Giardiasis may be a disease of the ecology of the GI tract
American Society for Microbiology News May 06, 2017
Colonization by the human and animal parasite, Giardia, changed the species composition of the mouse microbiome in a way that might be harmful.
The research was published in the journal Infection and Immunity.
ÂThis shift is generally characterized by more aerobic bacteria and less diversity of anaerobic species in the gastrointestinal tract, said coauthor Scott C. Dawson, Associate Professor of Microbiology and Molecular Genetics, the University of California, Davis. ÂThis suggests that Giardia infection could – at least in part – be an ecological disease, with parasite colonization disrupting the previously stable ecology of the gut.Â
Indeed, ÂWe found changes in the host microbial community throughout the entire gastrointestinal tract, said Dawson. These findings challenge the conventional wisdom that Giardia is a disease of the small intestine.
ÂWe infected mice with Giardia, sacrificed them at different times post–infection, and sequenced specific regions throughout the entire gastrointestinal tract using high–throughput 16S ribosomal RNA sequencing, said Dawson. This enabled the investigators to quantify the shifts in microbial diversity in each part of the GI tract, following infection. They also pre–treated one cohort of mice with antibiotics, to determine if that pretreatment resulted in different shifts in the microbiome as compared to those in mice not receiving antibiotics (it did so).
The various investigators had different motives for their interest in conducting this research, said Dawson. Steven M. Singer, of Georgetown University, Washington, DC, had previously noted that when mice were infected with a human Giardia, they had to be pre–treated with antibiotics in order for a robust infection to develop. ÂThat suggested that the gut microbiome had a protective effect in limiting giardiasis, said Dawson.
Furthermore, giardiasis is a major cause of sickness and malnutrition in developing nations, said Dawson, infecting an estimated 200 million in Africa, Asia, and Latin America, Âoften infecting children in communities without access to clean water. In the US, more than 15,000 cases were reported in 2012.
ÂWhile symptoms can be severe or even debilitating, the mechanism by which Giardia infection causes the disease symptoms remains unclear, said Dawson. ÂAs an anaerobic, fermenting, eukaryotic parasite, we reasoned that GiardiaÂs unique anaerobic metabolism may disturb host gut ecology.Â
Partly as a result of the unknown mechanism, there are few novel therapeutics, said Dawson. Moreover, even when treatment eradicates the parasite, GI symptoms may persist.
But if giardiasis really is an ecological disease, that raises the possibility that repopulating beneficial members of the gut microbiome could help treat this condition, said Dawson. ÂAlso, it is possible that certain types of gut commensal microbes could limit or inhibit early Giardia infection.Â
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The research was published in the journal Infection and Immunity.
ÂThis shift is generally characterized by more aerobic bacteria and less diversity of anaerobic species in the gastrointestinal tract, said coauthor Scott C. Dawson, Associate Professor of Microbiology and Molecular Genetics, the University of California, Davis. ÂThis suggests that Giardia infection could – at least in part – be an ecological disease, with parasite colonization disrupting the previously stable ecology of the gut.Â
Indeed, ÂWe found changes in the host microbial community throughout the entire gastrointestinal tract, said Dawson. These findings challenge the conventional wisdom that Giardia is a disease of the small intestine.
ÂWe infected mice with Giardia, sacrificed them at different times post–infection, and sequenced specific regions throughout the entire gastrointestinal tract using high–throughput 16S ribosomal RNA sequencing, said Dawson. This enabled the investigators to quantify the shifts in microbial diversity in each part of the GI tract, following infection. They also pre–treated one cohort of mice with antibiotics, to determine if that pretreatment resulted in different shifts in the microbiome as compared to those in mice not receiving antibiotics (it did so).
The various investigators had different motives for their interest in conducting this research, said Dawson. Steven M. Singer, of Georgetown University, Washington, DC, had previously noted that when mice were infected with a human Giardia, they had to be pre–treated with antibiotics in order for a robust infection to develop. ÂThat suggested that the gut microbiome had a protective effect in limiting giardiasis, said Dawson.
Furthermore, giardiasis is a major cause of sickness and malnutrition in developing nations, said Dawson, infecting an estimated 200 million in Africa, Asia, and Latin America, Âoften infecting children in communities without access to clean water. In the US, more than 15,000 cases were reported in 2012.
ÂWhile symptoms can be severe or even debilitating, the mechanism by which Giardia infection causes the disease symptoms remains unclear, said Dawson. ÂAs an anaerobic, fermenting, eukaryotic parasite, we reasoned that GiardiaÂs unique anaerobic metabolism may disturb host gut ecology.Â
Partly as a result of the unknown mechanism, there are few novel therapeutics, said Dawson. Moreover, even when treatment eradicates the parasite, GI symptoms may persist.
But if giardiasis really is an ecological disease, that raises the possibility that repopulating beneficial members of the gut microbiome could help treat this condition, said Dawson. ÂAlso, it is possible that certain types of gut commensal microbes could limit or inhibit early Giardia infection.Â
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