WHO geneva will already know because it is (or should be) explained in every introduction to virilogy lecture course. virulence and pathogenicity are completely different. the graph is precisely what we expect given natural selection, which favours virulence, and does not favour killing/isolating your host.
what is virulence?
how does pathogenicity (disease causing ability) relate to virulence (ability to do damage)?
Are virulence and pathogenicity really completely different?
I think you mean transmissability and virulence are completely different.
The natural selection argument is theoretically sound however The problem happens when you have the most significant transmission in a hospital environment you inadvertently select for nastier variants. This happened with the original SARS, which had been circulating widely in China and elsewhere for a many months without even being noticed, it mutates to be virulent enough to hospitalize someone, and then the more virulent strain runs through the hospital....IIRC it was the Prince of Wales Hospital Hong Kong then patients were sent to other hospitals and the whole thing was off to the races.
There is some evidence exactly the same thing happened with the current coronavirus, it was circulating before it maybe it mutated to become more virulent which meant it popped up in a hospital in Wuhan, it was then widely transmitted in the hospital leading to the very high CFRs initially seen.
It is interesting to wonder what lockdowns tend to select for, increased virulence and pathogenicity (leading to transmission in hospitals) or increased transmissability and reduced virulence?
Singapore can give you a partial answer on that, lockdown eliminated a reduced virulence strain which was replaced by a nastier imported strain.
how is a combination of mRNA that will break down in a couple of hours and ingredients found in plenty of other pharmaceuticals guaranteed to have long term effects? are you not just ignoring your own biases there?
If it doesn't have long term effects, positive, negative or otherwise and breaks down in a couple of hours that means it is a pretty worthless vaccine. Unless you get infected with covid a couple of hours post vaccination.
You are displaying your own bias there. You assume that long term effects are necessarily negative, they might be or they might be positive or they may be a mix of both and that is the unknown.
What is for certain is that the current Covid vaccines were developed very rapidly with corner cutting and rather less scrutiny of the results than is normal. I am not going to argue whether that was right or wrong. It is just a fact.
None of these vaccines are licensed, none have marketing authorization and it is unlikely any of the current ones ever will get a proper license or marketing authorization. Again that is just a fact.
It is a truism to say it is better to be lucky than good, lets hope pharma got lucky with the covid vaccines.
Personally I think it is likely we are going to see some unfortunate effects from some of these early vaccines when they are reviewed in a couple of years. There are very good reasons for the P1 P2 P3 trial system and it should all be backed with solid data, right now we have not got this so we are hoping to be lucky.