Originally Posted by
rsvman
I read through the entire paper that your article references. Interestingly, but not surprisingly, the part that the media chose to highlight was barely on the radar in the actual paper. The paper was about spread on cruise ships. I found some of the numbers actually fairly reassuring; despite being stuck together on fairly close quarters, about 80% of the passengers did not get infected. Spread among passengers was largely halted once they began limiting their contact aboard the ship, whereas spread among the crew (who had to continue to work) peaked AFTER contact/movement of passengers was limited.
The part about finding viral RNA on surfaces 17 days later was a single line in the article, and was attributed to "personal communication" (that's science speak for unpublished and unreviewed). It should be noted that coronavirus RNA is not infectious unless it is contained within the virus and its envelope. When an enveloped RNA virus dessicates, the virus becomes no longer communicable.
It is somewhat surprising that even RNA would survive that long, given the fact that there are RNAses everywhere (RNA is notorious for breaking down very quickly). It pays to remember, however, that RT-PCR testing done for coronavirus RNA only looks at two segments of the genome that together are about 100 nucleotides in length, and also that PCR logarithmically expands existing RNA. It is possible (and, in fact, in my opinion, likely) that not only was there no communicable viral material on those surfaces but also that there wasn't even any INTACT viral RNA on the surface; if small segments had not yet been broken down by environmental RNAses, PCR could still come back as positive. I have no way of knowing for sure, but I would be willing to bet that no infectious virus was in those cabins after 17 days. From a virologic standpoint, it's almost impossible to believe otherwise. Finally, testing was also done before any cleaning whatsoever was performed.
For those who don't know what PCR testing is or how it works, I'll give you a short primer (pun intended). If you already understand PCR testing, feel free to skip this part.
For simplicities' sake, let's look at the most common testing, PCR of DNA. (PCR stands for Polymerase Chain Reaction, by the way.)
Say you are looking for herpes simplex virus DNA in a sample taken from a skin lesion. You put the sample into a buffer, along with primers that match up to the DNA of virus, along with a soup of nucleotides and DNA polymerase (the polymerase is an enzyme that catalyzes the reproduction of DNA; the nucleotides are the building blocks of DNA). Then you put the sample into a machine. What the machine does is heat up the sample to a point at which the herpes DNA strands denature (essentially separate into two strands), at which point the sample begins to cool. As it cools, the polymerases in the "soup" start taking the nucleotides in the soup and matching them up to the separated strands. Thus, one strand of DNA becomes two, each new strand containing half of the old DNA and the other half the newly synthesized DNA. The sample is cooled down enough to make the entire process complete, then it is reheated again, which then separates the two strands, then it is cooled again, and the polymerases turn those two strands into FOUR. This process continues over and over again for multiple cycles, thus amplifying the sample many, many times over in logarithmic fashion. Sometimes they are cycled up to 30 or 40 times, turning even a single piece of DNA potentially into BILLIONS of pieces of DNA.
The main problem with PCR testing is false positives, precisely because amplification is so immense. Say, for example, that the person who had the skin lesion doesn't really have herpes infection, but the person who loads the PCR machine has occasional cold sores. If he/she is not wearing a mask when they load the sample, it would be simple for a tiny amount of herpes virus DNA to be accidentally inoculated into the sample (herpes DNA can be shed even when the person is not experiencing active cold sores).
Anyway, sorry for the long explanation. Many of you probably already knew all this. I certainly don't want to "talk down" to anybody. Some things I think people might want to know they really might not care about. It's hard to know, also, when I am oversimplifying things, or, conversely, going over people's heads. I apologize to anybody who feels like I am doing either of those things. I'm trying to walk the line between the two, but sometimes it's hard to know where that line is.