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Correlating WHO COVID-19 interim guideline 2020.5 and testing capacity, accuracy, and logistical challenges in Africa

Correlating WHO COVID-19 interim guideline 2020.5 and testing capacity, accuracy, and logistical challenges in Africa

Lydia Mosi1,2,3,&, Augustina Angelina Sylverken1,4,5, Kolapo Oyebola1,6,7, Kingsley Badu1,5, Natisha Dukhi1,8, Nowsheen Goonoo1,9, Priscilla Kolibea Mante1,10, Julien Zahouli1,11, Ebenezer Forkuo Amankwaa1,12, Mai Fathy Tolba1,13,14, Adeniyi Francis Fagbamigbe 1,15, Dziedzom Komi de Souza1,16, Damaris Matoke-Muhia1,17


1African Academy of Sciences Affiliates, Nairobi, Kenya, 2Department of Biochemistry, Cell and Molecular Biology, University of Ghana, Legon, Ghana, 3West African Centre for Cell Biology of Infectious Diseases, University of Ghana, Legon, Ghana, 4Kumasi Centre for Collaborative Research in Tropical Medicine, Kumasi, Ghana, 5Department of Theoretical and Applied Biology, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana, 6Nigerian Institute of Medical Research, Lagos, Nigeria, 7Department of Zoology, Faculty of Science, University of Lagos, Lagos, Nigeria, 8Human and Social Capabilities Division, Human Sciences Research Council, Cape Town, South Africa, 9Biomaterials, Drug Delivery and Nanotechnology Unit, Center for Biomedical and Biomaterials Research (CBBR), University of Mauritius, MSIRI Building, 80837 Reduit, Mauritius, 10Department of Pharmacology, Kwame Nkrumah University of Science and Technology, Kumasi, Ghana, 11Centre Suisse de Recherches Scientifiques en Côte d´Ivoire, Abidjan, Côte d´Ivoire, 12Department of Geography and Resource Development, University of Ghana, Accra, Ghana, 13Department of Pharmacology and Toxicology, Faculty of Pharmacy, Ain Shams University, Cairo 11566, Egypt, 14The Center of Drug Discovery Research and Development, Faculty of Pharmacy, Ain Shams University, Cairo, Egypt, 15Department of Epidemiology and Medical Statistics, Faculty of Public Health, College of Medicine, University of Ibadan, Ibadan, Nigeria, 16Noguchi Memorial Institute for Medical Research, College of Health Sciences, University of Ghana, Accra, Ghana, 17Centre for Biotechnology Research and Development, Kenya Medical Research Institute, Nairobi, Kenya



&Corresponding author
Lydia Mosi, Department of Biochemistry, Cell and Molecular Biology, University of Ghana, Legon, Ghana




Coronavirus disease 2019 (COVID-19), a severe acute respiratory syndrome caused by SARS-CoV-2 was declared a global pandemic by the World Health Organization (WHO) in March 2020. As of 21st April 2021, the disease had affected more than 143 million people with more than 3 million deaths worldwide. Urgent effective strategies are required to control the scourge of the pandemic. Rapid sample collection and effective testing of appropriate specimens from patients meeting the suspect case definition for COVID-19 is a priority for clinical management and outbreak control. The WHO recommends that suspected cases be screened for SARS-CoV-2 virus with nucleic acid amplification tests such as real-time Reverse Transcription-Polymerase Chain Reaction (rRT-PCR). Other COVID-19 screening techniques such as serological and antigen tests have been developed and are currently being used for testing at ports of entry and for general surveillance of population exposure in some countries. However, there are limited testing options, equipment, and trained personnel in many African countries. Previously, positive patients have been screened more than twice to determine viral clearance prior to discharge after treatment. In a new policy directive, the WHO now recommends direct discharge after treatment of all positive cases without repeated testing. In this review, we discuss COVID-19 testing capacity, various diagnostic methods, test accuracy, as well as logistical challenges in Africa with respect to the WHO early discharge policy.



