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Daniel Weir

@DanielWeirIAV

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MRC PhD Student @CVRinfo investigating the intercellular spread of influenza A viruses | Member of the @CVRHutchinson group.

Glasgow, Scotland
Joined January 2017
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@DanielWeirIAV
Daniel Weir
1 month
🚨🔎 Out now in @PLOSPathogens! 🔎🚨 This project has taken us @CVRinfo @UofGMVLS on a wild and wonderful journey. I am excited to share our story of how influenza A viruses (IAVs) exploit cell death to facilitate its covert spread. N/1
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@DanielWeirIAV
Daniel Weir
19 days
RT @BPoD_s: Flu virus spreads via tunnelling tubes it induces between cells: tube formation correlates with onset of apoptosis. 📷 @DanielWe….
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@DanielWeirIAV
Daniel Weir
22 days
RT @CVRinfo: 🦠 Influenza's Great Escape . New research from @DanielWeirIAV & colleagues reveals that flu viruses use secret tunnelling nano….
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@DanielWeirIAV
Daniel Weir
28 days
RT @SpyrosLytras: Can flu spread to another cell without ever exiting the first. one? Yes! Through little tunnels (TNTs) that form between….
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@DanielWeirIAV
Daniel Weir
1 month
To all the coauthors, Cal Bentley-Abbot, @JMcCowan97, @Onlycloney, @Robertslab1 and @CVRHutchinson, thanks for all your hard work! We are grateful for the funders, reviewers, @PLOS and our many fantastic colleagues @CVRinfo.
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@DanielWeirIAV
Daniel Weir
1 month
This work uncovers a novel way in which IAVs can exploit cell death to propagate infection. This time it does so by ensuring its continued spread after it has exhausted the life of its host cell, and the often hostile environment of the lung awaits.
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@DanielWeirIAV
Daniel Weir
1 month
Is apoptosis then required for IAV direct cell to cell spread? Well, not only do IAVs frequently undergo direct cell to cell spread, but this can almost be completely prevented with the inhibition of apoptosis! N/10
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@DanielWeirIAV
Daniel Weir
1 month
💡we found that whilst apoptosis alone had no effect, TLS induction by IAVs required both virus replication and the onset of apoptosis. Overall, our data reveals that apoptosis induced through IAV replication is responsible for the triggering of TLSs. N/9
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@DanielWeirIAV
Daniel Weir
1 month
🔍Clue 3: the induction of TLSs correlated with the onset of apoptosis. Furthermore, inhibition of apoptosis prevented the ability of IAVs to induce TLSs. However, induction of apoptosis with drugs, independent of infection, did not induce TLS formation. N/9
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@DanielWeirIAV
Daniel Weir
1 month
🔎Clue 2: induction of TLSs was consistent between IAV strains having either filamentous or spherical virion morphologies. This was in despite of several curious similarities between TLSs and budding IAV filaments. N/8
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@DanielWeirIAV
Daniel Weir
1 month
🔎Clue 1: the induction of TLSs did not occur through the release of paracrine innate immune signals, but did require intracellualr IAV replication. N/7
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@DanielWeirIAV
Daniel Weir
1 month
Satisfied that TLSs could be relevant to within host IAV spread, we set out to find how IAVs were triggering their formation. For this investigation we embarked on a systematic hunt for clues, using in vitro cell culture systems. N/6.
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@DanielWeirIAV
Daniel Weir
1 month
Firstly, we wanted to see if these structures formed at the natural site of IAV infection. We collaborated with the wonderful @Robertslab1 lab and we could see, for the first time, evidence of TNT-like structures (TLSs) forming from infected cells within the lungs of mice. N/5
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@DanielWeirIAV
Daniel Weir
1 month
One mechanism of IAV direct cell to cell spread in vitro is through the formation of long, thin and fragile membrane connections known as Tunnelling Nanotubes (TNTs). Impressively, IAVs trigger the formation of TNTs but it was unknown how they were doing this. N/4
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@DanielWeirIAV
Daniel Weir
1 month
Direct cell to cell spread of IAVs describes the mechanisms that deliver viral genomes to new cells, independent of a cell free virus particle. This can allow infection spread even in the presence of antiviral drugs and neutralising anitbodies. N/3
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@DanielWeirIAV
Daniel Weir
1 month
@CVRHutchinson we are fascinated about what makes IAVs infectious and what shapes it's within host spread. The complexity of this fundamental biology is underappreciated and many questions remain. A perfect example of this is the direct cell to cell spread of these viruses. N/2.
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@DanielWeirIAV
Daniel Weir
2 months
RT @SpyrosLytras: Sooo happy to finally have this one published!! (3 years in the making… 👀) A comprehensive investigation into the recency….
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@DanielWeirIAV
Daniel Weir
4 months
RT @annasimsbiol: I can't believe my second first-author paper has been published today, on my actual birthday!.Double celebrations tonight….
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@DanielWeirIAV
Daniel Weir
4 months
Congrats @annasimsbiol on your second 1st author paper! Working alongside you was a highlight of my time in Glasgow and it's so special to be one of your coauthors!.
@CVRHutchinson
Hutchinson Lab
4 months
Why can't these viruses be friends?.In a new study from her PhD @CVRinfo , @annasimsbiol shows that #SARSCoV2 infections segregate into distinct microdomains as they spread. But why? (1/N).
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@DanielWeirIAV
Daniel Weir
4 months
RT @CVRHutchinson: Why can't these viruses be friends?.In a new study from her PhD @CVRinfo , @annasimsbiol shows that #SARSCoV2 infections….
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