Tag Archives: Stress

Experts find remnants of ancient RNA viruses embedded inside reef-building corals

An international team of marine biologists has discovered the remnants of ancient RNA viruses embedded in the DNA of symbiotic organisms living inside reef-building corals.

The RNA fragments are from viruses that infected the symbionts as long ago as 160 million years. The discovery is described in an open-access study published this week in the Nature journal Communications Biology, and it could help scientists understand how corals and their partners fight off viral infections today. But it was a surprising find because most RNA viruses are not known for embedding themselves in the DNA of organisms they infect.

The research showed that endogenous viral elements, or EVEs, appear widely in the genomes of coral symbionts. Known as dinoflagellates, the single-celled algae live inside corals and provide them with their dramatic colors. The EVE discovery underscores recent observations that viruses other than retroviruses can integrate fragments of their genetic code into their hosts’ genomes.

So why did it get in there? It could just be an accident, but people are starting to find that these ‘accidents’ are more frequent than scientists had previously believed, and they’ve been found across all kinds of hosts, from bats to ants to plants to algae.”

Adrienne Correa, Study Co-Author, Rice University

That an RNA virus appears at all in coral symbionts was also a surprise.

“This is what made this project so interesting to me,” said study lead author Alex Veglia, a graduate student in Correa’s research group. “There’s really no reason, based on what we know, for this virus to be in the symbionts’ genome.”

The study was supported by the Tara Ocean Foundation and the National Science Foundation and led by Correa, Veglia and two scientists from Oregon State University, postdoctoral scholar Kalia Bistolas and marine ecologist Rebecca Vega Thurber. The research provides clues that can help scientists better understand the ecological and economic impact of viruses on reef health.

The researchers did not find EVEs from RNA viruses in samples of filtered seawater or in the genomes of dinoflagellate-free stony corals, hydrocorals or jellyfish. But EVEs were pervasive in coral symbionts that were collected from dozens of coral reef sites, meaning the pathogenic viruses were -; and probably remain -; picky about their target hosts.

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“There’s a huge diversity of viruses on the planet,” said Correa, an assistant professor of biosciences. “Some we know a lot about, but most viruses haven’t been characterized. We might be able to detect them, but we don’t know who serves as their hosts.”

She said viruses, including retroviruses, have many ways to replicate by infecting hosts. “One reason our study is cool is because this RNA virus is not a retrovirus,” Correa said. “Given that, you wouldn’t expect it to integrate into host DNA.

“For quite a few years, we’ve seen a ton of viruses in coral colonies, but it’s been hard to tell for sure what they were infecting,” Correa said. “So this is likely the best, most concrete information we have for the actual host of a coral colony-associated virus. Now we can start asking why the symbiont keeps that DNA, or part of the genome. Why wasn’t it lost a long time ago?”

The discovery that the EVEs have been conserved for millions of years suggests they may somehow be beneficial to the coral symbionts and that there is some kind of mechanism that drives the genomic integration of the EVEs.

“There are a lot of avenues we can pursue next, like whether these elements are being used for antiviral mechanisms within dinoflagellates, and how they are likely to affect reef health, especially as oceans warm,” Veglia said.

“If we’re dealing with an increase in the temperature of seawater, is it more likely that Symbiodiniaceae species will contain this endogenous viral element? Does having EVEs in their genomes improve their odds of fighting off infections from contemporary RNA viruses?” he said.

“In another paper, we showed there was an increase in RNA viral infections when corals underwent thermal stress. So there are a lot of moving parts. And this is another good piece of that puzzle.”

Correa said, “We can’t assume that this virus has a negative effect. But at the same time, it does look like it’s becoming more productive under these temperature stress conditions.”

Thurber is the Emile F. Pernot Distinguished Professor in Oregon State’s Department of Microbiology.

Source:
Journal reference:

Veglia, A. J., et al. (2023). Endogenous viral elements reveal associations between a non-retroviral RNA virus and symbiotic dinoflagellate genomes. Communications Biology. doi.org/10.1038/s42003-023-04917-9.