Perspective    Down


The pandemic caused by the Severe Acute Respiratory Syndrome Coronavirus 2 (SARS-CoV-2) continues to spread globally with varying global infection numbers (peaking at over 700,000 per day), leaving over 143 million infected (as of 21st April 2021) with more than 3 million associated deaths [1]. In Africa, as of March 9, 2021, almost 4 million cases and one hundred thousand deaths had been reported in 55 African union countries [2]. Based on the prevailing local/national policies regarding testing and the general epidemiology of SARS-CoV-2 within different countries, there are different approaches to testing suspected individuals. Suspected cases are usually categorized into 4 groups: (i) symptomatic (individuals with signs or symptoms consistent with COVID-19), (ii) asymptomatic (individuals without visible signs and symptoms of COVID-19 or recent known or suspected exposure to SARS-CoV-2 or those without known or suspected exposure to SARS-CoV-2), (iii) individuals being tested to determine the resolution of infection, (iv) individuals being tested for purposes of public health surveillance for SARS-CoV-2. The viral loads of individuals in each of these categories differ and are directly linked to the amount of exposure and immune status of these individuals [3]. A study has shown that the rate of false negatives is higher when testing is done very early or late during the infection [4]. In many instances, there are significant delays to testing and considering the acute period of the infection, testing samples backlogged beyond three weeks may likely impact accurate tracking of disease timelines and consequent discharge protocol.

Samples used for SARS-CoV-2 diagnosis are collected from the upper or lower respiratory tract and include nasal, nasopharyngeal, oropharyngeal swabs, sputum, lower respiratory tract aspirates, bronchoalveolar lavage, and nasopharyngeal wash/aspirate or nasal aspirate. The viral loads in each of these samples differ both in the stage of the infection and the appropriateness of the sampling technique used [5]. In early infections, upper respiratory tract samples are more suitable for diagnosis while in the late stage of infection, lower respiratory tract specimens are more reliable [6]. Viral loads in stool and urine are comparatively lower [5]. The viral loads within the different samples also differ based on the time taken to process after retrieval with the minimum being 24 hours for biopsies, an average of 2 days for most pharyngeal specimens and up to days for blood, stool and urine. Blood cultures are also useful in testing other complications of the infection. Currently, in Africa, most countries employ “smart screening” approaches with different testing strategies [7] for different purposes: routine surveillance, the port of entry screening and case diagnosis at health centres. There are also different types of tests available or being developed and African countries who are largely plagued with numerous health system challenges have to adapt and localise the specifications of these tests.

In a new policy directive, the WHO recommends direct discharge after treatment of all positive cases without repeated testing. In this review, we discuss local COVID-19 testing capacity in different countries, choice of diagnostic methods, testing accuracy, as well as logistical challenges in Africa with respect to the WHO early discharge policy. We highlight the challenges that are encountered logistically along the global supply chain to get access to testing materials, the differences in the testing methods across different countries and subsequent interpretation of results which ultimately affect testing accuracy. We also point out various challenges faced by African countries to the implementation of all WHO recommendations since the onset of the pandemic, largely due to apparent economic and logistic reasons. These include access to resources for diagnosis, treatment, and control particularly because most of the required logistics are not manufactured by most African countries and have to be shipped or transported from abroad. This article presents a comprehensive discussion on the relevance of the new WHO discharge policy on the inherent and current capacity of public health capacities and infection prevention strategies in different Africa countries in managing the SARS-CoV-2 pandemic. Finally, the article suggests possible ways in which different countries can mobilize the local and collaborative capacity to adhere to the recommendations by the WHO on public health responses to the pandemic.

Types of tests for COVID-19

The gold standard in curbing this pandemic is to have as many people tested in order to obtain a fair picture of the rate of infections, identify hotspots and isolate affected individuals in a timely manner for impactful Infection, Prevention and Control measures. In the early months of the COVID-19 pandemic several countries implemented the same lockdown strategies which heavily and negatively impacted on the economy and social lifestyle of many individuals. While this may seem a prudent strategy, there is wisdom in interrogating the impact of such approached to advise future interventions. As is evident, many developed countries are now careful to implement the same level of lockdown in the face of a second wave of infections. Similarly, it was thought early in the pandemic that nose masks were of no use in fighting the spread of the infection. Currently, the wearing of nose masks is strongly enforced. The recommendations by the WHO, whilst carefully crafted, remain guidelines to be implemented as they are or adopted to suit the local needs and policies of countries. Furthermore, the changing nature of policies and recommendations related to COVID-19 demand that any such policy or recommendation be carefully assessed before implementation. There are three main types of COVID-19 tests which include: molecular, antigen and antibody tests as highlighted below and summarized in Table 1.

