The DOI matches its Crossref record; 104 of the 105 references it cites were found in a registry or an index.
Reactive oxygen and nitrogen intermediates in the relationship between mammalian hosts and microbial pathogens
Open accessAbstract
This review summarizes recent evidence from knock-out mice on the role of reactive oxygen intermediates and reactive nitrogen intermediates (RNI) in mammalian immunity. Reflections on redundancy in immunity help explain an apparent paradox: the phagocyte oxidase and inducible nitric oxide synthase are each nonredundant, and yet also mutually redundant, in host defense. In combination, the contribution of these two enzymes appears to be greater than previously appreciated. The remainder of this review focuses on a relatively new field, the basis of microbial resistance to RNI. Experimental tuberculosis provides an important example of an extended, dynamic balance between host and pathogen in which RNI play a major role. In diseases such as tuberculosis, a molecular understanding of host–pathogen interactions requires characterization of the defenses used by microbes against RNI, analogous to our understanding of defenses against reactive oxygen intermediates. Genetic and biochemical approaches have identified candidates for RNI-resistance genes in Mycobacterium tuberculosis and other pathogens.
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?
The source backs part of the claim, not all of it — or backs it for a different population, condition or comparison.
In the citing paper
“In addition, NO causes the formation of reactive nitrogen species (such as peroxynitrite) which can damage mitochondrial function and which have been shown to have strong antifungal activity (26).”
From Inhibition of Classical and Alternative Modes of Respiration in Candida albicans Leads to Cell Wall Remodeling and Increased Macrophage Recognition (2019) · cites this paper as [26]
Experimental — accuracy not yet measuredThe cited source says what the claim attributes to it.
In the citing paper
“iNOS catalyzed high output formation of the labile radical NO by macrophages (Nathan and Shiloh, 2000; Bogdan, 2001) which exerts direct anti-microbial effector functions.”
From Iron at the interface of immunity and infection (2014) · cites this paper as Nathan and Shiloh, 2000
In the citing paper
“Using arginine and oxygen, the homodimeric NOS2 generates NO and citrulline, as one subunit transfers electrons between NADPH, FAD, flavin mononucleotide to the heme iron of the second subunit (56, 57).”
From Macrophage defense mechanisms against intracellular bacteria (2015) · cites this paper as [56]
In the citing paper
“NOX2 consists of five catalytic subunits, which assemble after phagocytosis thereby forming an active enzymatic complex producing superoxide anions and hydrogen peroxide along with the formation of hydroxyl radicals, the latter pathway being catalyzed by iron via the Fenton reaction (56, 59–61).”
From Macrophage defense mechanisms against intracellular bacteria (2015) · cites this paper as [56]
In the citing paper
“Both NOX2/gp91 phox and iNOS/ NOS2 are prototypical hemoproteins that use Fe-heme to catalyze the production of reactive oxygen species (ROS) and reactive nitrogen species (RNS), respectively [76].”
From The Iron age of host–microbe interactions (2015) · cites this paper as [76]
In the citing paper
“Moreover, extracellular hemoglobin may also exert protective effects based on NO and ONNO À detoxification [76,80,197].”
From The Iron age of host–microbe interactions (2015) · cites this paper as [76]
In the citing paper
“For example, generation of nitric oxide (NO•) by the inducible nitric oxide synthase (iNOS/NOS2) is a well established host defense mechanism that confers resistance to Salmonella, Leishmania or Mycobacteria (62).”
From Innate Nutritional Immunity (2018) · cites this paper as [62]
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
Nitric oxide as a secretory product of mammalian cells
Nathan, C. (1992) · The FASEB Journal · doi:10.1096/fasebj.6.12.1381691 · Cited by 4,350
Self-citationNITRIC OXIDE AND MACROPHAGE FUNCTION
MacMicking, J. D., Xie, Q. W., & Nathan, C. (1997) · Annual Review of Immunology · doi:10.1146/annurev.immunol.15.1.323 · Cited by 4,245
Self-citationPeroxynitrite oxidation of sulfhydryls.
Radí, R., Beckman, J. S., Bush, K., & Freeman, B. Α. (1991) · Journal of Biological Chemistry · doi:10.1016/s0021-9258(20)64313-7 · Cited by 2,492
An essential role for interferon gamma in resistance to Mycobacterium tuberculosis infection.