Japanese natto consumption may help realize a healthy and longer-living society

Health is wealth as the saying goes and new research now shows that it is possible to have a healthy, less stressed society through familiar and inexpensive foods. One such food might be the Japanese natto which is made from softened soybeans that have been boiled or steamed and fermented with a bacteria called Bacillus subtilis var. natto. Bacillus subtilis var. natto is found in soil, plants, animals, and the human stomach and intestines. Most of the natto consumed in Japan is made from the Miyagino strain.

A research group led by Professor Eriko Kage-Nakadai at the Graduate School of Human Life and Ecology, Osaka Metropolitan University, examined the effects of Bacillus subtilis var. natto consumption on the lifespan of the host using Caenorhabditis elegans worms. The researchers found that Caenorhabditis elegans fed Bacillus subtilis var. natto had a significantly longer lifespan than those fed the standard diet, and further elucidated that the p38 MAPK pathway and insulin/IGF-1-like signaling pathway, which are known to be involved in innate immunity and lifespan, were involved in the lifespan-enhancing effects of Bacillus subtilis var. natto. They also examined stress tolerance, which has been shown to have a correlation with longevity, and found that resistance to UV light and oxidative stress is enhanced.

For the first time, we were able to demonstrate the possibility of lifespan-extending effects of Caenorhabditis elegans through the ingestion of Bacillus subtilis var. natto. We hope that future experiments on mammals and epidemiological studies will help to realize a healthy and longer-living society if we can apply this research to humans.”

Professor Eriko Kage-Nakadai, Graduate School of Human Life and Ecology, Osaka Metropolitan University

The research results were published online in the Journal of Applied Microbiology on April 20, 2023.

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Source:
Journal reference:

Teramoto, N., et al. (2023) Impacts of Bacillus subtilis var. natto on the lifespan and stress resistance of Caenorhabditis elegans. Journal of Applied Microbiology. doi.org/10.1093/jambio/lxad082.

“Pandemic Brain”: The Silent Consequence of COVID-19 on Students

New research indicates that the decision-making skills of college students, including those set to graduate this spring, may have been adversely impacted by the COVID-19 pandemic.

A compact study carried out by The Ohio State University’s researchers revealed that students during the Fall semester of 2020 demonstrated less consistency in their decision-making processes compared to their peers from several preceding years who participated in analogous research.

The researchers compared responses to a hypothetical situation made by students during the pandemic to responses made by students in earlier studies. They found evidence that students in 2020 were more likely to cycle between going with their gut and more thoroughly mulling over their answers depending on how the scenario was described.

“Our theory is that feeling stressed by everything going on was limiting students’ resources to really evaluate the information that was presented to them,” said lead author Melissa Buelow, professor of psychology at Ohio State’s Newark campus.

The research also suggests that the prolonged and wide-ranging uncertainties that came with the global lockdown – far different from an acute stressor imposed in a lab – affected the brain region responsible for problem-solving and decision-making.

“I think that is one of the more important findings – that the stresses of everyday life can wax and wane, and they can potentially overwhelm your cognitive resources and you can see real downstream effects on everyday activities that require your energy and your effort,” Buelow said. “This study provides additional information to understand why students may have been having difficulty coming to class, focusing on class, and getting things turned in – because there was this global event affecting every part of their lives.”

Buelow conducted the study with Ohio State Newark psychology faculty members James Wirth and Jennifer Kowalsky. The research was published recently in the Journal of American College Health.

In autumn 2020, students on Ohio State’s campuses attended classes offered both virtually and in person with reduced density and continued physical distancing, wearing masks and undergoing routine COVID-19 testing. Students were presumed not to be infected with the coronavirus when they participated in this research.

Buelow and her colleagues were inspired to do the study after they referred to their own foggy thinking as “pandemic brain” in casual conversation.

“We said if we are experiencing this, we wonder if others were as well,” Buelow said. “And as we were collecting data, we heard in the popular press about this idea of the stress of COVID leading to difficulty with thinking, processing information and making decisions.”

