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https://s3.us-west-1.wasabisys.com/virusreports/2020/05/cropped-virus-favicon-32x32.png Bacteria Archives - Virus Reports https://virusreports.net/tag/bacteria/ 32 32 Gut bacteria could help diagnose diabetes https://virusreports.net/gut-bacteria-could-help-diagnose-diabetes/ https://virusreports.net/gut-bacteria-could-help-diagnose-diabetes/#respond Tue, 14 Jul 2020 15:23:11 +0000 https://virusreports.net/gut-bacteria-could-help-diagnose-diabetes/ A study of more than 4,000 people shows that gut bacteria fluctuate throughout the day and that this occurs to a lesser extent in people with type 2 diabetes. Doctors could potentially use these patterns to predict and diagnose diabetes.Share on PinterestA new study looks at the relationship between diabetes and gut bacteria.Circadian rhythms, which…

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A study of more than 4,000 people shows that gut bacteria fluctuate throughout the day and that this occurs to a lesser extent in people with type 2 diabetes. Doctors could potentially use these patterns to predict and diagnose diabetes.

Woman checking blood sugar levelShare on Pinterest
A new study looks at the relationship between diabetes and gut bacteria.

Circadian rhythms, which people sometimes refer to as the “body clock,” regulate patterns of sleep, alertness, temperature, and blood pressure, among other factors. These daily biological rhythms likely evolved to coordinate with light and food availability, but they also regulate internal metabolic processes.

Circadian rhythms are important to human health, and experts believe their long-term disruption to have various adverse consequences.

The possible health effects include obesity and type 2 diabetes. A growing body of evidence indicates a connection between circadian disruption and insulin resistance.

Building on this, a new study appearing in Cell Host & Microbe shows that diabetes is also associated with changes to the daily rhythms of the gut microbiome.

A team of researchers that the Technical University of Munich in Germany led showed that people with type 2 diabetes have fewer daily fluctuations in some of their gut bacteria and that these changes may serve to predict and diagnose the condition.

For many years, scientists have known that the circadian clock is crucial to human physiology. However, it is only recently that they have discovered its role in relation to the microbiome, which is the community of bacteria, viruses, and fungi that live in and on people — for instance, on the skin or in the gut.

Recent studies, for example, show that the community of gut bacteria fluctuates during the day, just like other circadian processes.

Some researchers believe that these regular changes to the microbiome are likely beneficial and that the loss of this daily rhythm could contribute to metabolic disorders, perhaps explaining the connection between circadian rhythms and diabetes.

To investigate this further, the team started by analyzing the microbiomes of almost 2,000 people over a period of 24 hours. Their results confirmed the regular oscillations of gut bacteria.

They then focused the study to include only the people with metabolic disorders, including obesity (defined as a body mass index, or BMI, of 30 or above), prediabetes, and type 2 diabetes.

They found that people with obesity and type 2 diabetes lost the rhythmic patterns of their gut bacteria. They also noted specific changes to the gut bacteria in people with diabetes.

Using a dataset of 2,039 people, the team started to detect particular changes to the microbiome that could serve as biomarkers to diagnose type 2 diabetes.

“When certain gut bacteria do not follow a day-night rhythm, so if their number and function does not change over the course of the day, this can be an indicator for [type 2 diabetes],”

– Silke Kiessling, co-author of the study

The researchers found 13 types of bacteria that did not change during the day in people with diabetes. They used these bacteria to train a mathematical model to detect whether a person has diabetes.

“Mathematical models also show that this microbial risk signature consisting of arrhythmic bacteria helps diagnosing diabetes,” explains first author Sandra Reitmeier.

When they tested the model on a new group of 699 people, it was able to predict not only who received a diagnosis of type 2 diabetes but also who was at risk of developing the condition.

The model was most effective in combination with BMI, which confirms the importance of obesity in diabetes onset.

