Quantitative analytical technique applied to histopathology of birds infected experimentally by the virus of chicken anemia virus
© García et al; licensee BioMed Central Ltd. 2008
Published: 15 July 2008
This research was conducted on ten glass slides selected from the histopathology evaluation chickens. Five slides of control's chickens healthy and five slides of chickens infected experimentally with chicken anemia virus (CAV slide) between one and twenty-one days post infection (PI), they were analyzed in magnifications of 200× and 400×. Histopathology showed severe bone marrow hypoplasia to complete aplasia, fully depletion of the erythrocytic and granulocytic series, both accompanied by space occupying adipocytic replacement. Foci of erythropoietic hyperplasia with intense mielopoietic activity, some hemocytoblast increased of size, with large nucleus. A quantitative analytical technique by Positive Pixel Count Algorithm was applied. It demonstrated that measures area stained of control slides were higher than CAV slides (Average: 61% vs. 25%, respectively). So, the control slides showed strong positivity, due to the presence of bigger quantity of cells of erythrocytic and granulocytic series. The CAV slides of seven days PI had high positivity (average: 94%), it was explained because the chicken anemia virus takes place severe lesions between ten to seventeen days PI, after 21 days PI the cellular regeneration is observed that is evidenced by means of focuses of erythroblastoid cells hyperplasia. This technique demonstrates in a quantitative way the severe decrease of the cellular components of the bone marrow in presence of the infection for CAV, supporting with numeric data the histology image evaluated by the pathologist. Therefore, it can be used as support to the histopathology of field samples to evaluate the presence of lesions taken place by CAV and this way to improve the quality and efficiency of the veterinary pathology services.
Chicken anemia virus (CAV) is a small, non-enveloped, single-stranded DNA virus, first isolated by Yuasa et al. (1979), a Gyrovirus, within the family Circoviridae . The virus causes aplastic anaemia, generalized lymphoid atrophy and increased mortality after infection of day-old susceptible chickens . The virus causes severe depletion of cortical thymocytes and erythroblastoid cells in the bone marrow, leading to immunodeficiency and anemia , because the VAIA lacks the necessary enzymes to reproduce its DNA in an independent way, it requires the cells to be divided very quickly . The Positive Pixel Count is a multipurpose algorithm that measures area and intensity of staining for two-colored slides. This technique is useful as support to improve the histopathology evaluation making it objective by means of quantitative analytical techniques and this way, to improve the quality and efficiency of the pathology services. The purpose of this study was to apply quantitative analytical technique to histopathology of birds infected experimentally by the virus of chicken anemia virus.
Materials and methods
10 glass slides stained with H&E, selected of the histopathology evaluations of chickens. Five slides coming from chickens healthy controls and five slides coming from chickens infected experimentally with chicken anemia virus (CAV slide) between one and twenty one days PI, they were analyzed in m agnifications of 200× and 400×.
Positive Pixel Count Algorithm (Aperio®)
Positive Pixel Count is a multipurpose algorithm that measures area and intensity of staining for two-colored slides. Pixels are classified according to colour and intensity of staining. Pixel counts (area) are calculated for strong positive (Red), positive (Orange), weak positive (Yellow), and negative (Blue) pixels. This is useful for measuring positivity as a fraction of total stained area.
Number of Strong Positive and Positivity (%) of Control slides and CAV slides in magnification 200× and 400×.
Number of Strong Positive
Number of Strong Positive
The results demonstrated that the number of Strong Positive and Positivity (%) of control slides were higher than CAV slides (Average: 61% vs. 25%, respectively). The control slides showed strong positivity, due to the presence of bigger quantity of erythroblastoid cells. The CAV slides of 7 days PI had high positivity (average: 94%), because the CAV produces the lesions but severe starting from the 10 days PI up 21 days PI, after the cellular regeneration is observed, being able to be evidenced by means of focuses of erythroblastoid cells hyperplasia.
This technique demonstrated in a quantitative way the severe decrease of the cellular components of the bone marrow in presence of the infection for CAV, supporting with numeric data the histology image evaluated by the pathologist. Therefore, it can be used as support to the histopathology of field samples to evaluate the presence of lesions taken place by CAV in the farms and this way to improve the quality and efficiency of the veterinary pathology services.
This article has been published as part of Diagnostic Pathology Volume 3 Supplement 1, 2008: New trends in digital pathology: Proceedings of the 9th European Congress on Telepathology and 3rd International Congress on Virtual Microscopy. The full contents of the supplement are available online at http://www.diagnosticpathology.org/supplements/3/S1
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