Research.Policy.News. The microbial sciences curated for you.
Research.Policy.News. The microbial sciences curated for you.
A portion of the antibiotics we consume are flushed down the toilet, either directly (not a good idea…) or by way of the human gastrointestinal tract. The antibiotics we increasingly feed to our meat sources may also end up at our local wastewater treatment facility. A recent metagnomic analysis reveals that bacteria containing a large number of antibiotic resistance genes (ARGs) and mobile elements (MEs) accumulate in our wastewater treatment plants, both in the activated sludge and anaerobic digestion processes. The ability of anaeorbic digestion to deactivate antibiotic resistant bacteria prior to biosolids utilization has been debated, and this study shows mixed results: anaeorbic digestion both increased and changed the overall abundance of ARGs but the number of MEs decreased. We should continue to monitor ARGs at our wastewater plants as we rely more heavily on antibiotics to protect and feed an ever growing human population.
Original article can be found here: http://www.sciencedirect.com/science/article/pii/S0043135417305651?via%3Dihub
When we talk about microbiomes, most people think of host-associated microbial communities. This makes sense because the term was first made popular by the Human Microbiome Project. Now, however, it has a broader meaning and refers to microbial communities everywhere, from buildings to natural hot springs. Microbial life can be found in the strangest places, and microbiome research is as diverse as the subjects it addresses.
Between June 17th and July 22nd, 2017, an international group of students will learn about the microbiome in yet another context: the earth’s history. For most of the time our planet has been in existence, only microbial life could thrive. How microbes survived and influenced the conditions of early earth is one of the key questions in the field of geobiology.
Caltech and USC’s Wrigley Institute are hosting the Agouron International Geobiology course, to give graduate students and postdocs the tools to reach beyond their own field and tackle this interdisciplinary problem. To chart our world’s history accurately, we must examine rock records and the biomarkers we find in them.
Taking water chemistry and microbiome samples at Mono Lake, CA
Curious? Check out more here or follow along with #GeoBio17 on twitter for ongoing updates!
Gut microbiota are different in male and female mammals, but no one has determined whether these differences are produced by innate variations in the male and female immune systems or whether immune system variations were produced by the microbiota in the gut. To find out, Fransen et al examined the immune systems of male and female germ-free (GF) mice and discovered that innate differences in immunity already existed, including higher levels of type 1 interferon signaling in GF females and much higher levels of the gut microbes Alistipes, Rikenella, and Porphyromonadaceae, that proliferate in the absence of innate immune defense mechanisms, in GF males. The team then transferred gut microbiota from conventional male and female mice into GF mice of the same gender or the opposite gender. The female GF mice developed gut inflammations that produced weight loss and DNA damage if they received microbiota from conventional males. The authors concluded that microbiota-independent differences in the immune systems of males and females exist and drive gut microbiome differences between the genders. They warned that these differences should be considered when designing treatment strategies to normalize gut microbiota caused by disease.
Original Article: Frontiers in Immunity 2017, Volume 8, Article 754.
The rise of multidrug-resistant bacteria in recent decades has increased the need for alternative antimicrobial treatments. Antimicrobial peptides offer a promising solution because they can target both gram-positive and gram-negative bacterial strains, some viruses, and fungi. Bioprospecting in wild animals, which have been exposed to a wide array of microbial assaults throughout their evolutionary history, has proven very useful in the identification of such peptides. In a recent article published in NPJ Biofilms and Microbiomes, Chung et al. 2017 identified a potential antimicrobial peptide in plasma collected from Komodo dragons (Varanus komodoensis). The team named the molecule DRGN-1 and created a synthetic version of it that demonstrated antimicrobial activity against both gram-negative Pseudomonas aeruginosa and gram-positive Staphylococcus aureus. It also inhibited the growth of biofilms and promoted wound healing.
