Unintelligent Design - How a Cell Division Error Sometimes Causes Cancers - Incompetence or Malevolence?

Chromosomes during mitosis (white). In orange, a centromere is visible consisting of two subdomains (arrows), each bound to a discrete bundle of microtubules (magenta).

Credit: Carlos Sacristan Lopez.
© Hubrecht Institute.

Two microscopy images of chromosomes. The left image shows chromosomes during mitosis (white). In orange, a centromere is visible consisting of two subdomains (arrows), each bound to a discrete bundle of microtubules (magenta). The right image depicts a dividing cancer cell showing a missegregating chromosome in the middle. The two centromere subdomains (arrows) of this chromosome appear split.

Credit: Carlos Sacristan Lopez. Copyright: Hubrecht Institute.

Research on centromere structure yields new insights.

Creationists, who, generally speaking, know little or nothing of biology and don't want to either because the risk of wondering it they could be wrong is far too great, are easily fooled by the frauds with a vested interest in keeping them simultaneously ignorant and imagining they have a deeper understanding than the millions of educated, working biomedical scientists who apply the Theory of Evolution every day of their working lives.

One thing they've been fooled into believing is that there is some sort of perfection in design inside a cell and that same designer is responsible for everything about living organisms.

But, in the last few years, under the onslaught of science, the frauds have needed to fall back from the demonstrably false notion of perfection of design in view if cancers, diseases and parasites, and now blame something for these obvious imperfections, which, by definition, could not be the products of a perfect designer god, do they have invented the biologically nonsensical notion of 'genetic entropy' and devolution caused by 'Sin' over which their omnipotent, omnibenevolent designer god is powerless.

And, again under the onslaught of science, the frauds have also conceded that evolution does indeed happen and happened at a massively accelerated rate to account for all the biodiversity produced by a small number of survivors of a genocidal flood just a few thousand years ago.

Unintelligent Designer News - How Creationism's Idiot Designer Continually Designs Different Solutions To The Same Problem

Squinting bush brown, Bicyclus anynana

Squinting bush brown, Bicyclus anynana

© Judy Gallagher (CC BY-SA)

New sex-determining mechanism in African butterfly discovered - News - University of Liverpool

Once sexual reproduction had become established in multicellular organisms, there was selection pressure to determine the gender of a developing embryo, so the result was either genetically male or genetically female. In humans and other mammals, for example, this is achieved by the XY Chromosomes, which, unlike all the other chromosomes (autosomes) are not paired. A zygote with 2X (homozygous) becomes a female and a zygote with XY (heterozygous) becomes male. Because the zygote gets either one or the other of these chromosomes from each parent these are the only combinations possible, so we never see a YY zygote.

Malevolent Design - Combatting The Highly Toxic, Tissue Destroying Spitting Cobra Venom

African black-necked spitting cobra, Naja nigricollis

Warren Klein via Wikimedia (CC BY-SA 3.0)

Black-necked spitting cobra, Naja nigricollis

© Marius Burger, CC0, via Wikimedia Commons

First effective treatment found for spitting cobra snakebite - Lancaster University

Snake venom is usually a potent cocktail of multiple different toxins, 'designed' to kill, mostly small vertebrate prey very quickly, so the snake can strike, then wait for the prey to become paralyzed or die before it can go very far.

The reason for this rich cocktail is an interesting piece of evolutionary biology that would embarrass any creationist with the courage to learn about it. It is the result of repeated arms races between the snake and its prey species. Not only that, but it involves new genetic information arising, by gene duplication and mutations - contrary to creationist dogma that such a thing is impossible.

As one prey species starts to evolve resistance there is selection pressure on the snake to change its venom to overcome the resistance or loose one source of food, but, there must be a balance between retaining one food species but loosing several others if the changed venom is less effective against them. Resistance usually arises when there is a change in receptor sites on cell surfaces, on which the venom acts so the active venom molecule doesn't bind to it.

Malevolent Design - How Creationism's Divine Malevolence Co-opted Red Squirrels To Spread Leprosy in Medieval England

Lepers having magic spells cast over them

Mycobacterium leprae

Ancient Mycobacterium leprae genome reveals medieval English red squirrels as animal leprosy host: Current Biology

Few places in Europe or elsewhere were more pious than Medieval England, but still creationism's pestilential malevolence continued to make people suffer with diseases such as bubonic plague, tuberculosis and the related leprosy. Even the extreme measures taken by believers to atone for imaginary transgressions that had brought about the Black Death had failed to assuage the putative designer god who was believed to be visiting this pestilence upon people.

The superstitious Bible-based belief in evil spirits and 'sin' as the cause of disease led to the social stigma that made the disease so feared and led to the isolation of sufferers in lepper colonies, and often reduced to begging to stay alive. Poor nutrition and poor sanitation led to a worsening of the condition and, although these counter-measures were visibly ineffective, such was the belief in the Bible that it was inconceivable that the disease could be caused by anything other than 'sin' and evil demons being permitted to enter the victim.

The modern equivalent of this victim-blaming superstition can be found in the modern creationist tactic of blaming 'Sin' and 'genetic entropy' for parasites, with demons being replaced by 'entropy' to make it sound sciencey. It is of course, Bible-based superstition without supporting evidence.

