News | Science Selections October 2013 | Volume 121 | Issue 10
Arsenic Handicap? Prenatal Exposure Worsens Influenza Infections in Young Mice
Carol Potera, based in Montana, has written for EHP since 1996. She also writes for Microbe, Genetic Engineering News, and the American Journal of Nursing.
Related EHP Article
Research in adult animals has provided evidence that exposure to inorganic arsenic may compromise immune responses to bacterial and viral infections.1 Arsenic exposure has also been associated with altered gene expression in lung tissue from mice, including reduced expression of genes involved in innate immune responses.2 But it’s still unclear how arsenic might modify acute inflammatory responses during early-life infections and the subsequent effects on lung structure and function.
Now Kathryn Ramsey, a respiratory physiologist at the Telethon Institute for Child Health Research in Subiaco, Western Australia, and her colleagues show that mice exposed to inorganic arsenic in utero and infected with influenza A soon after birth did not fight off the viral infection as well as unexposed mice. The arsenic-exposed mice also had more lung inflammation and airway damage. These findings, reported in this issue of EHP, strengthen the connection between early arsenic exposure and the development of chronic lung problems.3
Arsenic is a common contaminant of drinking water worldwide, and high exposures to the ubiquitous toxicant are known to increase the risk of lung, skin, bladder, and other cancers.4 The U.S. Environmental Protection Agency (EPA) has set a maximum contaminant level of 10 ppb for total arsenic in public drinking water supplies—that includes both inorganic and the less toxic organic forms of arsenic.5 Foods including rice, rice-based products, and apple juice also can be contaminated with inorganic arsenic, and diet may constitute a sizeable proportion of some people’s total exposure.6 Arsenic is not currently regulated in food, although the U. S. Food and Drug Administration recently proposed guidance for industry that levels of inorganic arsenic in apple juice not to exceed 10 ppb.7
In addition to cancer, inorganic arsenic has been linked to nonmalignant respiratory illnesses including chronic bronchitis, chronic obstructive pulmonary disease, and bronchiectasis in people, with lung cancer and bronchiectasis particularly linked to exposure in utero or during early childhood.8 Bronchiectasis is a progressive respiratory disease caused by repeated lower respiratory tract infections and exaggerated inflammatory responses to respiratory pathogens, which can lead to serious heart and lung problems.
In the current study, pregnant C57BL/6 mice drank either clean water or water contaminated with 100 ppb inorganic arsenic.3 One week after birth, some pups were intranasally inoculated with the H3N1 strain of influenza A. Pups of arsenic-exposed dams drank arsenic-treated water, and pups of unexposed dams drank clean water.3
One week after influenza infection, young mice exposed to both arsenic and influenza had viral titers and inflammatory responses that were 7–8 times higher than controls exposed to clean water and no influenza. At 8 weeks of age, the investigators measured cytokine levels in bronchoalveolar fluid to evaluate inflammatory responses and airway responsiveness to methacholine (a bronchoconstrictor). Mice exposed to both arsenic and influenza had significantly more airway resistance and greater deficits in lung mechanics than control mice.3
The effects of arsenic on immune function are unlikely to be relevant only to influenza, although the degree of lung damage may vary with other infections. For example, Ramsey says, exposure to different viruses may result in milder pathology. “We would like to combine arsenic exposure with repeated bacterial and viral infections to model the development of bronchiectasis throughout life,” she says.
“This is a great study that advances the field,” says Bruce Stanton, director of the Toxic Metals Superfund Research Program at Dartmouth College’s Geisel School of Medicine. He says the results suggest that infants and young children exposed to inorganic arsenic may be more susceptible to influenza infections and subsequent lung damage.
Although the 100-ppb arsenic exposure is relevant to water levels in some parts of the world, “it’s on the high side for the United States, where the EPA limit is 10 ppb,” says Stanton. However, the EPA standard does not cover private wells; by one estimate, as many as 25 million people in the United States who obtain their drinking water from private wells may be exposed to arsenic levels above the EPA standard.1
Stanton suggests repeating the mouse experiments with 10 ppb inorganic arsenic to see if the influenza response still worsens. Given current guidance on arsenic in drinking water and apple juice, “We’d want to know that,” says Stanton.
1. Kozul CD, et al. Low-dose arsenic compromises the immune response to influenza A infection in vivo. Environ Health Perspect 117:1441–1447 (2009); http://dx.doi.org/10.1289/ehp.0900911.
2. Kozul CD, et al. Chronic exposure to arsenic in the drinking water alters the expression of immune response genes in mouse lung. Environ Health Perspect 117(7):1108–1115 (2009); http://dx.doi.org/10.1289/ehp.0800199.
3. Ramsey KA, et al. Early life arsenic exposure and acute and long-term responses to influenza A infection in mice. Environ Health Perspect 121(10):1187–1193 (2013); http://dx.doi.org/10.1289/ehp.1306748.
4. Hughes MF, et al. Arsenic exposure and toxicology: a historical perspective. Toxicol Sci 123(2):305–332 (2011); http://dx.doi.org/10.1093/toxsci/kfr184.
5. EPA. Arsenic in Drinking Water [website]. Washington, DC:U.S. Environmental Protection Agency (updated 17 September 2013). Available: http://water.epa.gov/lawsregs/rulesregs/sdwa/arsenic/index.cfm [accessed 18 September 2013].
6. Kurzius-Spencer M, et al. Contribution of diet to aggregate arsenic exposures—an analysis across populations. J Expo Sci Environ Epidemiol; http://dx.doi.org/10.1038/jes.2013.37 [online 17 July 2013].
7. FDA. FDA Proposes “Action Level” for Arsenic in Apple Juice [press release]. Silver Spring, MD:U.S. Food and Drug Administration (12 July 2013). Available: http://goo.gl/Q3Z1yQ [accessed 18 September 2013].
8. Smith AH, et al. Increased mortality from lung cancer and bronchiectasis in young adults after exposure to arsenic in utero and in early childhood. Environ Health Perspect 114(8):1293–1296 (2006); http://dx.doi.org/10.1289/ehp.8832.
EHP is pleased to announce that it is now operating under a continuous publication workflow! As indicated in a previous announcement, continuous publication allows EHP to post new content online throughout the month, as each paper becomes ready for an issue. This gets content out to our readers much more quickly than the old issue-based model, and unlike our previous Advance Publication model, these are final, edited articles. (more…)
EHP is pleased to announce that Prenatal Exposure to Glycol Ethers and Neurocognitive Abilities in 6-Year-Old Children: The PELAGIE Cohort Study, published in EHP on 14 October 2016, has been selected by the Children’s Environmental Health Network (CEHN) as its May 2017 Article of the Month. CEHN Article of the Month summaries discuss the potential policy implications of current children’s environmental health research. The CEHN summary can be viewed here.
Among the Resources now available on our Children’s Health page is the text of Executive Order 13045, “Protection of Children from Environmental Health Risks and Safety Risks” (21 April 1997). The Executive Order noted the particular vulnerabilities of children to environmental hazards, codified the need to identify and alleviate such risks, and created the President’s Task Force on Environmental Health Risks and Safety Risks to Children to identify data resources and promote research in these areas. As we mark 20 years since the order was enacted, we can see how these efforts have produced important research and mitigation of hazards—a strong base for continued work on behalf of children’s environmental health.