Molecular Screening for Malaria among Blood Donors in a WHO Claimed Region of Egypt, Fayoum Governorate
1 Department of Clinical Pathology, College of Medicine, Fayoum University, Fayoum, Egypt.
2 College of Medicine, Princess Nourah bint Abdulrahman University, Riyadh, Saudia Arabia.
3 Department of Biological Sciences, Faculty of Science, King Abdulaziz University (KAU), Jeddah, Saudi Arabia.
4 Department of Genetics, Faculty of Agriculture, Ain Shams University, Cairo, Egypt.
5 Princess Al-Jawhara Al-Brahim Centre of Excellence in Research of Hereditary Disorders (PACER-HD), Faculty of Medicine, King Abdulaziz University (KAU), Jeddah, Saudi Arabia.
6 Department of Parasitology, College of Medicine, Ain Shams University, Egypt.
7 College of Medicine, Ain Shams University, Egypt.
8 Department of Zoology, College of Science, King Saud University, Riyadh, Saudi Arabia.
9 Chair Vaccines Research of Infectious Diseases, Faculty of Science, King Saud University, Riyadh, Saudi Arabia.
10 Department of Zoology and Entomology, Faculty of Science, Helwan University, Cairo, Egypt.
Received: August 13, 2017
Accepted: September 25, 2017
Mediterr J Hematol Infect Dis 2017, 9(1): e2017065 DOI 10.4084/MJHID.2017.065
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Background: Transfusion-transmitted malaria is undoubtedly a potential health hazard for blood recipients. Egypt is still on the prevention of reintroduction phase of malaria control program. Fayoum Governorate is considered one of the high-risk foci in Egypt due to its geology. However, no studies have been reported to evaluate the current status of subclinical Plasmodium infection based on sensitive molecular techniques. Moreover, screening of malaria is not listed within screening protocols of blood-borne pathogens in Fayoum blood banks.
Objective: To assess the current prevalence of subclinical Plasmodium
infection among blood donors of Fayoum inhabitants for transfusion
biosafety. To predict any possibility of the reemergence of malaria in
the governorate and the effectiveness of malaria control measures.
Results: All Fayoum inhabitants’ blood donors’ samples were negative for Plasmodium infection.
Fayoum Governorate was assigned as a high risk of malaria foci in Egypt during the last two decades, due to its geology,[1,10,11] the nature of its irrigation system which depends on a network of small canals, the presence of Quarun Lake, as well as the current changes in climate all over the country. All these conditions may have a direct impact on malaria transmission, facilitating the re-invasion of Anopheles arabiensis into the region which may come from other endemic areas of Africa such Sudan.
Although no autochthonous cases of Plasmodium infection have been reported officially in Fayoum Governorate or elsewhere in Egypt since 1998, some sporadic cases from Al-Fayoum, Siwa Oasis, and Cairo governorate were reported by Zaher et al., 2007 and El-Bahnasawy et al., 2010. Moreover, a recent outbreak occurred in southern Upper Egypt; Aswan Governorate during May 2014. Consequently, this supports the idea that malaria is reemerging in the country as reported by WHO-EMRO, 2016 and other researchers[2,5,12-17]
Transfusion-transmitted malaria, although uncommon, is considered a potential hazard for blood recipients. As post-transfusion clinical manifestations of malaria usually simulate other post-transfusion reactions, as a result of this simulation the most cases may be misdiagnosed. Moreover, donors who are subclinical carriers of Plasmodium become a reservoir for the parasite, maintaining its transmission in the community through blood donation. Hence, high sensitivity screening tests should be done to ensure blood transfusion biosafety for the recipient.
As far as we know, no previous studies have been reported based on sensitive molecular (PCR) techniques to assess the prevalence of Plasmodium infection in Fayoum inhabitants. Therefore, the current status of malaria is unclear in this high risk area of Egypt. In Egyptian blood transfusion centers, including Fayoum Governorate, screening of malaria parasite is not currently validated and not listed within screening protocols of blood-borne pathogens, although the risk of transfusion-transmitted malaria was still poorly documented in this high risk foci of Egypt.