Flynn, J. L., Chan, J., Triebold, K. J., Dalton, D. K., Stewart, T. A., & Bloom, B. R. (1993) · The Journal of Experimental Medicine · doi:10.1084/jem.178.6.2249 · Cited by 2,468
Multiple defects of immune cell function in mice with disrupted interferon-gamma genes.
Dalton, D., Pitts-Meek, S., Keshav, S., Figari, I., Bradley, A., & Stewart, T. (1993) · Science · doi:10.1126/science.8456300 · Cited by 2,015
Nitric oxide functions as a signal in plant disease resistance
Delledonne, M., Xia, Y., Dixon, R. A., & Lamb, C. J. (1998) · Nature · doi:10.1038/29087 · Cited by 1,859
Flynn, J. L., Goldstein, M. M., Chan, J., Triebold, K. J., Pfeffer, K., Lowenstein, C. J., Schrelber, R., Mak, T. W., & Bloom, B. R. (1995) · Immunity · doi:10.1016/1074-7613(95)90001-2 · Cited by 1,678
Immune Response in Mice that Lack the Interferon-γ Receptor
Huang, S., Hendriks, W. J. A. J., Althage, A., Hemmi, S., Bluethmann, H., Kamijo, R., Vilček, J., Zinkernagel, R. M., & Aguet, M. (1993) · Science · doi:10.1126/science.8456301 · Cited by 1,551
Defense gene induction in tobacco by nitric oxide, cyclic GMP, and cyclic ADP-ribose
Durner, J., Wendehenne, D., & Klessig, D. F. (1998) · Proceedings of the National Academy of Sciences · doi:10.1073/pnas.95.17.10328 · Cited by 1,320
DNA Deaminating Ability and Genotoxicity of Nitric Oxide and its Progenitors
Wink, D. A., Kasprzak, K. S., Maragos, C. M., Elespuru, R. K., Misra, M., Dunams, T. M., Cebula, T. A., Koch, W. H., Andrews, A. W., Allen, J. S., et al. (1991) · Science · doi:10.1126/science.1948068 · Cited by 1,243
Research works printed but not linked: 6
- S J Klebanoff Inflammation, eds J I Gallin, R Snyderman, D T Fearon, B F Haynes, C Nathan (Lippincott, Philadelphia), pp. 721–768 (1999).
- P Elsbach, J Weiss, O Levy Inflammation, eds J I Gallin, R Snyderman, D T Fearon, B F Haynes, C Nathan (Lippincott, Philadelphia), pp. 801–818 (1999).
- M A DeGroote, F C Fang Nitric Oxide and Infection, ed F C Fang (Kluwer/Plenum, New York), pp. 231–264 (1999).
- J Chan, J Flynn Nitric Oxide and Infection, ed F C Fang (Kluwer/Plenum, New York), pp. 281–310 (1999).
- B Gaston, J S Stamler Nitric Oxide and Infection, ed F C Fang (Kluwer/Plenum, New York), pp. 37–55 (1999).
- Bryk R. Griffin P. & Nathan C. (2000) Nature (London) in press.
Cited by
Sorted by citations
Items 901–1,000 of 1,000
Leukotrienes Produced in Allergic Lung Inflammation Activate Alveolar Macrophages
Silva, R. C., Landgraf, M. A., Hiyane, M. I., Pacheco‐Silva, Á., Câmara, N. O. S., & Landgraf, R. G. (2010) · Cellular Physiology and Biochemistry · doi:10.1159/000320555 · Cited by 15
Luo, Y., Xu, X., Ding, Z., Liu, Z., Zhang, B., Yan, Z.-Y., Sun, J., Hu, S., & Hu, X. (2008) · BMC Genomics · doi:10.1186/1471-2164-9-386 · Cited by 15
Errafiy, N., Ammar, E., & Soukri, A. (2013) · Journal of Essential Oil Research · doi:10.1080/10412905.2013.775681 · Cited by 15
Proteomic Analysis of Drug-Resistant Mycobacteria: Co-Evolution of Copper and INH Resistance
Chen, Y., Yang, F., Sun, Z., Wang, Q., Mi, K., & Deng, H. (2015) · PLoS ONE · doi:10.1371/journal.pone.0127788 · Cited by 16
Lebonville, C. L., Jones, M., Hutson, L. W., Cooper, L. B., Fuchs, R. A., & Lysle, D. T. (2016) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2016.04.005 · Cited by 15
The Hidden Face of Nitrogen Oxides Species: From Toxic Effects to Potential Cure?