And now, if you believe that stuff, there is evidence that creationism's putative designer god designed M. leprae to also infect red squirrels so they would act as a repository to spread leprosy. Red squirrels were common in those days and were often captured in the wild for pets or pelts. Their skins, when used for clothing, would have carried M. leprae and infected anyone who wore them - a brilliant strategy, if you hate people and want them to be sick, suffer and die.

Unintelligent Design News - How Creationism's Putative Designer 'Brilliantly' Designs Solutions To Problems It Supidly Designed

Two-spot spider mite, Tetranychus urticae

Two-spot spider mite (yellow form), Tetranychus urticae

Plants utilise drought stress hormone to block snacking spider mites | Sainsbury Laboratory

To start at the beginning because that's always a good place to start, plants need to get water and nutrients up to their leaves, so their 'designer' gave them a vascular system but without a pump, so, to maintain the upward flow, they need to evaporate away (or transpire) the water that just arrived in their leaves. They do this through tiny pores (or stomata; singular=stoma) that are just about visible to the naked eye, and clearly visible under a hand lens or a microscope.

These stomata are guarded by guard cells, one on either side, which can swell to close the stoma or shrink to allow the stoma to open, as the need arises.

However, these stomata are an open invitation to sap-sucking arthropods such as mites and aphids, which are cleverly designed, reputedly by the same designer that designed the stomata, which can push their mouthparts into the stoma to get at the nutrient-rich watery contents of the leaf.

So, having designed these sap-suckers to exploit the transport system it designed for plants, creationism's putative designer clearly saw the sap-suckers it had designed as a problem to be solved.

How it added this Heath-Robinson layer of additional complexity to solve the problem the earlier layer of complexity had caused is the subject of a research paper by a collaboration of researchers from the Centre for Plant Biotechnology and Genomics (CBGP), Spain, and Sainsbury Laboratory, Cambridge University (SLCU), Cambridge, UK and a news release from Cambridge University:

Malevolent Designer News - How Creationism's Favourite Pathogen Is Designed to Cause UTIs

Escherichia coli,
The usual cause of urinary tract infection (UTI)

UTI's will affect 50% of women at some time in their lives

How E. coli get the power to cause urinary tract infections | Michigan Medicine

Despite their protestations that their god doesn't create pathogens - some other creative entity does that, apparently - they have been in love with Escherichia coli, or E. coli ever since their guru and Deception Insitute flunky, Michael J Behe, persuaded them that he had 'proved' their god exists and designs things because he couldn't work out how the E. coli flagellum could have evolved - so God did it!

There problem then, courtesy of Michael J Behe is that they have accepted that, if there was a designer involved in E. coli's design, it is the god that Michael J Behe 'proved' designed it, so their god designs pathogens, and even designs clever way to make them good at making us sick.

With that in mind, which creationist is going to argue against Michael J Behe's clever 'proof' that their god designs things so must exist, and insist that it isn't also behind the newly discovered way it manages to cause urinary tract infections (UTIs)?

The discovery that they can live, reproduce, and do their nasty thing in the otherwise near-sterile urinary tract, was made by researchers at the laboratory of Professor Harry Mobley in the University of Michigan Medical School.

Having been filtered by the kidneys, while urine contains some chemicals such as metabolites, it is about as sterile as it gets, with anything in it entering through the urethral meatus, in women, stupidly placed near the anus and inside the vulva where it can become infected during sexual intercourse by a penis cleverly designed with a foreskin to harbour pathogens under.

It has now been discovered that E. coli is also cleverly 'designed' to grab the nutrients it needs but can't manufacture itself by have a highly efficient transport system for taking them from its victims at a rate of thousands of molecules a second. One of the genes responsible for this, codes for an enzyme known as ATP-binding cassette (ABC).

Typical of creationism's 'intelligent' [sic] designer, if you believe in such a thing, is the Heath-Robinson workaround for the lack of genes for manufacturing these amino acids, where the parasite needs an energy-intensive ATP-based transport system, complete with multi-layered back-up systems to keep them working - the needless waste and needless complexity, so typical of evolved systems and the antithesis of intelligently designed systems. The researchers have published their findings, open access, in the journal PNAS and explained them in a University of Michigan news release:

Antivaxxer Idiot News - How An mRNA Vaccine Is Proving Effective Against A Highly Malignant Brain Cancer

Sadeem Qdaisat, Dr. Hector Mendez-Gomez and Dr. Elias Sayour
discuss their new study.

Photo by Nate Guidry

Dr. Elias Sayour, Chong Zhao and Arnav Barpujari discuss the mRNA cancer vaccine developed at the University of Florida

New mRNA cancer vaccine triggers fierce immune response to fight malignant brain tumor - UF Health

Contrary to the bizarre antivaxxer claims that the mRNA vaccines used against the SARS-CoV-2 virus that causes COVID-19 somehow causes cancer, based on nothing more substantial than the fact that some people who developed cancer had previously been vaccinated, there is now an mRNA vaccine that is proving spectacularly effective against a highly malignant form of brain cancer.

Curiously, the fact that some people who developed cancer will previously have sung Christmas carols or eaten potatoes, is never given as a probable cause, but then few people who believe antivaxxer disinformation will understand statistics or statistical correlations.

The mRNA vaccine against the brain cancer known as Glioblastoma has shown very promising results in a small-scale study of four adults by scientists at Florida University, repeating the results of a trial in 10 dogs and preclinical trials in mice.

