MEET MY MAKER,
THE MAD MOLECULE
R
eturning to our mystery redhead in the movie theater—what else could we learn about her from a strand of hair or blood sample? Her DNA profile, resembling a supermarket barcode, is a monumental accomplishment, but it’s only a fraction of her story. For a fuller picture of her health and heredity, we would need to include the teeming seashores of her microbes, the rest of her being—in fact, more than her being. Another self, a shadow self. At any moment, she is inseparable from trillions of her single-celled, single-minded, naked companions, some of whom don’t have her best interests at heart.
When she weighed herself earlier today, she may have deducted a pound or two for clothes and shoes. But did she take into account the roughly three pounds of microorganisms that inhabit her crevices and innards? Probably not. She’d need an atomic scale to start with, and anyway microbes are shifty, jumping off her peninsulalike feet and climbing aboard elbows pell-mell; they’re not easy to tally.
Microbes are the most fruitful life form on Earth, colonizing all
sorts of ardent unspoken strangers, creating small sulfurous rumblings in the animal belly, reveling in the smell of fish and old shoes, and leaving aftertastes in the mouth stale as bus-station sandwiches. They’re also real workhorses, fluting the air until it’s breathable, promoting photosynthesis on the land and in the oceans, decomposing dead organisms and recycling their nutrients. In industry, we breed them to ferment dairy products and to process paper, drugs, fuel, vaccines, cloth, tea, natural gas, precious metals; they help mop up our oil spills. We yoke them like oxen and set them to work. But just as most of the mass in the universe (94 percent) is “dark matter,” this largest biomass on our planet escapes the naked eye, yet is the invisible Riviera of the visible world.
How remarkable it is that we’re not only renaming our age, we’re on the threshold of redefining ourselves as a completely different kind of animal than we ever imagined. For years, we thought DNA told the whole story. Instead we find that each person is a biological extravaganza of ten trillion microbes and one trillion human cells. It’s amazing we don’t slosh or disintegrate as we walk. Here’s the thing: on a microscopic level we do, while constantly adding new microbes from other people, plumes of dust, and the plants and animals we encounter.
In only the past ten years, our picture of a human being has evolved from a lone animal to a team of millions of life forms working in unison for mutual benefit. Unrelated people may be widespread from Tierra del Fuego to Quaanaaq, but there’s a movement afoot to classify human beings as “eusocial,” a single unit of highly sociable life forms who can’t survive all by themselves. Earth favors similar collectives—ants, bees, termites, coral, slime mold, naked mole rats, etc.—in which individuals pool their know-how to act for “the sake of the hive.” Thanks to the Web and social media, we’re discovering what a bustling rialto each person really is, and also how connected we all remain. Worlds within worlds, each of us is a unique ambulatory superorganism who belongs to one miscellaneous species living on the body of a colossal superorganism
of a planet in a waltz of innumerable galaxies sprinkled with other Gaia-like planets and likely their own life forms percolating with untold hangers-on.
A marvel of the Human Age is that, in the past decade alone, we’ve mapped both the DNA in our cells and the DNA in our microbes. In the hunt we’ve discovered that a true view of ourselves as a life form is more untidy than we thought, and unglimpsed by most of us, a cloud of entwined bugs and human cells in a semipermeable frame. Joshua Lederberg, the Nobel-laureate biologist who, in 2000, coined the term “microbiome,” defines it as “the menagerie of the body’s attendant microbes.” Amid the hoopla surrounding the Human Genome Project, he urged, “We must study the microbes that we carry within us and on our surfaces as part of a shared embodiment.”
If the Human Genome Project was a landmark feat of discovery, the Human Microbiome Project is gene cartography’s finest hour. NIH director Francis Collins compares it to “fifteenth-century explorers describing the outline of a new continent,” a triumph that would “accelerate infectious disease research in a way previously impossible.”
For five years, a consortium of eighty universities and scientific labs sampled, analyzed, and audited over ten thousand species that share our human ecosystem, thus mapping our “microbiome,” the normal microbial makeup of healthy adults. And the quest continues.
