2020•Journal of the Egyptian Society of ParasitologyOpen access

EFFICACY OF AZITHROMYCIN ON EXPERIMENTAL TOXOPLASMOSIS INFECTED MICE

Mona El-Sayed Nasr, Atef H. H. Abd El Hamid, Nagwa S. M. Aly, Ghada Helmy Omar, Ashraf Mohamed Barakat, Kawkab A. Ahmed, Safaa Hassanien Youssif, Gehan Abd El-Rahman Rashed

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Abstract

Toxoplasma gondii is an opportunistic protozoan that causes a devastating disease in immunocompromisedindividuals and congenitally infected neonates or children. This study evaluated theefficacy of early Azithromycin treatment of Toxoplasma gondii infected mice with cystogenic Me49 non-virulent strain. Fifty laboratory-bred female Swiss albino mice were divided into 5 groups:G1: Non-Infected, G2: Infected non-treated, G3: Infected and treated by Azithromycin 200mg/kg at 4th day post-infection for 3 days, G4: Infected and treated by Azithromycin 200mg/kg at4th day post-infection for 10 days & G5: Infected and treated by Spiramycin 200mg\kg at 4th daypost-infection for 2 weeks, brain cysts’ number, size and histopaholoical changes were assessedafter 3 months. Treatment with Azithromycin for 10 days decreased number and size of braincysts by 70% & 40% respectively without significant difference with Spiramycin treated micethat caused reduction by 74% & 50% respectively. Azithromycin treatment for 3 days caused theleast reduction by 51% & 21% respectively and Azithromycin treatment for 10 days decreasedthe histo-pathological changes in cerebral toxoplasmosis. Azithromycin treatment started at 4thday post-infection was effective than Spiramycin against T. gondii infection with a significant effecton cysts count and size and brain pathological changes. Azithromycin treatment for 10 daysgave better effect than 3 days.

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Toxoplasma gondii is an opportunistic protozoan that causes a devastating disease in immunocompromisedindividuals and congenitally infected neonates or children. This study evaluated theefficacy of early Azithromycin treatment of Toxoplasma gondii infected mice with cystogenic Me49 non-virulent strain. Fifty laboratory-bred female Swiss albino mice were divided into 5 groups:G1: Non-Infected, G2: Infected non-treated, G3: Infected and treated by Azithromycin 200mg/kg at 4th day post-infection for 3 days, G4: Infected and treated by Azithromycin 200mg/kg at4th day post-infection for 10 days & G5: Infected and treated by Spiramycin 200mg\kg at 4th daypost-infection for 2 weeks, brain cysts’ number, size and histopaholoical changes were assessedafter 3 months. Treatment with Azithromycin for 10 days decreased number and size of braincysts by 70% & 40% respectively without significant difference with Spiramycin treated micethat caused reduction by 74% & 50% respectively. Azithromycin treatment for 3 days caused theleast reduction by 51% & 21% respectively and Azithromycin treatment for 10 days decreasedthe histo-pathological changes in cerebral toxoplasmosis. Azithromycin treatment started at 4thday post-infection was effective than Spiramycin against T. gondii infection with a significant effecton cysts count and size and brain pathological changes. Azithromycin treatment for 10 daysgave better effect than 3 days.

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Available abstract

Toxoplasma gondii is an opportunistic protozoan that causes a devastating disease in immunocompromisedindividuals and congenitally infected neonates or children. This study evaluated theefficacy of early Azithromycin treatment of Toxoplasma gondii infected mice with cystogenic Me49 non-virulent strain. Fifty laboratory-bred female Swiss albino mice were divided into 5 groups:G1: Non-Infected, G2: Infected non-treated, G3: Infected and treated by Azithromycin 200mg/kg at 4th day post-infection for 3 days, G4: Infected and treated by Azithromycin 200mg/kg at4th day post-infection for 10 days & G5: Infected and treated by Spiramycin 200mg\kg at 4th daypost-infection for 2 weeks, brain cysts’ number, size and histopaholoical changes were assessedafter 3 months. Treatment with Azithromycin for 10 days decreased number and size of braincysts by 70% & 40% respectively without significant difference with Spiramycin treated micethat caused reduction by 74% & 50% respectively. Azithromycin treatment for 3 days caused theleast reduction by 51% & 21% respectively and Azithromycin treatment for 10 days decreasedthe histo-pathological changes in cerebral toxoplasmosis. Azithromycin treatment started at 4thday post-infection was effective than Spiramycin against T. gondii infection with a significant effecton cysts count and size and brain pathological changes. Azithromycin treatment for 10 daysgave better effect than 3 days.

Key concepts: Azithromycin, Spiramycin, Toxoplasmosis, Toxoplasma gondii, Medicine, Pathological, Internal medicine, Biology

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