Friday, April 04, 2025

Oxygen metabolism in bacteria arose before Earth’s Great Oxidation Event



Summary author: Walter Beckwith


American Association for the Advancement of Science (AAAS)




Bacteria may have adapted to oxygen well before Earth’s atmosphere was saturated with it, according to a new study. Researchers who traced microbial evolution over billions of years – using machine learning and other methods – show that the evolution of oxygen tolerance predated the Great Oxidation Event (GOE) and may have been crucial not only for the origin of oxygenic photosynthesis in Cyanobacteria but also for the evolution of the planet’s atmosphere. The findings underscore the dynamic relationship between biological evolution and Earth's geological history. Microbial life has dominated Earth’s history for at least 3.7 billion years. However, given the sparse presence of the planet’s first lifeforms in the fossil record, particularly in deep geological time, little is known about their evolution. In lieu of fossil evidence, researchers use geochemical records of microbial biological activity to estimate the ages of key bacterial lineages and their metabolic innovations. The GOE, ~2.4 billion years ago (Ga), marked the accumulation of atmospheric oxygen. This transformative event is thought to have been driven by the emergence of oxygenic photosynthesis – an evolutionary innovation attributed to Cyanobacteria that likely arose ~3.22 Ga. Yet despite this innovation that predated the GOE, it is thought that most life remained anaerobic until the GOE, when atmospheric oxygen levels began to rise. The extent to which aerobic life existed before the GOE remains a subject of debate and the evolutionary timelines of oxygen-adapted bacterial lineages remain poorly constrained. 

 

To address this gap, Adrián Davín and colleagues constructed a species tree of Bacteria using 1,007 genomes spanning bacterial taxonomy. Then, using machine learning and phylogenetic reconciliation, Davín et al. identified distinct evolutionary signatures for oxygen adaption in bacterial genomes and predicted lineages where ancestorial transitions from anaerobic to aerobic lifestyles occurred. This allowed the authors to trace the evolution of oxygen use in bacteria across deep time. According to the findings, early aerobic bacteria emerged before the GOE, around 3.22 to 3.25 Ga, suggesting that aerobic metabolism evolved in some lineages – likely the ancestors of cyanobacteria – before oxygenic photosynthesis emerged. Following the GOE, there was an intense diversification of aerobic metabolism, which contributed to higher rates of diversification in oxygen-adapted lineages compared to anaerobic ones.

Discovery of bacteria's defence against viruses becomes a piece of the puzzle against resistance




Umea University





Antibiotic resistance is a global health challenge that could overtake cancer mortality within a few decades. In a new study, researchers at Umeå University, Sweden, show that the emergence of resistance can be understood in the mechanism of how bacteria build up defences against being infected by viruses. It is about genes in the bacterium that interfere with the attacking virus's ability to multiply.

"A key to antibiotic resistance might be the use of viruses to kill bacteria, however, the systems that bacteria employ to defence themselves against viruses are unknown. Understanding these systems opens up for research into how we can break down the defence so that serious infection disease can be treated in the future," says Ignacio Mir-Sanchis, Assistant Professor at Umeå University and the study's lead author.

The Umeå researchers have studied the bacterium Staphylococcus aureus, which is a common but potentially fatal bacterium in cases such as septic shock and pneumonia. A subgroup of S. aureus has become multi-resistant to antibiotic treatment and thus poses a major danger to public health. In some countries, a quarter of S. aureus is now multi-resistant, in Sweden only one percent.

However, the bacteria themselves are vulnerable to infection by a type of virus called bacteriophages, or just phages. Throughout evolution, bacteria and phages have undergone an arms race in which phages infect bacteria, which in turn develop mechanisms to resist the attacks. Much of this defence is encoded in the part of the bacteria's genome that can easily be transferred between bacteria, the so-called mobilome. Such a transfer can mean that otherwise harmless bacteria can turn into lethal. This is because the mobilome often carries genes that are responsible for the production of toxins, i.e. toxic substances, and for resistance to antibiotics.

The research group has been able to identify a specific set of genes in S. aureus mobilome that confer immunity against infection with phages. This finding was possible thanks to Umeå University's cryoelectron microscope. These genes interfere with the ability of phages to spread and multiply. This happens because a key protein expressed by one of the genes forms a structure around an important protein encoded by the phage's genome, thereby blocking the phage's ability to copy its DNA and thus unable to infect more bacteria.

"The discovery of this mechanism could be a door opener to understand several aspects of bacterial pathogenesis. On the one hand, we now understand better how resistant bacteria defend themselves against viruses. On the other hand, because these set of genes also encode for toxins and antibiotic resistance genes, it may therefore turn out that this is an important piece of the puzzle in the fight against antibiotic resistance," says Ignacio Mir-Sanchis.

 

Bonobo communication shares compositional similarities with human language




Summary author: Walter Beckwith


American Association for the Advancement of Science (AAAS)




Wild bonobos – our closest living relatives – communicate using vocal calls organized in compositionally complex semantic structures that mirror key features of human language, according to a new study. The findings challenge long-held assumptions about the uniqueness of human language and open new avenues for understanding the evolution of communication. A hallmark characteristic of human language is its ability to combine discrete elements to form more complex, meaningful structures. This principle, known as compositionality, allows for the assembly of morphemes (the smallest unit of language with meaning) into words and words into sentences; the meaning of the whole is determined by its constituent parts and their arrangement. Compositionality can take two forms: trivial and nontrivial. In trivial compositionality, each word maintains its independent meaning. Nontrivial compositionality involves a more complex, nuanced relationship where meaning is not simply a direct sum of the words involved. Compositionality may not be unique to human language; studies in birds and primates have demonstrated that some animals are capable of combining meaningful vocalizations into  trivially compositional strucutres. However, to date, there is no direct evidence that animals use nontrivial compositionality in their communication.

 

Here, Mélissa Berthet and colleagues report strong empirical evidence that wild bonobos (Pan paniscus) use nontrivial compositionality in their vocal communication. Berthet et al. analyzed 700 recordings of bonobo vocal calls and call combinations and documented over 300 contextual features associated with each utterance. Employing a method derived from distributional semantics – a linguistic framework that measures meaning similarities between words – the authors analyzed these contextual features to infer the meanings of individual bonobo vocalizations and quantify their relationships. Then, to assess whether bonobo call combinations follow compositional principles, they applied a multi-step approach previously used to identify compositionality in human communication. Berthet et al. discovered that bonobo call types integrate into four compositional structures, three of which exhibit non-trivial compositionality, suggesting that bonobo communication shares more structural similarities with human language than previously recognized.