Depayras, S., Kondakova, T., Heipieper, H. J., Feuilloley, M. G. J., Orange, N., & Poc, C. D. (2018) · InTech eBooks · doi:10.5772/intechopen.75822 · Cited by 15
Nitric oxide-releasing compounds for the treatment of lung infections
Chiarelli, L. R., Degiacomi, G., Egorova, A., Makarov, V., & Pasca, M. R. (2020) · Drug Discovery Today · doi:10.1016/j.drudis.2020.10.027 · Cited by 15
Nitric oxide and ovarian function
Hattori, M. A., & Tabata, S. (2006) · Animal Science Journal · doi:10.1111/j.1740-0929.2006.00349.x · Cited by 15
Peroxynitrite detoxification by ferryl Mycobacterium leprae truncated hemoglobin O
Ascenzi, P., Marinis, E. D., Visca, P., Ciaccio, C., & Coletta, M. (2009) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2009.01.088 · Cited by 15
de Muñoz, F. G., Lanz‐Mendoza, H., & Hernández‐Hernández, F. D. L. C. (2007) · Archives of Insect Biochemistry and Physiology · doi:10.1002/arch.20174 · Cited by 15
Monmai, C., Kim, J.-S., & Baek, S.-H. (2022) · Nutrients · doi:10.3390/nu14194143 · Cited by 14
Host-directed therapy for bacterial infections -Modulation of the phagolysosome pathway-
Taya, T., Teruyama, F., & Gojo, S. (2023) · Frontiers in Immunology · doi:10.3389/fimmu.2023.1227467 · Cited by 14
Brucella spp. are facultative anaerobic bacteria under denitrifying conditions
Freddi, L., de la Garza-García, J. A., Dahouk, S. A., Occhialini, A., & Köhler, S. (2023) · Microbiology Spectrum · doi:10.1128/spectrum.02767-23 · Cited by 14
Dewan, A., Jain, C. M., Das, M., Tripathi, A. P., Sharma, A., Singh, H., Malhotra, N., Seshasayee, A. S. N., Chakrapani, H., & Singh, A. (2024) · Redox Biology · doi:10.1016/j.redox.2024.103285 · Cited by 16
Clinical characteristics and prognostic factors of pulmonary and extrapulmonary cryptococcosis
Tao, Z., Pu, Q., Shen, Y., Zhang, S., Wang, C., Hu, Z., Jin, Y., Zhu, X., & Weng, Y. (2024) · BMC Infectious Diseases · doi:10.1186/s12879-024-09895-9 · Cited by 15
Stokes, R. W., & Waddell, S. J. (2009) · Future Microbiology · doi:10.2217/fmb.09.94 · Cited by 14
Reiling, N., Homolka, S., Kohl, T. A., Steinhäuser, C., Kolbe, K., Schütze, S., & Brandenburg, J. (2017) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2017.09.009 · Cited by 15
Sousa, E. H. S., Carepo, M. S. P., & Moura, J. J. G. (2020) · Coordination Chemistry Reviews · doi:10.1016/j.ccr.2020.213476 · Cited by 14
Role of Base Excision Repair in Innate Immune Cells and Its Relevance for Cancer Therapy
Zhao, S., Habib, S. L., Senejani, A. G., Sebastian, M. M., & Kidane, D. (2022) · Biomedicines · doi:10.3390/biomedicines10030557 · Cited by 14
Ascenzi, P., Bolognesi, M., & Visca, P. (2007) · Biochemical and Biophysical Research Communications · doi:10.1016/j.bbrc.2007.04.024 · Cited by 14
Joseph, S. V., Madhavilatha, G. K., Kumar, R. A., & Mundayoor, S. (2012) · Applied and Environmental Microbiology · doi:10.1128/aem.01984-12 · Cited by 14
Dahiya, Y., Pandey, R. K., Bhatt, K. H., & Sodhi, A. (2010) · FEBS Letters · doi:10.1016/j.febslet.2010.09.009 · Cited by 14
Antioxidant supplementation enhances bacterial peritonitis in mice by inhibiting phagocytosis
