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11 August 2021 | Story André Damons | Photo Anja Aucamp
Prof Felicity Burt from the University of the Free State (UFS) and the National Health Laboratory Services (NHLS) holds an NRF-DST South African Research Chair in Vector-borne and Zoonotic Pathogens Research. She is also an expert on arbovirology in the UFS Division of Virology.

New variants of severe acute respiratory coronavirus 2 (SARS-CoV-2) have the potential to influence the size and duration of waves of infection and may prolong the duration of COVID-19’s stay with us. Despite the development of vaccines and the technology available to adapt vaccines in the future to address the emergence of new variants, it is extremely unlikely that COVID-19 will ever be eradicated.

The emergence of new variants has illustrated the importance of continually monitoring circulating variants for changes in viral proteins associated with cell binding (in other words, influencing entry of the virus into a cell) and immune responses (which would influence vaccine efficacy and reinfections). 

Prof Felicity Burt from the University of the Free State (UFS) and the National Health Laboratory Services (NHLS), who holds an NRF-DST South African Research Chair in Vector-borne and Zoonotic Pathogens Research, says the current vaccines are effective against severe disease, but do not prevent transmission. Hence, complete eradication of the virus is unlikely, as the virus will continue to circulate at low levels in the population even if high levels of vaccine coverage are achieved.  Prof Burt is also an expert on arbovirology in the UFS Division of Virology

“To date, the only pathogen that has been eradicated globally is the smallpox virus. This was achievable because of a highly efficacious vaccine and because smallpox caused a disease that was readily recognisable, enabling rapid isolation of afflicted patients. In contrast, a virus such as SARS-CoV-2 that can cause asymptomatic infections in which the person is unknowingly infected and able to shed and transmit the virus, is probably impossible to eradicate,” explains Prof Burt.  

Development of affordable treatment options remains important 

The current vaccines are, however, able to reduce the severity of the disease until a vaccine is available that prevents complete transmission of SARS-CoV-2; therefore, the development of affordable treatment options remains important. Novel therapeutics, such as an antiviral drug that interrupts replication of the virus, or monoclonal antibodies that neutralise the virus, would go a long way to contribute to the treatment of infections.  

“Currently, monoclonal antibody therapy is available in higher-income countries. Monoclonal antibodies mimic our natural antibody response, targeting specific regions of the virus, neutralising the virus, and stopping it from entering cells. Monoclonal antibodies have been used to treat other viral infections such as Ebola; however, they have significant limitations due to cost, availability, and high specificity, meaning that mutations in emerging variants could influence their efficacy. They are unlikely to be an affordable option in lower-income countries.”

Mutations become problematic

According to Prof Burt, viruses have a propensity to acquire mutations, or changes, in their genetic make-up during replication, and as expected, this virus has changed during the pandemic and will inevitably continue to mutate.

“These mutations become problematic if they influence the way the virus is transmitted between people, or if the disease profile changes and the virus causes a more severe disease, or if the changes result in a virus that is not recognised by the body's immune response.  In other words, the virus is capable of hiding from, or can escape, the immune response that a person has developed as a result of a previous natural infection or from vaccination. 

“If the virus has changed such that an existing immune response does not recognise it, then a person can become reinfected. Hence, changes in the ability to escape immunity are considered to confer an advantage to the virus. Although there are changes in all regions of the viral genes, we are concerned with changes that occur in the gene that codes for the spike protein. This protein is responsible for binding and entry of the virus into cells, hence changes in the spike protein that allow the virus to more readily enter cells are considered to be an advantage to the virus.” 

Variants of interest vs variants of concern

Prof Burt says there is now some evidence suggesting that antibodies produced in response to the Beta variant – the dominant variant during the second wave in South Africa – are less efficient at neutralising the Delta variant of the virus. In addition, there is evidence suggesting that the Delta virus can replicate to higher levels in the body, resulting in a higher viral load. Although the kinetics of each variant are still not completely understood, the combinations of higher viral load, and the potential for reinfections to occur will likely contribute towards a larger wave of infection.

“The World Health Organisation (WHO) and international partners characterise emerging variants as variants of concern (VOC) or variants of interest (VOI). Although there are multiple new variants globally, only a small proportion of these meet the definition. The Lambda variant, initially recognised in South America, is deemed a VOI. This is a level below VOC, indicating that it has mutations that are known or have the potential to affect the characteristics of the virus and that the prevalence is increasing in multiple countries over time. Currently, Lambda is not a concern in SA. In contrast, a VOC has the same characteristics as a VOI, but in addition, has one or more of the following: increased transmissibility or is associated with change in disease severity or clinical presentation, or the public health and social measures are less effective against the variant,” says Prof Burt.  

Vaccines will likely need to be adapted to accommodate future variants 

It is impossible to predict which variants may emerge next, explains Prof Burt. “Fortunately, although the current vaccines may not prevent mild disease, they have all been shown to reduce the incidence of severe disease and fatalities. The technology for adapting vaccines is available – but of course – if a vaccine has to be adapted, it will take some time for that to be available. As this virus is now well established globally and will continue to evolve over the years, it is likely that, in the future, vaccines will be required to be adapted to accommodate circulating variants.”

“Although there is some reduction in vaccine efficacy against the currently circulating variants, there are fortunately high levels of protection against severe disease and hospitalisation in people who have received the single-dose Johnson & Johnson vaccine or both doses of the Pfizer vaccine. In other words, they are fully vaccinated,” says Prof Burt. 