(i) Molecular tests

The SARS-CoV-2 genome encodes four structural proteins. The spike surface glycoprotein (S) mediates specific binding to the host cell receptors, the nucleocapsid (N) protein binds to the coronavirus RNA genome to make the nucleocapsid, the membrane (M) protein is the main structural protein that connects between the membrane and the capsid, and the small envelope (E) protein which is involved in the assembly and budding process of the coronavirus [8]. Among them, the genes for the N and E proteins are used as the targets for amplification in the rRT-PCR assay combined with the open reading frame 1 (ORF1) ab, and the RNA-dependent RNA polymerase (RdRP) gene. Nucleic acid amplification tests relying on real-time reverse polymerase chain reaction (rRT-PCR) is the most preferred method for diagnosis and confirmatory of SARS-CoV2 infection [4]. There are several commercially available rRT-PCR kits that supply a variety of premixed solutions for use and each of these has specific protocols [9, 10]. These kits are designed to amplify one and up to three of the four loci of interest in the genome of SARS-CoV2; the nucleocapsid (N), envelope (E), and spike (S) genes, and regions of the RNA-dependent RNA polymerase (RdRp) gene. Depending on the epidemiology of the infection within countries, WHO recommends positive results in at least two loci for highly affected areas and in one locus for areas of low incidence for accurate diagnosis [11]. In addition to rRT-PCR, droplet digital PCR has been tested for COVID-19 diagnosis [4]. Droplet digital PCR has the advantage of absolute quantification and previous studies have shown that it may be more sensitive for virus detection than RT-PCR [12]. Sequencing is highly encouraged to monitor viral genome mutations and molecular evolution; however, this comes with considerable cost implications. Loop-mediated isothermal amplification (LAMP) test is a type of rapid nucleic acid amplification which exhibits increased sensitivity and specificity and does not require expensive reagents or specialized equipment. LAMP is an ultrasensitive nucleic acid amplification method that can be used to detect small numbers of DNA or RNA templates within roughly an hour. The technique is based on the principle of the strand displacement reaction, which occurs under isothermal conditions with the generation of cauliflower-like DNA structures. As the target is recognized by six distinct primers, amplification of a target sequence by the LAMP method is highly specific. It is economical for coronavirus detection [13]. The development of clustered regularly interspaced short palindromic repeats (CRISPR) has led to rapid research expansion and disease detection. To help advance the diagnosis of COVID-19, the CRISPR-based SHERLOCK (Specific High Sensitivity Enzymatic Reporter UnLOCKing) [14] protocol has been developed among others.

(ii) Antigen tests

Antigen tests detect the presence of viral proteins in a biological sample, such as saliva or tissue swabbed from the nasal cavity. However, weak signals pose a challenge to antigen tests. Unlike PCR tests which amplify tagged DNA or RNA sequences, making it easy to reliably identify just a few copies of a virus, antigen tests do not amplify their protein signals, so they are inherently less sensitive. Furthermore, the antigen signals get diluted when samples are mixed with liquid needed for capillary action [15].

(iii)Antibody (serological) tests

Serological tests are most useful for exposure testing and other epidemiological studies. These immune-based ELISA or lateral-flow assays are useful in measuring levels of IgA, IgG, and/or IgM in serum and have predictive value in diagnosis albeit with low predictive value [16, 17]. The seroconversion rate to produce antibodies following exposure ranges from 1 to 3 weeks and varies significantly amongst individuals [18]. Additionally, cytokine and hemostatic analysis are beneficial for research purposes and understanding of other clinical complications of infection. However, the presence of antibodies does not indicate that an individual is protected from re-infection or has become free of the virus as there is limited understanding of the levels and persistence of antibodies necessary for protective immunity [19]. Antibody tests also are subject to false positives as they can create a positive test result if they react to a different type of coronavirus. Therefore, serology tests may not provide much information about an individual´s infectiousness or otherwise. New rapid point-of-care diagnostic tools now target the virus in saliva or mucus samples from the nose or throat.

Result interpretation and factors affecting testing accuracy

Real-time Reverse Transcription-Polymerase Chain Reaction methods have an advantage in detecting the SARS-COV-2 infection compared to rapid diagnosis since they detect 2-3 genes. However, there is a possibility of false negatives in the diagnosis given that mutations occur frequently in SARS-CoV-2 which may be a disadvantage of rRT-PCR -based methods. In order to overcome this challenge, it is important to simultaneously use two or more rRT-PCR diagnostic kits that detect different viral genes. Each rRT-PCR kit has a different cycle threshold for determining sample positivity with the ideal ranges between 10 and 45 [20]. Sample positivity is a combination of sample type, the threshold cycle (Ct) value and technicality of sampling technique, stage of infection, the kit type used and number of viral molecular targets (PCR primers). Thus, global standardization is of absolute necessity in differentiating between true positives, false positive and false negatives which range from 5-40% [21].