A clinical neuropsychologist, Buelow has used the Adult Decision Making Competence (ADMC) scale in her research for a decade. The tool presents numerous scenarios, framed in both positive and negative ways, and asks users to respond with their preferred solution or recommendation.

For this study, researchers compared data from a pre-pandemic sample of 722 undergraduates who had been assessed with the ADMC scale to data from 161 students who participated in one of two assessments during the 2020 fall semester.

The main finding: Instead of recognizing that ethics-based scenarios resulted in the same outcome whether presented as a gain or loss, students in 2020 were more likely to answer differently based on how the information was framed.

“Reliance on whether ‘this is a win’ versus ‘this is a loss’ really factored into decision making,” Buelow said.

Despite that inconsistency, the researchers noted that students in 2020 were as confident as pre-pandemic participants that their decisions on accuracy-based questions were correct.

“That struck us as interesting, with potential implications for the health and well-being of individuals adequately perceiving risk,” Buelow said. “Are individuals aware of what they do and don’t know, so to speak? And if you aren’t, does that lead to more risk?”

The researchers assessed another 72 students at two time points during the spring 2022 semester to gauge whether COVID-19 vaccination and loosened mask and distancing requirements lessened the pandemic’s effects on decision-making. Their exploratory analysis with this smaller sample found that students were still making less consistent decisions compared to pre-pandemic participants.

Buelow and colleagues are continuing to collect data to track changes in student decision-making over a longer period of time.

“Situational factors can affect why people make a good, advantageous decision versus a bad or risky decision, and that is an important context to have,” she said. “When we acutely stress individuals in the lab, we see a subsequent lowering of decision-making consistency. These findings really fit in with that – so we can theorize, in the absence of an acute lab stressor, that it was COVID, a much more global factor affecting every aspect of our lives, that affected cognition.”

Reference: “Poorer decision making among college students during the COVID-19 pandemic: Evidence for “pandemic-brain”” by Melissa T. Buelow, James H. Wirth and Jennifer M. Kowalsky, 28 March 2023, Journal of American College Health.
DOI: 10.1080/07448481.2023.2186129

Breast milk microbes shape infant gut health

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A new paper published in the Frontiers in Microbiology explores the contribution of human breast milk to the establishment of the infant gut microbiome.

Study: Human milk-associated bacterial communities associate with the infant gut microbiome over the first year of life. Image Credit: Pavel Ilyukhin / Shutterstock.com Study: Human milk-associated bacterial communities associate with the infant gut microbiome over the first year of life. Image Credit: Pavel Ilyukhin / Shutterstock.com

Introduction

Breastfeeding is encouraged as the first and exclusive food of infants for at least the first six months of life. In addition to its nutritional content, breast milk contributes significantly to the formation of the infant gut microbiome. This is because of its high content of immune cells, oligosaccharides carrying glycosyl residues, fatty acids, and some microbes.

Both breast milk bacteria and skin microbes from the maternal nipple reach and establish themselves in the infant’s gut. Bacteria may be shielded by secretory immunoglobulin A (sIgA) covering the immune system, thus allowing them to enter the gut intact.   

The infant gut microbiome (IGMB) is important for both infant development and immunity, as well as modulating conditions like atopy and body mass composition. However, earlier research on potential associations between the IGMB and breast milk microbiota has been limited to analyzing samples from corresponding time points.

The current study included almost 190 dyads from New Hampshire. Breast milk and infant stool samples were collected at around six weeks, four months, six months, nine months, and one year from birth, which allowed the scientists to identify correlations that developed over time.

What did the study show?

In the study population, with a mean age of 32 years, most were White and had a normal body mass index (BMI) during pregnancy. About 25% of deliveries occurred through Cesarean section (C-section), and antibiotic exposure prior to lactation occurred in over half of mothers.

Most babies were almost full term at birth, with only 3% being exposed to antibiotics by four months of life. By one year, about 30% of infants had been exposed to antibiotics.

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About 75% and 40% of infants did not receive any formula up to six weeks and four months, respectively. Most infants began eating solid food by six months.

