The PTS Ntr -KdpDE-KdpFABC Pathway Contributes to Low Potassium Stress Adaptation and Competitive Nodulation of Sinorhizobium fredii

The rhizobium-legume symbiosis is essential for sustainable agriculture by reducing nitrogen fertilizer input, but its efficiency varies under fluctuating soil conditions and resources. The nitrogen-related phosphotransferase system (PTS ) consisting of PtsP, PtsO, and PtsN is required for optimal n...

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Published inmBio Vol. 13; no. 3; p. e0372121
Main Authors Feng, Xue-Ying, Tian, Yu, Cui, Wen-Jing, Li, Yue-Zhen, Wang, Dan, Liu, Yanbo, Jiao, Jian, Chen, Wen-Xin, Tian, Chang-Fu
Format Journal Article
LanguageEnglish
Published United States 28.06.2022
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Abstract The rhizobium-legume symbiosis is essential for sustainable agriculture by reducing nitrogen fertilizer input, but its efficiency varies under fluctuating soil conditions and resources. The nitrogen-related phosphotransferase system (PTS ) consisting of PtsP, PtsO, and PtsN is required for optimal nodulation and nitrogen fixation efficiency of the broad-host-range Sinorhizobium fredii CCBAU45436 associated with diverse legumes, though the underlying mechanisms remain elusive. This work characterizes the PtsN-KdpDE-KdpFABC pathway that contributes to low potassium adaptation and competitive nodulation of CCBAU45436. Among three PtsN, PtsN is the major functional homolog. The unphosphorylated PtsN binds the sensory kinase KdpD through a non-canonical interaction with the GAF domain of KdpD, while the region covering HisKA-HATPase domains mediates the interaction of KdpD with the response regulator KdpE. KdpE directly activates the operon encoding the conserved high-affinity potassium uptake system. Disruption of this signaling pathway leads to reduced nodule number, nodule occupancy, and low potassium adaptation ability, but without notable effects on rhizoplane colonization. The induction of key nodulation genes and in host roots during early symbiotic interactions is impaired when inoculating the mutant that shows delayed nodulation. The nodulation defect of the mutant can be rescued by supplying replete potassium. Potassium is actively consumed by both prokaryotes and eukaryotes, and components of the PTS -KdpDE-KdpFABC pathway are widely conserved in bacteria, highlighting the global importance of this pathway in bacteria-host interactions. In all ecological niches, potassium is actively consumed by diverse prokaryotes and their interacting eukaryote hosts. It is only just emerging that potassium is a key player in host-pathogen interactions, and the role of potassium in mutualistic interactions remains largely unknown. This work is focused on the mutualistic symbiosis between rhizobia and legumes. We report that the nitrogen-related phosphotransferase system PTS , the two-component system KdpDE, and the high-affinity potassium uptake system KdpFABC constitute a pathway that is important for low potassium adaptation and optimal nodulation of rhizobia. Given the widely conserved PTS , KdpDE, and KdpFABC in bacteria and increasing knowledge on microbiome for various niches, the PTS -KdpDE-KdpFABC pathway can be globally important in the biosphere.
AbstractList The rhizobium-legume symbiosis is essential for sustainable agriculture by reducing nitrogen fertilizer input, but its efficiency varies under fluctuating soil conditions and resources. The nitrogen-related phosphotransferase system (PTS ) consisting of PtsP, PtsO, and PtsN is required for optimal nodulation and nitrogen fixation efficiency of the broad-host-range Sinorhizobium fredii CCBAU45436 associated with diverse legumes, though the underlying mechanisms remain elusive. This work characterizes the PtsN-KdpDE-KdpFABC pathway that contributes to low potassium adaptation and competitive nodulation of CCBAU45436. Among three PtsN, PtsN is the major functional homolog. The unphosphorylated PtsN binds the sensory kinase KdpD through a non-canonical interaction with the GAF domain of KdpD, while the region covering HisKA-HATPase domains mediates the interaction of KdpD with the response regulator KdpE. KdpE directly activates the operon encoding the conserved high-affinity potassium uptake system. Disruption of this signaling pathway leads to reduced nodule number, nodule occupancy, and low potassium adaptation ability, but without notable effects on rhizoplane colonization. The induction of key nodulation genes and in host roots during early symbiotic interactions is impaired when inoculating the mutant that shows delayed nodulation. The nodulation defect of the mutant can be rescued by supplying replete potassium. Potassium is actively consumed by both prokaryotes and eukaryotes, and components of the PTS -KdpDE-KdpFABC pathway are widely conserved in bacteria, highlighting the global importance of this pathway in bacteria-host interactions. In all ecological niches, potassium is actively consumed by diverse prokaryotes and their interacting eukaryote hosts. It is only just emerging that potassium is a key player in host-pathogen interactions, and the role of potassium in mutualistic interactions remains largely unknown. This work is focused on the mutualistic symbiosis between rhizobia and legumes. We report that the nitrogen-related phosphotransferase system PTS , the two-component system KdpDE, and the high-affinity potassium uptake system KdpFABC constitute a pathway that is important for low potassium adaptation and optimal nodulation of rhizobia. Given the widely conserved PTS , KdpDE, and KdpFABC in bacteria and increasing knowledge on microbiome for various niches, the PTS -KdpDE-KdpFABC pathway can be globally important in the biosphere.
