The DOI matches its Crossref record; 8 of the 8 references it cites were found in a registry or an index.
High-Affinity Zn2+Uptake System ZnuABC Is Required for Bacterial Zinc Homeostasis in Intracellular Environments and Contributes to the Virulence of Salmonella enterica
Abstract
To investigate the relevance of zinc in host-pathogen interactions, we have constructed Salmonella enterica mutant strains in which the znuA gene, which encodes the periplasmic component of the ZnuABC high-affinity Zn 2+transporter, was deleted. This mutation does not alter the ability of Salmonella to grow in rich media but drastically reduces its ability to multiply in media deprived of zinc. In agreement with this phenotype, ZnuA accumulates only in bacteria cultivated in environments poor in zinc. In spite of the nearly millimolar intracellular concentration of zinc, we have found that znuA is highly expressed in intracellular salmonellae recovered either from cultivated cells or from the spleens of infected mice. We have also observed that znuA mutants are impaired in their ability to grow in Caco-2 epithelial cells and that bacteria starved for zinc display decreased ability to multiply in phagocytes. A dramatic reduction in the pathogenicity of the znuA mutants was observed in Salmonella-susceptible (BALB/c) or Salmonella-resistant (DBA-2) mice infected intraperitoneally or orally. This study shows that the amount of free metals available for bacterial growth within the infected animal is limited, despite the apparent elevated concentration of free metals within cells and in plasma and suggests that Salmonella exploits the ZnuABC zinc transporter to maximize zinc availability in such conditions. These results shed new light on the complex functions of zinc in vertebrate and bacterial physiology and pave the way for a better comprehension of pathogenic mechanisms in Salmonella infections.
Overview
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Integrity signals
Registry
Cites
Statistics
Verification
Claims the paper makes
The claims and statistics of this paper haven’t been checked yet.
Run the check — free, no account needed. It reads the open-access text and checks the sources it cites.
Claims other papers make about this one
Each is checked against this paper’s own text: does it say what the citing paper says it does?
In the citing paper
“Under such circumstances, Salmonella maximizes zinc availability by taking use of the ZnuABC zinc transporter (Ammendola et al. 2007).”
From Nutritional Immunity in Wound Infection: Unveiling the Role of Dietary Elements in Host–Pathogen Interaction (2025) · cites this paper as Ammendola et al. 2007
Self-check
Percentages, sums and reported differences re-computed from the paper’s own numbers.
The self-check needs the paper’s full text.
Citations
Cites
Acute-Phase Proteins and Other Systemic Responses to Inflammation
Gabay, C., & Kushner, I. (1999) · New England Journal of Medicine · doi:10.1056/nejm199902113400607 · Cited by 6,734
Femtomolar Sensitivity of Metalloregulatory Proteins Controlling Zinc Homeostasis
Outten, C. E., & O'Halloran, A. T. V. (2001) · Science · doi:10.1126/science.1060331 · Cited by 1,489 · cited 6×
“Genetic and biochemical studies have shown that ZnuABC expression is repressed in cells containing adequate concentrations of zinc by the metallated form of Zur, a metalloregulatory DNA-binding protein with femtomolar sensitivity to free intracellular zinc (36, 37, 39).”
BackgroundInfluentialCounting the Zinc-Proteins Encoded in the Human Genome
Andreini, C., Banci, L., Bertini, I., & Rosato, A. (2006) · Journal of Proteome Research · doi:10.1021/pr050361j · Cited by 1,109
The ZnuABC high‐affinity zinc uptake system and its regulator Zur in Escherichia coli
Patzer, S. I., & Hantke, K. (1998) · Molecular Microbiology · doi:10.1046/j.1365-2958.1998.00883.x · Cited by 490 · cited 1×
“were initially reported in Escherichia coli (38, 39).”