“Apart from bacteria and their variations over the course of the day, other parameters, such as [BMI], play a role in being able to better predict a person’s future medical conditions,” adds senior author Prof. Dirk Haller.

The findings so far show a clear association between daily variations in the microbiome and type 2 diabetes, but they do not say anything about why the two are connected.

In the final part of their study, the researchers tried to answer this question by looking at changes to metabolism. They found 26 metabolic pathways that were associated with the lack of a microbial rhythm.

The same association existed for 19 of these pathways (73%) in a separate group of people with type 2 diabetes. These pathways included several that are known to influence sensitivity to insulin.

These common metabolic pathways suggest that the two states are functionally connected, although it is too early to say whether a disrupted microbiome actually causes diabetes.

While scientists do not yet fully understand the link between the microbiome and diabetes, the findings from this study suggest that a microbial risk score could be a new way to diagnose and predict the onset of type 2 diabetes.

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Do gut bacteria contribute to ethnic health disparities? https://virusreports.net/do-gut-bacteria-contribute-to-ethnic-health-disparities/ https://virusreports.net/do-gut-bacteria-contribute-to-ethnic-health-disparities/#respond Sun, 28 Jun 2020 13:22:28 +0000 https://virusreports.net/do-gut-bacteria-contribute-to-ethnic-health-disparities/ The bacteria living in our guts play a major role in health, and some studies have found an association between ethnicity and the makeup of these microbial communities. So will doctors of the future prescribe ethnicity-specific probiotics?Share on PinterestWe examine the evidence on the connection between ethnicity and the composition of gut bacteria.We share our…

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The bacteria living in our guts play a major role in health, and some studies have found an association between ethnicity and the makeup of these microbial communities. So will doctors of the future prescribe ethnicity-specific probiotics?

scientist working in labShare on Pinterest
We examine the evidence on the connection between ethnicity and the composition of gut bacteria.

We share our bodies with a vast community of bacteria. According to the latest estimate, the human body contains about 38 trillion bacterial cells and approximately 30 trillion human cells.

Scientists know that this community of gut bacteria, or microbiota, plays a role in healthy digestion and immune function. This has spurred sales of probiotics that manufacturers promote as boosting populations of “friendly” bacteria. Many of these products’ supposed health benefits remain unproven, however.

Studies have nonetheless found strong associations between particular species of gut bacteria and a range of diseases, including obesity, inflammatory bowel disease (IBD), and colorectal cancer.

Fecal transplants from healthy individuals can restore populations of beneficial gut bacteria and displace disease-causing species. For example, they have shown promise at suppressing Clostridium difficile, a bacterium that can cause life-threatening diarrhea and inflammation of the colon.

However, in June 2019, the Food and Drug Administration (FDA) issued a safety warning about the risk of developing bacterial infections due to transplanting fecal microbiota.

There is also some evidence that fecal transplants can treat a range of other disorders associated with disturbances in the microbiota, including IBD and obesity, among other diseases.

Each person’s gut microbiota is unique, but shared factors and characteristics, such as diet, age, sex, lifestyle, and genetics, influence it.

A study by scientists at Vanderbilt University in Nashville, TN, published in the journal PLoS Biology in 2018, found that a person’s ethnicity is a better predictor of the microbial community in their gut than other variables, such as body mass index (BMI), age, and sex.

Other research suggests that gut microbiota has associations with health disparities between ethnic and racial groups, such as increased incidence of colorectal cancer in African Americans and increased incidence of obesity and type 2 diabetes in Mexican Americans.

This raises the intriguing possibility that doctors could adjust a person’s bacterial communities — perhaps using fecal transplants or probiotics — according to their ethnicity or race.

The Vanderbilt University scientists studied data on the gut microbiota of almost 1,700 people from the American Gut Project and Human Microbiome Project, identifying 12 bacterial groupings, or taxa, that consistently varied between ethnic groups.