In all ecological niches, potassium is actively consumed by diverse prokaryotes and their interacting eukaryote hosts. It is only just emerging that potassium is a key player in host-pathogen interactions, and the role of potassium in mutualistic interactions remains largely unknown. ABSTRACT The rhizobium-legume symbiosis is essential for sustainable agriculture by reducing nitrogen fertilizer input, but its efficiency varies under fluctuating soil conditions and resources. The nitrogen-related phosphotransferase system (PTS Ntr ) consisting of PtsP, PtsO, and PtsN is required for optimal nodulation and nitrogen fixation efficiency of the broad-host-range Sinorhizobium fredii CCBAU45436 associated with diverse legumes, though the underlying mechanisms remain elusive. This work characterizes the PtsN-KdpDE-KdpFABC pathway that contributes to low potassium adaptation and competitive nodulation of CCBAU45436. Among three PtsN, PtsN 1 is the major functional homolog. The unphosphorylated PtsN 1 binds the sensory kinase KdpD through a non-canonical interaction with the GAF domain of KdpD, while the region covering HisKA-HATPase domains mediates the interaction of KdpD with the response regulator KdpE. KdpE directly activates the kdpFABC operon encoding the conserved high-affinity potassium uptake system. Disruption of this signaling pathway leads to reduced nodule number, nodule occupancy, and low potassium adaptation ability, but without notable effects on rhizoplane colonization. The induction of key nodulation genes NIN and ENOD40 in host roots during early symbiotic interactions is impaired when inoculating the kdpBC mutant that shows delayed nodulation. The nodulation defect of the kdpBC mutant can be rescued by supplying replete potassium. Potassium is actively consumed by both prokaryotes and eukaryotes, and components of the PTS Ntr -KdpDE-KdpFABC pathway are widely conserved in bacteria, highlighting the global importance of this pathway in bacteria-host interactions. IMPORTANCE In all ecological niches, potassium is actively consumed by diverse prokaryotes and their interacting eukaryote hosts. It is only just emerging that potassium is a key player in host-pathogen interactions, and the role of potassium in mutualistic interactions remains largely unknown. This work is focused on the mutualistic symbiosis between rhizobia and legumes. We report that the nitrogen-related phosphotransferase system PTS Ntr , the two-component system KdpDE, and the high-affinity potassium uptake system KdpFABC constitute a pathway that is important for low potassium adaptation and optimal nodulation of rhizobia. Given the widely conserved PTS Ntr , KdpDE, and KdpFABC in bacteria and increasing knowledge on microbiome for various niches, the PTS Ntr -KdpDE-KdpFABC pathway can be globally important in the biosphere.
