From the outset of the COVID-19 outbreak, testing for SARS-CoV-2 has been a priority. Initially just having a test for COVID-19 was a scientific success, enabled by the publication of the first viral genomic sequence in January 2020. As the pandemic has run its course many aspects of testing have been investigated. Here we highlight some of the key testing events that have taken place, and their outcomes.

Mass Covid Testing

Vo’, Italy – Mass testing in this Italian town was triggered by the reporting of the first COVID-19 death. With a population of 3275, Vo managed to test 86% in a first testing round, and 72% in a second round 2 weeks later. 2.6% were RT-PCR positive in the first round of tests, reducing to 1.2% in the second round. The organiser stated that ‘early identification of clusters and timely isolation of people testing positive suppressed transmission and curbed the epidemic’.

Wuhan – This COVID-19 mass testing event was orchestrated after the initial reactions to SARS-CoV-2 had been implemented and a stringent enforced lockdown had already successfully limited COVID-19 cases. In the last 2 weeks of May 2020 the nearly 10 million residents of Wuhan over 6 years old were tested using RT-PCR; pooled sensitivity was 73%, but no information provided for specificity. Asymptomatic cases reported numbered 300, with no new symptomatic cases found. Contact tracing of the 300 infected showed no cases of transmission. Pooling of five samples at a time were used to increase efficiency in some 23% of the samples. If a pooled sample was positive, all samples within the pool were re-tested as single samples.

Luxembourg – Here, RT-PCR was performed on pooled samples. Reportedly, sensitivity and specificity of the test protocol was 100%. Overall, 49% of the residential population were tested as well as 22% of cross border workers, totalling over half a million people. 850 positive cases were found and a further 249 identified through contact tracing. The study indicated that asymptomatic carriers are at least as infectious as symptomatic patients. It was reported that containment of future outbreaks will critically depend on early testing in sectors and geographical regions. Higher participation rates must be achieved, using targeted incentives and invitations.

COVID-19 Testing Site

 

Slovakia – 20000 medical and 40000 non-medical staff were used to administer 3 rounds of testing at the end of October 2020. The first round was a pilot and high prevalence areas were re-tested in the final round. In all, 5 million tests were performed, covering over 80% of the population. Samples taken by medical professionals used the SD Biosensor lateral flow rapid test, approved by WHO with a sensitivity of 95.5% (70-90% in the study) and specificity 99.2%. No confirmatory RT-PCR tests were perfomed. Over 50000 SARS-CoV-2 cases were positively identified, approximately 4% in the pilot, 1% in round 1 and 0.6% in round 2.

Qingdao, China – The events leading to the mass testing in Qingdao came from three people testing positive using RT-PCR, leading back to 2 asymptomatic dock workers whose transmission path couldn’t be followed further. Over 3 weeks nearly 11 million individuals over 5 years old were tested. To cover this many people pooling was used. The result was the identification of 12 positive cases. Public transport was only available to those with evidence of a negative test. No information was published on the specificity and sensitivity of the RT-PCR test.

Liverpool, UK – The objective was ‘to demonstrate massive asymptomatic cases can help identify far more cases and break the chain of transmission.’ Between the 6th and 26th November 108304 lateral flow tests (LFT) were carried out. Most tests were self-administered (military supervised) lateral flow tests from Innova. Some tests were repeated for quality assessment purposes with samples collected professionally and confirmed using PCR testing. Test sensitivity was substantially reduced depending on who carried out the tests; 78% when used by trained professionals, but only 58% when used by self-trained staff. Specificity was reportedly 99.93%, meaning false positives would be expected to be rare. Key workers, health and social care staff, school staff, and children aged 11 and over were targeted, but anyone could get tested, preferably at least twice within two weeks.

 

Table: Summary of SARS-CoV-2 mass testing events.

COVID Test Types

The variety of tests for SARS-CoV-2 are relatively well known thanks to media reporting.

The most sensitive is the RT-PCR test, we have described this in previous articles. RT-PCR uses engineered primers to amplify fragments of viral RNA present in the specimen and requires a laboratory. Sensitivity is high with figures ranging between 71-98%. However, this variation depends on multiple factors, including the diligence of sample collection, test type, swab type and time for which the sample is left in storage. The RT-PCR based mass testing events in China, taking place in a background of a small number of cases in the community, were seemingly effective in ending the outbreaks. 

Lateral flow tests to detect SARS-CoV-2 antigen came to the market more recently than RT-PCR tests, due to the fundamental timelines inherent in developing a new test of this type. However,  the technology has been around for years and is used in all manner of diagnostic tests, the most well known being pregnancy tests. Lateral flow tests  are relatively cheap to produce and can be tested on site with a result time varying between 5-30 minutes. This saving of time and money makes them an attractive option. Theoretically, they are extremely simple to perform and have the potential to be used by untrained individuals in any location, if the test protocol and instructions for use are simple enough. For SARS-CoV-2 specifically, some tests have now been approved by the US FDA for home-testing (Ellume and BINAX).

