Baby Bacteria

Sept. 26, 2014

By Medical Discovery News

Fetus in utero

While we know for sure that the bacteria living in and on us are key to our own well-being, more evidence suggests that we acquire our microbiomes before we’re even born. While a baby does acquire bacterial flora from its mother as it moves through the birth canal, scientists now think that our symbiotic, life-long relationships with bacteria begin in utero long before birth. They found bacteria living in the placenta, an organ previously thought to be sterile. They also discovered a baby’s bacteria to be similar to the bacterial flora of the mother’s mouth, making oral hygiene during pregnancy extra important.

An experiment in 2008 by Spanish scientists indicated that bacteria are acquired in some way before birth. They inoculated pregnant mice with labeled bacteria, which were then found in the meconium, the first bowel movement after birth. This was true even when the babies had been delivered by C-section. So scientists knew then that bacteria are acquired before birth and even without the birth canal, changing what we thought we knew about the womb.

Since then, scientists at Baylor College of Medicine have been studying the inside of the womb and birth canal in both humans and animals. They discovered that the vaginal microbiome changed during pregnancy, but it did not resemble that of newborns. So where did they get their bacteria from?

Baylor scientists then examined placentas from 320 women immediately after birth. Using DNA sequencing, they identified the individual types of bacteria each placenta contained. Comparing them to bacteria growing in and on the mothers, they found that the types of bacteria living in the mothers’ mouths most closely resembled those in their own placentas. Interestingly, the bacteria in the placenta consisted of high proportions of bacteria responsible for synthesizing vitamins and other nutrients, which probably benefits a developing fetus and newborn. So a fetus is first exposed to bacteria from the placenta, then at birth additional bacteria are introduced, and then again when babies are exposed bacteria on their parent’s skin, in breast milk, and in their environment.

Other studies have shown the influence of the microbiome on a mother and her baby. In one experiment, monkeys who ate a high-fat diet while pregnant and lactating produced babies with different proportions of bacteria in their guts than those of monkeys fed a normal diet. The short- and long-term consequences of abnormal maternal and infant microbiomes are not yet known, but it’s speculated that these changes could influence the metabolism of the infant and the development of metabolic disorders.

Science is increasingly aware of the role and importance the microbiome has in various parts of the body and the part it plays in human health and disease.

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What Makes a Male?

May 16, 2014

By Medical Discovery News

What makes a male?

Despite centuries of women being celebrated for siring sons, or scorned for failing to produce an heir, it is actually men who determine a baby’s gender. Women give each of their offspring an X chromosome, but the male can give an X or a Y chromosome to create a female (XX) or male (XY), respectively. But how much of the Y chromosome is required to make a male? It turns out only two genes are needed to create a male mouse, a species that determines gender the same as humans. 

Humans have 23 pairs of chromosomes, one of which is the sex chromosome. Chromosomes contain lots and lots of genes, all which carry instructions that tell different parts of the body what to do. In males, the Y chromosome carries a gene called SRY that encodes the Sex-determining region Y (also abbreviated SRY) protein. This protein, as its name suggests, will decide the sex of future offspring. Consequently, this one single gene, SRY, is all that’s required to produce an anatomically male mouse. However, these male mice are infertile because they lack some of the genes involved in sperm production.

That’s where another gene called Eif2s3y comes in. With this second gene, male mice can at least generate sperm cell precursors known as round spermatids, but not mature sperm. To fully develop sperm, the mice need both copies of this gene. One is toward the end of the Y chromosome and the other version is on the X chromosome.

So with only two genes from the Y chromosome, male mice are able to produce immature sperm. Scientists used an assisted in vitro fertilization technique to treat male infertility by injecting the round spermatids directly into the eggs of female mice. The round spermatids fertilized the eggs nine percent of the time. In comparison, sperm from natural-born male mice fertilized eggs 26 percent of the time. The offspring born from these efforts developed into normal, healthy, fertile adult mice. 

Even though only two genes from the Y chromosome are required to produce fertile adult mice, the Y chromosome is still important. More genes are required to produce fully mature, motile sperm capable of fertilizing an egg without intervention. The Eif2s3y gene may play a role in some forms of male infertility in humans. With this new data, therapies could be invented to encourage the development of functional sperm that could reproduce through in vitro methods. Injecting round spermatid into eggs is not currently an option for humans due to technical and safety issues, but this technique is likely to get better with additional research. 

The genetic information contained in the Y chromosome plays important roles in reproduction by controlling the development of sperm and normal fertilization and will continue to do so, negating suggestions that it is being eliminated by evolution or rendered useless by in vitro fertilization. For now at least, men remain indispensable.