Author Jiao, Jian
Feng, Xue-Ying
Cui, Wen-Jing
Wang, Dan
Tian, Yu
Li, Yue-Zhen
Chen, Wen-Xin
Tian, Chang-Fu
Liu, Yanbo
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Cites_doi 10.1073/pnas.77.12.7347
10.1128/AEM.03454-15
10.1038/nrmicro.2017.171
10.1038/nature22970
10.1073/pnas.0609897104
10.1094/MPMI-02-18-0031-R
10.1073/pnas.0600912103
10.1110/ps.041232805
10.1038/sj.emboj.7601471
10.1128/jb.173.2.687-696.1991
10.1128/mSystems.01299-20
10.1126/science.3291115
10.1016/S0014-5793(99)00288-4
10.1105/tpc.114.131607
10.1371/journal.ppat.1007591
10.1111/j.1469-8137.2010.03261.x
10.1111/j.1365-2958.2012.08176.x
10.1094/MPMI.2001.14.7.848
10.1128/MMBR.00001-14
10.1111/j.1365-2958.2009.06704.x
10.1002/bies.202000108
10.1128/mBio.03193-19
10.1111/mmi.13751
10.1016/j.tibs.2006.12.004
10.1007/s00018-010-0317-7
10.1099/mic.0.068700-0
10.1128/JB.00569-15
10.1111/1462-2920.13948
10.1159/000375497
10.1080/09687688.2019.1638977
10.1046/j.1365-2958.1999.01402.x
10.1128/AEM.00717-19
10.1159/000369809
10.1111/j.1574-6976.2011.00314.x
10.1371/journal.ppat.1003201
10.1111/j.1574-6968.2008.01262.x
10.1111/1758-2229.12323
10.1146/annurev-micro-091018-054627
10.1126/scisignal.aaz2970
10.1128/JB.01567-08
10.1111/j.1365-2958.2012.08014.x
10.1099/mic.0.075226-0
10.1126/science.aat1743
10.1128/IAI.00641-20
10.1111/j.1469-8137.2007.02015.x
10.1007/s00239-019-09915-2
10.1016/j.tim.2010.02.003
10.1105/tpc.19.00279
10.1111/mmi.12312
10.1073/pnas.1917471117
10.1128/JB.00813-15
10.1093/molbev/msr121
10.1016/0378-1119(93)90611-6
10.1515/hsz-2015-0123
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References e_1_3_2_26_2
e_1_3_2_49_2
e_1_3_2_28_2
e_1_3_2_41_2
e_1_3_2_20_2
e_1_3_2_43_2
e_1_3_2_22_2
e_1_3_2_45_2
e_1_3_2_24_2
e_1_3_2_47_2
e_1_3_2_9_2
e_1_3_2_16_2
e_1_3_2_37_2
e_1_3_2_7_2
e_1_3_2_18_2
e_1_3_2_39_2
e_1_3_2_10_2
e_1_3_2_31_2
e_1_3_2_52_2
e_1_3_2_5_2
e_1_3_2_12_2
e_1_3_2_33_2
e_1_3_2_58_2
e_1_3_2_3_2
e_1_3_2_14_2
e_1_3_2_35_2
e_1_3_2_56_2
e_1_3_2_50_2
e_1_3_2_27_2
e_1_3_2_48_2
e_1_3_2_29_2
e_1_3_2_21_2
e_1_3_2_42_2
Miller JH (e_1_3_2_54_2) 1972
e_1_3_2_23_2
e_1_3_2_44_2
e_1_3_2_25_2
e_1_3_2_46_2
Begon M (e_1_3_2_40_2) 2021
e_1_3_2_15_2
e_1_3_2_38_2
e_1_3_2_8_2
e_1_3_2_17_2
e_1_3_2_59_2
e_1_3_2_6_2
e_1_3_2_19_2
e_1_3_2_30_2
e_1_3_2_32_2
e_1_3_2_51_2
Vincent JM (e_1_3_2_53_2) 1970
e_1_3_2_11_2
e_1_3_2_34_2
e_1_3_2_57_2
e_1_3_2_4_2
e_1_3_2_13_2
e_1_3_2_36_2
e_1_3_2_2_2
Qin J (e_1_3_2_55_2) 2014; 8
References_xml – ident: e_1_3_2_57_2
  doi: 10.1073/pnas.77.12.7347
– ident: e_1_3_2_30_2
  doi: 10.1128/AEM.03454-15
– ident: e_1_3_2_28_2
  doi: 10.1038/nrmicro.2017.171
– ident: e_1_3_2_14_2
  doi: 10.1038/nature22970
– ident: e_1_3_2_43_2
  doi: 10.1073/pnas.0609897104
– ident: e_1_3_2_37_2
  doi: 10.1094/MPMI-02-18-0031-R
– ident: e_1_3_2_38_2
  doi: 10.1073/pnas.0600912103
– ident: e_1_3_2_41_2
  doi: 10.1110/ps.041232805
– volume-title: Experiments in molecular genetics
  year: 1972
  ident: e_1_3_2_54_2
  contributor:
    fullname: Miller JH
– ident: e_1_3_2_21_2
  doi: 10.1038/sj.emboj.7601471
– ident: e_1_3_2_48_2
  doi: 10.1128/jb.173.2.687-696.1991
– ident: e_1_3_2_33_2
  doi: 10.1128/mSystems.01299-20
– ident: e_1_3_2_3_2
  doi: 10.1126/science.3291115
– ident: e_1_3_2_49_2
  doi: 10.1016/S0014-5793(99)00288-4
– volume-title: Ecology: From individuals to ecosystems
  year: 2021