Goswami, M., Sharma, D., Khan, N. M., Checker, R., Sandur, S. K., & Jawali, N. (2013) · Journal of Medical Microbiology · doi:10.1099/jmm.0.067173-0 · Cited by 14
Kurtz, S. L., & Elkins, K. L. (2015) · Clinical and Vaccine Immunology · doi:10.1128/cvi.00301-15 · Cited by 14
A comparative analysis of the DNA recombination repair pathway in mycobacterial genomes
Singh, A., Bhagavat, R., Vijayan, M., & Chandra, N. R. (2016) · Tuberculosis · doi:10.1016/j.tube.2016.04.011 · Cited by 14
Li, S., Li, P., Zhang, L., Hu, W., Wang, M., Liu, Y., Tang, G., Wang, D., BiJun, Z., & Yan, J. (2017) · PLoS ONE · doi:10.1371/journal.pone.0178618 · Cited by 14
Inhibitory Effect of NO-Releasing Ciprofloxacin (NCX 976) on Mycobacterium tuberculosis Survival
Ciccone, R., Mariani, F., Cavone, A., Persichini, T., Venturini, G., Ongini, E., Colizzi, V., & Colasanti, M. (2003) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.47.7.2299-2302.2003 · Cited by 14
Cerquetti, M. C., Goren, N., Ropolo, A., Grasso, D., Giacomodonato, M. N., & Vaccaro, M. I. (2002) · Infection and Immunity · doi:10.1128/iai.70.2.964-969.2002 · Cited by 14
Zeng, J., Yang, Z., Zhong, Y., Zheng, Y., Hao, J., Luo, G., & Yan, Q. (2022) · Scientific Reports · doi:10.1038/s41598-022-17387-6 · Cited by 13
Fatima, S., Zaki, A., Madhav, H., Khatoon, B. S., Rahman, A., Manhas, M. W., Hoda, N., & Syed, M. A. (2023) · RSC Advances · doi:10.1039/d3ra01893h · Cited by 13
Cryptosporidiosis in a Zoonotic Gastrointestinal Disorder Perspective
Balendran, T., Iddawela, D., & Lenadora, S. (2024) · Journal of Tropical Medicine · doi:10.1155/2024/6439375 · Cited by 13
Fusconi, M., Greco, A., Cattaneo, C. G., Ciofalo, A., Ralli, M., & VINCENTIIS, M. D. (2018) · Infection Genetics and Evolution · doi:10.1016/j.meegid.2018.03.018 · Cited by 13
Mycobacterium tuberculosis Rv0991c Is a Redox-Regulated Molecular Chaperone
Becker, S. H., Ulrich, K., Dhabaria, A., Ueberheide, B. M., Beavers, W. N., Skaar, E. P., Iyer, L. M., Aravind, L., Jakob, U., & Darwin, K. H. (2020) · mBio · doi:10.1128/mbio.01545-20 · Cited by 13
Regulation of Rfa2 phosphorylation in response to genotoxic stress in C andida albicans
Gao, J., Wang, H., Wong, A. H., Zeng, G., Huang, Z., Wang, Y., Sang, J., & Wang, Y. (2014) · Molecular Microbiology · doi:10.1111/mmi.12749 · Cited by 13
Nasal nitric oxide in children with adenoidal hypertrophy: A preliminary study
Torretta, S., Bossi, A., Capaccio, P., Marchisio, P., Esposito, S., Brevi, A., & Pignataro, L. (2010) · International Journal of Pediatric Otorhinolaryngology · doi:10.1016/j.ijporl.2010.03.025 · Cited by 13
Wang, Z., Tejero, J., Wei, C., Haque, M. M., Santolini, J., Fadlalla, M., Biswas, A., & Stuehr, D. J. (2011) · Journal of Inorganic Biochemistry · doi:10.1016/j.jinorgbio.2011.11.015 · Cited by 13
Jowkar, F., Dehghani, F., & Jamshidzadeh, A. (2010) · Journal of Dermatological Treatment · doi:10.3109/09546634.2010.495380 · Cited by 13
Lee, E., Kim, S., Kwon, S., Kim, S., Nam, Y., & Kim, K. (2004) · Diseases of Aquatic Organisms · doi:10.3354/dao058255 · Cited by 13
Vanin, A. F., & Чазов, Е. И. (2011) · BIOPHYSICS · doi:10.1134/s0006350911020321 · Cited by 13
Relationship of nitric oxide and protein carbonyl in tuberculosis.