Despite reduced effectiveness and potential for vaccine breakthrough, it is still important for people to be vaccinated, as it reduces viral load and duration of virus shedding. Less viral replication means that the virus has less chance to mutate, with less chance of new variants emerging.   

News Archive

Verslag: SA studente atletiek (Afrikaans)
2005-04-28

Absa-kovsieatletiek
SA studente atletiekkampioenskap - 22 en 23 April 2005 Johannesburg Universiteit

 

Weereens baie goed!!! Dit is hoe ons die Kovsieatlete se vertonings op en af van die baan af kan beskryf. Die 22 medaljes vanjaar teenoor die 25 van 2004, die 14 van 2003 en die 10 van 2002 spreek boekdele, veral as ons in ag neem dat ons in die laaste week 4 van ons top atlete weens beserings verloor het (Antonie Rossouw, Nico Oosthuizen, Jaco Claasen en Renè Kalmer).

Ons het op 20 April om 09:00 vanaf Pelliespark per bus na Johannesburg vertrek en tuisgegaan in die Randburg Road Lodge hotel.

'n Totaal van 43 atlete – 18 vroue en 25 mans het die Kovsies verteenwoordig (spanlys aangeheg).

Die bestuurspan het bestaan uit Danie Cronjé bestuurder mans, Sarina Cronjé bestuurder vroue, Bertus Pretorius afrigter mans, Ans Botha afrigter vroue, Hendrik Cronjé (Video), Jan du Toit, Sidney van Biljon, DB Prinsloo sportbestuurder.

Die mediese span het bestaan uit Dr. Org Strauss en Daleen Lamprecht(bio).

Die volgende lede van die ABSA KOVSIESPAN het medaljes verwerf.

GOUD    
     
Jan vd Merwe  400   46,37
     
Johan Cronjé    1500 mans   3:50.20
     
Boy Soke  10000   30:23,40
     
Charlene Henning   Driesprong vroue  12.62m
     
Francois Potgieter      Tienkamp  6862 punte
     
Magdel Venter    Diskusgooi vroue     46.94m
     
Kovsiespan mans   4x400 Aflos  3:10,17
     
(Dirk Roets, Francois Lötter, Johan Cronjé, Jan van der Merwe)
     
     
SILWER    
     
Charlene Henning  Verspring vroue    6,16m
     
Magdel Venter  Gewigstoot vroue  13,21m
     
Sanè du Preez   Hamergooi vroue     44,71m
     
Boy Soke     5000m    14:36,60
     
Francois Potgieter  110 Hekkies mans    14,00sek
     
Christine Kalmer  1500m vroue    4:35,40
     
Cobus Marais    3000m hindernis   9:32,80
     
     
BRONS    
     
Gustav Kukkuk     110 Hekkies mans    14.00sek
     
Mariana Banting    Driesprong vroue  12.36m
     
Helen-Joan Lombaard   Sewekamp vroue    3354 punte
     
Clive Wessels   Paalspring   4,05m
     
Johan Cronjé  800m  1:52,01
     
Kovsiespan vroue   4x100 Aflos    47,56
     
(Denise Polson, Elmie Hugo, Carlene Henning, Minette Albertse)
     
Kovsiespan mans    4x100 Aflos   42,21
     
( Tiaan Pretorius, Gustav Kukkuk, Marno Meyer, Wiaan Kriel)
     
     
Kovsies wat ook onder die eerste 8 geëindig het sien as volg daaruit:
     
     
4de Plek    
     
Mariana Banting   Hoogspring vroue  1.70m
     
Stefan van Heerden   Driesprong  15,12m
     
Elmie Hugo   200m   24,12sek
     
Ronè Reynecke     400m  57,31sek
     
     
5de Plek    
     
Jackie Kriel    100 Hekkies    13,90sek
     
Jackie Kriel     400 Hekkies   65,40sek
     
Riana Rossouw    Gewigstoot    10,59m   
     
Kenny Jooste   Verspring   7,23m
     
Elmie Hugo    100m  11,86sek
     
Helen-Joan Lombard  Paalspring    3,25m
     
Ronè Reynecke     800m   2:17,58
     
Christine Kalmer   5000m      17:38,32
     
     
6de Plek    
     
Tiaan Pretorius  Verspring   7,21m
     
Francois Pretorius    800m     1:52,67
     
Riana Rossouw   Spiesgooi      38,12m
     
Kovsiespan vroue   4x400 Aflos  4:06,56
     
(Ronè Reynecke, Denise Polson, Lise du Toit, Elmie Hugo)
     
     
7de Plek    
     
Gerda Rust    Hamergooi   36,37m
     
Schalk Roestoff     1500m      3:55,80
     
Francois Lotter    400m       47,94
     
Pienaar j v Rensburg    10000m   32:12,21
     
Kovsie mans  ”A”  en  B span  4x400     3:15,44
     
     
8ste Plek    
     
Charles le Roux   Verspring   7,06m
     
Tiaan Pretorius  Driesprong  14,06m

In die spankompetisie het die Vroue 4de geëindig en die mans 4de. In die algehele kompetisie het die Kovsies ook die 4de plek behaal (aangeheg).

Die gees en gedrag van die toergroep was uitstekend en was die atlete goeie ambassadeurs vir die Kovsies.

Danie Cronjé     Sarina Cronjé
Spanbestuurder  Mans   Spanbestuurder Vroue

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