The researchers have found that each of us contains a hundred trillion microbial cells—ten times more than our human cells. When they peered deeper and compared the genes, they realized that we carry about three million genes from bacteria—360 times more than our own human code. Among the hundred or so large groups of bacteria, only four specialize in the human body. They’ve been sidekicks for so long that over time our fate has fused with theirs.
So, odd as it sounds, most of the genes responsible for human survival don’t descend from the lucky fumblings of sperm and egg, don’t come from human cells at all. They belong to our fellow travelers,
the bacteria, viruses, protozoans, fungi, and other lowlife that dine, scheme, swarm, procreate, and war all over us, inside and out. Vastly more bacteria than anything else. All alone our moviegoer could be arrested for unlawful assembly. She doesn’t propel a solid body but a walking ecosystem.
They also learned that we all carry pathogens, microorganisms known to spark disease. But in healthy people, the pathogens don’t attack; they simply coexist with their host and the rest of the circus tumbling and roaring inside the body. The next mystery to crack is what causes some to turn deadly, which will revamp our ideas about microbes and malady.
We’ve known about bacteria for 350 years, ever since a seventeenth-century Dutch scientist, Antonie van Leeuwenhoek, slipped some of his saliva under a homemade microscope, which he had crafted with lenses made from whiskers of glass, and espied single-celled organisms crawling, sprawling, flailing about in the suburbs of our gums. He named them animalcules and peered at them through a vast array of lenses (an avid microscoper, he made over five hundred).
In the nineteenth century Louis Pasteur proposed that healthy microbes might be vital, and their absence spur illness. By the time tiny viruses were discovered, only a hundred years ago, people were already driving cars and flying airplanes. But we didn’t have the tools to study the every-colored, shifting, scented shoal of microbes we swim in, play in, breathe in all the day long. Some cross the oceans on dust plumes. Acting as condensation nuclei, they jostle rain or snow until it falls from clouds. Far from being empty, the air, like the soil, throbs with flecks and dabs of life, more like an aerial ecosystem than a conveyor belt for clouds.
We need to reimagine the air, not as a desolate ether but as a lively, largely invisible, ecosystem. As we peer through its glassy expanse to a far trail or up at a billowing cloud, nothing blocks our view, the whole corridor looks vacant, and yet it’s a community pulsing with life. Our eyes merely slide over its tiniest tenants. The sky is really
another kind of ocean, and even though we sometimes used to refer to “oceans of air,” we imagined barren currents; we didn’t realize how life-soaked the waves really are.
When David Smith and his colleagues at the University of Washington sampled two large dust plumes that had sailed across the Pacific from Asia to Oregon, they were surprised to find thousands of different species of microbes in the plumes, plus other aerosols, dust particles, and pollutants. All suspended and wafting around the planet, tromboning and floating, interacting with life.
In this panoramic new portrait, the Anthropocene body is no longer an entity that’s separate from the environment, like a balloon we pilot through the world, avoiding obstacles, but an organism that’s in constant conversation with its environment, a life-and-death dialogue on such a minute level that we’re not aware of it. It recognizes the mad microscopic mosaics we really are, molecular bits who trace their origins to simple one-celled blobs, then cellular flotillas that grew by engulfing others in life’s oceanic swap meet. Evolving this way and that, nabbing traits, shedding traits, we went haywire in slow motion over millions of years. Maybe our cells, however much they evolve, retain a phantom sense of those early days as colonial bodies with a shared purpose, more like amoebas or slime mold than mammals. We’re beginning to accept the idea of gypsy organisms that fanfare around us, making catlike raids on each other in dark simmering thickets, species as different from one another as animals adapted to rainforest, arctic, ocean, prairie, or desert. For we, too, have hillocks and estuaries, bogs and chilly outposts, sewers and pulsing rivers for them to quarrel and carouse in.
Even inside our own cells, we house more twitchy bacteria than anything else, because our mitochondria and chloroplasts were once primitive bacterial cells. They’ve sponged off us for so long that they can no longer exist on their own. Some our body welcomes with open pores because they handle metabolic melodies we couldn’t even hum on our own. It amazes me that we’ve survived with such grace, since we’re born dottily deficient, lacking vital survival skills such as
how to digest the very foods we eagerly wolf down. An omnivorous diet helped us endure icy forests and bright broiling terra-cotta landscapes, but we don’t have all the enzymes we need to absorb those foods; our microbes assist.