Testing capacity and logistical challenges (implementation)

In considering whether the WHO recommendation is the best strategy for Africa, it is important to consider the testing needs and how this is influenced by the logistics, procurement, and testing capacity of different countries. Having considered Africa´s response to COVID-19, it is becoming obvious that the “test, test and test” mantra is not achievable in many African countries as there are significant challenges procuring the necessary reagents and supplies for the needed testing [22]. The dependency of the continent on external suppliers has significantly limited its ability to increase its testing capacity [23]. This is despite the pooled procurement of tests facilitated by the WHO global access to COVID-19 tools [24]. It is important to note that while the majority of cases on the continent are reported in only a few countries, the presumptive low case reportage in other countries is not necessarily due to the absence of cases but the unavailability of the required diagnostic capacity, supplies and the challenges in procurement [25]. As expertly stated by the director of Africa CDC - Dr. John Nkengasong: “If you don´t test, you don´t find”. So far, South Africa and Ghana accounted for nearly half of the testing on the continent [26]. But even in these countries, there are challenges. For example, in Ghana, pooled testing from several cases has been used to conserve testing kits, and it is only when a pool result is positive that samples are followed up individually. Even in Ghana, testing sites acknowledge the limitations associated with the pooling strategy. In South Africa where large-scale community screening and testing were implemented, challenges with massive backlogs and two-week turnaround time for results have been reported, with rippling effects on the health system [22]. Further, Africa´s testing capacity is nowhere compared to other regions. By March 9, 2021, 31.7 million PCR tests for COVID-19 had been conducted in Africa with a population of more than 1 billion people [2]. Europe on the other hand had carried out over 500 million tests [27] for a population of slightly about 741 million as at April 2021

As a result of the pandemic and the need to ramp up testing, Africa has experienced severe logistics challenges in procuring the necessary testing kits for COVID-19, thus lagging in the diagnostic market. “The collapse of global cooperation and a failure of international solidarity have shoved Africa out of the diagnostics market [28].“ African countries are therefore struggling to find the tests they need, even when the resources are available [29]. Beyond the logistical challenges linked to getting the tests where needed, other challenges in access to rural and densely populated urban areas, limitations on healthcare personnel and facilities, distrust of healthcare workers, and stigma associated with the virus itself, also affect the ability of African countries to test as many people as possible [30]. While, there are several initiatives through the WHO global pool procurement mechanism [24] or the Africa CDC´s Partnership to Accelerate COVID-19 Testing [23], it is becoming increasingly clear that most countries on the African continent will not be able to circumvent the logistics challenges quickly enough to provide enough testing to all patients (either suspected or recovering from infection). “In light of these challenges, we have proposed in Table 2 [31], some corresponding solutions.“


Suspected cases of COVID-19 should always be validated by laboratory tests. While RT-PCR still remains the gold standard, issues related to laboratory infrastructure, human resources, supply chain management, and the stockpile of laboratory consumables/reagents need some consideration before Africa adopts the recent WHO discharge protocol or even comes up with a context-specific protocol with the WHO´s as a guideline. Recommendations are that suspected samples are handled under biosafety cabinet, or BSL-2 for RT-PCR) and BSL-3 at the minimum for viral cultures [11]. The infrastructural design of such laboratories not forgetting servicing contracts of equipment may pose a challenge for many African countries since most of these equipments are either assembled or manufactured by and in Western countries. The manufacturers of PCR platforms (such as Roche, Abbott, Hologic, Thermo Fisher, and Cepheid) cannot scale up production quickly enough. And even if they could, chances are that Western countries may be their highest priority. This will mean most cases may not even be sampled let alone tested if these requirements are not met. Beyond infrastructure is trained personnel with the needed expertise and knowledge in not only performing rRT-PCR but importantly, interpreting rRT-PCR results depending on the positivity rates of communities within countries.

The global supply chain is always vital to provide laboratory supplies to ensure timely testing and issuance of test results of suspected cases. However, this is currently heavily fractured and restricted supplies of test reagents and consumables are making it difficult to mobilise capacity. To avert this, efficient humanitarian aid corridors and services to assure the timely provision of laboratory supplies may be an option. A more sustainable option will be a WHO-validated rapid diagnostic test that could provide a faster and cheaper alternative to PCR [11] which can easily be manufactured in African countries considering the continent´s limited manufacturing capacity. While it may be prudent as recommended by the WHO to test suspected cases for other respiratory pathogens using routine laboratory procedures, as recommended in local management guidelines for community-acquired, one wonders how many countries are able to implement this.

Recommendations in line with an early discharge protocol

The WHO recommendations for early discharge have been proposed after careful consideration of the current global epidemiological state of the SARS-CoV-2 pandemic. They are also largely driven by the economics and other logistical challenges surrounding the Infection Prevention and Control (IPC) strategies within different countries. Africa faces its own sets of challenges compared to other developed nations. The state of the healthcare system, socio-economic and political situation in each African country will inform the level of measures to be implemented. Recent evidence, as this pandemic unfolds, seems to suggest that Africa has been spared the brunt of COVID-19 associated mortalities. In view of this, many countries have started opening gradually to allow some sense of normalcy back. However, all these actions must be done cautiously and in the light of the suggested WHO guidelines. Bearing in mind the science behind the infection during all the stages of infection and associated viral shedding risks, it seems appropriate to maintain the current early discharge regimen.



Competing interests Up    Down

The authors declare no competing interests.



Acknowledgments Up    Down

All authors are affiliates of the African Academy of Sciences (AAS). The AAS Affiliates fellowship program comprises a cohort of early and mid-career scientists who have demonstrated excellence in their development and application of science in Africa. The diversity of the group brings on board young African research leaders with expertise in a variety of cross cutting disciplines. The group has recently published a policy document on “Securing Africa´s health sovereignty: why investing in science and innovation matters” and are well positioned to interrogate evidence to shed light on WHO's policies. We acknowledge the mentorship of the AAS.



Tables Up    Down

Table 1: summary of diagnostics tests for COVID-19 (adapted from [8])

Table 2: proposed solutions to challenges to COVID-19 testing in African countries



References Up    Down

  1. John Hopkins University of Medicine. Corona Virus Resource Centre. (Eds) 2021.

  2. Africa Centers for Disease Control. Outbreak Brief 26: COVID-19 Pandemic. 9 March 2021. (Eds) (2021).

  3. Guan WJ, Ni ZY, Hu Y, Liang W-H, Ou C-Q, Jian-Xing HEet al. Clinical Characteristics of Coronavirus Disease 2019 in China. N Engl J Med. 2020 Apr 30;382(18):1708-1720. PubMed | Google Scholar

  4. Zou L, Ruan F, Huang M, Liang L, Huang H, Hong Z et al. SARS-CoV-2 Viral Load in Upper Respiratory Specimens of Infected Patients. N Engl J Med. 2020 Mar 19;382(12):1177-1179. PubMed | Google Scholar

  5. Wang W, Xu Y, Gao R, Lu R, Han K, Wu G et al. Detection of SARS-CoV-2 in Different Types of Clinical Specimens. JAMA. 2020 May 12;323(18):1843-1844. PubMed | Google Scholar

  6. Wang X, Tan L, Wang X, Liu W, Lu Y, Cheng L et al. Comparison of nasopharyngeal and oropharyngeal swabs for SARS-CoV-2 detection in 353 patients received tests with both specimens simultaneously. Int J Infect Dis. 2020 May;94:107-109 Epub 2020 Apr 18. PubMed | Google Scholar

  7. James D. Ramping up early detection of COVID-19 with limited resources: the role of pool testing. In: The International Gowth Centre. (Eds) (Ghana, 2020).

  8. UptoDate, Caliendo Angela M, E HK. Coronavirus disease 2019 (COVID-19): Diagnosis. In: Topic 128404 Version 11.0. Hirsh Martin S., Allyson, B (Eds) (2021).

  9. Nalla AK, Casto AM, Huang MW, Perchetti GA, Sampoleo R, Shrestha L et al. Comparative Performance of SARS-CoV-2 Detection Assays Using Seven Different Primer-Probe Sets and One Assay Kit. J Clin Microbiol. 2020 May 26;58(6):e00557-20. PubMed | Google Scholar

  10. Yu F, Yan L, Wang N, Yang S, Wang L, Tang Y et al. Quantitative Detection and Viral Load Analysis of SARS-CoV-2 in Infected Patients. Clin Infect Dis. 2020 Jul 28;71(15):793-798. PubMed | Google Scholar

  11. World Health Organization. Laboratory testing for coronavirus disease 2019 (COVID-19) in suspected human cases. (Eds) (World Health Organization, 2020).