Three breast milk microbiome types (BMTs) were identified in the six-week breast milk samples. These could be differentiated by the relative proportions of four bacterial genera, including Streptococcus, Staphylococcus, Pseudomonas, and Acinetobacter, as well as by the microbial diversity.

At six weeks, the gut microbiome in infants exhibited four six-week infant gut microbiome types (6wIGMTs). These had different abundances of Bifidobacterium, Bacteroides, Clostridium, Streptococcus, and Escherichia/Shigella.

The 6wIGMT correlated with the 6wBMT in male infants and those born by C-section. Notably, the same microbe was likely to be the most abundant within the dyads at this point.

By age one, the predominant difference in microbiome composition was due to Bacteroides. There was no association between the 6wBMT and 12mIGMT, which is likely due to the intake of solid foods by infants at this age. The transition to a primarily solid diet causes the infant microbiome to be dominated by other microbes, such as Bifidobacterium and Bacteroidetes, both of which are more abundant in the adult gut.

At six weeks, the BMT was associated with 6wIGMT in all infants but more strongly in male infants born by C-section. Male infants also had a higher proportion of microbes from breast milk present in their stool.

While infants delivered by C-section have a reduced colonization by maternal stool microbiota, their colonization by breast milk microbiota is higher than vaginally delivered infants.”

This could be due to the reduced microbial diversity and Bacteroides depletion in the IGMB of C-section-delivered infants, which makes it easier for breast milk microbes to colonize the gut.

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Male infants appeared to show a greater effect of the breast milk microbes on their gut microbiome. This may be because they exhibit less microbial diversity, with fewer Clostridiales and more Enterobacteriales abundance than is observed in female infants. The male infant’s gut microbiota is also more susceptible to stress and environmental exposures.

Overall, the breast milk microbial communities correlated most strongly with those found in infant stool samples that were collected at a later time point. For example, Pantoea in breast milk at four and six months was correlated with infant stool collected at nine and twelve months, respectively. These findings require further validation in future research.

What are the implications?

The identification of microbial clusters in human milk and infant feces that were shared within the mother-infant pair at six weeks is a striking finding in this study. The delay in cluster sharing and the association with C-section were associated with stronger correlations.

The findings of this study agree with earlier reports on the associations of various microbes in breast milk and the infant gut. Notably, the current study adds to previous data by identifying correlations between different taxa in these two sites.

The scientists postulate that microbes within communities may show direct interactions, such as the transmission of a microbe present in the infant oral cavity to the breast in this case, as well as the intake of breast milk by the infant. In addition, they may show indirect interactions through nutrients like fatty acids and milk sugars or other bacterial metabolites that influence both communities.

With the observed shift in breast milk microbial diversity over time, long-term studies may be needed to understand the breadth of microbial exposures during infancy. The change in IGMTs over time should also be better characterized and their relevance assessed.

These results suggest that milk microbial communities have a long-term effect on the infant gut microbiome both through sharing of microbes and other molecular mechanisms.”

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Journal reference:
  • Lundgren, S. N., Madan, J. C., Karagas, M. R., et al. (2023). Human milk-associated bacterial communities associate with the infant gut microbiome over the first year of life. Frontiers in Microbiology. doi:10.3389/fmicb.2023.1164553.

Most kids recover from Lyme disease within six months of completing antibiotic treatment

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A majority of parents of children diagnosed with Lyme disease reported that their kids recovered within six months of completing antibiotic treatment, according to a new joint study from Children’s National Research Institute and the National Institute of Allergy and Infectious Diseases (NIAID), part of the National Institutes of Health, published in Pediatric Research. The findings, based on Lyme disease treatment outcome data from 102 children in the United States, also revealed that a notably small percentage of children took longer than six months to recover and experienced a significant impact on their daily functioning.

