Life has survived for more than three billion years because it is robust, and almost no mutations can easily outwit the defense mechanisms built up through eons of exposure to potential pathogens.
–Lawrence M. Krauss
Every second, every minute of your life, your body is under attack. This may be strange to think about, but millions of bacteria, as well as myriad other parasites, are attempting at this very moment to invade the sanctum of your body. Do not be offended, these creatures do not do this out of any sense of malice. They are simply driven by the two greatest necessities of life – survival and reproduction.
Ever since the first cells arose in the hot, steamy, soup that was our earth’s oceans billions of years ago, organisms have competed fiercely for the same limited resources. Some cells devised ways to halt the growth of or outright kill other cells, while others entered complex beneficial (mutualistic) or harmful (parasitic) interactions with each other. With time, two kinds of life forms emerged – parasites, who attack other organisms to their own benefit and the other’s loss, and hosts, who suffer from the parasites’ attack. A much larger class is that of pathogens – any organism that can directly cause disease in a host is called a pathogen. Host defense mechanisms have, therefore, evolved over eons to outsmart parasites and pathogens. Plants have specialized signaling systems to fight invading bacteria, and multicellular animals like human beings have an immune system with several tiers of defense to combat infection. Yet, at the same time, the parasites have been evolving too, devising sneakier and subtler ways of evading the host’s defense pathways to gain entry and live undetected. Life can, in fact, be described as a continuous arms race between hosts and their parasites, where neither gains the upper hand on the other, even after centuries of creating sophisticated arsenals for the purpose.
This continuous struggle has given rise to some truly ingenious forms of biological innovation. A recent study from Xuezhi Zhang and colleagues, working in a collaboration between the University of Geneva, Switzerland, and Baylor College of Medicine, USA, sheds light on a remarkable and evolutionarily ancient line of defense employed by a class of social amoeba. Simply put, the defense consists of casting a net formed of DNA molecules over bacteria and killing them slowly with poisons embedded in the net.
Before going further, let us take a look at the remarkable microorganism Zhang et al. performed their study on. Dictyostelium discoideum, the slime mold, is an amoeba, member of a heterogenous group of single-celled microbes united by the lack of a fixed body shape. Most of you would have observed amoebae in your high school biology class, or must have seen them in pictures (or if you watched Cartoon Network in the 90s, you might remember the amoeba boys from The Powerpuff Girls). Amoeba can create pseudopodia – false feet – that they can use to engulf their prey whole before digesting it. Dictyostelium, however, is a different kind of amoeba. When food (which for Dicty, consists primarily of bacteria) is available in plenty, Dictyostelium behaves like any other amoeba, happily swallowing prey as it moves through the soil. However, when food becomes scarce, this little microbe undergoes a fascinating transformation. Hundreds, and often thousands of Dictyostelium cells come together to form a single body, called a slug (named so both because of their shape and the slime trails they leave behind). Slugs can contain up to 100,000 individual Dictyostelium cells, are 1-2mm in length, which means they can be seen with the naked eye, and can move as a single body towards stimuli like light or nutrients. The slug travels for days, and once it reaches a suitable environment, it forms a mushroom-like fruiting body, with a stalk and a spore head, which then releases thousands of spores into the environment. The spores germinate to give rise to brand new mature and independent Dictyostelium cells. In doing so, Dictyostelium, like other slime molds, occupies a unique boundary region between unicellular and multicellular organisms.
Here’s a video of Dictyostelium in action.
Dictyostelium can be grown in the lab on agar plates with lawns of bacteria to serve as food. Depleting the medium of nutrients causes individual amoeba to aggregate and form slugs, which can be studied as they are, or disaggregated to look at individual cells. Zhang and colleagues observed that as the slug moved through an area containing the pathogenic bacteria Klebsiella pneumoniae, it released a cloud of DNA into the surroundings. This DNA could be stained and visualized by a dye called propidium iodide. When the researchers took the slug apart, they found that the extracellular DNA is released almost exclusively by a class of cells called sentinel cells (S-cells). Sentinel cells have previously been shown to act as specialized immune cells for the Dictyostelium slug, capable of phagocytosing (swallowing) and killing bacteria in the slug’s immediate surroundings. The scientists confirmed that the extracellular material was DNA by adding a special enzyme that digests and degrades DNA to the medium, and observing that the stained cloud does, indeed, disappear.