“If you look at common factors associated with gut microbiome differences, such as gender, weight, or age, you find many inconsistencies in the types of gut bacteria present,” said biologist Seth Bordenstein, senior author of the study.

“But when we compare differences by patients’ self-declared ethnicities, we find stable and consistent features of bacteria present in the gut.”

Bordenstein directs the Vanderbilt Microbiome Initiative, a collaboration between five Vanderbilt schools and colleges investigating the human microbiome: the collective genetics of our microbiota.

The ultimate objective of the initiative is to develop probiotic treatments as a form of precision medicine tailored to the genetics, metabolism, and microbiome of particular individuals or groups.

“You may buy probiotics over the counter at a drugstore, but those are unlikely to affect your microbiome in a substantial way,” said Bordenstein. “They often are at too low a dose, and they may not even be viable bacteria. Moreover, one size may not fit all.”

“But with more of this kind of research, we can hone in on the relevant differences and doses of bacteria that may reverse illness or prevent it from developing in the first place.”

The majority of the bacteria identified in the study are partly heritable. Heritability is a measure of the extent to which differences between people’s genes account for differences in their characteristics, or traits — in this case, their gut microbiota.

The research at Vanderbilt suggests that self-identified ethnicity, which is partly determined by the genes a person inherited from their parents, plays a role in the type of bacteria that live in their guts. This, in turn, may help to shape their effect on health.

But human beings are much more than the product of their genes. A complex interplay of genetic and environmental influences determines who we are, and the relationship between ethnicity, health, and gut microbiota is no exception.

The ethnic group with which people identify encompasses not just genetics but also a wide range of cultural factors, including the food they have eaten since childhood. Scientists know that these factors influence not only our gut microbiota but also our metabolic health.

A study in 2015, for example, found evidence that the gut microbiota of Mexican Americans has associations with their high risk of obesity and type 2 diabetes.

But it is important to note that other environmental and behavioral factors also contribute to this increased risk, including diet and levels of physical activity.

The picture gets even more complicated with the addition of the socioeconomic influences on health that unequally affect different ethnic or racial groups. These include income, educational opportunities, and access to healthcare.

So how much of a role does ethnicity really play in the makeup of our microbiota, and by extension in the health disparities that exist between different ethnic groups?

The study by Bordenstein and his colleagues encompassed the whole of the United States. The many regional differences introduced many confounding variables into the analysis.

Researchers at the University of Amsterdam in the Netherlands limited these variables by focusing on a relatively small geographical region.

They studied 2,084 individuals living in the same city who identified as belonging to one of six ethnic groups: Moroccan, Turkish, Ghanaian, African Surinamese, South Asian Surinamese, and Dutch.

In 2018, they reported in Nature Medicine that ethnicity was the strongest determinant of differences in the subjects’ gut microbiota. Its influence was more significant than alcohol consumption, age, smoking, diet, and education levels, for example.

Nonetheless, ethnicity’s sole contribution to differences between individuals was only 2.5–3%, after accounting for other variables, such as diet.

The researchers identified some subtle differences. They identified that Dutch people harbored relatively high concentrations of the Christensenellaceae group of bacteria. In contrast, the South-Asian Surinamese people had relatively low levels.

The researchers describe Christensenellaceae as highly heritable bacteria that have associations with greater diversity in the overall gut microbiota. Scientists have linked their presence to several health benefits, including lower BMI and less risk of IBD.

However, scientists remain unsure of how ethnicity underlies its influence on the microbiome.

In conclusion, the authors write:

“Ethnicity comprises many different aspects — genetics, cultural habits, migration (for example, socioeconomic status, health care and antibiotics use, early-life environment) — which may all contribute to shaping the gut microbiota … Although the influence of genetics is likely low (2–8% heritability) compared to environmental factors, especially diet, it may participate in building diverse profiles of gut microbiota that would be further refined by the environment.”

According to this view, the shared genetic inheritance of a particular ethnic group initiates subtle differences in their gut bacteria. Shared environmental influences then amplify these differences.