Definitive determination of the prevalence of asymptomatic Plasmodium infection in a general population and blood-donors, in particular, is like to help in updating the screening operating policy and procedures (SOP) for blood recipient safety as well as reviewing health policy decisions.
Undoubtedly, molecular-based assays are about 100 fold greater sensitivity compared to microscopy or RDTs at detecting malaria parasite, especially in subclinical infections with detection limits as low as 5 parasites/µl. Our study was conducted to detect the 18S rRNA gene of Plasmodium parasite. This study aimed to assess the current prevalence of subclinical Plasmodium infection in blood donors at a public blood bank of the University hospital in Fayoum Governorate, Egypt. Furthermore, this study could provide to give accurate, current epidemiological data on malaria in Fayoum Governorate considering the changes in climate, so evaluating the effectiveness of national malaria control measures.
Material and Method
Sample collection. Blood samples were obtained from each donor as a whole venous blood on EDTA, and as a dried blood sample by finger prick, where 2 drops of capillary blood were spotted onto Whatman®31ETCHR filter paper (Whatman, Piscataway, NJ). Filtered papers were air dried at room temperature and kept in separate clean zipper bags until further processing. All blood samples were screened as routine for ABO grouping and serological screening tests, including HCV, HBV, HIV, and Syphilis.
Malaria testing. A) Microscopic examination: was done using thick and thin blood films stained with Giemsa according to WHO competency assessment protocol. Immunological rapid diagnostic test (BinaxNOW Malaria Test; Binax, Inc., Scarborough, ME, USA), was used for primary detection of malaria antigen positive cases.
B) DNA extraction: DNeasy Blood and Tissue kit, Cat no. 69504 (Qiagen, Valencia, CA, USA) was used as per manufacturer’s instructions with some modifications. Whatman filter paper was cut into strips (almost 1 cm2) and put into a 1.5 mL Eppendorf tube. The concentration of extracted DNA was measured using a Nanodrop 2000 (Thermo Fisher Scientific Inc, CA, USA).
C) PCR amplification: Conventional PCR amplification was performed using 10 ng of extracted DNA with purity 1.7 to 2 in a total volume of 25 μL reaction volume using master mix (Go Taq green 2x master mix, Promega, USA) with primers (Bioneer, Korea) rPLU6 (5’- TTA AAA TTG TTG CAG TTA AAA CG 3’) and rPLU5 (5’-CCT GTT GTT GCC TTA AAC TTC-3); as described by Gal et al., 2001. Glyceraldehyde-3-phosphate dehydrogenase (GAPDH) with accession number NG 007073, GAPDH-F (5’- AGG TGG TCT CCT CTG ACT TCA AC-3’), GAPDH-R (5’- CGC CAG ACC CTG CAC TTT T-3’) was designed in this study with amplicon size 150 bp.
As the cycle conditions began with an initial denaturing period at 95°C for 5 min, followed by 35 cycles of 94°C for 30 s, 58°C for 1 min, and 72°C for 1 min, with a final extension for 5 min at 72°C. PCR amplicon was separated on 1% agarose gel (Agarose, LE, Analytical Grade, Promega, USA). The presence of the 1200 amplicon was detected in the gel under UV light after its staining with Invitrogen TM SYBER TM Safe.
D) Statistical methods: Data were collected, coded and analyzed using IBM SPSS software, version 23 software (IBM, Armonk, NY, USA). The result of simple descriptive analysis of numbers and percentages for qualitative data were tabulated. Graphs were produced using Excel software.
|Figure 1. Distribution of ABO blood groups among blood donors.|
|Figure 2. Prevalence of HCV, HBV and HIV among blood donors.|
PCR results on Agarose gel showed that all samples were negative for 18 S ssrRNA Plasmodium gene. For PCR validation, malaria positive control was used for each run which gives band at 1200 bp. In addition, a housekeeping gene (GAPDH), which was used as an internal control for PCR negative samples for testing the integrity of DNA, revealed clear positive PCR band at 150 bp (Figure 3 and 4).