The vaccine successfully, and very quickly, reprograms the immune system to produce highly specific antibodies against the tumour. Intelligent design proponents (or 'cdesign proponentcists' as they have been known since the Kitzmiller trial) might like to explain why the immune system, supposedly intelligently designed to protect us, needs to be artificially reprogrammed by human medical science.

The trick has been to create clusters of nanoparticles of lipid-enclosed mRNA wrapped around one another like a miniature onion. These means the mRNA will be released slowly and reprogram the immune system more effectively than a single burst would. The specific mRNA is tailor-made for the patient's tumour and creates antibodies against specific tumor proteins, in the same way the mRNA anti-COVID vaccines target the virus's spike proteins, so is specific to that particular cancer.

The results are reported in the journal Cell and are also explained in a University of Florida Health News release:

In a first-ever human clinical trial of four adult patients, an mRNA cancer vaccine developed at the University of Florida quickly reprogrammed the immune system to attack glioblastoma, the most aggressive and lethal brain tumor.

The results mirror those in 10 pet dog patients suffering from naturally occurring brain tumors whose owners approved of their participation, as they had no other treatment options, as well as results from preclinical mouse models. The breakthrough now will be tested in a Phase 1 pediatric clinical trial for brain cancer.

Reported May 1 in the journal Cell, the discovery represents a potential new way to recruit the immune system to fight notoriously treatment-resistant cancers using an iteration of mRNA technology and lipid nanoparticles, similar to COVID-19 vaccines, but with two key differences: use of a patient’s own tumor cells to create a personalized vaccine, and a newly engineered complex delivery mechanism within the vaccine.

“Instead of us injecting single particles, we’re injecting clusters of particles that are wrapping around each other like onions, like a bag full of onions,” said senior author Elias Sayour, M.D., Ph.D., a UF Health pediatric oncologist who pioneered the new vaccine, which like other immunotherapies attempts to “educate” the immune system that a tumor is foreign. “And the reason we’ve done that in the context of cancer is these clusters alert the immune system in a much more profound way than single particles would.”

Among the most impressive findings was how quickly the new method, delivered intravenously, spurred a vigorous immune-system response to reject the tumor, said Sayour, principal investigator of the RNA Engineering Laboratory within UF’s Preston A. Wells Jr. Center for Brain Tumor Therapy and a UF Health Cancer Center and McKnight Brain Institute investigator who led the multi-institution research team.

“In less than 48 hours, we could see these tumors shifting from what we refer to as ‘cold’ — immune cold, very few immune cells, very silenced immune response — to ‘hot,’ very active immune response,” he said. “That was very surprising given how quick this happened, and what that told us is we were able to activate the early part of the immune system very rapidly against these cancers, and that’s critical to unlock the later effects of the immune response.”

Glioblastoma is among the most devastating diagnoses, with median survival around 15 months. Current standard of care involves surgery, radiation and some combination of chemotherapy.

The new publication is the culmination of promising translational results over seven years of studies, starting in preclinical mouse models and then in a clinical trial of 10 pet dogs that had spontaneously developed terminal brain cancer and had no other treatment options. That trial was conducted with owners’ consent in collaboration with the UF College of Veterinary Medicine. Dogs offer a naturally occurring model for malignant glioma because they are the only other species that develops spontaneous brain tumors with some frequency, said Sheila Carrera-Justiz, D.V.M., a veterinary neurologist at the UF College of Veterinary Medicine who is partnering with Sayour on the clinical trials. Gliomas in dogs are universally terminal, she said.

After treating pet dogs that had spontaneously developed brain cancer with personalized mRNA vaccines, Sayour’s team advanced the research to a small Food and Drug Administration-approved clinical trial designed to ensure safety and test feasibility before expanding to a larger trial.

In a cohort of four patients, genetic material called RNA was extracted from each patient’s own surgically removed tumor, and then messenger RNA, or mRNA — the blueprint of what is inside every cell, including tumor cells — was amplified and wrapped in the newly designed high-tech packaging of biocompatible lipid nanoparticles, to make tumor cells “look” like a dangerous virus when reinjected into the bloodstream and prompt an immune-system response. The vaccine was personalized to each patient with a goal of getting the most out of their unique immune system.

“The demonstration that making an mRNA cancer vaccine in this fashion generates similar and strong responses across mice, pet dogs that have developed cancer spontaneously and human patients with brain cancer is a really important finding, because oftentimes we don’t know how well the preclinical studies in animals are going to translate into similar responses in patients,” said Duane Mitchell, M.D., Ph.D., director of the UF Clinical and Translational Science Institute and the UF Brain Tumor Immunotherapy Program and a co-author of the paper. “And while mRNA vaccines and therapeutics are certainly a hot topic since the COVID pandemic, this is a novel and unique way of delivering the mRNA to generate these really significant and rapid immune responses that we’re seeing across animals and humans.”

While too early in the trial to assess the clinical effects of the vaccine, the patients either lived disease-free longer than expected or survived longer than expected.

The 10 pet dogs lived a median of 139 days, compared with a median survival of 30 to 60 days typical for dogs with the condition.