Another study appears to contradict this view, however. It suggests that our current environment has a more profound influence on our gut microbiota than our genes.

A 2018 study published in Nature found that the microbiomes of genetically unrelated individuals who share a household have significant similarities, whereas blood relatives who have never lived together do not.

The researchers at the Weizmann Institute of Science in Rehovot in Israel analyzed the microbiomes of 1,046 healthy individuals of six different ethnicities: Ashkenazi, North African, Middle Eastern, Sephardi, Yemenite, and mixed ancestry.

They found that while their genetic ancestry did not have a statistically significant effect on their microbiomes, more than 20% of its variability had links to other factors that the scientists took into consideration, including diet and lifestyle.

According to this line of evidence, ethnicity by itself has no more than a subtle effect on our microbiota, whereas factors such as diet and the people with whom we live play much more prominent roles.

This would seem to argue against doctors choosing probiotic treatments based on a person’s ethnicity because it would not be precise. Genuine precision medicine would entail individualizing the treatment to a person’s individual genetic, microbiotic, and lifestyle characteristics, rather than using their ethnicity as a convenient proxy.

Race-based medicine has a controversial recent history in the U.S.

In 2005, the FDA approved the first race-based medicine — a drug combination called BiDil for treating heart failure in Black patients. The patent on BiDil expired in 2020.

At the time, there was some evidence that Black people responded better to this treatment than the standard therapy.

Critics of the decision argued that its one-size-fits-all approach meant that some Black patients might receive a treatment that didn’t work for them, while non-Black patients might not have access to a potentially effective treatment.

Jonathan Kahn, a law professor at Northeastern University School of Law in Boston, MA, and the bioethicist Pamela Sankar at the University of Pennsylvania have claimed that the decision to develop BiDil as a race-based medicine had more to do with securing a patent than precision medicine.

One final consideration in the question of whether ethnic probiotics might work is genetic variability.

Genome research has found that there is more genetic variation within human populations than between them. This calls into question the whole notion of race or ethnicity as a useful biological construct.

It suggests that geographical ancestry may not be a reliable proxy for a person’s genetic makeup, let alone all the other factors that contribute to their health, such as diet, exercise, and the kinds of bacteria living inside them.

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Gut bacteria linked to brain blood vessel abnormality https://virusreports.net/gut-bacteria-linked-to-brain-blood-vessel-abnormality/ https://virusreports.net/gut-bacteria-linked-to-brain-blood-vessel-abnormality/#respond Sun, 21 Jun 2020 11:22:04 +0000 https://virusreports.net/gut-bacteria-linked-to-brain-blood-vessel-abnormality/ A new study shows that gut bacteria have links to an abnormality in a brain blood vessel that can increase the chances of stroke.Share on PinterestResearchers have examined the gut microbiome and found connections with a brain blood vessel abnormality.New research has found a link between cavernous angiomas (CA), a type of brain blood vessel…

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A new study shows that gut bacteria have links to an abnormality in a brain blood vessel that can increase the chances of stroke.

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Researchers have examined the gut microbiome and found connections with a brain blood vessel abnormality.

New research has found a link between cavernous angiomas (CA), a type of brain blood vessel abnormality, and the gut microbiome’s composition.

The study further supports emerging research on the significance of the microbiota-gut-brain axis, which is the relationship between bacteria in the gut and how the brain functions.

According to one article, CA are a type of abnormal blood vessel in a person’s brain. Estimates show that 0.5% of the population has them. Of these, 40% become symptomatic, sometimes due to the vessel hemorrhaging.

Symptoms can include headaches, visual disturbances, seizures, or stroke.

Doctors can monitor CA with frequent magnetic resonance imaging (MRI) scans. Some people may require surgery.

Scientists know that CA have a genetic component, so a person may inherit certain gene variants that make developing CA more likely.