Lyme disease is the most common vector-borne disease in the United States, with most cases caused by the bacterium Borrelia burgdorferi transmitted through the bites of infected blacklegged or deer ticks. Children between the ages 5 and 9 years account for a large proportion of the approximately 476,000 Lyme disease cases diagnosed and treated annually in the United States. Common symptoms of Lyme disease include: fever; headache; fatigue; and a distinct skin rash called erythema migrans. Without treatment, the infection can spread to joints, the heart and the nervous system. Antibiotic treatment resulting in full recovery is successful in most Lyme cases. For some, however, symptoms of pain, fatigue, or difficulty thinking persist or return after antibiotic treatment. Symptoms that substantially reduce levels of activity and impact quality of life for more than six months after treatment are classified as post-treatment Lyme disease (PTLD) syndrome.

This research studied the long-term outcomes of children with Lyme disease through a cross-sectional evaluation using validated surveys. The study collected survey responses from the parents of 102 children ages 5 to 18 years who had been diagnosed with Lyme disease between six months and 10 years before enrollment. Adolescents ages 10 to 18 years old were also invited to complete adolescent-specific questionnaires. According to these parent survey responses, 75% of children fully recovered within six months of completing treatment: 31% of all children recovered within one month; 30% recovered in one-to-three months; and 14% recovered in four-to-six months. Approximately 22% of children in the study experienced at least one symptom that persisted six or more months after completing treatment; of those, 9% had symptoms classified as PTLD syndrome. Six percent of the children were not fully recovered at the time of the survey, with 1% experiencing symptoms significant enough to impair daily functioning, the authors noted.

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According to the authors, this study supports previous data showing an excellent overall prognosis for children with Lyme disease, which should help alleviate understandable parental stress associated with lingering non-specific symptoms among infected children. They note that the findings of this study can help clinicians manage families’ expectations about the varying post-treatment recovery times of pediatric Lyme disease patients. The researchers suggest this new data could help reduce the potential for families seeking dangerous alternative therapies for children who experience prolonged recovery times. PTLD syndrome remains poorly understood in children and adults, and more research is needed to better understand these prolonged symptoms and identify treatment targets, according to the authors.

This study was supported through a partnership between NIAID and the Children’s National Research Institute (CNRI). Researchers at the Center for Translational Research at CNRI and the NIAID Laboratory of Clinical Immunology and Microbiology conducted the study.

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Source:
Journal reference:

Monaghan, M., et al. (2023). Pediatric Lyme disease: systematic assessment of post-treatment symptoms and quality of life. Pediatric Research. doi.org/10.1038/s41390-023-02577-3.

Researchers report surprising first steps that promote resistance to commonly prescribed antibiotics

Antibiotic resistance is a global health threat. In 2019 alone, an estimated 1.3 million deaths were attributed to antibiotic resistant bacterial infections worldwide. Looking to contribute a solution to this growing problem, researchers at Baylor College of Medicine have been studying the process that drives antibiotic resistance at the molecular level.

They report in the journal Molecular Cell crucial and surprising first steps that promote resistance to ciprofloxacin, or cipro for short, one of the most commonly prescribed antibiotics. The findings point at potential strategies that could prevent bacteria from developing resistance, extending the effectiveness of new and old antibiotics.

Previous work in our lab has shown that when bacteria are exposed to a stressful environment, such as the presence of cipro, they initiate a series of responses to attempt to survive the toxic effect of the antibiotic.”

Dr. Susan M. Rosenberg, co-corresponding author, Ben F. Love Chair in Cancer Research and professor of molecular and human genetics, biochemistry and molecular biology and molecular virology and microbiology at Baylor

She also is program leader in Baylor’s Dan L Duncan Comprehensive Cancer Center (DLDCCC). “We discovered that cipro triggers cellular stress responses that promote mutations. This phenomenon, known as stress-induced mutagenesis, generates mutant bacteria, some of which are resistant to cipro. Cipro-resistant mutants keep on growing, sustaining an infection that can no longer be eliminated with cipro.”

Cipro induces breaks in the DNA molecule, which accumulate inside bacteria and consequently trigger a DNA damage response to repair the breaks. The Rosenberg lab’s discoveries of the steps involved in stress-induced mutagenesis revealed that two stress responses are essential: the general stress response and the DNA-damage response.

