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Background - Definitions
1. Obesity
Obesity has emerged as an epidemic, especially in the United States. It is a complex
disorder that involves an excessive amount of fat in the body.
It is often accompanied by a variety of chronic medical problems, including diabetes,
heart disease, hypertension (high blood pressure), and dyslipidemia (high cholesterol).
The study of microbiota is one that is paid a significantly lesser amount of attention in
comparison to the topic of obesity in popular science, despite its equal and interrelated
importance.
2. Microbiota/Microbiome
The microbiome is the totality of microbial population (culture-independent) in a
particular ecological niche or community (ocean, soil, body site, etc).
If the human intestinal micro biome is disrupted, then you have dysbiosis - disruption
of intestinal bacteria that have adverse effects on homeostasis and metabolism.
Hypothesis
Most reports attribute the obesity epidemic to factors such as excess food energy intake, changes in diet and
eating behavior, and increasing sedentary life style. Undoubtedly, these factors contribute, they do not
account for the rapid increase in obesity rates weve seen over the last two decades.
Recently, a series of studies have described the role of intestinal microbiota on body metabolism and energy
balance, and how its disruption (known as dysbiosis) could adversely affect body physiology and health.
If this mechanism disruption of the intestinal microbiota occurred at the population level, it could actually
explain the obesity epidemic.
It is important to note that the livestock use of antimicrobial agents has sharply increased in the USA over
the same 20-year period of the obesity epidemic and its sharp rise.
HYPOTHESIS: the American human intestinal microbiota may have been disrupted by chronic, widespread
exposures to low-residue antimicrobial drugs that have increasingly entered our food chain and the
environment over the last 20years. These exposures can be contributing to the obesity epidemic - they
could be the missing link to our explanation of the epidemic.
Procedure
The hypothesis and conclusion is based on a review of relevant literature.
1. First, they searched PubMed by cross-referencing the word obesity with the
following terms: epidemic, prevalence, diet, calorie intake, nutrients, physical activity,
lifestyle, host factors, genetics, antibiotics/antimicrobial agents, antibiotic residues in
food, antibiotics in plants, antibiotic growth promoters, environmental release of
antibiotics, animal husbandry, animal feed, gut microbiome/microbiota, and
metagenome.
2. Then they found more references by reviewing the cited references from the primary
articles.
3. They excluded abstract reports or conference proceedings. Articles not available
electronically were sought at the University of California library collections.
*The search was limited to publications in English up to August 2013.
- Food animal industry gradually adopts practice of administering subtherapeutic doses of antibiotics as
growth promoters.
- How do they gain weight anyway?
1. Suppression of subclinical infections and overt diseases which promotes general health of the animal
and hence better nutrition.
2. Stimulation of growth of bacteria in the gut that synthesize essential nutrients.
3. Suppression of microbes that compete with the host for nutrients.
4. Improvement in intestinal absorption of nutrients.
- Thus, if humans are indeed chronically exposed to low-dose antibiotics from the environment,
there is a good reason to believe that they, like the chicks, can gain weight.
- The next relevant question would be, how does exposure to antibiotics contribute to alteration in
intestinal microbial population?
Trasande et al. examined the long-term effect of antibiotic exposures in the first 2years of life of
children born in Avon, United Kingdom between 1991 and 1992. They found that exposure to
antibiotics during the first 6months of life, but not during 614 or 1523months was
consistently associated with a later increase in BMI.
Blaser and Falkow have suggested that the accelerated disappearance of the normal human
microbial community, such as Helicobacter pylori in the stomach, due in part to the human use of
antibiotics to treat peptic ulcer disease, may be contributing to post-modern conditions, including
obesity.
In a 10-month prospective experimental study of three human subjects given two courses of
ciprofloxacin, Dethlefsin and Relman showed that the gut microbiota was rapidly altered with
the antimicrobial drug exposure.
Future Research
What needs to be done:
1. The impact of antibiotic exposures on the gut microbiota ecology and body
physiology needs to be examined at the population level.
2. There needs to be a comparison of gut microbiota of populations residing near
farms or regions where animals are administered antibiotics versus those living
away from those places to reveal microbiota population structures associated with
differences in body physiology.
3. The practice and trend of use of antibiotics as growth promoters in animal
husbandry needs to be assessed to examine the relevance of this hypothesis to the
obesity epidemic in these other regions of the world.
4. A more systematic and comprehensive analysis of antimicrobial residues in food
and the environment is needed.
Conclusion
- Today, the core gut microbiota of many Americans may be substantially
different from that of most Americans living before the 1950s.
- Chronic exposures to low-residue antimicrobial drugs in food could disrupt
the equilibrium state of intestinal microbiota and cause dysbiosis that can
contribute to changes in body physiology.
- Thus, the obesity epidemic in the United States may be partly driven by the
mass exposure of Americans to food containing low-residue antimicrobial
agents.