Do we need to screen Egyptian voluntary blood donors for toxoplasmosis?
Asian Pacific Journal of Tropical Disease • 2016
معلومات البحث
المؤلفون
Nagwa Mostafa El-Sayed1*, Maha Mohamed Abdel-Wahab1, Shereen Magdy Kishik2, Naglaa Fathy Alhusseini3
الكلمات المفتاحية
Toxoplasma gondii
Blood donors
ELISA
PCR
المجلة العلمية
Asian Pacific Journal of Tropical Disease
الناشر
elsevier
المجلد
6
العدد
(4):
الصفحات
260-264
publication.type
International
رابط البحث
Not Available
المواد المرفقة
Not Available
الملخص
Objective: To determine the value of voluntary blood donors screening in diagnosing
asymptomatic toxoplasmosis in an attempt to reduce the risk of this infection in Egyptian
immunocompromised recipients.
Methods: Serum samples from 300 healthy voluntary blood donors were analyzed for anti-
Toxoplasma antibodies [immunoglobulin G (IgG) and immunoglobulin M (IgM)] using ELISA
and detection of Toxoplasma gondii (T. gondii) parasitemia was done by real-time quantitative
PCR (qrtPCR).
Results: Frequency of T. gondii infection in 300 healthy blood donors was 101 (33.67%), 10
(3.33%), 18 (6.00%) by ELISA IgG, IgM and qrtPCR, respectively. It was found that 8 of 18
(44.4%) donor samples positive by qrtPCR contained IgM anti-T. gondii, conversely 8 of 10
(80%) IgM-positive samples were positive for T. gondii DNA. There was a highly significant
increase in detection of recent Toxoplasma infection using PCR over IgM ELISA by 55.6%.
At the same time, T. gondii parasitemia was detected in 11 of 101 (10.90%) donor samples
positive by IgG ELISA and in 7 of 199 (3.50%) negative donor samples for anti-T. gondii IgG
antibodies. On the other hand, the negative results obtained by both qrtPCR and ELISA in 192
(64%) subjects ruled out the infection in those donors.
Conclusions: It might be appropriate to include the screening of blood and blood products for T.
gondii in the pre-transfusion blood testing schedule in Egypt. Also, molecular screening should
be carried out on the blood being transfused to immunocompromised patients.
asymptomatic toxoplasmosis in an attempt to reduce the risk of this infection in Egyptian
immunocompromised recipients.
Methods: Serum samples from 300 healthy voluntary blood donors were analyzed for anti-
Toxoplasma antibodies [immunoglobulin G (IgG) and immunoglobulin M (IgM)] using ELISA
and detection of Toxoplasma gondii (T. gondii) parasitemia was done by real-time quantitative
PCR (qrtPCR).
Results: Frequency of T. gondii infection in 300 healthy blood donors was 101 (33.67%), 10
(3.33%), 18 (6.00%) by ELISA IgG, IgM and qrtPCR, respectively. It was found that 8 of 18
(44.4%) donor samples positive by qrtPCR contained IgM anti-T. gondii, conversely 8 of 10
(80%) IgM-positive samples were positive for T. gondii DNA. There was a highly significant
increase in detection of recent Toxoplasma infection using PCR over IgM ELISA by 55.6%.
At the same time, T. gondii parasitemia was detected in 11 of 101 (10.90%) donor samples
positive by IgG ELISA and in 7 of 199 (3.50%) negative donor samples for anti-T. gondii IgG
antibodies. On the other hand, the negative results obtained by both qrtPCR and ELISA in 192
(64%) subjects ruled out the infection in those donors.
Conclusions: It might be appropriate to include the screening of blood and blood products for T.
gondii in the pre-transfusion blood testing schedule in Egypt. Also, molecular screening should
be carried out on the blood being transfused to immunocompromised patients.
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