The next step, through support from the Food and Drug Administration and the CureSearch for Children’s Cancer foundation, will be an expanded Phase I clinical trial to include up to 24 adult and pediatric patients to validate the findings. Once an optimal and safe dose is confirmed, an estimated 25 children would participate in Phase 2, said Sayour, an associate professor in the Lillian S. Wells Department of Neurosurgery and the department of pediatrics in the UF College of Medicine, part of UF Health.

For the new clinical trial, Sayour’s lab will partner with a multi-institution consortium, the Pediatric Neuro-Oncology Consortium, to send the immunotherapy treatment to children’s hospitals across the country. They will do this by receiving an individual patient’s tumor, manufacturing the personalized vaccine at UF and sending it back to the patient’s medical team, said Sayour, co-leader of the Immuno-Oncology and Microbiome research program at the UF Health Cancer Center.

Despite the promising results, the authors said one limitation is continued uncertainty about how best to harness the immune system while minimizing the potential for adverse side effects.

“I am hopeful that this could be a new paradigm for how we treat patients, a new platform technology for how we can modulate the immune system,” said Sayour, the Stop Children's Cancer/Bonnie R. Freeman Professor for Pediatric Oncology Research. “I am hopeful for how this could now synergize with other immunotherapies and perhaps unlock those immunotherapies. We showed in this paper that you actually can have synergy with other types of immunotherapies, so maybe now we can have a combination approach of immunotherapy.”

Graphic abstract

Highlights

• RNA-LPAs mimic dangerous emboli for lymphoreticular entrapment and systemic immunity
• Systemic immunity resets both the peripheral and intratumoral milieu via IFNAR1/RIG-I
• RNA-LPAs are safe and effective tumor re-modulators in canines with spontaneous gliomas
• RNA-LPAs reprogram the TME and elicit adaptive immunity in human GBM patients

Summary Cancer immunotherapy remains limited by poor antigenicity and a regulatory tumor microenvironment (TME). Here, we create “onion-like” multi-lamellar RNA lipid particle aggregates (LPAs) to substantially enhance the payload packaging and immunogenicity of tumor mRNA antigens. Unlike current mRNA vaccine designs that rely on payload packaging into nanoparticle cores for Toll-like receptor engagement in immune cells, systemically administered RNA-LPAs activate RIG-I in stromal cells, eliciting massive cytokine/chemokine response and dendritic cell/lymphocyte trafficking that provokes cancer immunogenicity and mediates rejection of both early- and late-stage murine tumor models. In client-owned canines with terminal gliomas, RNA-LPAs improved survivorship and reprogrammed the TME, which became “hot” within days of a single infusion. In a first-in-human trial, RNA-LPAs elicited rapid cytokine/chemokine release, immune activation/trafficking, tissue-confirmed pseudoprogression, and glioma-specific immune responses in glioblastoma patients. These data support RNA-LPAs as a new technology that simultaneously reprograms the TME while eliciting rapid and enduring cancer immunotherapy.

Mendez-Gomez, Hector R.; DeVries, Anna; Castillo, Paul; et al.(2024)
RNA aggregates harness the danger response for potent cancer immunotherapy Cell https://doi.org/10.1016/j.cell.2024.04.003

© 2024 Cell Press.
Reprinted under the terms of s60 of the Copyright, Designs and Patents Act 1988.

---

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This book presents the reader with multiple examples of why, even if we accept Creationism's putative intelligent designer, any such entity can only be regarded as malevolent, designing ever-more ingenious ways to make life difficult for living things, including humans, for no other reason than the sheer pleasure of doing so. This putative creator has also given other creatures much better things like immune systems, eyesight and ability to regenerate limbs that it could have given to all its creation, including humans, but chose not to. This book will leave creationists with the dilemma of explaining why evolution by natural selection is the only plausible explanation for so many nasty little parasites that doesn't leave their creator looking like an ingenious, sadistic, misanthropic, malevolence finding ever more ways to increase pain and suffering in the world, and not the omnibenevolent, maximally good god that Creationists of all Abrahamic religions believe created everything. As with a previous book by this author, "The Unintelligent Designer: Refuting the Intelligent Design Hoax", this book comprehensively refutes any notion of intelligent design by anything resembling a loving, intelligent and maximally good god. Such evil could not exist in a universe created by such a god. Evil exists, therefore a maximally good, all-knowing, all-loving god does not.

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Uninteligent Design - Bacteria Have A Defence Against The Viruses Designed To Infect Them

Bacterium infected by phage viruses

Illustration: Getty Images

Structural model at atomic resolution of bacteriophage T4

Dr. Victor Padilla-Sanchez, PhD via Wikimedia (CC BY-SA 4.0)

Study details a common bacterial defense against viral infection

Creationism's latest hobbyhorse, designed by Michael J Behe to revive the flagging fortunes of his Discovery Institute’s Wedge Strategy and the abysmal failure of his Intelligent [sic] Design ploy to get creationism inserted into the US public school science curricula at US taxpayers' expense, is the silly notion of 'genetic entropy' and 'devolution'.

This unintelligently designed strategy contains the seeds of its own failure at being regarded as a science because it starts off with the assumption that all species were created perfectly by a perfect creator, in compliance with Christian superstition, and so any mutation must be devolutionary away from that perfection. Mutations are called 'genetic entropy', so incorporating the idiotic notion that genetic 'information' is subject to the same law of physics as energy, so the Second Law of Thermodynamic make evolution impossible.