Some of the downstream steps of the process that leads to increased mutagenesis have been revealed previously by the Rosenberg lab and her colleagues. In this study, the researchers discovered the molecular mechanisms of the first steps between the antibiotic causing DNA breaks and the bacteria turning on the DNA damage response.

“We were surprised to find an unexpected molecule involved in modulating DNA repair,” said first author Dr. Yin Zhai, postdoctoral associate in the Rosenberg lab. “Usually, cells regulate their activities by producing specific proteins that mediate the desired function. But in this case, the first step to turn on the DNA repair response was not about activating certain genes that produce certain proteins.”

Instead, the first step consisted of disrupting the activity of a protein already present, RNA polymerase. RNA polymerase is key to protein synthesis. This enzyme binds to DNA and transcribes DNA-encoded instructions into an RNA sequence, which is then translated into a protein.

“We discovered that RNA polymerase also plays a major role in regulating DNA repair,” Zhai said. “A small molecule called nucleotide ppGpp, which is present in bacteria exposed to a stressful environment, binds to RNA polymerase through two separate sites that are essential for turning on the repair response and the general stress response. Interfering with one of these sites turns off DNA repair specifically at the DNA sequences occupied by RNA polymerase.”

“ppGpp binds to DNA-bound RNA polymerase, telling it to stop and backtrack along the DNA to repair it,” said co-corresponding author Dr. Christophe Herman, professor of molecular and human genetics, molecular virology and microbiology and member of the DLDCCCC. The Herman lab found the repair-RNA-polymerase connection previously, reported in Nature.

Rosenberg’s lab discovered that DNA repair can be an error-prone process. As repair of the broken DNA strands progresses, errors occur that alter the original DNA sequence producing mutations. Some of these mutations will confer bacteria resistance to cipro. “Interestingly, the mutations also induce resistance to two other antibiotic drugs the bacteria have not seen before,” Zhai said.

“We are excited about these findings,” Rosenberg said. “They open new opportunities to design strategies that would interfere with the development of antibiotic resistance and help turn the tide on this global health threat. Also, cipro breaks bacterial DNA in the same way that the anti-cancer drug etoposide breaks human DNA in tumors. We hope this may additionally lead to new tools to combat cancer chemotherapy resistance.”

Other contributors to this work include P.J. Minnick, John P. Pribis, Libertad Garcia-Villada and P.J. Hastings, all at Baylor College of Medicine.

Source:
Journal reference:

Zhai, Y., Minnick, P. J., Pribis, J. P., Garcia-Villada, L., Hastings, P. J., Herman, C., & Rosenberg, S. M. (2023). ppGpp and RNA-polymerase backtracking guide antibiotic-induced mutable gambler cells. Molecular Cell. doi.org/10.1016/j.molcel.2023.03.003.

Possible pathways of C. auris emergence and the hypothetical role of interspecies transmission

In a recent study published in the journal Clinical Microbiology and Infection, researchers in Spain, summarized the current understanding of the emergence and ecologic niches of Candida auris.

Study: Climate change, animals, and Candida auris: insights into the ecological niche of a new species from a one health approach. Image Credit: Kateryna Kon/Shutterstock.com
Study: Climate change, animals, and Candida auris: insights into the ecological niche of a new species from a one health approach. Image Credit: Kateryna Kon/Shutterstock.com

Background

C. auris was first identified in a Japanese inpatient in 2009. The United States (US) Centers for Disease Control and Prevention (CDC) categorized the pathogen as an urgent threat. Moreover, C. auris has been designated as a fungal pathogenic species of critical concern by the World Health Organization (WHO) in their fungal priority list in October 2022.

Five clonally distinct clades of this fungus emerged independently and concurrently on three continents. Whole-genome sequencing of 47 isolates identified many single nucleotide polymorphisms (SNPs) with minimal intra-regional genetic diversity, suggesting a near-contemporary emergence in distinct geographic locations.

In the present study, the authors discussed the likely pathways of the emergence of C. auris and the role of inter-species transmission. In doing so, the study postulates that climate change has played a major role in high thermotolerant C. auris emergence. Thus, hypothesizing that climate change induced an environmental ancestor to become pathogenic through thermal adaptation.