COVID-19 negative Lateral Flow test result

 

Lateral flow tests can also be used to identify human anti-SARS-CoV-2 antibodies present in samples, sometimes known as antibody tests or serology tests. However, these can not be used to determine if an individual has a current SARS-CoV-2 infection, only if the individual has ever had an infection. These tests have potential to be used to identify individuals who have already been infected and built up some immunity, and could therefore be a lower priority for vaccination. However, this would be a controversial use of such tests and no country has thus far decided to do this, despite the current context of a shortage of vaccine doses and an urgent drive to protect as many vulnerable people as possible. 

Mass testing analysis

The success of mass testing events is challenging to ascertain; the testing events are ambitious and complex operations featuring innumerable variables. In particular, where mass testing events are carried out alongside a “lockdown”, it is difficult to separate the results of the two and thus understand which element was responsible for any subsequent reduction in infections. It can be said that each mass testing event, in coordination with a lockdown, appeared to reduce numbers of positive covid tests, at least in the short-term.

Overall, RT-PCR is accurate but time consuming and costly. Pooling testing is a cost effective method of testing large numbers using RT-PCR. Lateral flow tests are cheap to produce and give fast results but lack accuracy. Multiple tests performed on the same individuals at different time points could help improve the accuracy. 

The experience of self-administered tests in Liverpool versus the professionally administered tests carried out China and Slovakia highlights the importance of medical expertise. Samples collected by trained professionals provide more accurate results than samples gathered by individuals. The new FDA approved Ellume and Abbott Binax tests are the first home test kits available, reporting sensitivity and specificity of 92% and 100%, respectively, and results within 20 minutes. But their use comes with a caveat in the form of a “Telehealth Proctor”. At present even the most user friendly tests available require supervision for best results; it remains to be seen whether they can be simplified to the extent that they can be performed effectively without this. 

The lateral flow tests used in Liverpool, were found to only confirm half of all COVID-19 cases identified by RT-PCR tests. It has been suggested this is understandable in low viral load cases, which may be less infectious, but it also missed 3 of 10 in higher viral load cases (based on Ct values below 25). These tests have been strongly criticised and called unfit for purpose by some,  but from a public health perspective it can be argued it is better to find 50% of cases rather than none. The UK government has announced more mass testing in COVID-19 high prevalence areas and it remains to be seen how it will modify its approach using the learning points from the Liverpool testing. 

Mass testing is an important tool in defeating SARS-CoV-2. The logistical challenges involved are exceedingly complex (and expensive) and few governments have thus far attempted them. If sensitive and user-friendly lateral flow tests can be developed we expect to see great demand for public and private sector test settings such as schools, airports, universities, care homes and cruise ships.  

Logical Biological provides swabs/serum/plasma for use in test development

At Logical Biological we supply nasopharyngeal/oropharyngeal/nasal SARS-CoV-2, FluA and Flu B swabs available in UTM, Inactivating TM, saline or dry frozen. Negative swabs and COVID-19 / pre-COVID saliva are also available. Typically, our swabs are provided together a Ct value measured from a ‘companion swab’ taken simultaneously. We also provide serum and plasma samples from individuals infected with SARS-CoV-2 and other respiratory infectious diseases.

Swabs table
Table: Products available from Logical Biological

What are Ct values?  

In quantitative PCR (qPCR) and reverse transcriptase quantitative PCR (RT-qPCR), the cycle threshold (Ct) value is the number of nucleic acid amplification cycles required for the signal generated by the amplification of a specific target DNA to cross a set threshold. Labelling the DNA primers with a fluorescent tag is what makes this PCR ‘real time’; as the target genetic material increases with each amplification cycle so does the fluorescence signal.

The lower the amplification cycles required to meet the threshold, the higher the level of target nucleic acid (and thus virus in the case of SARS-CoV-2) in the patient sample. Therefore Ct values are inversely related to viral load. Within a specific test the Ct value result is compared to a value often known as a ‘cut-off’. A value lower than the cut-off is a positive result (for COVID-19 meaning the patient most likely has the infection), whereas a value higher than the cut-off is a negative result.

 

Many of Logical Biological’s COVID-19 swab samples are tested using Thermo-Fisher Taqpath, which has a positive cut-off of Ct ≤37. In that test, a sample with a Ct of 36 would be a low positive. At the other end of the range, Ct values below 20 would be considered a strong positive, and we have infrequently seen values below 15.

Ct values and COVID-19 

The course of SARS-CoV-2 infection shows viral levels vary throughout the duration of the disease, peaking a few days after symptom onset. Correspondingly RT-qPCR Ct values should alter depending on the timeline of an individuals infection. The lower the Ct values the increased probability the patient is near to peak-infection. However there are multiple practical factors unrelated to the actual infection that may also affect the Ct value achieved.

Correspondence between development of viral load during SARS-CoV-2 infection, clinical course and positivity of quantitative rRT-PCR assays (r = real-time). (Lippi et al, 2020).

qPCR/RT-qPCR Ct value variables include but are not limited to:

  1. Swabbing protocol
  2. Swabbing technique
  3. Swab type
  4. Swab brand
  5. Sample storage time
  6. Sample storage conditions
  7. UTM/VTM brand
  8. RNA extraction method
  9. PCR reagents used
  10. PCR test kit used
  11. Patient days since infection
  12. Patient viral load
  13. Environmental contamination
  14. Standard quantification curves

With so many variables any comparison of Ct values between individuals has obvious limitations.