This is supposed to make creationists think Darwin must have been wrong because mutations can't improve fitness, being devolutionary, not evolutionary because of 'genetic entropy'. It ignores the fact that only an improvement in fitness in a given environment can produce more descendants than a deleterious mutation because fitness is defined as the ability to survive and reproduce. How increased fitness can be defined as a reduction in perfection is never explained because Behe 'forgot' to define 'perfection' leaving his marks to assume it means something made by their god.

And this daft notion is now cited by creationists to explain why an intelligent, omniscient and supposedly omnibenevolent god would design parasites. These are now explained as devolved from some initial perfection because of 'genetic entropy' made possible by Adam & Eve's 'sin' - Which is not religious superstition, because it was a historical fact! Got it!

So, we now have an explanation for bacteria, viruses and other parasites, that absolved creationism's god of any responsibility for them while blaming humans for their 'devolution'. However, the problem for this childish nonsense arises when we have parasites on those parasites, such as viruses that infect bacteria - how are bacteria responsible for Adam & Eve's sin and if they aren't why are they being punished for it?

Then it gets even more bizarre when we discover that many bacteria have mechanisms for protecting themselves from these viruses. How can 'devolution' produce an improvement in the organism's ability to survive and reproduce, and in what sense is an improvement a reduction in perfection?

Unintelligent Design - How the Periodic Cicadas Evolved

17-year cicada, Magicicada septendecim

Image: © Ed Reschke-Stone/Getty Images

13-year cicada, Magicada tridecima

Billions of cicadas are about to emerge from underground in a rare double-brood convergence

If it hasn't happened yet, it will do soon. The largest brood of 13-year locusts is about to emerge simultaneously with the mid-western brood of 17-year locusts - and even that only happens every 221 years.

The mathematically-minded will have noticed something about the periodicity of these insects - they are prime numbers (i.e. numbers that are only divisible by themselves and 1) ad there is a very good evolutionary reason for this - it makes it harder for a potential predator to synchronise with these emergencies because, since there are no periods that would coincide exactly with these primes other than the prime itself and a 2, 3, 4 or more period would only coincide with an emergence of these cicadas every 26, 39 and 52 years respectively for the 13-year locust, longer for the 17-year locust.

Because these broods only emerge in the same year, they form an effectively isolated genetic population and yet these two broods appear to be identical in appearance, song and genetics, so it will be interesting to see how they interact, although they occupy different geographical areas, so overlap is relatively rare.

As a strategy to avoid predation, this takes some beating in terms of intelligent stupid design, but there is a nasty little twist to the story, as I will relate later...

In the following article reprinted from The Conversation under a creative commons license, John Cooley, Assistant Professor of Ecology and Evolutionary Biology, University of Connecticut, USA and Chris Simon, Senior Research Scientist of Ecology and Evolutionary Biology, University of Connecticut, USA explains the significance of this event from the point of view of ecologists and evolutionary biologists. Their article has been reformatted for stylistic consistency:

Malevolent Design News - The Superbug, Clostridium Difficile (C. Diff), May Be Developing Resistance to Vancomycin - Design or Evolution?

Clostridium difficile (C. diff)

Treatment for Deadly Superbug C. diff May Be Weakening - University of Houston

The latest rabbit hole Michael J Behe has driven the creation cult into is the daft notion of 'Genetic Entropy'. This was introduced following the failure of the Discovery Institute to trick the courts in the USA into declaring that 'Intelligent [sic] Design' is real science and so should be foist on impressionable children in science class at taxpayers’ expense.

The notion of 'Genetic Entropy' plays on what used to be presented as an anti-evolution argument - the Second Law of Thermodynamics, which says that a closed system tends to disorder (increased entropy), so evolution can't increase order and complexity. This ignores the fact that Earth is not a closed system, of course, and relies on the scientific illiteracy of its target marks. And it looks nice and sciencey - something that creationists all crave while purporting to reject science.

So, Genetic Entropy starts off with the assumption that every species was created perfect and then, because Adam and Eve allowed 'Sin' to enter the world, these 'perfect' genes have been getting progressively less perfect. Now, this isn't Bible literalism, obviously, because that would make 'Genetic Entropy' religion, not science! Got it!

I posted this in an Evolution Vs Creation Facebook group. Creationists appear to be pretending not to have seen it.

The problem then is, how can increasing 'entropy' lead to greater fitness in a given environment? It can't of course because unlike the random process of mutation, there is no selective element which can produce more descendants from a worse genome, and unless it is getting worse, in what possible sense of the word can it be getting less perfect?

So, faced with something like increasing bacterial resistance to antibiotics, creationists in Michael J Behe's latest rabbit hole have only two ways to go. They can't argue that increased entropy is leading to an improved genome (from the perspective of the bacterium) because that would mean 'genetic entropy' is leading towards greater perfection. That then leaves them with the unenviable choice of design or evolution, and for design, read 'malevolence' because increasing antibiotic resistance increases the ability of the bacterium to make us sick, and any omniscient designer would know that.

IOW, Michael J Behe's attempt to resuscitate the Discovery Institute's flagging 'Wedge Strategy' has resulted in his fundamentalist cult having to choose between the twin 'evils' of blasphemy or evolution!