Kulkarni, A., & Madrasi, N. A. (2008) · PubMed · Cited by 13
Innate sensing and cell-autonomous resistance pathways in Legionella pneumophila infection
Naujoks, J., Lippmann, J., Suttorp, N., & Opitz, B. (2017) · International Journal of Medical Microbiology · doi:10.1016/j.ijmm.2017.10.004 · Cited by 16
Nitric oxide produced by NOS2 copes with the cytotoxic effects of superoxide in macrophages
Kobayashi, S., Homma, T., & Fujii, J. (2021) · Biochemistry and Biophysics Reports · doi:10.1016/j.bbrep.2021.100942 · Cited by 13
Nitric oxide research in agriculture: bridging the plant and bacterial realms
COHEN, M. F., Mazzola, M., & Yamasaki, H. (2006) · Springer eBooks · doi:10.1007/1-4020-4389-9_5 · Cited by 13
Nitric oxide and lysozyme production as an impact to Clostridium perfringens mastitis
Osman, K. M., El-Enbaawy, M. I., Ezzeldin, N. A., & Hussein, H. M. G. (2009) · Comparative Immunology Microbiology and Infectious Diseases · doi:10.1016/j.cimid.2009.09.001 · Cited by 13
Attack on the Scourge of Tuberculosis: Patented Drug Targets
Vohra, R., Gupta, M., Chaturvedi, R., & Singh, Y. P. (2006) · Recent Patents on Anti-Infective Drug Discovery · doi:10.2174/157489106775244127 · Cited by 13
Tarasenko, O., Scott, A., Soderberg, L. S. F., Ponnappan, U., & Alusta, P. (2009) · Glycoconjugate Journal · doi:10.1007/s10719-009-9248-7 · Cited by 13
Burge, E. J., Gauthier, D. T., & Veld, P. A. V. (2004) · Comparative Biochemistry and Physiology Part C Toxicology & Pharmacology · doi:10.1016/j.cca.2004.03.007 · Cited by 13
General Metabolism and Biochemical Pathways of Tubercle Bacilli
Wheeler, P. R., & Blanchard, J. S. (2004) · Wiley eBooks · doi:10.1128/9781555817657.ch20 · Cited by 13
Khan, H., Paul, P., Goar, H., Bamniya, B., Baid, N., & Sarkar, D. (2024) · eLife · doi:10.7554/elife.92136 · Cited by 12
Mycobacterium tuberculosis and host interactions in the manifestation of tuberculosis
Abbasnia, S., Asnaashari, A. M. H., Sharebiani, H., Soleimanpour, S., Mosavat, A., & Rezaee, S. A. (2024) · Journal of Clinical Tuberculosis and Other Mycobacterial Diseases · doi:10.1016/j.jctube.2024.100458 · Cited by 14
Stempinski, P. R., Irizarry, P. R., McConnell, S. A., Lopes, L. C. L., Santos, S. R. D., Wear, M. P., & Casadevall, A. (2025) · Fungal Biology · doi:10.1016/j.funbio.2025.101544 · Cited by 12
Probiotic modulation of key immune macromolecules in shrimp
Abo‐Al‐Ela, H. G., Mahdi, S., Angthong, P., & Rungrassamee, W. (2025) · Microbial Pathogenesis · doi:10.1016/j.micpath.2025.107463 · Cited by 12
Pupylation-dependent and -independent proteasomal degradation in mycobacteria
Imkamp, F., Ziemski, M., & Weber-Ban, E. U. (2015) · BioMolecular Concepts · doi:10.1515/bmc-2015-0017 · Cited by 12
Foderaro, J. E., & Konopka, J. B. (2021) · Infection and Immunity · doi:10.1128/iai.00670-20 · Cited by 12
Molecular feature of neutrophils in immune microenvironment of muscle atrophy
You, Z.-Q., Huang, X.-Y., Xiang, Y., Dai, J.-X., Jiang, J.-J., & Xu, J.-G. (2022) · Journal of Cellular and Molecular Medicine · doi:10.1111/jcmm.17495 · Cited by 11
Thakur, R. S., Basavaraju, S., Khanduja, J. S., Muniyappa, K., & Nagaraju, G. (2015) · Journal of Biological Chemistry · doi:10.1074/jbc.m115.671164 · Cited by 12