Photo Credit: Tatiana Morozova
Chung, EMC, Dean, SN, Propst, CN, Bishop, BM, van Hoek, ML. (2017) Komodo dragon-inspired sythetic peptide DRGN-1 promotes wound-healing of a mixed-biofilm infected wound. npj Biofilms and Microbiomes, 3:9 doi:10.1038/s41522-017-0017-2
Anaerobic ammonium oxidation (anammox) is one of the most energy efficient biotechnologies for removing nitrogen from high-strength ammonium wastewaters. The system works using a combination of heterotrophic and anammox bacteria, but the specific metabolite exchange reactions between them in the anammox microbiome are poorly understood. The team used metagenomics and metatranscriptomics to explore these interactions and determined that the anammox bacteria provide amino acids and B-vitamins essential for anaerobic respiration and growth, and the protein-degrading heterotrophic bacteria liberate the amino acids and vitamins from the anammox matrix as well as scavenging and disposing of the cell debris and peptides anammox bacteria produce. The anammox bacteria Brocadia and the heterotrophic bacteria Chlorobi were the most dominant organisms, followed by heterotrophic bacteria affiliated with Chloroflexi, Bacteroidetes, and Proteobacteria.
The original article can be found here.
Quorum sensing, the production and detection of chemical signals produced when a critical mass of bacteria (a quorum) is present, allows bacterial cells to communicate with each other and coordinate their activities. Quorum sensing can happen between cells of the same species or between different species. One well-studied example of quorum sensing is bioluminescence in the bobtail squid using the bacteria Aliibivibrio fischeri. Producing light is energy-expensive, so these bacteria only do so when there are enough individuals collected to make the light visible when they glow.
The signaling molecules bacteria use to determine how many cells are present are generally made in their cytoplasms and then secreted into their environment. These molecules are different for each organism. How the molecules reach other cells is not fully understood, particularly if they cannot dissolve in water.
One option is membrane vesicles, bubbles of cell membrane enclosing fluid. We know that bacteria in some environments, such as the ocean, make a lot of these. This paper demonstrates that quorum sensing can occur via membrane vesicles in Paracoccus denitrificans, a gram-negative bacteria that is part of nitrate reduction. A strain of Paracoccus that was not able to produce a signaling molecule was able to produce a quorum sensing response when supplemented with membrane vesicles from the wild-type strain. Although this study focused on only one microbe, the results suggest that membrane vesicles may be an important mechanism of communication in microbiomes!
Colorectal cancer (CRC) is among the most common human cancers, and routine screening is recommended by the Department of Health and Human Services. There is now evidence of a relationship between gut bacteria and the development of these malignancies. The first clue was the association between the chronic gastritis caused by Helicobacter pylori infections in the stomach and low-grade, B-cell gastric lymphoma of the mucosa-associated lymphoid tissue. Clinicians also noted that patients who had Streptococcus bovis infections developed CRC, and research has proven that this is more than an anecdotal association. Several other organisms are associated with human colorectal cancer as well, including Fusobacteria and E. coli. There is a direct relationship between the abundance of these organisms and cancer, and also with the stage of disease and the presence of lymph node metastases. In contrast, Roseburia and Lachnospiraceae levels are lower in people with CRC.
Although the small bowel is significantly longer than the colon, cancers of the small bowel are much less common. Some researchers think the discrepancy occurs because there are almost one million times as many bacteria in the colon as in the small bowel, and this theory spurred more investigation into the role of gut microbiota in CRC development.
Studies in mice and rats have strengthened the case for a microbial contribution to colorectal cancer. Mice with genetic mutations that predispose them to CRC had less tumor growth if they were kept germ free and/or received antibiotics. A “dysbiotic” gut microbiome has also been found that induces colitis and CRC in mice and is transmissible, suggesting that gut bacteria induce inflammation and the resulting cell turnover leads to DNA damage and cancer.