Many recent reports seemed to suggest that malaria is reemerging in Egypt, due to current climate changes, and the recently discovered malaria outbreak in a specific region of the country. Recently, the Military Fever Hospital research group recorded that 12.5% out of 36 malaria-infected cases were from Fayoum governorate. Similarly, many studies have reported sporadic malaria-infected cases in Fayoum.[5,13-17,25]
In accordance, Kamel et al. who assessed the prevalence of malaria in Fayoum governorate among patients admitted Fayoum fever hospitals using rapid diagnostic tests (RDTs- ABON PLUS), pointed out that malaria control program in South Egypt – including the Fayoum Governorate – should be strengthened to prevent reintroduction of malaria. Kamel et al. further recommended the need to evaluate the validity of the RDT results of their study using more sensitive technique.
Several studies support the higher sensitivity of PCR assay compared to microscopy and RDTs to roll out infection and to monitor the success of control programs in low transmission areas. Hence, a study highlighted the urgency to use a sensitive PCR based molecular assay to determine the current malaria status in the high risk areas of Egypt.
Many molecular assays are available for detection of Plasmodium pathogens. However, it is challenging to select the most ideal and appropriate method for screening of blood donors, that can screen a large number of samples with a higher sensitivity and easily performed technique. Since using PCR based pooling strategy reduces the number of assays needed when screening for infectious diseases, individual PCR testing of dried blood spot samples allows pathogen detection despite its higher efforts and cost. Therefore, in the present study, PCR of dried blood spot samples was used, due to its sensitivity, to validate the results obtained from microscopic evaluation and rapid immunologic assay for malaria antigen.
Regarding the sensitivity of detection, Bharti et al. (2009) who assessed PCR based pooling strategy with a pool size of 10, reported six positives cases out of 200 ‘negative’ malaria samples using microscopic detection. Furthermore, Taylor et al. (2010) reported 35 positive samples out of 1,092 negative cases with microscopy. Lima GF et al. (2016) reported in a study conducted to assess four different molecular assays in detecting Plasmodium pathogens that the sensitivity of pooled samples is not ideal (86.7%) mainly when used for blood transfusion screening, and more efforts still need to improve the assays used for detection low-density parasitemia. Another study pointed out that PCR using dried blood spot from filter paper was able to detect almost one-fifth and one-third of Plasmodium presences that were missed by RDT and microscopy, respectively.
In contrast to the previously mentioned studies which were claimed the high probability of reemergence of malaria in Upper Egypt (including Fayoum), the present study’s results made it clear by using PCR based assay for detecting 18S ssrRNA Plasmodium gene. The results demonstrated no subclinical malarial infection in the sample group as no Plasmodium DNA genome was detected in any of the donors’ blood samples. The results obtained in our study were confirmed by using an internal control gene (GAPDH) to check the quality of DNA extraction and to assure that there were not misleading results due to the poor DNA quality or no DNA at all.
In response to recent studies suggesting the possibility of re-emergence of malaria in the area,[5,9,13-17] the results of our study support the idea that all cases of malaria previously reported in the Fayoum governorate[8,25] are imported from outside.
In the present study, the prevalence of blood groups O+, O-, A+, A-, B+, B-, AB+, AB-, A2B, and A2 among donors was 27.4 %, 4%, 33%, 2.2%, 20.7%, 2.2%, 7.8%, 1.3%, 1%, and 0.3% respectively. Similar prevalence have been reported in another study carried out all over 26 governorates of Egypt, as the frequency of groups O+, O-, A+, A-, B+, B-, AB+, and AB- was 27.5%, 2.3%, 33.6%, 2.7%, 22%, 1.8%, 9.3%, 0.7% respectively.
In light of the results of our study, we may assume that the current control and preventive measures applied under the umbrella of the WHO and Egyptian MOH were able to control malaria, at least during the time of the study, in the Fayoum Governorate. However further comprehensive study is recommended to screen and stratify the results according to age to substantiate the assume eradication of the infection. Regular monitoring is still needed.
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