Binjawadagi, B., Dwivedi, V., Manickam, C., Torrelles, J. B., & Renukaradhya, G. J. (2011) · Viral Immunology · doi:10.1089/vim.2011.0040 · Cited by 12
Pinto, R., Leotta, L., Shanahan, E. R., West, N. P., Leyh, T. S., Britton, W. J., & Triccas, J. A. (2012) · The Journal of Infectious Diseases · doi:10.1093/infdis/jis751 · Cited by 12
Saldarriaga, Ó. A., Travi, B. L., Choudhury, G. G., & Melby, P. C. (2012) · Journal of Leukocyte Biology · doi:10.1189/jlb.1010568 · Cited by 12
Fischer, K. J., Yajjala, V. K., Bansal, S., Bauer, C. D., Chen, R., & Sun, K. (2019) · The Journal of Immunology · doi:10.4049/jimmunol.1801471 · Cited by 12
Rao, Z., Cao, H.-J., Shi, B., Liu, X., Luo, J., & Zeng, N. (2019) · Journal of Pharmacology and Experimental Therapeutics · doi:10.1124/jpet.118.255893 · Cited by 12
Dutta, A., Mazumder, M., Alam, M., Gourinath, S., & Sau, A. K. (2019) · Biochemical Journal · doi:10.1042/bcj20190545 · Cited by 12
Zou, S., Zhang, Q., & Gong, J. (2020) · Microorganisms · doi:10.3390/microorganisms8040559 · Cited by 12
Noncoding RNAs: modulators and modulatable players during infection-induced stress response.
Chattopadhyay, P., Vasudevan, J. S., & Pandey, R. (2021) · Briefings in Functional Genomics · doi:10.1093/bfgp/elaa026 · Cited by 9
Adaptive Immunity and Genetics of the Host Immune Response
Roberts, C. W., Prasad, S., Khaliq, F., Gazzinelli, R. T., Khan, I. A., & McLeod, R. L. (2013) · Elsevier eBooks · doi:10.1016/b978-0-12-396481-6.00025-8 · Cited by 12
Nezami, N., Ghorbanihaghjo, A., Rashtchizadeh, N., Argani, H., Tafrishinejad, A., Ghorashi, S., & Hajhosseini, B. (2011) · Atherosclerosis · doi:10.1016/j.atherosclerosis.2011.03.025 · Cited by 12
Kang, J., Cheun, H., Kim, J., Moon, S.-U., Park, S., Kim, T., Sohn, W., & Na, B. (2008) · Parasitology Research · doi:10.1007/s00436-008-1041-1 · Cited by 12
Steenkamp, D. J., & VOGT, R. N. (2003) · Analytical Biochemistry · doi:10.1016/j.ab.2003.10.011 · Cited by 12
The Role of Vitamin D in Innate Immunity
Liu, P. T. (2011) · Elsevier eBooks · doi:10.1016/b978-0-12-381978-9.10093-9 · Cited by 12
Fu, J., Zong, G., Zhang, P., Gu, Y., & Cao, G. (2017) · Current Microbiology · doi:10.1007/s00284-017-1394-8 · Cited by 12
Alba, A., Tetreau, G., Chaparro, C., Sánchez, J., Vázquez, A. A., & Gourbal, B. (2019) · Developmental & Comparative Immunology · doi:10.1016/j.dci.2019.103463 · Cited by 12
Crystallization and preliminary analysis of active nitroalkane oxidase in three crystal forms
Nagpal, A., Valley, M. P., Fitzpatrick, P. F., & Orville, A. M. (2004) · Acta Crystallographica Section D Biological Crystallography · doi:10.1107/s0907444904013289 · Cited by 12
Role of Salmonella surface components in immunomodulation of inflammatory mediators
Choudhary, A., Tiwari, R. P., Koul, A., Chanana, V., Gupta, S., & Rishi, P. (2005) · Molecular and Cellular Biochemistry · doi:10.1007/s11010-005-4506-x · Cited by 12
Mendelow, B., Cegielski, P., Dhansay, M. A., Gevers, W., Gray, C. M., Gray, G., Grobler, L., Hussey, G. D., McMurray, D. N., Msamanga, G., et al. (2007) · SUNScholar (Stellenbosch University) · Cited by 12
Pandey, R. K., Dahiya, Y., & Sodhi, A. (2011) · Microbes and Infection · doi:10.1016/j.micinf.2011.11.004 · Cited by 11