In the distant past, as Earth bloomed with primitive life, strings and mounds of twinkling single-celled bacteria discovered the mutual benefits of teamwork and became allies. Others took a bolder and more violent step—they gobbled each other up. It’s only at that stage that lilacs, marine iguanas, wombats, and humans became possible. As multicelled organisms grew more and more complex, the imprisoned bacteria adapted and thrived, until they became vital cogs of each complex cell.
The consensus now among evolutionary biologists is that we can’t separate “our” body from those of our resident microbes, which have been fiddling in subtle ways with our nature as a species for millions of years, and influence our health and happiness to a previously unimagined degree. Study after study is showing that microbes profoundly affect our moods, life spans, personalities, and offspring. They influence not only
how
we are but
who
we are. How strange that we feel whole, one person whom we can wash and dress and conduct internal monologues with, though most of us is not only invisible but not even what we’re used to defining as human. Planet Human offers a dizzying array of habitats for the unseen and the unforeseen, the hominid and microbial.
Only very recently has the scientific community acknowledged the extent to which our microbes might indeed affect our evolution, and by
our
I mean the whole
mespucha
, as they say in Yiddish (the term in biology-speak is “holobiont”). Not just individuals but all their microscopic relatives with their relative points of view. Some hijack our free will, divert our behavior, and become matchmakers. A wasp study is offering fresh insights. By definition, members of a species can mate and produce live offspring. But researchers studying several species of jewel wasp (loaded with ninety-six different kinds of gut bacteria) have discovered that microbes can determine
whether unions between different wasp species will succeed. When two distinct species of wasps mated, their offspring kept dying. Until recently, we would have said such a fertility problem was genetic. We know now that it can be microbial. When researchers changed the wasps’ microbes, the species bred favorably and hybridized. Evolution can be detoured by a mob of hidden persuaders.
Once again from the insect world, recent experiments with fruit flies are showing another way microbes can be at the helm, and the too-real possibility that bacteria have played a vital, even scary, role in our evolution. Consider how microbes control the love life of concupiscent humans and lusty fruit flies alike. Ilana Zilber-Rosenberg and her colleagues at Tel Aviv University’s Department of Molecular Microbiology and Biotechnology have discovered that the bacteria inside the gut of a fruit fly sway its choice of mates.
Fruit flies raised on either molasses or starch prefer to mate with others on the same diet. But when the flies are dosed with antibiotics, which kills the microbes in their gut, they’re no longer picky and will mate with any willing male. Among fruit flies, sexy males know all the right dance moves, but they also have to smell sexy, and their pheromone-cologne is modified by the microbes inhabiting the fly. For both humans and fruit flies, the love-wizards of smell are the symbiotic microbes that brew pheromones for us, their larger hosts. Scent rules in human courtship, too, especially among females looking for a mate. Although men seldom report such fussy responses to their partner’s natural smell, women so often do that it’s become a romantic cliché: “There just wasn’t any chemistry.”
Tinker with microbes and you alter stud capital, which in turn alters the genes of the female’s offspring, and so on as generations disrobe or unfold their wings. The object of natural selection isn’t a single plant or animal, Zilber-Rosenberg proposes, but its whole milieu, the host organism plus its microbial communities, including all the parasites, bacteria, fungi, viruses, and other bugs that call it home.
Fruit flies make appealing test subjects because we share such a
bevy of mating behaviors. The dinner date, for instance. What’s the quickest way to a man’s heart? Forget Cupid’s arrow. According to Mom-wisdom, it’s coaxed by a cozy meal, in a penumbra of pleasure that mingles the fragrant food with the cook. If men are anything like fruit flies—and who’s to say they’re not at times; heaven knows women are—Mom was right. For female fruit flies, a dinner date is the ultimate rush. And rush it literally is, since they only live about twenty-five days and can’t afford to be shy.
Live fast and die
is their mantra, and they need a handy food supply if their large new brood is to survive. Female fruit flies prefer males who favor the same chow. Still, the males need to be in the right mood, and the females are surprisingly picky and manipulative given their short career.