Cargando…
Cationic Amino Acid Transporters and Salmonella Typhimurium ArgT Collectively Regulate Arginine Availability towards Intracellular Salmonella Growth
Cationic amino acid transporters (mCAT1 and mCAT2B) regulate the arginine availability in macrophages. How in the infected cell a pathogen can alter the arginine metabolism of the host remains to be understood. We reveal here a novel mechanism by which Salmonella exploit mCAT1 and mCAT2B to acquire...
Autores principales: | , , , , , , , |
---|---|
Formato: | Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2010
|
Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2997073/ https://www.ncbi.nlm.nih.gov/pubmed/21151933 http://dx.doi.org/10.1371/journal.pone.0015466 |
_version_ | 1782193265756340224 |
---|---|
author | Das, Priyanka Lahiri, Amit Lahiri, Ayan Sen, Minakshi Iyer, Namrata Kapoor, Nisha Balaji, Kithiganahalli Narayanaswamy Chakravortty, Dipshikha |
author_facet | Das, Priyanka Lahiri, Amit Lahiri, Ayan Sen, Minakshi Iyer, Namrata Kapoor, Nisha Balaji, Kithiganahalli Narayanaswamy Chakravortty, Dipshikha |
author_sort | Das, Priyanka |
collection | PubMed |
description | Cationic amino acid transporters (mCAT1 and mCAT2B) regulate the arginine availability in macrophages. How in the infected cell a pathogen can alter the arginine metabolism of the host remains to be understood. We reveal here a novel mechanism by which Salmonella exploit mCAT1 and mCAT2B to acquire host arginine towards its own intracellular growth within antigen presenting cells. We demonstrate that Salmonella infected bone marrow derived macrophages and dendritic cells show enhanced arginine uptake and increased expression of mCAT1 and mCAT2B. We show that the mCAT1 transporter is in close proximity to Salmonella containing vacuole (SCV) specifically by live intracellular Salmonella in order to access the macrophage cytosolic arginine pool. Further, Lysosome associated membrane protein 1, a marker of SCV, also was found to colocalize with mCAT1 in the Salmonella infected cell. The intra vacuolar Salmonella then acquire the host arginine via its own arginine transporter, ArgT for growth. The argT knockout strain was unable to acquire host arginine and was attenuated in growth in both macrophages and in mice model of infection. Together, these data reveal survival strategies by which virulent Salmonella adapt to the harsh conditions prevailing in the infected host cells. |
format | Text |
id | pubmed-2997073 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2010 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-29970732010-12-10 Cationic Amino Acid Transporters and Salmonella Typhimurium ArgT Collectively Regulate Arginine Availability towards Intracellular Salmonella Growth Das, Priyanka Lahiri, Amit Lahiri, Ayan Sen, Minakshi Iyer, Namrata Kapoor, Nisha Balaji, Kithiganahalli Narayanaswamy Chakravortty, Dipshikha PLoS One Research Article Cationic amino acid transporters (mCAT1 and mCAT2B) regulate the arginine availability in macrophages. How in the infected cell a pathogen can alter the arginine metabolism of the host remains to be understood. We reveal here a novel mechanism by which Salmonella exploit mCAT1 and mCAT2B to acquire host arginine towards its own intracellular growth within antigen presenting cells. We demonstrate that Salmonella infected bone marrow derived macrophages and dendritic cells show enhanced arginine uptake and increased expression of mCAT1 and mCAT2B. We show that the mCAT1 transporter is in close proximity to Salmonella containing vacuole (SCV) specifically by live intracellular Salmonella in order to access the macrophage cytosolic arginine pool. Further, Lysosome associated membrane protein 1, a marker of SCV, also was found to colocalize with mCAT1 in the Salmonella infected cell. The intra vacuolar Salmonella then acquire the host arginine via its own arginine transporter, ArgT for growth. The argT knockout strain was unable to acquire host arginine and was attenuated in growth in both macrophages and in mice model of infection. Together, these data reveal survival strategies by which virulent Salmonella adapt to the harsh conditions prevailing in the infected host cells. Public Library of Science 2010-12-03 /pmc/articles/PMC2997073/ /pubmed/21151933 http://dx.doi.org/10.1371/journal.pone.0015466 Text en Das et al. http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Das, Priyanka Lahiri, Amit Lahiri, Ayan Sen, Minakshi Iyer, Namrata Kapoor, Nisha Balaji, Kithiganahalli Narayanaswamy Chakravortty, Dipshikha Cationic Amino Acid Transporters and Salmonella Typhimurium ArgT Collectively Regulate Arginine Availability towards Intracellular Salmonella Growth |
title | Cationic Amino Acid Transporters and Salmonella Typhimurium ArgT Collectively Regulate Arginine Availability towards Intracellular Salmonella Growth |
title_full | Cationic Amino Acid Transporters and Salmonella Typhimurium ArgT Collectively Regulate Arginine Availability towards Intracellular Salmonella Growth |
title_fullStr | Cationic Amino Acid Transporters and Salmonella Typhimurium ArgT Collectively Regulate Arginine Availability towards Intracellular Salmonella Growth |
title_full_unstemmed | Cationic Amino Acid Transporters and Salmonella Typhimurium ArgT Collectively Regulate Arginine Availability towards Intracellular Salmonella Growth |
title_short | Cationic Amino Acid Transporters and Salmonella Typhimurium ArgT Collectively Regulate Arginine Availability towards Intracellular Salmonella Growth |
title_sort | cationic amino acid transporters and salmonella typhimurium argt collectively regulate arginine availability towards intracellular salmonella growth |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2997073/ https://www.ncbi.nlm.nih.gov/pubmed/21151933 http://dx.doi.org/10.1371/journal.pone.0015466 |
work_keys_str_mv | AT daspriyanka cationicaminoacidtransportersandsalmonellatyphimuriumargtcollectivelyregulatearginineavailabilitytowardsintracellularsalmonellagrowth AT lahiriamit cationicaminoacidtransportersandsalmonellatyphimuriumargtcollectivelyregulatearginineavailabilitytowardsintracellularsalmonellagrowth AT lahiriayan cationicaminoacidtransportersandsalmonellatyphimuriumargtcollectivelyregulatearginineavailabilitytowardsintracellularsalmonellagrowth AT senminakshi cationicaminoacidtransportersandsalmonellatyphimuriumargtcollectivelyregulatearginineavailabilitytowardsintracellularsalmonellagrowth AT iyernamrata cationicaminoacidtransportersandsalmonellatyphimuriumargtcollectivelyregulatearginineavailabilitytowardsintracellularsalmonellagrowth AT kapoornisha cationicaminoacidtransportersandsalmonellatyphimuriumargtcollectivelyregulatearginineavailabilitytowardsintracellularsalmonellagrowth AT balajikithiganahallinarayanaswamy cationicaminoacidtransportersandsalmonellatyphimuriumargtcollectivelyregulatearginineavailabilitytowardsintracellularsalmonellagrowth AT chakravorttydipshikha cationicaminoacidtransportersandsalmonellatyphimuriumargtcollectivelyregulatearginineavailabilitytowardsintracellularsalmonellagrowth |