The scientists’ next experiments revealed the unique function of this strange extracellular net. When the researchers added tiny bacteria-sized beads to the medium around the Dictyostelium slug cells, they quickly became trapped and concentrated at the areas with the nets, showing that these nets can effectively trap particles of a similar size. At the same time, when these nets were formed in a bacterial lawn, the bacteria in the vicinity could be seen to die. When an enzyme that could degrade DNA was added to the medium along with the net-forming cells, the bacteria could no longer be killed as effectively.
Now, this is not the first report of extracellular DNA based traps that serve an immune function. Neutrophils are specialized white blood cells that patrol our bodies and move quickly to sites of infection. There, they release antimicrobial substances, as well as swallow microorganisms whole by a process called phagocytosis. In 2004, Brinkmann and colleagues, at the lab of Arturo Zychlinksy at the Max Planck Institute for Infection Biology, Germany, discovered a new mechanism of anti-microbial activity by neutrophils, which they named as Neutrophil Extracellular Traps, or NETs. NETs are strands of DNA dotted with antimicrobial proteins and enzymes that trap and kill pathogenic organisms when released at the site of infection. Later, this process was shown to occur in a number of other immune cells, including another type of white blood cells called eosinophils. Though first described in mammals, later studies showed that this process also occurs in chicken, fish and even invertebrates like crabs, mussels and sea anemone. The current study by Zhang et al., however, is the first report of such a process occurring in a single-celled organism, pushing back the evolutionary ancientness of the process by several millions of years,
The process of extracellular trap formation by immune cells like neutrophils is called ETosis, and it is one of the early steps of programmed cell death, a kind of altruistic suicide that these cells undergo following an infection. You can also get a sense of this when you consider that the DNA that neutrophils extrude in order to form extracellular traps is made up primarily of nuclear DNA, which is kinda important for cells. However, in their experiment, Zhang and colleagues did not observe significant numbers of Dictyostelium Sentinel cells dying off as they produced extracellular traps. Upon testing, the nets were found to contain almost exclusively mitochondrial DNA, which is DNA contained in organelles called mitochondria (these are small compartments inside the cell that generate energy for the cell to function). Mitochondrial DNA is also important for the cell; however, it is much more numerous and definitely much more expendable than nuclear DNA. While Dictyostelium cells are also capable of apoptosis – the altruistic self-sacrifice for the greater good that we talked about earlier – this does not seem to be necessary for producing extracellular traps.
Other aspects of the extracellular trap response seem to be remarkably conserved between Dictyostelium and multicellular organisms. Reactive oxygen species (ROS), which are oxygen-derived free radicals often used as a toxic antimicrobial substance by immune cells, was shown to be produced by the Dictyostelium Sentinel cells, and reducing ROS levels by a ROS ‘scavenger’, significantly improved bacterial survival. In mammals, toll-like receptors are a type of protein that sense and recognize foreign bacterial particles. The homolog of such genes in Dictyostelium, TirA, appeared be critical for the production of extracellular DNA traps, and Dictyostelium mutants lacking it were much more susceptible to bacterial infection in later stages of their life cycles.
Amoeba diverged from other animals approximately 1 billion years ago. Since then the two lineages have evolved separately, though often in the same environments, with the latter following the path of greater complexity and going on to create multicellular creatures as large as the blue whale, while the former remained restricted to the scale of a few micrometers (sometimes millimeters). Yet, as this study shows, the mechanisms of host defense against parasites possibly predate even this ancient divergence, and continue to help both us and Dictyostelium in our lifelong struggles for existence.
Zhang X, Zhuchenko O, Kuspa A, Soldati T (2016) Social amoebae trap and kill bacteria by casting DNA nets. Nat Commun 7:1–9
*Image by Zhang X, Zhuchenko O, Kuspa A, Soldati T (2016) Social amoebae trap and kill bacteria by casting DNA nets. Nat Commun 7:1–9 [CC BY 4]
**Image by Urban CF, Ermert D, Schmid M, Abu-Abed U, Goosmann C, et al. 2009 Neutrophil Extracellular Traps Contain Calprotectin, a Cytosolic Protein Complex Involved in Host Defense against Candida albicans. PLoS Pathog 5(10): e1000639. doi:10.1371/journal.ppat.1000639 [CC BY 2.5]
Graduate student and part-time science blogger. I am currently working on my PhD in neuroscience. In my spare time, I like to indulge my insatiable book addiction, browse the crazy alleys of reddit, and window-shop for gadgets.