However, previous research on mice has shown that the gut microbiome may also affect CA. The microbiome is the collective genome of approximately 100 trillion micro-organisms, primarily bacteria, that live in a person’s gut.

While scientists have suggested a link between the gut microbiome and CA, more detail about what type of microbiome a person with CA has is not available, and few studies have looked at human subjects.

The authors of the present study, which is available in nature communications, wanted to determine what type of bacteria people with CA have, and whether different types of CA correlated to different gut microbiomes.

To do this research, the authors of the present study conducted an advanced genomic analysis of the stool samples of 122 people with at least one identified CA. They compared these samples to a control group matched for age and sex who did not have any CA.

The study found that the CA group had more gram-negative gut bacteria, whereas the control group had more gram-positive gut bacteria.

Further, the study found that particular types of gut bacteria were more prevalent in people with CA, even after they had accounted for possible confounding factors, such as sex, geographic location, or genetics.

The study also identified that the gut bacteria in the people with CA also produced more lipopolysaccharide molecules. The authors noted a link with the production of CA in mice.

As well as indicating a link between types of bacteria and the presence of CA, the study also demonstrated that the composition of some gut bacteria could help identify how aggressive CA might be.

Finally, the study made clear that analyzing the particular type of microbiomes in combination with blood plasma could help clinicians determine the severity of a person’s brain disorder.

The authors suggest that further research should involve larger cohorts and follow-up assessments. They also suggest that it may be valuable to look at the effects of diet on the microbiome and consequently, on CA.

While the research clarifies a link between the gut microbiome and CA, precisely how the two relate is not yet clear.

The microbiota-gut-brain axis is at the forefront of current health science research, and the relationship between the gut and the brain is complex.

However, the study provides further evidence for the importance of the gut-brain relationship and offers more detail on the specifics of CA in relation to gut bacteria.

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6,000 Strains of Bacteria Under 1 Roof https://virusreports.net/6000-strains-of-bacteria-under-1-roof/ https://virusreports.net/6000-strains-of-bacteria-under-1-roof/#respond Mon, 08 Jun 2020 14:08:30 +0000 https://virusreports.net/6000-strains-of-bacteria-under-1-roof/ In the winter of 1915, Pvt. Ernest Cable arrived at the Number 14 Stationary Hospital in Wimereux, France, in bad shape. The British army’s soldiers stationed on the Western Front of World War I were being ravaged by a variety of microscopic enemies. For Private Cable, it was Shigella flexneri, the bacterium that causes dysentery.A…

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In the winter of 1915, Pvt. Ernest Cable arrived at the Number 14 Stationary Hospital in Wimereux, France, in bad shape. The British army’s soldiers stationed on the Western Front of World War I were being ravaged by a variety of microscopic enemies. For Private Cable, it was Shigella flexneri, the bacterium that causes dysentery.

A military bacteriologist named Lt. William Broughton-Alcock took a sample of S. flexneri from Private Cable’s body after he died on March 13, 1915. It was likely kept alive in agar, sealed under paraffin wax, and was eventually renamed NCTC 1 when it became the very first specimen added to Britain’s National Collection of Type Cultures, the oldest library of human bacterial pathogens in the world devoted to sharing strains with other scientists. The collection turned 100 this year.

Managed by Public Health England, the N.C.T.C. holds about 6,000 bacterial strains representing more than 900 species that can infect, sicken, maim and kill us. (Strains are genetic variants of a species.) Of the nearly 800 registered culture collections in 78 countries, it’s one of only a few dedicated to clinically relevant bacteria — that is, to species that make us sick.

About half of the microorganisms in the world’s culture collections are bacteria, dwarfing the number of viruses and fungi. While many scientists today are focused on fighting the spread of the novel coronavirus, bacteria continue to outmaneuver our immune systems and antibiotics. We think of them as invaders in our world, but really, we live in theirs.