The latest twist in the evolutionary arms race between bacteria and human medical science is in the increasing weakness of the antibiotic of choice for Clostridium difficile (C. diff), vancomycin, against which C. diff appears to be developing resistance. This was discovered by researchers at the University of Houston College of Pharmacy, Texas, USA, who have just published their findings in the Journal Clinical Infectious Diseases, sadly behind a paywall with only the abstract available. However, their work is described in a University of Houston news release:

Unintelligent Design - The Brilliant Way Bacteria Evade Our Immune System - Malevolent Design or Incompetent Designer?

Burkholderia thailandensis (purple) uses cellular components (yellow) to form membrane protrusions from one host cell to another (green).

Burkholderia pseudomallei, a Gram-negative rod, straight or slightly curved, with bipolar staining

The enemy within: How pathogens spread unrecognized in the body - Biozentrum

Here's a conundrum for intelligent [sic] design creationists. Scientists working at Biozentrum, University of Basel, Switzerland with colleagues in the Department of Biochemistry, National University of Singapore, have discovered how the bacterium, Burkholderia pseudomallei that causes the serious tropical disease, melioidosis, manages to evade our immune systems to make us sick.

What information do you have on the origins of the bacterium Burkholderia pseudomallei and what it causes in humans? Burkholderia pseudomallei is a Gram-negative bacterium that causes melioidosis, a potentially fatal infectious disease primarily found in Southeast Asia and Northern Australia. The bacterium is commonly found in soil and water in endemic regions. It was first identified by Alfred Whitmore and C.S. Krishnaswami in 1912 in Rangoon, Burma (now Yangon, Myanmar). The name "melioidosis" is derived from the Greek word "melis," meaning "distemper of asses," as the disease was initially identified in horses. B. pseudomallei can infect humans and a wide range of animals through various routes, including inhalation, ingestion, or through breaks in the skin. In humans, it can cause a spectrum of symptoms ranging from localized skin abscesses and fever to more severe forms of pneumonia, septicemia (bloodstream infection), and multiple organ abscesses. Melioidosis can be challenging to diagnose due to its diverse clinical manifestations and can mimic other diseases, making it important for clinicians in endemic areas to consider it when evaluating patients with febrile illnesses. Treatment of melioidosis typically involves prolonged antibiotic therapy with drugs such as ceftazidime, meropenem, or imipenem, followed by oral antibiotics such as trimethoprim-sulfamethoxazole to prevent relapse. However, antibiotic resistance in B. pseudomallei is a growing concern, particularly in regions where the disease is endemic. Prevention strategies include avoiding contact with contaminated soil and water, wearing protective clothing during outdoor activities, and practicing good wound care.

The conundrum is, was this malevolently designed or is it the result if incompetent design?

The problem for creationists is that they believe the human immune system was intelligently designed to protect us from the bacteria and other organisms their putative designer god had designed to make us sick, and yet not only does it not work as intended but many of the harmful parasites from which we suffer seem to have been designed to avoid our immune system, some of them by ingenious ways, like the bacterium in question, B. pseudomallei.

It's hard to reconcile the difference between a designer who can't design a functional immune system and one who is genius enough to design some of the extremely clever and sophisticated mechanisms for evading our immune system. The idea that these could be one and the same entity is almost laughable unless the answer is that the inadequate immune system and the ingeniously designed parasites are all part of the same malevolent plan to make us sick.

What B. pseudomallei does to avoid being detected by the immune system, once it gets inside a cell, is cause the cell to make special tubes connected to other cells, through which it can pass without going outside the cell again, where it would be recognised as a pathogen. In this way it spreads throughout a tissue without the victim's immune system even being aware of it.

The research team have published their findings, in the open access, online Cell Press journal, Cell Host & Microbe and explain it in a press release from The University of Basel, Biozentrum:

Malevolent Designer News - How Creationism's 'Intelligent Designer' COULD Have Designed Us To Survive A Heart Attack - But Chose Not To

Zebra fish, Danio rerio

Source: Encyclopædia Britannica

Why can zebrafish regenerate damaged heart tissue, while other fish species cannot? – @theU

If you're foolish enough to believe the claims of creationist frauds that we were intelligently designed by an omniscient, omnibenevolent god, then the work of four researchers at Utah University, USA, should be a cause for concern.

They have shown how the zebra fish is 'designed' to survive a heart attack by repairing the damaged cardiac muscle unlike humans and other mammals who replace the damaged muscle with non-functional scar tissue, which can cause several life-limiting problems for those who survive the initial attack.

Just to recap; a heart attack is caused when an artery supplying blood to the heart muscle becomes blocked, so depriving the muscle of oxygen. Unless cleared very quickly, the muscle will die and will be replaced with scar tissue which lacks the contractile ability of cardiac muscle. How much this affects the functioning of the heart will depend on how much muscle was damaged.
How the zebra fish heart is able to repair itself is the subject of an open access paper in the journal Biology Open and of a news release from Utah University:

Malevolent Designer News - How The Monkeypox Virus (MPVX) Was Redesigned To Make It More Contagious

Monkeypox virus

Monkeypox virus (MPXV)

New Research Defines Specific Genomic Changes Associated with the Transmissibility of the Monkeypox Virus | Mount Sinai - New York


Why did the monkeypox virus (MPXV) suddenly become much more contagious in 2022 to transform it from a relatively harmless, low-level infection of humans and other animals into a potential pandemic virus?