Hypothetical emergence due to global warming

Global warming is proposed as the likely explanation for the independent and contemporary emergence of distinct C. auris clades. Few fungal species are pathogenic in endothermal animals and humans; very few fungi thrive at mammals’ high basal temperatures, creating a thermal barrier preventing infections.

Several reports suggest that increasing environmental temperatures due to climate change may result in the selection of thermotolerant fungal lineages that can circumvent the thermal barrier and infect/colonize endothermic animals.

One study showed that C. auris could grow at elevated temperatures than its close phylogenetic relatives. In addition, the remarkable halotolerance exhibited by this fungus suggested that it could have previously existed as an environmental species in wetlands/marshes.

These ancestors might have become pathogens in humans after gaining thermotolerance due to climate change adaptation. Nevertheless, this hypothesis cannot explain the geographic dispersion of the independently evolved clades of C. auris.

Ecological niche(s) of C. auris

The first environmental isolates of C. auris were reported in 2021 from a salt marsh in the Andaman Islands and recently in Colombian estuaries. Notably, one of the isolates was less multidrug-resistant and less heat-tolerant.

It was also significantly different from clinical isolates suggesting a higher similarity to its wild ancestors from marine ecosystems.

C. auris also exhibits high-stress resistance, allowing for continued survival in stressful environments. This plasticity might contribute to its emergence and growing prevalence. Further, this fungus was detected in stored but not freshly pickled apples in India, suggesting a new human transmission pathway and a possible selection route for drug-resistant isolates in agriculture, storage, and supply chains.

Isolation from animal cultures or the environment has not been documented yet. Nonetheless, a study employing in silico DNA metabarcoding screened the internal transcribed spacer region in public datasets.

DNA metabarcoding identified partial matches in non-human sources, such as activated sludge, air dust, the ear canal of a dog with otitis, peanut fields, and the skin of newts. This provided evidence of the ubiquitous presence of the fungus in anthropogenic and natural environments.

One Health approach to understand and manage C. auris

One Health is an integrative, collaborative, multi/trans-disciplinary approach for sustainable balance and optimization of the health of humans, animals, and ecosystems.

Zoophilic fungi and, hypothetically, C. auris might have a dual life cycle wherein host, and environmental reservoirs may serve as durable sources of propagules. This might contribute to the global rise of emergent fungal diseases across continents.

Concluding remarks

The striking plasticity and the ability of C. auris to adapt to harsh environments could allow the fungus to thrive in sludge, wastewater, and fresh/marine waters.

Global warming, the impact of changes in the environment and human population, and indiscriminate antifungal use in agriculture might have led to C. auris evolving into a much more resistant/invasive pathogen that can infect/colonize endothermic animals.

Aquatic marine hosts could have spread primitive strains to humans. Therefore, adopting the One Health approach can help understand the relationship between animal/human health and ecological changes as factors in the emergence and transmission of fungal pathogens.

Journal reference:

Unlocking Academic Success: How Pre-Pandemic Campus Sports Boosted Resilience During Lockdowns

A history of participating in campus recreational sports can offset stress and contribute to academic competence even during high-stress periods such as a pandemic lockdown, shows a new study.

Researchers at the University of Waterloo found that participation in activities such as fitness classes and intramural and drop-in sports before the COVID-19 pandemic was linked to lower levels of stress and higher levels of perceived competence to handle challenges and master school workload during the lockdown.

The study used factor and regression analyses based on self-reported responses from 116 students active in campus recreational sports at two-time points – January 2020, before the pandemic and April 2020, after COVID lockdowns.

“Our findings suggest that the impact of campus recreational activities on reducing stress went beyond the obvious physical health benefits and contributed to overall well-being even down the line,” said Steven Mock, a researcher in the department of Recreation and Leisure Studies.

“It’s possible that students who had learned how to deal with challenges and losses in the context of sport and recreational activity developed key skills such as adaptability that helped them manage with pandemic-related setbacks.”

