The effect of 3-nitrooxypropanol, a potent methane inhibitor, on ruminal microbial gene expression profiles in dairy cows

Author:

Pitta Dipti W.,Indugu Nagaraju,Melgar Audino,Hristov Alexander,Challa Krishna,Vecchiarelli Bonnie,Hennessy Meagan,Narayan Kapil,Duval Stephane,Kindermann Maik,Walker Nicola

Abstract

Abstract Background Enteric methane emissions from dairy cows are an environmental problem as well as a gross feed energy loss to the animal. Methane is generated in the rumen by methanogenic archaea from hydrogen (H2) + carbon dioxide and from H2 + methanol or methylamines. The methanogenic substrates are provided by non-methanogens during feed fermentation. Methane mitigation approaches have yielded variable results, partially due to an incomplete understanding of the contribution of hydrogenotrophic and methylotrophic archaea to methanogenesis. Research indicates that 3-nitrooxypropanol (3-NOP) reduces enteric methane formation in dairy cows by inhibiting methyl-coenzyme M reductase (MCR), the enzyme responsible for methane formation. The purpose of this study was to utilize metagenomic and metatranscriptomic approaches to investigate the effect of 3-NOP on the rumen microbiome and to determine the fate of H2 that accumulates less than expected under inhibited methanogenesis. Results The inhibitor 3-NOP was more inhibitory on Methanobrevibacter species than methanol-utilizing Methanosphaera and tended to reduce the gene expression of MCR. Under inhibited methanogenesis by 3-NOP, fluctuations in H2 concentrations were accompanied by changes in the expression of [FeFe] hydrogenases in H2-producing bacteria to regulate the amount of H2 production. No previously reported alternative H2 sinks increased under inhibited methanogenesis except for a significant increase in gene expression of enzymes involved in the butyrate pathway. Conclusion By taking a metatranscriptomic approach, this study provides novel insights on the contribution of methylotrophic methanogens to total methanogenesis and regulation of H2 metabolism under normal and inhibited methanogenesis by 3-NOP in the rumen.

Funder

DSM Nutritional Products

USDA

Publisher

Springer Science and Business Media LLC

Subject

Microbiology (medical),Microbiology

Reference59 articles.

1. Intergovernmental Panel on Climate Change. Summary for policy makers of IPCC special report on global warming of 1.5°C approved by governments [Internet]. 2018. Available from: https://www.ipcc.ch/2018/10/08/summary-for-policymakers-of-ipcc-special-report-on-global-warming-of-1-5c-approved-by-governments/. Cited2/17/22.

2. Gerber PJ, Steinfeld H, Henderson B, Mottet A, Opio C, Dijkman J, et al. Tackling climate change through livestock – a global assessment of emissions and mitigation opportunities [Internet]. Food and Agriculture Organization of the United Nations (FAO), Rome. 2013. Available from: https://www.fao.org/3/i3437e/i3437e.pdf. Cited 1/12/22.

3. Saunois M, Bousquet P, Poulter B, Peregon A, Ciais P, Canadell JG, et al. The global methane budget 2000–2012. Earth Syst. Sci. Data. 2016;8(2):697–751. https://doi.org/10.5194/essd-8-697-2016.

4. Johnson KA, Johnson DE. Methane emissions from cattle. J Anim Sci. 1995;73(8):2483–92. https://doi.org/10.2527/1995.7382483x.

5. Hristov AN, Oh J, Firkins JL, Dijkstra J, Kebreab E, Waghorn G, et al. Special topics—mitigation of methane and nitrous oxide emissions from animal operations: I. A review of enteric methane mitigation options. J Anim Sci. 2013;91(11):5045–69. https://doi.org/10.2527/jas.2013-6583.

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