To propose hydroxyproline (HYP) content as a novel and efficient biomarker for quantifying granulomatous lesions in PCM.
- To establish HYP as a marker for assessing disease severity in experimental fungal infections.
Main Methods:
- Infection of B10.A mice with *P. brasiliensis* and subsequent omentum tissue collection after 15 days.
- Histopathological analysis of omentum for granuloma assessment.
- High-performance liquid chromatography (HPLC) analysis of deproteinized and derivatized omentum tissue to quantify HYP levels.
Main Results:
- Infected mice exhibited disseminated paracoccidioidomycotic lesions and significantly higher HYP levels compared to uninfected controls.
- Histopathology revealed marked collagen deposits in infected mice, correlating with elevated HYP.
- A positive correlation was observed between the number and morphology of granulomatous lesions and measured HYP levels.
Conclusions:
- Hydroxyproline (HYP) quantification serves as an effective method for evaluating disease intensity in experimental *P. brasiliensis* infection.
- This HYP measurement technique can be a valuable tool for monitoring disease evolution and potentially fungal load.
- The proposed methodology may also be applicable to other diseases involving significant fibrin degradation.