  ident: e_1_3_2_40_2
  contributor:
    fullname: Begon M
– volume: 8
  start-page: 791
  year: 2014
  ident: e_1_3_2_55_2
  article-title: A genetic composition analysis of soybean sibling varieties Jidou17 and Ji nf58
  publication-title: Aust J Crop Sci
  contributor:
    fullname: Qin J
– ident: e_1_3_2_51_2
  doi: 10.1105/tpc.114.131607
– ident: e_1_3_2_22_2
  doi: 10.1371/journal.ppat.1007591
– ident: e_1_3_2_36_2
  doi: 10.1111/j.1469-8137.2010.03261.x
– ident: e_1_3_2_9_2
  doi: 10.1111/j.1365-2958.2012.08176.x
– ident: e_1_3_2_50_2
  doi: 10.1094/MPMI.2001.14.7.848
– ident: e_1_3_2_7_2
  doi: 10.1128/MMBR.00001-14
– ident: e_1_3_2_16_2
  doi: 10.1111/j.1365-2958.2009.06704.x
– ident: e_1_3_2_11_2
  doi: 10.1002/bies.202000108
– ident: e_1_3_2_32_2
  doi: 10.1128/mBio.03193-19
– ident: e_1_3_2_47_2
  doi: 10.1111/mmi.13751
– ident: e_1_3_2_4_2
  doi: 10.1016/j.tibs.2006.12.004
– ident: e_1_3_2_12_2
  doi: 10.1007/s00018-010-0317-7
– ident: e_1_3_2_19_2
  doi: 10.1099/mic.0.068700-0
– ident: e_1_3_2_23_2
  doi: 10.1128/JB.00569-15
– ident: e_1_3_2_31_2
  doi: 10.1111/1462-2920.13948
– ident: e_1_3_2_46_2
  doi: 10.1159/000375497
– ident: e_1_3_2_15_2
  doi: 10.1080/09687688.2019.1638977
– ident: e_1_3_2_58_2
  doi: 10.1046/j.1365-2958.1999.01402.x
– ident: e_1_3_2_39_2
  doi: 10.1128/AEM.00717-19
– ident: e_1_3_2_8_2
  doi: 10.1159/000369809
– ident: e_1_3_2_2_2
  doi: 10.1111/j.1574-6976.2011.00314.x
– volume-title: A manual for the practical study of root nodule bacteria
  year: 1970
  ident: e_1_3_2_53_2
  contributor:
    fullname: Vincent JM
– ident: e_1_3_2_27_2
  doi: 10.1371/journal.ppat.1003201
– ident: e_1_3_2_34_2
  doi: 10.1111/j.1574-6968.2008.01262.x
– ident: e_1_3_2_18_2
  doi: 10.1111/1758-2229.12323
– ident: e_1_3_2_5_2
  doi: 10.1146/annurev-micro-091018-054627
– ident: e_1_3_2_45_2
  doi: 10.1126/scisignal.aaz2970
– ident: e_1_3_2_25_2
  doi: 10.1128/JB.01567-08
– ident: e_1_3_2_17_2
  doi: 10.1111/j.1365-2958.2012.08014.x
– ident: e_1_3_2_42_2
  doi: 10.1099/mic.0.075226-0
– ident: e_1_3_2_52_2
  doi: 10.1126/science.aat1743
– ident: e_1_3_2_26_2
  doi: 10.1128/IAI.00641-20
– ident: e_1_3_2_35_2
  doi: 10.1111/j.1469-8137.2007.02015.x
– ident: e_1_3_2_44_2
  doi: 10.1007/s00239-019-09915-2
– ident: e_1_3_2_6_2
  doi: 10.1016/j.tim.2010.02.003
– ident: e_1_3_2_29_2
  doi: 10.1105/tpc.19.00279
– ident: e_1_3_2_20_2
  doi: 10.1111/mmi.12312
– ident: e_1_3_2_10_2
  doi: 10.1073/pnas.1917471117
– ident: e_1_3_2_24_2
  doi: 10.1128/JB.00813-15
– ident: e_1_3_2_59_2
  doi: 10.1093/molbev/msr121
– ident: e_1_3_2_56_2
  doi: 10.1016/0378-1119(93)90611-6
– ident: e_1_3_2_13_2
  doi: 10.1515/hsz-2015-0123
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Snippet The rhizobium-legume symbiosis is essential for sustainable agriculture by reducing nitrogen fertilizer input, but its efficiency varies under fluctuating soil...
In all ecological niches, potassium is actively consumed by diverse prokaryotes and their interacting eukaryote hosts. It is only just emerging that potassium...
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Title The PTS Ntr -KdpDE-KdpFABC Pathway Contributes to Low Potassium Stress Adaptation and Competitive Nodulation of Sinorhizobium fredii
URI https://www.ncbi.nlm.nih.gov/pubmed/35491828
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