It is still unclear whether any particular gut organism causes or prevents CRC. In the human studies published to date, samples were collected from CRC patients at the time of their initial therapeutic surgery and compared to healthy control microbiota sampled at a single time point, so it was not possible to determine whether the microbiome seen at surgery was present before the malignancy developed or was due to mucosal disruption and inflammation caused by the cancer.
More studies that look at gut microbiota before cancer develops and follow participants over a number of years will be necessary to determine whether cancer causes dysbiosis or vice versa. It will also be important to factor diet into the equation because there appears to be a strong link between the consumption of red meat, processed meat, and CRC.
When we think about single-celled organisms, we don’t typically imagine them behaving in ways that align with traditional ecological theory; but would it really be surprising if, upon closer inspection, we found that microbial communities operating within host ecosystems did, in fact, exhibit the same patterns as ecosystems that contain multicellular organisms? Welsh and his colleagues think that this is the case. In a recent study published in PeerJ, the team decided to address the extent to which one phenomenon in particular – apex predation as a stabilizing force in ecological communities – applies to communities at the microbial level.
To do this, Welsh and colleagues designed an experiment in which vibrio bacteria (Vibrio coralliilyoticus) were experimentally introduced to the greater star coral (Montastraeidea cavernosa) either in the presence or absence of the bacterial predator Halobacteriovorax. Although V. coralliilyoticus is widespread in tropical environments and is a species to which M. cavernosa might be exposed, it does not naturally associate with greater star corals. For this experiment, it was chosen as an alien invader to which the coral and its native microbiome might succumb. In contrast, Halobacteriovorax has been found at low abundance in nearly 80 percent of M. cavernosa corals surveyed in the wild, and is considered to be a member of the greater star coral’s core microbiome.
When V. coralliilyoticus was introduced to the experimental M. cavernosa group that did not contain Halobacteriovorax, Welsh at al. (2017) found that the coral’s microbiome became quite disturbed. Not only did V. coralliilyoticus proliferate, so did the native bacteria Rhodobacteria and Cytophagales, possibly due to the opening of niche space within the coral host. However, when greater star corals were exposed to V. coralliilyoticus in the presence of Halobacteriovorax, no significant difference between the experimental and control microbiomes was observed.
Just as wolves control deer and sharks control other fish populations, Halobacteriovorax seems able to operate as a top-down abundance control mechanism for both native bacteria and potential alien invaders. Similar relationships have also been observed in both human and mouse models (Gupta et al. 2016, and Shatzkes et al. 2017). Such ecological phenomenon are not typically described in the microbial literature, but may be much more common than previously thought.
This research can be found at PeerJ 5:e3315; DOI 10.7717/peerj.3315.
Image from www.xkcd.com
If you are looking for new metabolic pathways, you don’t need to look in exotic environments. Kwong, Zheng, and Moran of the University of Texas at Austin have found that a bacterial symbiont of honey bee guts, Snodgrassella alvi, uses a variant of the tricarboxylic acid (TCA) cycle previously associated only with vinegar production. This variant cycle appears to be an adaption to environments rich in acetate (the active ingredient of vinegar). The team found that the variant has evolved several times so it can work in a variety of organisms, including the human gut microbiome.
Image by Charlesjsharp (Own work, from Sharp Photography, sharpphotography) [CC BY-SA 3.0 (http://creativecommons.org/licenses/by-sa/3.0)], via Wikimedia Commons
Thirteen microbiome projects that will produce preliminary data for grant funding and support research infrastructure at the university have been funded by the UW-Madison Microbiome Initiative. The eight research projects include the contribution of gut microbes to Alzheimer’s disease, using the microbiome to reduce antibiotic resistance in children, the way a resident brain microbe prevents weight gain, gut microbial metabolism and host epigenetics, and harnessing microbiomes to manage the global nitrogen cycle. There is also a community enhancement project on the microbiome of the upper airway and respiratory infections. Fifty-eight faculty members representing six schools and colleges will collaborate on the projects.
The original article can be found here: http://news.wisc.edu/new-campus-initiative-targets-microbiome-research
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