BackgroundMeasurement of invasion by gentamicin resistance
Elsinghorst, E. A. (1994) · Methods in Enzymology · doi:10.1016/0076-6879(94)36030-8 · Cited by 342
Forbes, J. R., & Gros, P. (2003) · Blood · doi:10.1182/blood-2003-02-0425 · Cited by 288
Bjarnason, J., Southward, C. M., & Surette, M. G. (2003) · Journal of Bacteriology · doi:10.1128/jb.185.16.4973-4982.2003 · Cited by 173
A nutritive view on the host–pathogen interplay
Schaible, U. E., & Kaufmann, S. H. E. (2005) · Trends in Microbiology · doi:10.1016/j.tim.2005.06.009 · Cited by 106
Research works printed but not linked: 46
- 10.1128/IAI.69.4.2549-2557.2001 · DOI
- 10.1016/j.febslet.2004.06.008 · DOI
- 10.1016/S0168-6445(03)00041-X · DOI
- 10.1093/ajcn/68.2.425S · DOI
- 10.1128/IAI.70.8.4721-4725.2002 · DOI
- 10.1016/j.jmb.2007.01.041 · DOI
- 10.1111/j.1574-6968.2001.tb10781.x · DOI
- 10.1128/JB.00173-07 · DOI
- 10.1016/S1367-5931(98)80064-1 · DOI
- 10.1128/jb.175.6.1687-1696.1993 · DOI
- 10.1074/jbc.R600011200 · DOI
- Cousins, R. J. 1989. Systemic transport of zinc, p. 79-93. In C. F. Mills (ed.), Zinc in human biology. Springer-Verlag, London, England.
- 10.1073/pnas.120163297 · DOI
- 10.1093/nar/11.6.1645 · DOI
- 10.1073/pnas.83.14.5189 · DOI
- 10.1016/S0966-842X(01)02098-4 · DOI · Paper page
- 10.1016/S0378-1097(03)00131-9 · DOI
- 10.1016/j.mib.2005.02.001 · DOI
- 10.4049/jimmunol.172.12.7750 · DOI
- 10.1111/j.1462-5822.2004.00451.x · DOI
- 10.1093/jn/133.5.1452S · DOI
- 10.1292/jvms.66.1059 · DOI
- 10.1128/IAI.71.6.3020-3027.2003 · DOI
- Klasing, K. C. 1984. Effect of inflammatory agents and interleukin 1 on iron and zinc metabolism. Am. J. Physiol.247:901-904.
- 10.1128/IAI.67.10.5060-5068.1999 · DOI
- 10.1073/pnas.0502257102 · DOI · Paper page
- 10.1016/S0021-9258(19)52451-6 · DOI
- 10.1074/jbc.272.46.29033 · DOI
- 10.1006/geno.1994.1458 · DOI
- 10.1016/j.bbamcr.2006.05.007 · DOI
- 10.1021/bi0155448 · DOI
- 10.1074/jbc.M001775200 · DOI
- 10.1016/0966-842X(93)90036-Q · DOI
- 10.1128/JB.01531-06 · DOI
- 10.1146/annurev.micro.54.1.881 · DOI · Paper page
- 10.1038/nrmicro1046 · DOI · Paper page
- 10.1093/ajcn/68.2.447S · DOI · Paper page
- 10.1046/j.1365-2958.2002.03145.x · DOI
- 10.1073/pnas.261348198 · DOI
- 10.1002/jlb.58.4.382 · DOI
- Vidal, S. M., E. Pinner, P. Lepage, S. Gauthier, and P. Gros. 1996. Natural resistance to intracellular infections: Nramp1 encodes a membrane phosphoglycoprotein absent in macrophages from susceptible (Nramp1 D169) mouse strains. J. Immunol.157:3559-3568. · DOI · Paper page
- 10.1146/annurev.nutr.23.011702.073054 · DOI
- 10.1128/JB.187.18.6333-6340.2005 · DOI
- 10.1128/IAI.01957-05 · DOI
- 10.2741/1317 · DOI
- 10.2144/06404RR02 · DOI
Cited by
Sorted by citations
Nutritional immunity: transition metals at the pathogen–host interface
Hood, M. I., & Skaar, E. P. (2012) · Nature Reviews Microbiology · doi:10.1038/nrmicro2836 · Cited by 1,535
Nutritional immunity beyond iron: a role for manganese and zinc
Kehl-Fie, T. E., & Skaar, E. P. (2010) · Current Opinion in Chemical Biology · doi:10.1016/j.cbpa.2009.11.008 · Cited by 634
Transcriptional regulation by Ferric Uptake Regulator (Fur) in pathogenic bacteria
Troxell, B., & Hassan, H. M. (2013) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2013.00059 · Cited by 500
Liu, J. Z., Jellbauer, S., Poe, A. J., Ton, V., Pesciaroli, M., Kehl-Fie, T. E., Restrepo, N. A., Hosking, M. P., Edwards, R. A., Battistoni, A., et al. (2012) · Cell Host & Microbe · doi:10.1016/j.chom.2012.01.017 · Cited by 328