Paniccia, J. E., Lebonville, C. L., Jones, M., Parekh, S. V., Fuchs, R. A., & Lysle, D. T. (2018) · Brain Behavior and Immunity · doi:10.1016/j.bbi.2018.07.024 · Cited by 11
Limón, G., Samhadaneh, N. M., Pironti, A., & Darwin, K. H. (2023) · mBio · doi:10.1128/mbio.00363-23 · Cited by 11
Roy, H. S., Neethu, K. M., Rajput, S., Sadhukhan, S., Gowri, V., Dar, A. H., Monga, M., Salaria, N., Guha, R., Chattopadhyay, N., et al. (2023) · Chemistry - A European Journal · doi:10.1002/chem.202301748 · Cited by 11
Instantaneous Inactivation of Herpes Simplex Virus by Silicon Nitride Bioceramics
Pezzotti, G., Ohgitani, E., Ikegami, S., Shin‐Ya, M., Adachi, T., Yamamoto, T., Kanamura, N., Marin, E., Zhu, W., Okuma, K., et al. (2023) · International Journal of Molecular Sciences · doi:10.3390/ijms241612657 · Cited by 11
Involvement of thioredoxin domain-containing 5 in resistance to nitrosative stress
Lee, H., Hitchcock, T. M., Park, S., Mi, R., Kraft, J. D., Luo, J., & Cao, W. (2010) · Free Radical Biology and Medicine · doi:10.1016/j.freeradbiomed.2010.06.012 · Cited by 11
Gutierrez, F. R. S., Pavanelli, W. R., Medina, T. D. S., Silva, G. K., Mariano, F. S., Guedes, P. M. D. M., Mineo, T. W. P., Rossi, M. A., Cunha, F. Q., & Silva, J. S. (2013) · Microbes and Infection · doi:10.1016/j.micinf.2013.10.007 · Cited by 11
Carli, C. B. D. A., Quilles, M. B., Maia, D. C. G., Lopes, F. C. M., Santos, R. R., Pavan, F. R., Leite, C. Q. F., Calvo, T. R., Vilegas, W., & Carlos, I. Z. (2010) · Pharmaceutical Biology · doi:10.3109/13880200903303471 · Cited by 11
Fundová, P., Filipovský, T., Funda, D. P., Hovorka, O., Holý, R., Navara, M., & Tlaskalová‐Hogenová, H. (2008) · Folia Microbiologica · doi:10.1007/s12223-008-0089-8 · Cited by 11
Seal, A., Suh, H., Jansen, L. T., Summers, L. G., & Kavouras, S. A. (2018) · Elsevier eBooks · doi:10.1016/b978-0-12-814556-2.00011-7 · Cited by 14
Brown, A. J. P., Cowen, L. E., Pietro, A. D., & Quinn, J. (2017) · ASM Press eBooks · doi:10.1128/9781555819583.ch21 · Cited by 11
Bacterial Copper Resistance and Virulence
Pontel, L. B., Checa, S. K., & Soncini, F. C. (2015) · Springer eBooks · doi:10.1007/978-3-319-18570-5_1 · Cited by 11
Sannella, A. R., Gradoni, L., Persichini, T., Ongini, E., Venturini, G., & Colasanti, M. (2003) · Antimicrobial Agents and Chemotherapy · doi:10.1128/aac.47.7.2303-2306.2003 · Cited by 11
The N‐terminal pre‐A region of Mycobacterium tuberculosis 2/2HbN promotes NO ‐dioxygenase activity
Pesce, A., Bustamante, J. P., Bidon‐Chanal, A., Boechi, L., Estrin, D. A., Luque, F. J., Sebilo, A., Guertin, M., Bolognesi, M., Ascenzi, P., et al. (2015) · FEBS Journal · doi:10.1111/febs.13571 · Cited by 11
DeLeo, F. R., & Nauseef, W. M. (2015) · Elsevier eBooks · doi:10.1016/b978-1-4557-4801-3.00008-4 · Cited by 11
Crosstalk Between Sphingomyelinases and Reactive Oxygen Species in Mycobacterial Infection
Wu, Y., Gulbins, E., & Grassmé, H. (2017) · Antioxidants and Redox Signaling · doi:10.1089/ars.2017.7050 · Cited by 11
Gautam, K., Negi, S., & Saini, V. (2021) · Free Radical Research · doi:10.1080/10715762.2021.1892091 · Cited by 11
Requirement for multiple activation signals by anti-inflammatory feedback in macrophages
