Seeing lots of analyses scraping GISAID data and looking at variant sequences / total sequences. I've heard chatter in my corner of the world that "Wow, Michigan really has a variant problem." Do we? Short thread about putting the epidemiology back in genomic epidemiology 1/x
In Michigan, who uploads sequence data? Vast majority comes from our awesome State Lab and then my lab. Since 1/1, my lab has uploaded 1146 to GISAID. Don't know State Lab numbers but at least 2x that. There are 600+ B.1.1.7 from Michigan, according to CDC 2/x
Why is that important? Well you need to know how sequencing is done. My lab is sequencing broadly in our area - we do every positive that we can get our hands on. We've been getting sequences uploaded on > 25% of cases since September. We've done better since January. 3/x
So that is a really good sample, albeit from a smallish region. The State Lab sequences broadly across the State, but will also do a lot of sequencing for specific contact traces or outbreaks. This is important for the data. 4/x
If you sequence more, you will find more. So total variant cases can be misleading if you don't control for number of cases or number of cases sequenced. But how cases are selected for sequencing can also lead to bias. See this note on outbreak.info. 5/x
How does the splay out in Michigan. Well. Look at this, also from outbreak.info. See that huge spike in percent of cases with variant? What's up with that? 6/x
State lab sequenced a major outbreak of B.1.1.7 in a prison. Don't know final numbers, but at least 90 cases from the very start of the outbreak. This is major ascertainment issue. State sequences an outbreak is not representative sample. 7/x
freep.com/story/news/loc…
How do things look with a broad sample from a small area (Washtenaw County, 367,000 residents with a major University)? We've had 6.5% of our sequences as B.1.1.7, most tied to an outbreak in our campus community. 8/x
The last two sequencing runs (weekly) of 192 samples, we've had approximately <10% B.1.1.7. 9/x
Hope you've found this interesting. It's important to understand the data you're using in order to draw conclusions. Especially important if data are being used for policy decisions. One way to get a better sense of the data is to actually ask the people who generate it. 10/x
To answer my question, "Do we have a variant problem?" Maybe. Certainly would like there to be fewer variants around my neck of the woods. But, not sure it's worse in Michigan than elsewhere around the country. 11/x
Adding to this thread. Folks pointing to helix data. I’ve learned that this is non overlapping with data from state public health labs (which in MI is substantial). Also can’t figure out denominator on helix site (percent of how many?) or how they sample States. Anyone know?

• • •

Missing some Tweet in this thread? You can try to force a refresh
 

Keep Current with Lauring Lab

Lauring Lab Profile picture

Stay in touch and get notified when new unrolls are available from this author!

Read all threads

This Thread may be Removed Anytime!

PDF

Twitter may remove this content at anytime! Save it as PDF for later use!

Try unrolling a thread yourself!

how to unroll video
  1. Follow @ThreadReaderApp to mention us!

  2. From a Twitter thread mention us with a keyword "unroll"
@threadreaderapp unroll

Practice here first or read more on our help page!

More from @LauringLab

18 Mar
Teaching virus evolution to grad students tomorrow. Just reread the assigned paper. I think it's relevant to the discussion on immunocompromised hosts and VOC. Like most things COVID, we forget lessons from other viruses 1/x
journals.plos.org/plospathogens/…
Those who know me know that I love geeking out on within-host evolution and I love geeking out on poliovirus. So I will try to hold myself in check. Briefly, oral poliovirus OPV is live attenuated virus vaccine, so it replicates in gut and shed in stool. Thus, it evolves. 2/x
See recent work from @alvalesano @mt2fus @famulare_mike and others on this. It's long been recognized that individuals with primary immunodeficiencies related to antibody generation can have prolonged "infections" with OPV. 3/x
cell.com/cell-host-micr…
Read 11 tweets
20 Jan
Happy to share out latest preprint on SARS-CoV-2 within host diversity. Brief thread.
biorxiv.org/content/10.110…
We've been interested in within-host diversity for some time. It's important for understanding how mutations accumulate over time (relevant for how variants arise). Important for understanding how likely it is for variants to transmit and potentially for inferring trx chains 2/x
We looked at inpatients and outpatients. First we measured viral load. Why? Cause we're interested. But it's also a big factor in looking at diversity within hosts (spoiler alert). Another important (unique?) thing in our study is we analyzed data by day from symptom onset 3/x
Read 11 tweets
29 Dec 20
Unfortunately very few - any? - studies that I’ve seen relating viral load to outcome stratify by day post infection or symptom onset. This is big issue (viral load varies by day and people vary in when they get tested in disease course for many reasons). nytimes.com/live/2020/12/2…
For example, here’s data from my lab showing viral load by day for outpatients (purple) vs hospitalized patients (green). All tests were on presentation. If you just look at viral load on presentation, outpatients were higher - they were just tested earlier.
H/t to @Kalee_Rumfelt in my lab who did the chart review. Most studies don’t have day post symptom onset because it’s hard to retrieve. You typically don’t get it in data pulls from EMR. You have to go into chart notes one by one.
Read 4 tweets
24 Dec 20
Been thinking more about this piece from @kakape this morning and have some thoughts to share. So thought I'd do a Xmas eve thread about SARS-CoV-2/COVID19 and immunocompromised hosts. (1/x)
sciencemag.org/news/2020/12/u…
I emphasize that I respect the stated opinions out there and don't have doubts about data or what they may show. Just feel there's a perspective missing from the conversation. What can I bring to conversation? I am an infectious disease physician and study virus evolution. (2/x)
I have taken care of patients with COVID19 who have a range of immunocompromising conditions. I have also published on within host evolutionary dynamics of viruses. We published a preprint in Sept and subsequent JID paper on long term evolution in lymphoma patient. (3/x)
Read 20 tweets
20 Dec 20
With the news of this new variant and discussions of what it means for vaccines, keep thinking about this article from @SCOTTeHENSLEY and Yewdell (who very much needs a Twitter account). Short thread.

science.sciencemag.org/content/326/59…
First question from ID docs and many virologists I know is “OMG, what does this mean for vaccines.” We grow up in this pathogen vs. immune system paradigm that is sometimes distracting from issues at play. (2)
Many variants have been reported to escape this serum or that monoclonal. But large scale selection of a variant at this point is probably not driven by immune system (just not that much immunity around). (3)
Read 10 tweets

Did Thread Reader help you today?

Support us! We are indie developers!


This site is made by just two indie developers on a laptop doing marketing, support and development! Read more about the story.

Become a Premium Member ($3/month or $30/year) and get exclusive features!

Become Premium

Too expensive? Make a small donation by buying us coffee ($5) or help with server cost ($10)

Donate via Paypal Become our Patreon

Thank you for your support!

Follow Us on Twitter!