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Influence of inflammation on parasitism and area of experimental amoebic liver abscess: an immunohistochemical and morphometric study
© Costa et al; licensee BioMed Central Ltd. 2011
- Received: 27 October 2010
- Accepted: 28 February 2011
- Published: 28 February 2011
The influence of inflammation on the number of trophozoites and on the murine amoebic liver abscess area following infection with Entamoeba histolytica and E. dispar was evaluated. Immunohistochemistry and digital morphometry were used to identify and quantify the trophozoites, neutrophils, macrophages, and lesions. Positive correlation was observed between the number of trophozoites and inflammatory cells. A significant decrease in parasitism and inflammation in groups treated with dexamethasone was observed. The scarceness or absence of trophozoites in the treated groups suggest the importance of the inflammatory response in the production of amoebic hepatic abscesses in spite of the inherent virulence of the parasite being decisive in the establishment of the lesion.
- Inflammatory Infiltrate
- Hepatic Parenchyma
- Hepatic Necrosis
- Entamoeba Histolytica
Amoebiasis is a disease caused by the protozoan Entamoeba histolytica through oral infection by cysts followed by colonization or tissue invasion by trophozoites in the large intestine. Annually, about 50 million people are infected, causing approximately 100,000 deaths . After the colonic mucosa is damaged, the trophozoites may reach the bloodstream and liver, producing the amoebic hepatic abscess, which is the most common extra-intestinal form of amoebiasis . The typical amoebic lesion is characterized by a liquefactive necrosis zone with edges consisting of cellular debris and polymorph-histiocitary inflammatory infiltrate. Such necrosis is produced by trophozoite derivatives, such as amoebapores (polypeptides capable of forming pores in the hosts' cells), cysteine proteinases (enzymes that cleave collagen, elastin, fibrinogen, and laminin), and galactose/N-acetylgalactosamine lectin (Gal/GalNac) (a CD59 like molecule capable of inhibiting the C5b-9 complex of the complement, inducing apoptosis and stimulating the production of IL-1α, IL-1β, and IL-8).
Controversial results have been published about the role of inflammation on the pathogenesis of amoebic necrosis. The inflammatory infiltrate in amoebiasis is very discrete when compared to intense necrosis, suggesting that the inflammatory cells are destroyed, releasing their enzymatic content into the hepatic parenchyma . Radiation-induced leucopenia in hamsters followed by trophozoites inoculation led to the reduction of inflammatory processes, hepatic necrosis, and parasitism . On the other hand, mice infected with E. histolytica and previously treated with anti-neutrophil monoclonal antibodies developed liver necrosis with the same dimensions as those of the control group, and those lesions were probably produced by products secreted by the amoeba itself .
Considering the doubts that still persist about amoebic pathogenesis, we assessed the influence of inflammation in necrosis and in hepatic parasitism in mice inoculated with E. histolytica. For comparison purposes, we used the non-pathogenic species E. dispar, which can produce experimental lesions similar to those of E. histolytica and that has contributed to the understanding of the pathogenesis of amoebiasis [5, 6]. Trophozoites from both strains, neutrophils, and macrophages were identified by immunohistochemistry and quantified by digital morphometry.
All procedures were conducted according to principles established by the Ethics Committee on Animal Experimentation of the UFMG. Ten Swiss mice were intra-hepatically inoculated with 250,000 trophozoites of the EGG strain of E. histolytica or MCR strain of E. dispar, previously identified by zymodeme and PCR [7, 8]. Half of the animals were previously treated with two doses (0.5 mg/Kg) of dexamethasone, subcutaneously, 24 and 01 h before inoculation (Groups EGG-DEX and MCR-DEX) and, the other half received only buffered saline (Groups EGG and MCR).
The animals were euthanized on the second day of infection, three slices of the left lobe of the liver were collected, fixed in buffered formaldehyde 10%-pH 7.2, and scanned by a Sony MVC-CD400/CD250 digital camera for the morphometry of the amoebic necrosis. After dehydration, clearing and paraffin embedding of the slices, 4 μm thick cuts were obtained and stained with Haematoxylin and Eosin (H&E).
Using a JVC-TK 1270 microcamera (JVC, Japan) and a 40× objective lens, 30 random images of immunohistochemical reactions against trophozoites were scanned, covering a total of 1.6 × 106 mm2 analyzed hepatic parenchyma for the counting of trophozoites by that software. The macrophages and neutrophils were quantified on the edges of the necrosis using the same methodology. The distribution of continuous variables was assessed by the Shapiro-Wilk test, and this indicated normal distribution in all cases. Thus, the Student t test was used for comparison between groups, and differences with p < 0.05 were considered statistically significant. Data were expressed as mean ± standard deviation for parametric variables. The Pearson r was used for correlation analysis.