Scientists from Mount Sinai, New York, USA, in collaboration with researchers from the Carlos III Health Institute (ISCIII) in Madrid, Spain believe they have worked out the answer to this puzzle - a substantive change in the DNA virus' genome.

Creationists will reject the idea that this change was an evolutionary change driven by environmental selectors, despite the obvious explanation of the observed facts that this explanation offers because their cult dogma states that changes in genomes only happen if caused by their putative intelligent [sic] designer, although, to be fair to creationists, some of them will betray the religious nature of creationism by blaming viruses and these sorts of changes in their genomes on another creator, called 'Sin' to make it compliant with fundamentalist beliefs in a literal Bible.

But these apologists are continually undermined by those fundamentalists who generally, in their kind, caring and compassionate way, greet every new epidemic as their god's punishment for something they don't like. This will usually be some far-right political hobbyhorse in the USA, the way HIV was greeted with great jubilation by Christians as a 'Gay Plague', sent to punish homosexuals, and COVID-19 was declared to be God's punishment on New Yorkers for voting for Democrats.

However, those few creationists intelligent enough to realise they should be supporting the Discovery Institutes efforts to disguise creationism as science, will avoid these excuse, but they are then left with either evolution by natural selection, or intelligent [sic] design, so let's go with those who claim to see their god's hand in these viruses, so at least have managed to avoid the blasphemy of believing in two or more creators, while presenting their allegedly loving god as a pestilential malevolence.

Malevolent Designer News - How Creationism's Divine Malevolence Creates Genetic Defects

UC Irvine-led research team builds first tandem repeat expansions genetic reference maps – UCI News

Creationists assure us that creating new genetic information is impossible without magic performed by the magic creator because they have been sold some half-baked notion that genetic information follows the same laws of physics as energy, so can't be created according to the Third Law of Thermodynamics.

The fact that this is demonstrably wrong since gene duplication is readily observable doesn't stop them trotting out the same refuted claims time after time, but then to a creationist, having a claim refuted is not seen as a reason not to try to get away with it again later. You'll see this repeatedly as an apologist fraud such as William Lane Craig, Ken Ham or Michael J Behe will be comprehensively refuted in a public debate one day, only to try the self-same argument a day or two later on a different opponent in front of a different audience.

Sadly for creationists, however, this tactic leads them down a cul-de-sac where they are left arguing that DNA duplication must have been intelligently designed and, so they will also claim, evidence of intelligent design is evidence that their favourite god (and no other!) exists.

Malevolent Designer News - New Discovery Unravels Malaria Invasion Mechanism

Malaria-infected red blood cells

Photo: AdobeStock

Plasmodium falciparum in a blood smear.

New Discovery Unravels Malaria Invasion Mechanism

Medical science just took a step forward in the continuing arms race between it and creationism's divine malevolence to try to prevent its parasite, Plasmodium falciparum from killing 600,000 people, mostly children, a year, mostly in Africa.

Creationists who use the traditional excuse that it's not their god who designs parasites but another intelligent designer - Sin - should refresh their memories of Michael J Beh's 'proof' that their god exists by falsely claiming that anti-malarial drug resistance in P. falciparum must have been intelligently designed because the (wrong) mathematical model he used gave the infinitesimally small probability it was intelligently designed to give, so could not have evolved.

So, they can't have it both ways: if evidence of design in parasites, no matter how spurious, is evidence for their god then their god is responsible for the design of those parasites. If not, then Michael J Behe's carefully concocted 'proof' is nothing of the sort.

The alternative is the blasphemous claim that there is another supernatural deity with powers to create living things, over whom their god has no power or authority.

So, while creationists are struggling with trying to hold two mutually exclusive views simultaneously, biomedical scientists are trying to unravel the devilishly clever way this parasite overcomes our defences to do what creationists must believe it was designed to do - make us sick and increase the suffering in the world.

This is the latest breakthrough medical science has just announced.

It was made by researchers from by the Swiss Tropical and Public Health Institute (Swiss TPH) and Griffith University’s Institute for Glycomics, led by Professor Gerd Pluschke of Swiss TPH. Their discovery concerns the way the parasite gains access to the red blood cells to begin their destruction. It is published, open access, in Cell Reports and is explained in a Swiss PTH news release:

Malevolent Designer News - How Creationism's Divine Malevolence Designed The CCHF Virus To Kill Us

CCHF Virus

New study shows how the Crimean-Congo haemorrhagic fever virus enters our cells | Karolinska Institutet

Creationists traditionally have a schizophrenic attitude towards viruses. On the one hand, they blame them all on the biblical myth of 'The Fall', so betraying the fact that creationism is not a science like they claim it to be, but fundamentalist Christianity.

On the other hand, as we saw in the early days of the COVID-19 pandemic, they declared it to be their god's divine punishment for whatever their hobbyhorse was at the time - abortion, same-sex marriage, New Yorkers electing a Democrat, etc., etc., as though their god would inflict a punishment on the whole world for the actions of politicians in America or the way Americans in New York voted. Creationism is nothing if not parochial and ignorant!

Malevolent Designer - How Creationism's Putative Designer COULD Have Given Us A Mechanism to Prevent Heart Attacks But Chose Not To

Naked mole-rat, Heterocephalus glaber

Photo: TxanTxunai via Wikimedia Commons

Naked mole rats, Heterocephalus glaber - uniquely able to resist cardiac damage.