At the beginning of winter 2020, stress levels for students were generally low. Managing academic demands, building new relationships, and trying to achieve personal goals were the top three stressors at that time.

“Students had just come back from the holiday break, their academic workload was still low, and they were not anticipating any societal disruption such as COVID-19,” said co-author Narges Abdeahad, a former PhD candidate in the department of Recreation and Leisure Studies.

By April 2020, after lockdowns had begun, the overall level of stress had increased to above the midpoint, and the top stressors had changed to online delivery of quizzes and exams, the influence of the pandemic on their lives, and managing academic demands.

“We also found that graduate students and, even more so, international students had very low participation in campus recreational sports pre-pandemic, which has wellness implications for these two groups of students,” said Abdeahad.

“Since campus recreational sports appear to help develop lifelong skills that offset stressful events, educational institutions should consider including campus recreational sports as a strategy to enhance student mental health and well-being.”

Reference: “The role of past campus recreational sports participation in predicting students’ stress and competence during the COVID-19 pandemic” by Narges Abdeahad and Steven Mock, 6 February 2023, Journal of Leisure Research.
DOI: 10.1080/00222216.2023.2165203

Study provides evidence for a strong role of autophagy in controlling intracellular infections

Researchers at the Francis Crick Institute have found that the body’s process of removing old and damaged cell parts, is also an essential part of tackling infections that take hold within our cells, like TB.

If this natural process can be harnessed with new treatments, it could present an alternative to, or improve use of antibiotics, especially where bacteria have become resistant to existing drugs.

In their study, published in Nature Microbiology today, ahead of World TB Day on the 24th March, the team studied genes key to bacteria’s ability to evade autophagy, a pathway that cells use to destroy themselves when they are under stress or infected.

They engineered human immune cells called macrophages from specialist stem cells called induced pluripotent stem cells, which have the ability to become any cell type in the body. They then used genome editing tools to manipulate the macrophages ability to perform autophagy. When genes key to autophagy were removed and the cells were infected with Mycobacterium tuberculosis (bacilli that cause TB), the bacterial infection took hold, replicating more within the engineered cells and causing mass host cell death.

These results are evidence for a strong role of autophagy in controlling intracellular infections like TB. If this pathway can be boosted or strengthened, it could be a new avenue for tackling antibiotic resistance, by making existing antibiotic drugs more effective or presenting an alternative to drugs in cases where bacteria have evolved resistance.

I first studied the role of autophagy in infection during my PhD, so it’s incredible to see renewed interest in this field. Using the latest technologies, we’ve been able to show a key role for this pathway in controlling infection.

As immunotherapies have harnessed the immune system to fight cancer, boosting this immune defense with a host-directed therapy, could be a valuable new tool in the fight against infections, particularly those becoming resistant to antibiotics.”

Max Gutierrez, Head of the Host-Pathogen Interactions in Tuberculosis Laboratory at Francis Crick Institute

The team also validated their results using macrophages isolated from blood samples, confirming the importance of autophagy in human defenses.

Beren Aylan, joint first author and PhD student at the Crick together with Elliott Bernard and Enrica Pellegrino, said: “Antibiotic resistance is a huge threat to our health so it’s incredibly important to understand how our bodies fight infection and where there might be room for improvement.

“TB is a great example of where targeting our own immune defenses could be really effective, because it takes a very long course of different antibiotic treatments to effectively remove the infection. Anything that can be done to more effectively remove bacteria, could also make a huge difference to the cost and accessibility of treatments.”

The team are now planning to screen for drug compounds that could be used to boost autophagy in a targeted way.

“Boosting the autophagy pathway isn’t as simple as it might seem,” adds Max. This is because all parts of the body use autophagy as a way to recycle old and damaged cells. In order to safely increase autophagy in the location of infections, we need to target the pathway in macrophages alone.”

Source:
Journal reference:

Aylan, B., et al. (2023). ATG7 and ATG14 restrict cytosolic and phagosomal Mycobacterium tuberculosis replication in human macrophages. Nature Microbiology. doi.org/10.1038/s41564-023-01335-9