Self-citationHood, M. I., Mortensen, B. L., Moore, J. L., Zhang, Y., Kehl-Fie, T. E., Sugitani, N., Chazin, W. J., Caprioli, R. M., & Skaar, E. P. (2012) · PLoS Pathogens · doi:10.1371/journal.ppat.1003068 · Cited by 255
Kehl-Fie, T. E., Zhang, Y., Moore, J. L., Farrand, A. J., Hood, M. I., Rathi, S., Chazin, W. J., Caprioli, R. M., & Skaar, E. P. (2013) · Infection and Immunity · doi:10.1128/iai.00420-13 · Cited by 213
Host resistance factor SLC11A1 restricts Salmonella growth through magnesium deprivation
Cunrath, O., & Bumann, D. (2019) · Science · doi:10.1126/science.aax7898 · Cited by 177
Severe Zinc Depletion of Escherichia coli
Graham, A. I., Hunt, S., Stokes, S. L., Bramall, N., Bunch, J., Cox, A. G., McLeod, C. W., & Poole, R. K. (2009) · Journal of Biological Chemistry · doi:10.1074/jbc.m109.001503 · Cited by 156
Bobrov, A. G., Kirillina, O., Fetherston, J. D., Miller, M. C., Burlison, J. A., & Perry, R. D. (2014) · Molecular Microbiology · doi:10.1111/mmi.12693 · Cited by 149
Remy, L., Carrière, M., Derré‐Bobillot, A., Martini, C., Sanguinetti, M., & Borezée‐Durant, E. (2013) · Molecular Microbiology · doi:10.1111/mmi.12126 · Cited by 139
Bayle, L., Chimalapati, S., Schoehn, G., Brown, J., Vernet, T., & Durmort, C. (2011) · Molecular Microbiology · doi:10.1111/j.1365-2958.2011.07862.x · Cited by 137
Nutrient Zinc at the Host–Pathogen Interface
Lonergan, Z. R., & Skaar, E. P. (2019) · Trends in Biochemical Sciences · doi:10.1016/j.tibs.2019.06.010 · Cited by 129
Stork, M., Bos, M. P., Jongerius, I., de Kok, N., Schilders, I., Weynants, V. E., Poolman, J. T., & Tommassen, J. (2010) · PLoS Pathogens · doi:10.1371/journal.ppat.1000969 · Cited by 141
Petrarca, P., Ammendola, S., Pasquali, P., & Battistoni, A. (2010) · Journal of Bacteriology · doi:10.1128/jb.01310-09 · Cited by 129
Self-citationTransition metal ions at the crossroads of mucosal immunity and microbial pathogenesis
Diaz-Ochoa, V. E., Jellbauer, S., Klaus, S., & Raffatellu, M. (2014) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2014.00002 · Cited by 129
Sabri, M., Houle, S., & Dozois, C. M. (2009) · Infection and Immunity · doi:10.1128/iai.01082-08 · Cited by 118
Siderophore-mediated zinc acquisition enhances enterobacterial colonization of the inflamed gut
Behnsen, J., Zhi, H., Aron, A. T., Subramanian, V., Santus, W., Lee, M. H., Gerner, R. R., Petras, D., Liu, J. Z., Green, K. D., et al. (2021) · Nature Communications · doi:10.1038/s41467-021-27297-2 · Cited by 101
Mortensen, B. L., & Skaar, E. P. (2013) · Frontiers in Cellular and Infection Microbiology · doi:10.3389/fcimb.2013.00095 · Cited by 99
Metallothionein: a Potential Link in the Regulation of Zinc in Nutritional Immunity
Rahman, M. T., & Karim, M. M. (2018) · Biological Trace Element Research · doi:10.1007/s12011-017-1061-8 · Cited by 77
Lonergan, Z. R., Nairn, B. L., Wang, J., Hsu, Y.-P., Hesse, L. E., Beavers, W. N., Chazin, W. J., Trinidad, J. C., VanNieuwenhze, M. S., Giedroc, D. P., et al. (2019) · Cell Reports · doi:10.1016/j.celrep.2019.01.089 · Cited by 76
Cerasi, M., Liu, J. Z., Ammendola, S., Poe, A. J., Petrarca, P., Pesciaroli, M., Pasquali, P., Raffatellu, M., & Battistoni, A. (2014) · Metallomics · doi:10.1039/c3mt00352c · Cited by 75
Self-citationCorbett, D., Wang, J., Schuler, S., Lopez-Castejon, G., Glenn, S., Brough, D., Andrew, P. W., Cavet, J. S., & Roberts, I. S. (2012) · Infection and Immunity · doi:10.1128/iai.05904-11 · Cited by 71