FMD - Secrets of the naked mole-rat: new study reveals how their unique metabolism protects them from heart attacks - Queen Mary University of London

Part of creationists mythology is the belief that humans stand at the pinnacle of creation, being the supreme creation of their putative designer. Even those who accept the evidence for evolution, like to imagine that somehow evolution was intended to result in humans being at the apex of it.

As you would expect of creationism, those beliefs are counter-factual and so are not supported by the evidence, and, if they are to be believed, paints their putative creator god in a very poor light, not the least because of the very many examples of where, if it had created humans and all the other species, humans come off at best second best, having inferior versions of organs and processes compared to many other species. I list several of these in my popular, illustrated book, The Malevolent Designer: Why Nature's God is not Good, for example, the superior eye of the peregrine falcon, the superior immune system of bats and the fact that elephants and sharks rarely get cancer.
Now we have the example of naked mole rats which are able to suffer anoxia without sustaining damage to their cardiac muscles, so they rarely have heart attacks.

The damage during a heart attack, i.e., when a cardiac artery is blocked by a blood clot, is cell death due to being deprived of oxygen. But Naked mole rats have a unique cardiac metabolism and unique genes, that enable their cardiac muscle cells to survive a period of anoxia.

The reason for this, and the mechanism creationism's creative god could have given humans if it were real and is as omnibenevolent as creationists like to pretend, was discovered by researchers from London, Pretoria and Cambridge, led by Dr. Dunja Aksentijevic of the Centre for Biochemical Pharmacology, William Harvey Research Institute, Bart’s and the London Faculty of Medicine and Dentistry, Queen Mary University of London, London, UK.

The team have just published their findings, open access, in the journal Nature Communications. It is also explained in a Queen Mary University news release:

Malevolent Design - How The Malaria Parasite is 'Designed' To Evolve And Outwit Medical Science

The Malaria parasite generates genetic diversity using an evolutionary ‘copy-paste’ tactic.

Credit: Karen Arnott/EMBL-EBI,
Isabel Romero Calvo/EMBL

The malaria parasite generates genetic diversity using an evolutionary ‘copy-paste’ tactic | EMBL

Devotees of creationism’s divine malevolence would be conflicted by this news if they understood it, because it shows the creative genius of any intelligent designer who could come up with this system, but, it looks like it did so (if you believe it couldn't happen naturally) by setting up an evolutionary process that creationists are obliged by dogma to believe doesn't work.

The news is that the organisms that causes malaria, Plasmodium falciparum, is 'designed' to quickly find a way to overcome the anti-malarial drugs medical science has developed to cure people suffering from it and to prevent others from getting malaria, by evolving very quickly.

The discovery was by researchers at European Molecular Biology Laboratory's (EMBL’s) European Bioinformatics Institute who have identified a mechanism of ‘copy-paste’ genetics that increases the genetic diversity of the parasite at accelerated time scales. This helps solve a long-standing mystery regarding why the parasite displays hotspots of genetic diversity in an otherwise unremarkable genetic landscape. Copy-paste' is a way of doing something creationists insist is impossible without the aid of god-magic of increasing the genetic information in a genome and making it available for evolution by mutation and selection without any loss of function in the original copied genes.

The team have recently published their finding in the open access journal PLOS Biology and describe it in an EMBL news item:

Unintelligent Malevolence - Pathogens 'Designed' to Beat Medical Science In Two Different Ways

Acinetobacter baumannii

Escherichia coli

Acinetobacter baumannii seen under a scanning electron-microscope

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Escherichia coli

What makes a pathogen antibiotic-resistant? | Sanford Burnham Prebys

One of todays examples of the stupidity of creationism is something of a novelty. Usually, by applying the central tenets of creationism, any putative designer of living things like parasites either appears malevolent (and sometime it has to be said, malevolent at a near genius level in the ways it finds to make us and other animals sick) or it looks incompetent in that its 'solutions' are often to problems of its own making and more often than not to solutions it designed for one side of an arms race which it now trets as problems for the other side.

But today's example can only be described as an example of incompetent malevolennce, as creationism's putative designer, faced with the same 'problem' of medical science developing antibiotics effective against two different species of pathogen, set about designign two completely different 'solutions' to this problem. - Talk about re-inventing the wheel!

The pathogens are: Escherichia coli and Acinetobacter baumannii.

Creationists will probably be familiar with Escherichia coli (E. coli) because they believe their guru, Michael J Behe, 'proved' their god exists by claiming (falsely) that E. coli's flagellum must have been intelligently designed because he didn't know it evolved out of a pre-exiting structure and couldn't think how else it could have evolved. But then such is the standard of creationist apologetics!

What Behe had unwitting done was destroy the traditional excuse creationists use to explain pathogens like E. coli by blaming them on another 'designer' called 'Sin' which somehow creates living organisms although the creationit designer god is the only entitiy capable of designing livign things, so any example of 'intelligent design, real or imaginary, if 'proof' of this designer god's existance.

So, what creationists are now left with is an E.coli with a flegellum designed by their god to make it better at making us sick, and now resitant to antibiotics to help it win against medical science trying to prevent it makign us sick!

But what creationists are less likely to be familiar with is the pathogen, Acinetobacter baumannii, so here is a little background: