This is crucial because the misuse of antibiotics in livestock farming has been a major driver of antimicrobial resistance (AMR), a global health crisis. When antibiotics are overused or improperly applied in animals, bacteria can evolve to become resistant, rendering these life-saving drugs ineffective for treating infections in humans and animals alike.
It has always been a perversity that life-saving reserve antibiotics were ever permitted to prop up the grotesque machinery of the modern food industry—a system built on global-scale animal cruelty.
Penicillin production was revolutionized when it moved to Peoria, IL and found the famous cantelope:
https://www.pjstar.com/story/news/local/2019/04/25/peoria-pl...
If those import markets were open European producers would struggle to compete with US-agri due to its sheer volume and lack of interest in animal welfare and/or disease control. The UK specifically suffered issues in the past with such issues via "Mad Cow Disease" in the 90s and has attempted to reform its practices as a consequence.
Conversely US agri still seems to ignore these existential nightmares, as most recently seen with Bird Flu and the new administration's troubling ideas with how to deal with it (e.g. the suggestion to avoid culls in order to "find resistent birds").
We couldn't even convince everyone to wear masks, this won't be an issue people will rise up in mass protests for... People are literally being kidnapped and thrown into detention centers without due process and there are not massive protests.
It takes a lot to make people protest, this ain't a battle for it.
I dread it when any generic medication I get is made in india or china since the fda doesn't meaningfully regulate/test their stuff
Kill it three different ways at once and it cannot adapt fast enough to leave dna fragments for the next microbe to pick up and continue the work.
AFAIK there is a new class of molecules specific to thwarting the resistance mechanism that makes the bacteria susceptible again in ways that cannot be out evolved. I'm looking for the general name for this technique - I do remember reading about it.
Regarding this detail, there has been only one pandemic recently and it has not been attributed to 'meat agriculture', though it may have involved wild meat.
https://en.wikipedia.org/wiki/Sirolimus
https://pmc.ncbi.nlm.nih.gov/articles/PMC9634974/
(Full disclosure - spent my PhD working with macrolides including this one. It's an amazing origin story for a compound...)
Antibiotic resistance is as much a political problem as a biology one.
Formulas for "antibiotics of last resort" (I would consider a newly designed one in this category) should not be sent to Pharma companies of these countries, rather, the antibiotics should be pre-dosed and mailed over from a country who can maintain the integrity of the formula in a limited fashion to keep their effectiveness high so they can continue to serve patients years into the future.
It sucks, but we've watched antibiotics be abused so badly that babies are born into hospitals where they catch resistant infections nearly right after childbirth. I blame the antibiotics-for-every-cough medical practices common in some countries (I've seen this happen myself!)
However for children the number that die of infection in the UK is double that of cancer deaths - ( ~15% versus ~7% ) - and that's in an advanced economy.
Infection is a big problem.
In terms of barriers to making treatments - yes in part there is a problem with the right financial incentives - but it's not the only problem - finding molecules that simultaneously kill bacteria, won't be rapidly evolved around, and are safe to take isn't that easy. Then you have the problem of selectivity between bacteria - how many different sorts will it work with - 'good' verus 'bad' bacteria etc. Then you have the problem of being able to make the molecule at scale etc.
The good news is there is a constant bacteria on bacteria, fungus on bacteria chemical war going on - hence the paper.
The question is shouldn't we explore it more?
Put dangerous bacteria in contact with other bacteria, fungi, viruses, prisons, viroids, archaea and see what kill them, how and why?
I don’t know that it’s helpful to have such a blunt and un-nuanced take.
Theres no “certain oligarchy” that holds a single patent on "chemotherapy" as a broad concept, as it encompasses various chemical treatments for cancer. specific chemotherapy drugs and methods are patented by pharmaceutical companies and research institutions, for example:
- NanOlogy LLC: holds a patent for a method involving injecting large surface area microparticle taxanes directly into the tumor, combined with systemic delivery of immunotherapeutic agents.
- Johns Hopkins University: assigned patent rights for a method related to cancer treatment to Becton-Dickinson & Company, which then sublicensed them to Baxter.
- University of Cincinnati Clermont College: has a patent for breakthrough chemotherapy technology involving nanocarriers.
- Northeastern University: reports a patented molecule, WYC-209, that eliminates cancer cells.
They must be making some novel improvements, though. Those original patents from the '60s are long expired by now.
Antibiotics are lazy. Sure, some people have to die, but at least you didn't have to spend any time taking samples of the actual infection.
phages are found in large quantities in mucus, where they seemingly contribute to the barrier function of mucus by preying on any bacteria that try go cross
https://pubmed.ncbi.nlm.nih.gov/23690590/
https://www.pnas.org/doi/10.1073/pnas.1508355112
https://journals.asm.org/doi/10.1128/mbio.01984-19
this might be adaptable for therapeutics
Antibiotics are found by isolating a compound some i.e. fungi naturally produces. We figure out how to produce the compound and don't fill people with fungi to produce it. Bacteriophages are already the analogy to the compound itself.
So we should be investing heavily in creating and distributing all variety of bacteriophage for all our common bacterial infections. 20k deaths/year from MRSA in the USA alone, 120k infections/year in USA and many of the survivors are left with life-long complications.
And since antibiotics still work (for now), there's not all that much money in phage research. If we do get to the point where we "run out" of antibiotics due to bacterial resistance, I imagine phage research will become a lot more attractive as a destination for research funding.
Still, highly recommend people watch it. Great animation and art style, good writing and characterization, music is pretty rad and it's quite the trip at times.
Then again, the idea behind "28 Days Later" was that everyone got a cancer vaccine and turned into zombies...
We have been lucky that we have found a few pathways that are not in human (read mammals) that are in bacteria we worry about. However bacteria just finds a different pathway and odds are that is a pathway in humans and so we can't use it because it would kill humans as well.
And if you do spend the $1bn to get there, you end up like Achaogen. For anyone in this field, read this teardown of Achaogen: https://www.nature.com/articles/s41599-024-03452-0
I learned about it through this video, but there's a lot to explore beyond this: https://www.youtube.com/watch?v=2ig6ktJGTWk
It sounds like the main problem is a for-profit healthcare system.
Gotta love capitalism.