The Acinetobacter baumannii Znu System Overcomes Host-Imposed Nutrient Zinc Limitation
Hesse, L. E., Lonergan, Z. R., Beavers, W. N., & Skaar, E. P. (2019) · Infection and Immunity · doi:10.1128/iai.00746-19 · Cited by 59
Ilari, A., Alaleona, F., Tria, G., Petrarca, P., Battistoni, A., Zamparelli, C., Verzili, D., Falconi, M., & Chiancone, E. (2014) · Biochimica et Biophysica Acta (BBA) - General Subjects · doi:10.1016/j.bbagen.2013.10.010 · Cited by 55
Self-citationEndopeptidase Regulation as a Novel Function of the Zur-Dependent Zinc Starvation Response
Murphy, S. G., Alvarez, L., Adams, M. C., Liu, S., Chappie, J. S., Cava, F., & Dörr, T. (2019) · mBio · doi:10.1128/mbio.02620-18 · Cited by 46
Maurakis, S., Keller, K., Maxwell, C. N., Pereira, K., Chazin, W. J., Criss, A. K., & Cornelissen, C. N. (2019) · PLOS Pathogens · doi:10.1371/journal.ppat.1007937 · Cited by 45
Ilari, A., Alaleona, F., Petrarca, P., Battistoni, A., & Chiancone, E. (2011) · Journal of Molecular Biology · doi:10.1016/j.jmb.2011.04.036 · Cited by 41
Rosadini, C. V., Gawronski, J. D., Raimunda, D., Argüello, J. M., & Akerley, B. J. (2011) · Infection and Immunity · doi:10.1128/iai.05135-11 · Cited by 38
Kumar, P., Sannigrahi, S., & Tzeng, Y.-L. (2012) · Infection and Immunity · doi:10.1128/iai.05208-11 · Cited by 39
Competition for Manganese at the Host–Pathogen Interface
Kelliher, J. L., & Kehl-Fie, T. E. (2016) · Progress in Molecular Biology and Translational Science · doi:10.1016/bs.pmbts.2016.05.002 · Cited by 34
High-Throughput Screen for Identifying Small Molecules That Target Fungal Zinc Homeostasis
Simm, C., Luan, C.-H., Weiss, E., & O'Halloran, T. (2011) · PLoS ONE · doi:10.1371/journal.pone.0025136 · Cited by 34
Stocks, C. J., von Pein, J. B., Curson, J. E. B., Rae, J., Phan, M.-D., Foo, D., Bokil, N. J., Kambe, T., Peters, K. M., Parton, R. G., et al. (2021) · Journal of Leukocyte Biology · doi:10.1002/jlb.2hi0420-160r · Cited by 28
Quan, G., Xia, P., Lian, S., Wu, Y., & Zhu, G. (2020) · Veterinary Research · doi:10.1186/s13567-020-00854-1 · Cited by 22
Castelli, S., Stella, L., Petrarca, P., Battistoni, A., Desideri, A., & Falconi, M. (2013) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2012.11.073 · Cited by 15
Chen, C., Hu, X., He, D., He, X., & Shen, L. (2025) · Food Science & Nutrition · doi:10.1002/fsn3.70854 · Cited by 6
Salmonella: Invasion, Evasion & Persistence
Chami, B., & Bao, S. (2012) · Salmonella - Distribution, Adaptation, Control Measures and Molecular Technologies · doi:10.5772/30443 · Cited by 3
Metadata
- Authors
- Ammendola, S., Pasquali, P., Pistoia, C., Petrucci, P., Petrarca, P., Rotilio, G., & Battistoni, A.
- Affiliations
- Department of Biology, University of Rome Tor Vergata, 00133 Rome, Italy
- Department of Food Safety and Veterinary Public Health, Istituto Superiore di Sanità, 00161 Rome, Italy
- Venue
- Infection and Immunity
- Publisher
- American Society for Microbiology
- Published
- 2007-12
- Volume
- 75
- Issue
- 12
- Pages
- 5867-5876
- ISSN
- 0019-9567
- 1098-5522
- Cited by
- 235
- References
- 8
- Language
- en
About these checks
Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.
Statistics and arithmetic are recomputed, not judged.
Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.
What counts as a claim ›How we measure confidence ›How we check this ›
Are you an author, or do you see a problem with this page? Request a review