“On any possible, reasonable or fair criterion,” wrote Stephen Jay Gould, the evolutionary biologist “bacteria are — and always have been — the dominant forms of life on Earth.”

The collection supplies many of the world’s clinical microbiologists with authenticated microbial strains of known origin. These scientists study how bacteria evolve, test safety protocols for infectious pathogens, develop vaccines, anticancer drugs and treatments for metabolic diseases, and study the ever-increasing problem of antimicrobial resistance.

Private Cable’s killer, for instance, was brought back to life from its freeze-dried form by Kate Baker, a microbiologist at the University of Liverpool, and her colleagues, part of an effort to understand how S. flexneri has evolved over the past century. It still kills about 164,000 people every year, most of them children.

The team sequenced the NCTC 1’s genome and then compared it with other strains isolated in 1954, 1984 and 2002. Only 2 percent of the bacterium’s genome had changed over the century, but those changes were associated with higher virulence, immune evasion and greater antimicrobial resistance.

When researchers like Dr. Baker discover a new species or strain, they can deposit it in the N.C.T.C.

“Their science can then be reproducible, because other people can study it,” said Sarah Alexander, the collection’s lead scientist and curator. “There may be new applications for those strains.”

“From my perspective, it is one of the most important collections worldwide,” said Jörg Overmann, the director of the German Collection of Microorganisms and Cell Cultures, one of the world’s largest and most diverse.

Image

Credit…National Infection Service, Public Health England

The collection first opened in London in 1920 at the Lister Institute of Preventive Medicine. Its first 200 cultures — including Private Cable’s — were deposited by Sir Frederick William Andrewes, a pathologist who studied dysentery throughout World War I.

The organization sent 2,000 strains to various institutions for free over the next year. The bacteria were delivered alive, teeming on a medium of agar made from Dorset egg yolks and sealed with paraffin wax.

Safety protocols weren’t in place yet: In 1922, three N.C.T.C. researchers caught Tularemia, or rabbit fever, during an experiment in which they’d rubbed the spleen of a guinea pig infected with Francisella tularensis on the scarified skin of a healthy guinea pig.

The collection was transferred to a farmhouse north of London in 1939, a lucky move as the institute was bombed during World War II. In 1947, the curator honed the collection to medical and veterinary strains. The collection began charging scientists two shillings and sixpence per strain — about $5 today.

In the following decades, the growing collection moved back to London and raised its prices. Today it is a nonprofit that’s self-supporting through the sale of strains, which usually cost between $85 and $375.

“I need to make sure the collections are scientifically relevant and financially robust,” said Julie Russell, the head of culture collections at Public Health England, which also has collections of pathogenic viruses and fungi.

The N.C.T.C. holds many bacteria relevant to medical breakthroughs. Alexander Fleming, who discovered penicillin, deposited 16 strains into the collection between 1928 and 1948. Fleming sourced NCTC 4842, the bacterium Haemophilus influenzae, from his own nose. Betty Hobbs, a noted expert on food poisoning who identified Clostridium perfringens as the culprit behind many food-borne illnesses, deposited more than 20 related strains.

A subset of its holdings is the Murray Collection, assembled by Everitt George Dunne Murray in the first half of the 20th century from the stool, urine, blood, cerebrospinal fluid and other bodily products of sick people across the world. The sub-collection’s 683 strains span the period when antibiotics entered into general use.

“It gives us this snapshot of an era for which we don’t have much information but that is critical for understanding how we’ve got to the antimicrobial crisis that we’re in today,” Dr. Baker said.

The collection has also sequenced the genomes of about half the strains, making that data available publicly for genetic research.

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Credit…Public Health England

In 2019, the collection sent 3,803 ampuls of bacteria to 63 countries. Among the most requested genera, were Clostridium (a leading cause of infectious diarrhea), E. coli (360 strains, some dangerous, others harmless), Staphylococcus (causing infections ranging from mild to fatal), Mycobacteriaceae (responsible for tuberculosis and leprosy, among others) and Salmonella (from contaminated food).

