Carnivorous Nepenthes Pitchers with Less Acidic Fluid House Nitrogen-Fixing Bacteria

被引:1
|
作者
Bittleston, Leonora S. [1 ,5 ]
Wolock, Charles J. [2 ,5 ]
Maeda, Junko [3 ]
Infante, Valentina [3 ]
Ane, Jean-Michel [3 ,4 ]
Pierce, Naomi E. [5 ,6 ]
Pringle, Anne [3 ,7 ]
机构
[1] Boise State Univ, Dept Biol Sci, Boise, ID 83725 USA
[2] Univ Washington, Dept Biostat, Seattle, WA USA
[3] Univ Wisconsin Madison, Dept Bacteriol, Madison, WI USA
[4] Univ Wisconsin Madison, Dept Agron, Madison, WI USA
[5] Harvard Univ, Dept Organism & Evolutionary Biol, Cambridge, MA 02138 USA
[6] Harvard Univ, Museum Comparat Zool, Cambridge, MA USA
[7] Univ Wisconsin Madison, Dept Bot, Madison, WI USA
关键词
carnivorous plant; convergent evolution; microbial ecology; nitrogen fixation; symbiosis; trade-off; 16S RIBOSOMAL-RNA; DINITROGEN FIXATION; PLANT; CAPTURE; EFFICIENCY; DIVERSITY; RESOURCE; HOST; PREY; MICROBIOME;
D O I
10.1128/aem.00812-23
中图分类号
Q81 [生物工程学(生物技术)]; Q93 [微生物学];
学科分类号
071005 ; 0836 ; 090102 ; 100705 ;
摘要
Carnivorous pitcher plants are uniquely adapted to nitrogen limitation, using pitfall traps to acquire nutrients from insect prey. Pitcher plants in the genus Sarracenia may also use nitrogen fixed by bacteria inhabiting the aquatic microcosms of their pitchers. Here, we investigated whether species of a convergently evolved pitcher plant genus, Nepenthes, might also use bacterial nitrogen fixation as an alternative strategy for nitrogen capture. First, we constructed predicted metagenomes of pitcher organisms from three species of Singaporean Nepenthes using 16S rRNA sequence data and correlated predicted nifH abundances with metadata. Second, we used gene-specific primers to amplify and quantify the presence or absence of nifH directly from 102 environmental samples and identified potential diazotrophs with significant differential abundance in samples that also had positive nifH PCR tests. Third, we analyzed nifH in eight shotgun metagenomes from four additional Bornean Nepenthes species. Finally, we conducted an acetylene reduction assay using greenhouse-grown Nepenthes pitcher fluids to confirm nitrogen fixation is indeed possible within the pitcher habitat. Results show active acetylene reduction can occur in Nepenthes pitcher fluid. Variation in nifH from wild samples correlates with Nepenthes host species identity and pitcher fluid acidity. Nitrogen-fixing bacteria are associated with more neutral fluid pH, while endogenous Nepenthes digestive enzymes are most active at low fluid pH. We hypothesize Nepenthes species experience a trade-off in nitrogen acquisition; when fluids are acidic, nitrogen is primarily acquired via plant enzymatic degradation of insects, but when fluids are neutral, Nepenthes plants take up more nitrogen via bacterial nitrogen fixation.IMPORTANCE Plants use different strategies to obtain the nutrients that they need to grow. Some plants access their nitrogen directly from the soil, while others rely on microbes to access the nitrogen for them. Carnivorous pitcher plants generally trap and digest insect prey, using plant-derived enzymes to break down insect proteins and generate a large portion of the nitrogen that they subsequently absorb. In this study, we present results suggesting that bacteria living in the fluids formed by Nepenthes pitcher plants can fix nitrogen directly from the atmosphere, providing an alternative pathway for plants to access nitrogen. These nitrogen-fixing bacteria are only likely to be present when pitcher plant fluids are not strongly acidic. Interestingly, the plant's enzymes are known to be more active under strongly acidic conditions. We propose a potential trade-off where pitcher plants sometimes access nitrogen using their own enzymes to digest prey and at other times take advantage of bacterial nitrogen fixation. Plants use different strategies to obtain the nutrients that they need to grow. Some plants access their nitrogen directly from the soil, while others rely on microbes to access the nitrogen for them.
引用
收藏
页数:13
相关论文
共 50 条
  • [31] INHIBITION BY ACETYLENE OF CONVENTIONAL HYDROGENASE IN NITROGEN-FIXING BACTERIA
    SMITH, LA
    HILL, S
    YATES, MG
    NATURE, 1976, 262 (5565) : 209 - 210
  • [32] Regional distributions of nitrogen-fixing bacteria in the Pacific Ocean
    Church, Matthew J.
    Bjorkman, Karin M.
    Karl, David M.
    Saito, Mak A.
    Zehr, Jonathan P.
    LIMNOLOGY AND OCEANOGRAPHY, 2008, 53 (01) : 63 - 77
  • [33] Plant flotillins are required for infection by nitrogen-fixing bacteria
    Haney, Cara H.
    Long, Sharon R.
    PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA, 2010, 107 (01) : 478 - 483
  • [34] DETOXIFICATION OF MERCURY AND ORGANOMERCURIALS BY NITROGEN-FIXING SOIL BACTERIA
    RAY, S
    GACHHUI, R
    PAHAN, K
    CHAUDHURY, J
    MANDAL, A
    JOURNAL OF BIOSCIENCES, 1989, 14 (02) : 173 - 182
  • [35] DEHYDROGENASE AND NITROGEN-FIXING ACTIVITY OF PEA NODULE BACTERIA
    ROMEIKO, IN
    DUBOVENK.EK
    MALINSKA.SM
    MIKROBIOLOGIYA, 1972, 41 (02): : 247 - &
  • [36] EFFECT OF NITROGEN-FIXING BACTERIA ON MINERALIZATION IN RAW HUMUS
    SUNDSTROM, KR
    HUSS, K
    OIKOS, 1975, 26 (02) : 147 - 151
  • [37] INOCULATION OF RICE WITH NITROGEN-FIXING BACTERIA - PROBLEMS AND PERSPECTIVES
    RAO, VR
    JENA, PK
    ADHYA, TK
    BIOLOGY AND FERTILITY OF SOILS, 1987, 4 (1-2) : 21 - 26
  • [39] ENRICHMENT AND ISOLATION OF NEW NITROGEN-FIXING HYDROGEN BACTERIA
    MALIK, KA
    SCHLEGEL, HG
    FEMS MICROBIOLOGY LETTERS, 1980, 8 (02) : 101 - 104
  • [40] ASSOCIATION OF NITROGEN-FIXING BACTERIA WITH CERTAIN PLANTATION CROPS
    GOVINDAN, M
    PURUSHOTHAMAN, D
    NATIONAL ACADEMY SCIENCE LETTERS-INDIA, 1985, 8 (06): : 163 - 165