Ray, J. C. J., & Kirschner, D. E. (2006) · Journal of Theoretical Biology · doi:10.1016/j.jtbi.2005.11.037 · Cited by 11
Kim, H.-G., Park, E.-H., & Lim, C. (2005) · Molecules and Cells · doi:10.1016/s1016-8478(23)13197-9 · Cited by 11
Antioxidant Phytochemicals as Novel Therapeutic Strategies against Drug-Resistant Bacteria
Gangwar, B., Kumar, S., & Darokar, M. P. (2023) · Biochemistry · doi:10.5772/intechopen.108220 · Cited by 11
Nevière, R., Trinh-Duc, P., Hulo, S., Edmé, J. L., Dehon, A., Boleslawski, E., Dharancy, S., & Lebuffe, G. (2016) · Transplant International · doi:10.1111/tri.12861 · Cited by 10
DNA lesions and repair in trypanosomatids infection
Repolês, B. M., Machado, C. R., & Florentino, P. T. V. (2020) · Genetics and Molecular Biology · doi:10.1590/1678-4685-gmb-2019-0163 · Cited by 11
Acuña, S. M., Zanatta, J. M., Bento, C. D. A., Floeter‐Winter, L. M., & Muxel, S. M. (2022) · Non-Coding RNA · doi:10.3390/ncrna8010017 · Cited by 10
IFN-induced cell-autonomous immune mechanisms in the control of intracellular protozoa
Skariah, S., Sultan, A. A., & Mordue, D. G. (2022) · Parasitology Research · doi:10.1007/s00436-022-07514-7 · Cited by 10
Jeon, S. M., Kim, Y. J., Nguyen, T. Q., Cui, J., Hanh, B. T. B., Silwal, P., Kim, J. K., Kim, J., Oh, D., Jang, J., et al. (2022) · Virulence · doi:10.1080/21505594.2022.2138009 · Cited by 10
Antibacterial and Therapeutic Effects of Houttuynia cordata Ethanol extract for Murine Salmonellosis
Kim, D., Lim, J.-J., Lee, J.-J., Jung, W.-C., Shin, H.-J., Lee, H.-J., Kim, G. S., & Kim, S. (2008) · Korean Journal of Environmental Agriculture · doi:10.5338/kjea.2008.27.2.156 · Cited by 10
Metadata
- Authors
- Nathan, C., & Shiloh, M. U.
- Affiliations
- Cornell University (US)
- Venue
- Proceedings of the National Academy of Sciences
- Publisher
- National Academy of Sciences
- Published
- 2000-08
- Volume
- 97
- Issue
- 16
- Pages
- 8841-8848
- ISSN
- 0027-8424 (ISSN-L)
- 1091-6490
- PMC
- PMC34021
- OpenAlex
- W2113120391
- Cited by
- 1,469
- References
- 105
- Citations by year
- 2026: 26 · 2025: 29 · 2024: 42 · 2023: 32 · 2022: 49 · 2021: 42 · 2020: 59 · 2019: 51 · 2018: 56 · 2017: 62 · 2016: 66 · 2015: 64 · 2014: 72 · 2013: 70 · 2012: 81
- FWCI
- 4.65
- Type
- journal article
- Language
- en
- Open access
- green
- europepmc.org
- Locations
- Proceedings of the National Academy of Sciences (publishedVersion)
- Europe PMC (PubMed Central) (publishedVersion)
- PubMed Central (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Life Sciences › Immunology and Microbiology › Immunology › Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Health Sciences › Medicine › Infectious Diseases › Tuberculosis Research and Epidemiology
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Molecular Biology › Redox biology and oxidative stress
- Keywords
- reactive oxygen species, reactive nitrogen intermediates, host-pathogen interaction, inducible nitric oxide synthase, NADPH oxidase, inducible nitric oxide, Mycobacterium tuberculosis, tuberculosis, knockout mice, innate immunity
- MeSH terms
- Animals, Humans, Mammals, Mycobacterium tuberculosis, Nitrogen, Reactive Oxygen Species, Nitric Oxide Synthase, NADPH Oxidases, Mice
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