They’re shipped from a distribution center outside London under strict protocols, with safe handling instructions. Most bacteria are biosafety level two or three, which means they can cause serious or lethal diseases but have a cure. Level 4, the deadliest, includes only viruses.

The collection is also growing at a good clip.

“We receive anywhere between 50 and 200 strains a year from all sorts of sources,” said Jake Turnbull, a microbiologist at the collection.

Some are newly discovered, called type strains. Others are deposited from historical collections, or by scientists who retire or shift their research focus and want their strains to have a future.

New specimens are cultured on agar to make sure they’re alive and uncontaminated, suspended in a sugar-rich cryoprotectant broth, freeze-dried at about minus 28 degrees Fahrenheit for 3 to 4 hours, plugged with sterilized cotton, flame sealed in an evacuated glass ampul and stored at 39 degrees. Not all specimens survive long-term storage.

“The process we use is very similar to the one developed in the 1930s,” Ms. Russell said.

Each sample must come with a description of its origin, identification and special characteristics that are added to a searchable database.

“Fifty years ago, you may just get a handwritten letter with a strain,” Dr. Alexander said. “Now we may get a strain that’s had its whole genome sequenced.”

They accept 90 percent of samples they receive. Most are strains that are currently circulating, responsible for outbreaks or have novel antimicrobial resistance profiles.

One 2018 acquisition was NCTC 14208, a strain of Neisseria gonorrhoeae swabbed from the throat of a British man who recently contracted gonorrhea. The sexually transmitted disease, which infects nearly 80 million people every year, is becoming nearly untreatable.

“Evolutionarily, it’s quite an amazing bacterium,” Dr. Alexander said. “It has a lot of horizontal gene transfer. They swap antimicrobial resistance genes between the strains.”

The man had been given ceftriaxone and azithromycin — the only remaining treatment for the infection — but the bacteria beat them both. Another treatment eventually cured him.

In 2019, the collection sent 28 strains of N. gonorrhoeae to dozens of researchers. The strain from the British man, referred to as “super gonorrhea,” went to six.

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Credit…Anna Dumitriu

In late February, the collection got a visit from Anna Dumitriu, who became its first artist-in-residence in 2018. Her work, often done in collaboration with scientists, frequently incorporates microorganisms.

She and a reporter observed the extraction of the super gonorrhea’s DNA in an N.C.T.C. molecular biology lab ahead of getting a lesson from Dr. Alexander on proteomics, a tool for studying antibiotic resistance that involves analyzing bacterial proteins.

“The loves of my life are chlamydia and gonorrhea,” Dr. Alexander, who has researched STDs for years, said during the session.

In anticipation of collection’s 100th anniversary, Ms. Dumitriu created the raw-silk “Plague Dress,” impregnated with killed Yersinia pestis bacteria, which she extracted from the collection’s samples with Dr. Alexander’s help.

She also observed the process of how a strain becomes part of the collection, using a penicillin-resistant strain of Staphylococcus aureus swabbed from her own nose, à la Alexander Fleming, and added to the collection as NCTC 14139.

“I’ve used it in quite a lot of artworks and installations,” Ms. Dumitriu said.

She isn’t sure yet what creative expression the super gonorrhea strain will yield.

Antimicrobial resistance is likely to be one of the most pressing public health concerns for years to come. Of the 49 antibiotics currently in development, only four have been approved, and less than a quarter come from novel drug classes.

The samples being studied, donated and preserved in the N.C.T.C. and other culture collections will almost certainly play a role in medical breakthroughs decades in the future, just as Private Cable’s has a century after he died.

Dr. Alexander is keenly aware of this long-term view. Scientists who place their microorganisms in the collection “leave their legacy,” she said.

“You immortalize your science. We’re very much hopeful that in a hundred years’ time, people may be able to access strains that scientists deposited a hundred years ago.”

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