Clinical Use of Covid-19 Ct data

Cycle threshold values are beginning to be used for COVID-19 patients as there is a suggested relationship between viral load and prognosis. Lower Ct values have been linked to a worse course of illness and poorer outcomes. Clinicians have been  encouraged to interpret the SARS-CoV-2 RT-qPCR test results and consider the Ct value where appropriate.

A positive PCR test alone does not correlate with infectivity (Tom and Mina, 2020); a positive test with high Ct value may indicate the patient is not infectious. If this information could be used to inform patient isolation decisions it could transform quarantine restrictions and take significant steps in reducing the already extensive economic consequences of the pandemic, not to mention the mental health implications of isolation. Conversely, low Ct values may indicate a high level of infectiousness, acting as a signal to healthcare professionals to ensure the patient remains isolated and avoid releasing them into the general population until their Ct value increases sufficiently. The challenge here is reliably using Ct values to determine infectiousness.

Contradictory research regarding viral load and shedding in asymptomatic cases require further investigation. Measuring asymptomatic Ct values provided evidence of little difference when compared to symptomatic cases, implying similar viral load. On the other hand, other researchers found asymptomatic cases tested had no viable SARS-CoV-2 virus and no evidence of viral transmission for these carriers. This particular study should be viewed in the context of the virus persisting undetected in a population (Wuhan) where non-pharmaceutical interventions had been used to almost eradicate the virus from the population over a relatively long period of time; selection for a weakened strain may have occurred.

Ct values and disease diagnosis test development

While the value of Ct values to clinicians is debatable, they definitely have utility in in vitro diagnostic (IVD) assay development. Assay sensitivity can be defined as the proportion of true positive samples that actually test positive. SARS-CoV-2 test makers are motivated to produce sensitive tests able to even detect virus in patient samples where the viral load is low. Lateral Flow SARS-CoV-2 antigen test manufacturers, for example, may use patient samples with known RT-qPCR Ct values to determine how the samples test in their assay. Samples with very low Ct counts (high viral loads) would be expected to test positive, but by testing samples with increasing Ct counts (lower viral loads) assay developers can assess the performance of their test, understand what viral loads correspond with a failure of their test to detect, and work to optimise assay performance where necessary.

Conclusions

Ct values have limited use in clinical settings. A multitude of variables impact on the viral load and a separate large set of variables impact on patient outcomes (e.g. age). Ultimately Ct values are not easily comparable between assays or patients. It is possible they can be used to assist patient prognosis in some circumstances where a full clinical history is available. 

However, in vitro diagnostic assay developers find Ct values useful as a way of quickly determining the lower limit of detection of the tests they are developing. In this way, Ct data has a great value in contributing to the development of sensitive tests. 

Available from Logical Biological

At Logical Biological we supply nasopharyngeal/oropharyngeal/nasal SARS-CoV-2, FluA and Flu B swabs available in Universal Transport Medium (UTM), Inactivating Transport Medium (ITM), saline or in dry frozen format. Negative swabs and COVID-19 / pre-COVID saliva are also available, as are serum and plasma. Typically, our swabs are provided together a Ct value measured from a ‘companion swab’ taken simultaneously. For UTM & ITM we can provide remnant samples at your preferred Ct values.

Swabs table

Table: Products available from Logical Biological

This article covers swab type and selection, transport products and medium enabling a smooth transfer of patient samples to the laboratory for analysis. Additionally, we discuss the implications of cycle thresholds and whether they should be assessed in patient prognosis.


Swabs

Swabs come in all shapes and sizes and some favourites have become well known in recent months:

  • Nasal Swab: needs to be inserted at least 1cm into the naris (nostril), directed upwards. May cause sneezing.
  • Nasopharyngeal Swab: one method is to measure the distance from the corner of the nose to the front of the ear, then half it. This is the approximate distance the nasopharyngeal swab should be entering the nasal cavity. Use the medial side of the septum as a guide and gently rotate to facilitate insertion. The swab should run parallel to the palate and needs to be left in place for ‘several seconds’. Taking a sample is a skill in itself. The complexity and invasive nature of this test paired with lack of discrepancy compared to nasal swab results has lead to a shift in favour of nasal swabs. May cause sneezing and watering eyes.
  • Oropharyngeal Swab: enters through the oral cavity (mouth). This swab aims to take material from the tonsils and the oropharyngeal wall (back of the throat), and avoids touching the tongue, teeth and gums. May cause retching.  

nasopharyngeal swab, oropharyngeal swab, nasal swab

Generally the shape of these swabs are incredibly similar, essentially long shafted cotton buds. The tips can be selected to best accommodate the chosen antigen or marker of interest and the shafts chosen for access purposes. Options include long-armed pharmaceutical grade cotton buds, or perhaps Rayon or Dacron swabs are better suited if considering a dry swab. Rayon swabs are made from synthetic fibres spun from wood pulp, whereas Dacron is made from polystyrene. Swabs destined for transport medium require different properties such as polyester or foam, they can be made less or more absorbent, have different porosities and have good ‘release’ factors. Canadian researchers investigated how specific these swabs need to be especially in the current pandemic with supplies at a premium. They determined swab type had limited impact on test results.


Transport Medium

Having collected samples with wisely chosen swabs, samples must be secured in transport medium to make their way to the lab. Again there are many choices. Generally used, Universal Transport Medium (aka UTM) will protect and conserve samples. This is a well know method and low risk regarding the preservation of the sample. Examples are the BD universal viral transport system, which can accommodate storage at room temperature or at +4°C, and Copan UTM, which contains proteins for virus stablisation, plus buffer, antibiotics and antimycotics. 

Other media can provide more specific care depending on sample consistency, for example Viral Transport Medium (VTM) has specific ingredients suited to the transport of viral content. However, UTMs are also suitable for virus sample maintenance and the ingredients list of VTMs is similar. Generon outline a mix including heat inactivated fetal bovine serum, gentamicin and amphotericin B, an antifungal agent. Some recipes suggest including additional calcium and magnesium. If you are making your own sterility can be ensured by filtration or using sterile ingredients and aseptic technique upon mixing. A newer alternative is the Inactivated Transport Medium (ITM), or Molecular Transport Medium.


Inactivation – Health & Safety

It is not a large leap to identify the advantages of using ITM, and in fact there has been a call for this to take place with SARS-CoV-2 from back in April. From a UK perspective, SARS-CoV-2 is classified as Hazard Group 3 (HG3) by the UK Advisory Committee for Dangerous Pathogens. The Containment Level 3 list of requirements for low-risk handling of active HG3 infectious organisms are long and require specialist facilities, including:

  • Maintenance of a negative air pressure
  • HEPA systemic exhaust air extraction and filtration 
  • Sealable laboratory to enable fumigation

For SARS-CoV-2 research and assay development, the ability to transport and analyse inactivated viral samples potentially negates the need for such stringent containment measures. This would assist COVID-19 test developers because they would no longer need to access Containment Level 3 / BSL 3 facilities as part of their test development. Such facilities are few and far between and potentially extremely expensive to access. The CDC advises transport of inactivated COVID-19 samples in a nucleic acid extraction buffer. The nucleic acids remain intact and identifiable, the medium inactivates the protein cap (using guanidine thiocyanate and N-Lauroylsarcosine (sodium) in ethanol) and renders the virus unable to reinfect. Of course, each user will need to abide by their local risk assessments and satisfy themselves that their choice of ITM truly inactivates the virus. Inactivation may denature the antigen of interest so users would need to be sure that the ITM would be compatible with their project objectives. Users should also seek specialist advice on the containment measures required when using any ITM. Logical Biological offers SARS-CoV-2 remnant swabs inactivated in NEST Scientific ITM.


Cycle Threshold Values

With an inactivated sample safely in the lab, the molecular components are ready to be amplified and analysed. Cycle Threshold (Ct) values are important as the quantitative unit of measurement in PCR methodologies and using them in diagnostic testing can be invaluable for patient prognosis. Essentially the lower the number of amplification cycles required to reach a threshold level for the target gene is, the higher the level of target nucleic acid (and thus virus in the case of SARS-CoV-2) in the patient sample; Ct values are inversely related to viral load. Generally speaking a very high Ct value indicates a low amount of target nucleic acid in the sample, and the possibility of environmental contamination should be borne in mind. Often a Ct value of around 34 is the cut-off point for a patient to be considered positive for the infection. Many of Logical Biological’s COVID-19 swab samples are tested using Thermo-Fisher Taqpath, which has a positive cut-off of Ct ≤37. At the other end of the range we have infrequently observed Ct values as low as 9, with Ct values below 15 considered an extremely strong positive. Some Logical Biological clients wish to access a selection of swabs with a range of different Ct values, to ensure that their assay is able to detect the various different ‘strengths’ of infection. This is something we have been able to accommodate readily

SARS-COV-2 PCR Ct values have been analysed and the scientific and clinical communities are assessing if indeed Ct values, that are not often reported in clinical results, should be included and used as a marker for future prognosis. As an example please refer to Rao et al, 2020. 

 

Available from Logical Biological

At Logical Biological we supply nasopharyngeal/oropharyngeal/nasal SARS-CoV-2, FluA and Flu B swabs available in UTM, Inactivating TM, saline or dry. Negatives, and COVID-19 / pre-COVID saliva is also available.

 

Swabs table
Table: Products available from Logical Biological

At the outset of the 2019 SARS-CoV-2 / COVID-19 epidemic, diagnostic immunoassay manufacturers focused on developing anti-SARS-CoV-2 IgM & IgG tests.
While the epidemic has progressed to become a global pandemic, diagnostic test developers’ efforts have also evolved. Recently, we have noticed an increase in interest for patient material positive for Human anti-SARS-CoV-2 IgA. This article will take a look at the difference between the different immunoglobulin sub-classes and seek to understand test developers’ interest in human IgA antibodies specific to SARS-CoV-2.

 

SARS-CoV-2 Antibody Tests

In a recent article we have explained the reason for interest in tests to detect SARS-CoV-2 specific antibodies. Previously infected individuals may be expected to express antibodies specific to SARS-CoV-2. Therefore antibody tests have utility for serology studies that seek to understand how many in the population have previously been infected, and may also have future use as companion tests for vaccinated populations to understand if satisfactory immune responses have been generated. Furthermore, one idea early in the pandemic which hasn’t gained much traction was to mitigate some of the economic impact by identifying and liberating from freedom of movement constraints, i.e. “lockdown”, those individuals who have already been infected by the virus and may therefore be immune from future infections.

 

Types of Immunoglobulin

There are 5 major classes of immunoglobulins. These are IgG, IgM, IgA, IgD, and IgE, each with its own structure based around the classic antibody “Y” shape consisting of Heavy and Light chains.

 

IgG

The most common class of immunoglobulin, present in the largest amounts in blood and tissue fluids, and the most commonly detected type in diagnostic infectious disease tests.

IgM

The initial class of Immunoglobulin made by B cells following exposure to an antigen, commonly present as a receptor on the B cell surface. Typically the earliest class of immunoglobulin detectable before levels wane. However, the situation can vary for different infections and different individuals, e.g. in Lyme Disease and Toxoplasmosis which we have covered in previous articles.

IgA

The main class of antibody found in many bodily secretions including tears and saliva, respiratory and intestinal secretions. Typically, IgA is not as stable as IgG despite being synthesized in large amounts

IgE

IgE is present in low concentrations in the blood. IgE antibodies stimulate a histamine response when binding allergens and play a crucial role in allergy testing; allergen specific IgEs produced in response to exposure to a given allergen can be readily detected in human serum or plasma and are diagnostic of specific allergies.

IgD

IgD is present on the surface of most B cells early in their development but only limited amounts are released into circulation

 

Why Test for IgA?

Whereas early studies of SARS-CoV-serological responses focused on IgG and IgM responses, some papers have suggested COVID-19 IgA may be the most readily detectable of the immunoglobulins in COVID-19 patients and detection of it can serve to increase test sensitivity.

Back in March 2020 Guo et al reported that IgM and IgA appeared earlier than IgG while IgG titres were highest followed by IgA and then IgM.

In a May 2020 article, Jääskeläinen et al. analysed sera from 39 patients and determined that IgA levels were higher than IgG in most cases. In many cases, the IgA level was high enough for the patient to test positive whereas the IgG level was below the threshold for a positive test result. Euroimmun SARS-CoV-2 IgG and IgA kits were used, which are suitable for detection in serum and plasma.

In August 2020 Beavis et al showed 68 out of 82 SARS-CoV-2 PCR positive patients were positive for SARS-CoV-2 IgA whereas 55 out of 82 were positive for SARS-CoV-2 IgG. For patients tested 0, 1 or 2 days after symptom onset the vast majority were negative for IgG whereas most were positive for IgA.

 

 

Timelines of IgG and IgA results from SARS-CoV-2 PCR positive patients (from Beavis et al.)

 

Infantino et al., have recommended the use of IgA tests in order to enhance diagnostic sensitivity of COVID-19 serology tests. They found that IgA levels reached concentrations higher than those observed for IgG and IgM and were often positive in IgM negative patients. Therefore, IgA could shorten the amount of time needed post-infection for virus positive patients to test antibody positive.

SARS-CoV-2 IgG, IgA and IgM in SARS-CoV-2 patients who were initially IgM negative

 

Saliva testing

Collecting blood and converting to serum or plasma in order to detect antibodies is a fairly straightforward process, but perhaps not as straightforward as collecting saliva. Since IgA tends to be present in saliva, detection of  SARS-CoV-2 specific human IgA could theoretically be performed on saliva. Recent studies have confirmed that SARS-CoV-2 IgA is detectable in the saliva of COVID-19 patients.  Another paper in pre-print suggests that antibody levels in serum and saliva do not correlate particularly well so testing in both matrices would enhance test sensitivity even further.

 

Closing the serology gap

If the time window between viral infection and antibody detectability is short enough (e.g. 0-2 days post-infection) the utility of SARS-CoV-2 serology tests could greatly increase. With many countries struggling to expand molecular PCR testing capacity to the levels needed, serology tests carried out using different technology and by different laboratories/personnel to PCR tests, would be additive to the existing COVID-19 test capacity. The price per test would also likely be significantly lower. Unfortunately, it would be hard to tell from the test results exactly when the patient had become infected, especially as antibody levels post-infection vary greatly between individuals, so the utility of such a test is still in doubt.

Interestingly, SARS-CoV-2 IgA also has potential as a prognostic marker, being associated with more severe disease.

 

Conclusion

Data from several sources suggests that the detection of SARS-CoV-2 IgA in addition to the other immunoglobulins (IgG and IgM) represented in SARS-CoV-2 antibody tests  can increase the sensitivity of COVID-19 tests when compared with tests to detect anti-SARS-CoV-2 IgG and/or IgM .

Logical Biological offers serum and plasma samples with measured positive levels of SARS-CoV-2 IgA, IgM and IgG as well as SARS-CoV-2 positive swabs.

With the world’s attention focused on SARS-CoV-2 and the serious impact COVID-19 is having both on our health and on society as a whole, it is worth noting that humans have in fact co-existed with numerous coronaviruses (CoVs) for millions of years. It is little understood how these related viruses have such startlingly different effects on infected individuals but some researchers have found evidence that mild CoV infection offers some protection from SARS-CoV-2. Could it be that the common cold may actually be a useful ally in our struggle to combat COVID-19?

It is only in recent years, after the emergence of SARS-CoV, that coronaviruses have been considered a significant threat to human health; before this time it was thought coronaviruses caused only mild respiratory infections in humans. HCoV-229E, HCoV-NL63, HCoV-OC43 and HCoV-HKU1 are all endemic in the human population1,2,3,4, causing 15-30% of respiratory tract infections each year and are mostly experienced as a mild cold by those infected. Only rarely do they lead to lower respiratory tract infections in high-risk individuals. This is in marked contrast to SARS-CoV, MERS-CoV and of course the current headliner SARS-CoV-2.

 

Two individuals with possible endemic human Coronavirus infection

 

There is a clear distinction between the endemic, mild disease-causing Human CoVs and the three newly emerged, highly debilitating CoVs. With the latter all due to recent jumps from animal hosts it is clear that zoonotic diseases can be highly debilitating to the human immune system. However, with some individuals being exposed to the novel zoonotic CoVs and only eliciting mild symptoms, is there any chance that the endemic, older strains may be serving up some protection that explains this variability in disease progression?

Tantalisingly, this has been suggested by a recent study published in Science by Jose Mateus and colleagues5. Using samples from unexposed individuals the team were able to identify memory CD4+ T cells that cross-reacted with the four common cold coronaviruses and to SARS-CoV-2, suggesting that previous infection with a milder coronavirus may produce CD4+T cells that can also protect against COVID-19. In accordance with this finding it was also recently found that children that had developed a serious form of COVID-19, called multisystem inflammatory syndrome (MIS-C) carried no antibodies to two of the common endemic coronaviruses, unlike children who had suffered only mild COVID-19 symptoms6. The authors speculated that this lack of protection may have played a role in the serious disease progression seen in these small number of cases.

Another interesting study analysed the CoV-specific antibody repertoires in children and adults and found these to be qualitatively different between these two groups. The anti-HCoV IgG specificities in children were more likely to target regions that are functionally important and structurally conserved in the viral spike and nucleocapsid with some appearing to be broadly cross-reactive across human CoVs7. This fascinating insight into differences in the immune response between adults and children could in part explain why COVID-19 disease is much milder in younger members of the population as well as hinting at the possibility of cross-reactivity of antibodies generated to previous mild CoV infection.

Although highly speculative at the moment, the cross-reactivity of antibodies generated to mild endemic CoVs may in part explain the huge variance in COVID-19 disease states. Perhaps in a COVID-19 future we will embrace catching a common cold each year, celebrating the antibodies it has gifted us to protect against its more dangerous relatives.

 

Antibodies that cross-react between coronavirus strains may be highly desirable in the population but for in vitro diagnostic SARS-CoV-2 antibody tests it is essential that such tests do not detect antibodies individuals have raised against the other endemic CoVs. The FDA publishes a list of potentially cross-reacting markers that manufacturers of SARS-CoV-2 antibody tests wishing to gain Emergency Use Authorisation should ensure are not recognised by their test. These include antibodies to the 4 circulating human CoVs as well as antibodies raised against various other infectious diseases.

Patient/donor serum and plasma specimens collected before the COVID-19 pandemic and containing measured levels of these potential cross-reactors are available at Logical Biological.

The current US FDA list (as of 23rd September 2020) is:

anti-Influenza A IgG & IgM
anti-Influenza B IgG & IgM
anti-HCV (IgG and IgM)
anti-Hepatitis B Virus (HBV) IgG & IgM
anti-Haemophilus influenzae IgG & IgM
anti-229E Alpha Coronavirus
anti-NL63 Alpha Coronavirus
anti-OC43 Beta Coronavirus
anti-HKU1 Beta Coronavirus 
ANA (Anti-Nuclear Antibodies)
anti-Respiratory Syncytial Virus (RSV) IgG & IgM
anti-HIV

 

Logical Biological has gained ISO 9001:2015 certification. We have always operated a Quality Management System based on the ISO 9001 system, and now we have the certificate to prove we are fully ISO 9001 compliant. This emphasises our commitment to Quality processes and products.

Logical Biological specialises in provision of human biospecimens.

 

Two types of tests for SARS-CoV-2 currently predominate. The first are molecular tests, based on PCR technology, that detect the presence of viral nucleic acid and therefore indicate a current infection. The second are serology tests that are designed to detect anti-SARS-CoV-2 antibodies (usually IgG) generated by the immune systems of individuals who have been infected in the past.

RT-PCR to detect SARS-CoV-2 virus is relatively slow and requires specialist laboratories. At the outset of the pandemic, testing capacity was too low to meet the needs of governments, and even 6 months later demand for tests can outstrip supply in areas where there is a surge of infections. At the end of June 2020 Quest Diagnostics, a key player in COVID-19 testing in the USA, announced that only the highest risk patients could get a test result faster than 3-5 days. Other companies reported similar issues.

Alternatives to slow and expensive procedures such as RT-PCR testing do exist. Rapid tests based on Lateral Flow technology have been put forward as a faster, cheaper, low technology alternative to RT-PCR testing. However, this technology is fundamentally of lower sensitivity than PCR-based testing; while PCR is able to exponentially increase the signal until it is detectable, Lateral Flow (also known as immunochromatography) tests have little scope for signal amplification.

An example of Lateral Flow rapid tests

There is also the question of what tissue type to use for the testing. While many rapid tests use serum or plasma derived from blood as the sample of choice, that would only be a suitable matrix for SARS-CoV-2 testing if the virus was present in samples from infected individuals. In the case of SARS-CoV-2 it would seem that blood (and therefore serum and plasma) is not suitable. In a March 2020 JAMA paper, Wang et al. reported that using RT-PCR, SARS-CoV-2 was only identified in 3 out of 307 blood samples (1%) collected from up to 205 patients in China.

Since the virus is thought to be spread by droplets in coughing and sneezing, saliva has been considered a high potential sample type for rapid tests. It does seem that in many cases the virus is present in saliva samples – a recent paper by Azzie et al. in the Journal of Infection has determined that in a cohort of 25 patients with severe COVID-19, virus was detectable in the saliva of all 25 of them via RT-PCR. The Cycle Threshold values ranged from 18 to 32 with a mean average of 27. The extent to which the virus is present in asymptomatic patients remains to be determined.

A further challenge around rapid antigen detection in saliva or other sample types is sensitivity. RT-PCR is highly sensitive and theoretically able to detect a very low number of viruses. However, in a recent study by Mizuno et al. on >100 patients, virus was only detected in 11.7% of them using a rapid antigen test (Fujirebio) compared to up to 82% using molecular diagnostic tests.

Intriguingly, faeces and rectal swabs have a high potential as a positive sample type; in a review article Bwire et al. reported positive rates of 32.8% and 87.8%, respectively. Rectal swabs have a vastly superior positive rate according to this review than both nasopharyngeal (45.5%) and oropharyngeal (7.6%) swabs. Although they are perhaps not so amenable to drive-through testing(!), they have some potential for self-testing at home.

Our surprising conclusion is that stool samples may be the best matrix for rapid SARS-CoV-2 virus testing. Serum and plasma are clearly not suitable and saliva, which is perhaps the most convenient alternative, may have a lower viral load than stools. A further challenge with both stools and saliva is that they are likely to need diluting into a suitable liquid prior to testing, to enable them to flow down the test strip. This would reduce the test sensitivity even further .

If rapid tests cannot reach the levels of sensitivity of RT-PCR tests, do they have any utility? Some believe that they do. If it was possible to make such a cheap and easy test that everyone in the country could be tested, say, 1 or 2 times every day, it could be that at some point in the infection cycle those carrying infections would have a high enough viral load to test positive using a low sensitivity test. In the context of this pandemic where a large proportion of those infected never find out due to being asymptomatic or not ill enough to get tested, this may be of value, and is presumably why companies continue to pursue the holy grail of SARS-CoV-2 rapid testing.

Logical Biological provides human patient material for SARS-CoV-2 relevant to both virus and serology testing. This includes nasal swabs with quantitative PCR results, saliva and serum/plasma.

Here at Logical Biological we care about reducing our environmental impact. We are lucky to work in a rural location and get to see lots of wildlife around our HQ at Discovery Park. A few days ago, we were able to put our environmentally conscious aims into practice when we saved a Green Woodpecker. We noticed the beautiful bird, caught upside down with its legs tangled in synthetic nesting material high up on the outside of the building.

 

The trapped woodpecker

 

We at Logical Biological will not stand idly by whilst a woodpecker is in distress, so we sprang into action and… called Discovery Park reception! Some heroes arrived with a ladder to retrieve the woodpecker, whilst Logical Biological provided the crucial pair of scissors required in the untangling process.

 

Untangling the woodpecker

 

Although our levels of customer service are second to none, we are not expecting to win awards for our wildlife photography any time soon! However, here is a picture so you can see what a Green Woodpecker (Picus viridis) looks like when it is not being saved by the team at Logical Biological.

 

The European Green Woodpecker (Picus viridis)

 

 

We are in the midst of the most significant global pandemic since the 1918-19 Influenza pandemic, over 100 years ago. The 2020 pandemic has been caused by a Coronavirus, named SARS-CoV-2, which confers a severe respiratory illness (COVID-19) on a proportion of those infected. The virus is readily transmissible from human to human with many of those infected showing no or mild symptoms, meaning it is hard to know who has been infected.

The virus has resulted in severe economic impacts because many countries have adopted “lockdown” policies in order to limit its spread by limiting interaction between individuals. One idea for mitigating some of the economic impact has been to identify and liberate from lockdown those individuals who have already been infected by the virus and may therefore be immune from future infections. As yet, it is not known for sure if previous infection by the virus renders individuals immune from future viral challenge, nor how long such immunity would last for. However, for this idea to be viable, diagnostic tests that can identify the SARS-CoV-2 antibodies in the human blood are required. Such tests have been made by innumerable manufacturers but they vary greatly in their performance.

 

At what stage are antibodies exhibited?

To understand the value of SARS-CoV-2 antibody tests we need to know who exhibits what antibodies, and when. It is assumed that the vast majority of individuals will have a detectable antibody response, regardless of whether or not they are symptomatic. The below data suggests IgG and IgM antibodies are detectable 1-3 weeks after SARS-CoV-2 symptom onset.