  12. Lieberman JA, Pepper G, Naccache SN, Huang ML, Jerome KR, Greninger AL. Comparison of Commercially Available and Laboratory-Developed Assays for In Vitro Detection of SARS-CoV-2 in Clinical Laboratories. J Clin Microbiol. 2020 Jul 23;58(8):e00821-20. PubMed | Google Scholar

  13. Kashir J, Yaqinuddin A. Loop mediated isothermal amplification (LAMP) assays as a rapid diagnostic for COVID-19. Med Hypotheses. 2020;141:109786.

  14. Joung J, Ladha A, Saito M et al. Point-of-care testing for COVID-19 using SHERLOCK diagnostics. medRxiv. 2020 May 8;2020.05.04.20091231. PubMed | Google Scholar

  15. Service RF. Fast, cheap tests could enable safer reopening. Science. 2020 May 8;2020.05.04.20091231. PubMed | Google Scholar

  16. Guo L, Ren L, Yang S, Xiao M, De Chang, Fan Yang et al. Profiling early humoral response to diagnose Novel Coronavirus Disease (COVID-19). Clin Infect Dis. 2020 Jul 28;71(15):778-785. PubMed | Google Scholar

  17. Zhao J, Yuan Q, Wang H, Liu W, Liao X, Su Y et al. Antibody responses to SARS-CoV-2 in patients of novel coronavirus disease 2019. Clin Infect Dis. 2020 Nov 19;71(16):2027-2034. PubMed | Google Scholar

  18. Meyer B, Drosten C, Muller MA. Serological assays for emerging coronaviruses: challenges and pitfalls. Virus Res. 2014 Dec 19;194:175-83. PubMed | Google Scholar

  19. Long QX, Tang XJ, Shi QL, Li Q, Deng H-J, Yuan J et al. Clinical and immunological assessment of asymptomatic SARS-CoV-2 infections. Nat Med. 2020 Aug;26(8):1200-1204. PubMed | Google Scholar

  20. Chang MC, Hur J, Park D. Interpreting the COVID-19 Test Results: a guide for Physiatrists. Am J Phys Med Rehabil. 2020 Jul;99(7):583-585. PubMed | Google Scholar

  21. Theel ES, Slev P, Wheeler S, Couturier MR, Wong SJ, Kadkhoda K. The Role of Antibody Testing for SARS-CoV-2: Is There One? J Clin Microbiol. 2020 Jul 23;58(8):e00797-20. Google Scholar

  22. Wadvalla BA. How Africa has tackled COVID-19. BMJ. 2020 Jul 16;370:m2830. PubMed | Google Scholar

  23. Ondoa P, Kebede Y, Loembe MM, Bhiman JN, Tessema SK, Sow A et al. COVID-19 testing in Africa: lessons learnt. Lancet Microbe. 2020 Jul;1(3):e103-e104. PubMed | Google Scholar

  24. World Health Organization. Access to COVID-19 tools (act) accelerator. (Eds) (2020).

  25. Kobia F, Gitaka J. COVID-19: Are Africa's diagnostic challenges blunting response effectiveness? AAS Open Res. 2020 Apr 17;3:4. Google Scholar

  26. Reuters Graphics, Houreld Kathearine, Lewis David, McNeil Ryan, Samuel G. Understanding COVID-19,Virus exposes gaping holes in Africa´s health systems. (Eds) (2020).

  27. Statistia. Number of coronavirus (COVID-19) tests carried out in Europe as of April 20, 2021, by country. (Eds) (2021).

  28. Nkengasong J. Let Africa into the market for COVID-19 diagnostics. Nature. 2020 Apr;580(7805):565. PubMed | Google Scholar

  29. The New Humanitarian, April. Z. African countries struggle to find the coronavirus test kits they need. (Eds) (2020).

  30. Atlantic Council, Bruton Bronwyn, Neil E. Barriers to mass testing for COVID-19 in Africa. (Eds) (2020).

  31. BU-LABnet. Buruli Ulcer Laboratory Network. Buruli Ulcer Laboratory Network. (Eds) (2021).