To exclude the possibility of amebicidal activity of dexamethasone, the growth inhibition of E. histolytica and E. dispar cultures associated with the drug was assessed. For this, 240,000 trophozoites were grown in 6 mL of medium at 37°C and associated with dexamethasone in concentrations ranging of 40 to 800 mg/mL for 48 hours. The tests were done in triplicate and repeated one time. There was no interference of drugs on the growth and development of cultures even in higher concentrations.
Hepatic amoebic lesions were detected in all animals inoculated with E. histolytica or E. dispar. Within 48 hours of infection, the lesion was macroscopically visible in the left lobe; it had a yellowish-white color and was well defined.
The mean and the standard deviation of the hepatic necrosis area in animals inoculated with E. histolytica of groups EGG and EGG-DEX were 2.95 ± 1.91 mm2 and 1.32 ± 0.44 mm2, respectively. In animals inoculated with E. dispar of groups MCR and MCR-DEX, they were 4.63 ± 2.96 mm2 and 2.62 ± 1.71 mm2, respectively. Although the mean area of necrosis proved to be arithmetically smaller in animals from both groups treated with dexamethasone, this difference between treatment groups was not significant by the Student's t-test (p > 0.05). The reduction of inflammation was associated with a small decrease in the necrotic area showing that necrosis in the untreated groups was mainly due to amoebic products. The secretion of amoebapores, cystein-proteinases, and Gal/GalNac lectin by the trophozoites also results in the destruction of neutrophils and the consequent liberation of their toxic products, which may play an important role in the amplification of amoebic lesions .
The quantitative analysis showed a significant decrease of macrophages on the edges of the necrosis zone of the animals in the MCR-DEX group (p < 0.05). The mean and the standard deviation of the number of macrophages in animals inoculated with E. dispar from groups MCR and MCR-DEX were 23 ± 8.91 and 5.8 ± 5.67, respectively. A positive correlation was observed between the fall in the number of trophozoites and the reduction in the number of macrophages in the necrotic zone (r = 0.6217; p = 0.0017) and the reduction in the number of neutrophils in the hepatic parenchyma (r = 0.3939; p = 0.04). In groups EGG (12.4 ± 3.4) and EGG-DEX (9.2 ± 8.2) there was no significant reduction in the number of macrophages at the edge of the lesion.
As expected, the treatment with dexamethasone reduced the inflammatory infiltrate, but, paradoxically, the number of trophozoites and necrotic area were smaller. Such results suggest that the inflammation normally observed during the amoebic pathogenesis favors the multiplication of trophozoites and, consequently, leads to an increase in the dimensions of the amoebic abscess area. It is possible that leukocytes and/or their products stimulate the transcription of amoebic toxic substances, amplifying the lesion. Additionally, a study performed with trophozoites marked with radioactivity showed that less resistant trophozoites were destroyed by inflammation, favoring the proliferation of more virulent parasites . This probable selection of parasites by the inflammatory process has also been indicated by our studies with the experimental model of amoebic liver abscess in hamster [13, 14]. In animals inoculated with either E. histolytica or E. dispar small numbers of trophozoites were found in the liver parenchyma after 12 hours of infection. However, within 24 hours of infection a significant increase of trophozoites was observed in mice infected with both species of amoebae (7 and 130 times in E. histolytica and E. dispar, respectively), showing that, although both produce experimental lesions, their mechanisms of adaptation to the host are different. Perhaps the lowest number of trophozoites observed in E. histolytica infection would be related to its higher virulence. E. histolytica produces greater amount and variety of proteolytic substances, leading not only to the destruction of host tissue but also of amoebae. No significant reduction observed in the number of macrophages at the edge of the lesion in the EGG group leads us to speculate that these cells are not major factors involved in virulence selection on E. histolytica.
The visualization of residual trophozoites with positive immunohistochemical staining for immunoglobulins and complement, suggests that these elements may be involved in the selection of more resistant parasites . Genotype differences from E. histolytica and E. dispar in stool- and liver abscess-derived samples from the same patients [15, 16] corroborate the selection hypothesis.
In spite of the earlier published controversial results about the importance of the inflammatory response in the production of amoebic hepatic abscesses, our results emphasise the crucial role of inflammation in pathogenesis and establishment of the lesion.
This work was supported by FAPEMIG (Fundação de Amparo à Pesquisa do Estado de Minas Gerais) and CNPq (Conselho Nacional de Desenvolvimento Científico e Tecnológico). The authors are grateful to João da Costa Viana, Jacqueline Vanessa C.C. de Moura and Gislene Arlindo da Silva for technical assistance.
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