Detection of IgG, IgM and Neutralising (NT) antibodies over time since symptom onset.
Taken from a pre-print published online by Borremans et al., (2020)

 

Why 100% test specificity is essential for SARS-CoV-2

Logical Biological received some CE-marked SARS-CoV-2 IgG and IgM antibody tests a few weeks ago (we won’t name the manufacturer). In the pack insert these tests reported 97% specificity, which sounds high, but what does it mean in the context of the proportion of people who actually have been infected in the population? Specificity can be defined as the number of true negative cases that actually return a negative test result.

As can be seen in the tables below, if 1 person is selected at random and tests positive using a 97% specificity test when the prevalence within the population is low, it is much more likely that a positive test result is a false positive than a true positive.

Even with a 99.6% specificity test, such as those now available in a leading UK high street pharmacist, there is a clear threat of false positives, the proportion of false positives to actual positives reducing as the true number of infected within the population increases. One serology study, performed in Santa Clara, California, received criticism that the specificity of the test was too low, at only 99.5%. Only with 100% can we be fully confident that the positive test result is a true positive. Fortunately, such tests are now becoming available, such as one developed by Ortho Clinical Diagnostics.

The tables below consider a random selection of the population. Individuals may feel more confident about a positive result they receive if they have also shown the classical symptoms.

97% Specificity

% of population prev. infected Test Specificity True positives (per 1000) Expected False positives (per 1000)
0.1% 97.0% 1 30
1% 97.0% 10 30
10% 97.0% 100 30
100% 97.0% 1000 30

 

99.6% Specificity

% of population prev. infected Test Specificity True positives (per 1000) Expected False positives (per 1000)
0.1% 99.6% 1 4
1% 99.6% 10 4
10% 99.6% 100 4
100% 99.6% 1000 4

 

100% Specificity

% of population prev. infected Test Specificity True positives (per 1000) Expected False positives (per 1000)
0.1% 100.0% 1 0
1% 100.0% 10 0
10% 100.0% 100 0
100% 100.0% 1000 0

 

Sensitivity

Sensitivity of a test can be defined as the proportion of those genuinely bearing a marker (such as SARS-CoV-2 antibodies) who test positive for it. In the context of SARS-CoV-2 antibody tests, results from low sensitivity tests are less “dangerous” than results from low specificity tests. Low specificity tests could result in a situation where susceptible individuals who have wrongly tested positive, believing themselves to be both immune and non-infective, stop taking precautions to protect themselves and others, leading to further infections. On the other hand, low sensitivity tests would likely result in previously-infected individuals who have wrongly tested negative continuing to be cautious and since they have already had the infection would not be able to contribute to further spread in any case.


Table shows theoretical results of a 97% sensitivity test

% of population prev. infected Test sensitivity True positives (per 1000) Expected positives based on 97% sensitivity
0.1% 97.0% 1 0.97
1% 97.0% 10 9.7
10% 97.0% 100 97
100% 97.0% 1000 970

 

 

How many people have actually been infected by SARS-CoV-2?

One of the countries most affected by the pandemic has been Spain. The government of Spain has recently performed a serological study (results published on 13th May 2020) where they assessed the blood of 70,000 individuals. The most affected province showed 14.2% positive tests whereas the least affected regions were at less than 2%. The overall figure for previously-infected individuals in Spain was assessed to be approximately 5%. The test looked for both IgG and IgM antibodies. In the context of the above information, it should be noted that the test used was reported to show 100% specificity and 79% sensitivity for IgG. This means it would miss 21% of those previously infected and also may miss some people in the early stages of infection. It was wise of them to choose a 100% specificity test, and in the context of a serological survey to assess prevalence within a large population, the results can be adjusted to account for the low sensitivity of the test.

Data from other countries is in line with that from the Spanish study. For example, study results announced on April 23rd from another of the world’s major hotspots, New York State, USA, found 21% of people to be antibody positive in New York City. High figures (10-20%) were also seen in other areas while outside of the most-affected areas in the state the average prevalence was 3.6%.

 

Conclusion

The prevalence of SARS-CoV-2 in some locales is 2-20%. At the upper end of this range the % of positive tests that would be false when using a 97% specificity test would be significant and unacceptably high. At the low end of this range there would be more false positives returned than true positives, rendering such a test completely useless. Beware SARS-CoV-2 antibody tests with <100% specificity.

 

Available from Logical Biological

  • SARS-CoV-2 PCR positive serum/plasma/swabs
  • SARS-CoV-2 IgG positive serum/plasma – 1ml samples and bulk units
  • SARS-CoV-2 IgM positive serum/plasma – 1ml samples and bulk units
  • Pre-Covid19 serum/plasma from normal healthy donors – any quantity

Due to the dynamic nature of the SARS-CoV-2 pandemic this blog post will be out of date shortly after it is written.

As we move into 2020, one thing we’d like to do at Logical Biological is find a greener way of dealing with polystyrene box waste. The material has fantastic properties making it ideal for use in shipping biological reagents around the world. It is incredibly lightweight, a great insulator and it can withstand some knocking around, so it is no surprise that our industry uses so much of it. The downside is that most EPS boxes are treated as single-use and are destined for landfill or incineration. How can we get rid of them in a way that minimises environmental impact? We’d love to know how people would feel about receiving goods in re-used EPS boxes where it is safe to do so. Any other suggestions on this topic are very welcome! You can contact us on infoATlogicalbiological.com or follow this link to complete the web form.

Logical Biological, December 2019