- Research article
- Open Access
Distinct roles for nitric oxide in resistant C57BL/6 and susceptible BALB/c mice to control Burkholderia pseudomallei infection
© Breitbach et al; licensee BioMed Central Ltd. 2011
- Received: 25 August 2010
- Accepted: 16 March 2011
- Published: 16 March 2011
Burkholderia pseudomallei is the causative agent of melioidosis, an emerging bacterial infectious disease in tropical and subtropical areas. We recently showed that NADPH oxidase but not nitric oxide (NO) contributes to resistance in innately resistant C57BL/6 mice in a B. pseudomallei respiratory infection model. However, the function of NO for resistance was shown to differ among distinct strains of mice and proved also to be stage dependent in various infection models. The present study therefore aimed to examine the role of NO in a systemic infection model of melioidosis and to test whether the function of NO differs among innately resistant C57BL/6 and susceptible BALB/c mice after B. pseudomallei infection.
C57BL/6 iNOS-/- mice that were intravenously infected with B. pseudomallei survived several weeks, whereas most of the wild type animals succumbed during this period. The bacterial burden in liver and spleen was significantly higher in wild type animals compared to iNOS-/- mice 13 days after challenge. In contrast, BALB/c mice that were treated with amminoguanidine to inhibit NO expression in vivo showed significantly enhanced mortality rates and higher bacterial loads in liver and spleen compared to control animals. The bactericidal function of IFN-γ stimulated C57BL/6 iNOS-/- macrophages were not altered after B. pseudomallei infection, but BALB/c macrophages exhibited reduced killing activity against the pathogen when NO was inhibited.
Our present data indicate a dual role of NO among resistant and susceptible mouse strains after B. pseudomallei infection. NO mediated mechanisms are an essential component to control the infection in susceptible BALB/c mice. In contrast, NO production in B. pseudomallei infected C57BL/6 mice rather harmed the host likely due to its detrimental effects.
- Nitric Oxide
- Bacterial Load
- Infection Model
- Bone Marrow Derive Macrophage
- Bacterial Burden
Nitric oxide (NO) is a free radical molecule that can be expressed by several cell types including fibroblasts, hepatocytes, and phagocytes via nitric oxide synthases. NO exhibits many pleiotropic functions, among these microbicidal activity, and a role in immune regulation are of special interest after infection with parasites, bacteria or viruses. Release of NO can restrict the growth of several pathogens in the host [1–5], but is also known to cause nonspecific damage in host cells that can lead to an exacerbation after infection [2, 6]. A rather protective or damaging function for NO was also described to be dependent on the stage of infection or the background mouse strain in several murine infection models [4, 6–9].
Burkholderia pseudomallei comprises a facultative intracellular gram-negative rod and is the causative agent of melioidosis, an emerging infectious disease of humans and animals in certain areas of the tropics and subtropics . The infection is thought to be acquired by inoculation into minor cuts, abrasions, or inhalation after contact with contaminated water or soil . Clinical manifestations are variable, ranging from inapparent to localized chronic infections and fulminant acute septicemias with high mortality rate .
Several reports could show that the inbred mouse strains C57BL/6 and BALB/c differed in their outcome after B. pseudomallei challenge [13–15]. Irrespective whether mice were infected intravenously or via inhalation, the LD50 of C57BL/6 mice was 100-fold higher compared to BALB/c mice [13, 14]. In addition, BALB/c mice exhibited significantly higher bacterial loads in liver and spleen already 12 h after intravenous infection compared to C57BL/6 mice . Thus, C57BL/6 mice are considered to represent a relatively resistant mouse strain in murine melioidosis, whereas BALB/c mice are highly susceptible. We previously have shown that macrophages were essential for resistance in both BALB/c and C57BL/6 mice to control B. pseudomallei infection . By further investigating bactericidal effector molecules of macrophages, we could not find any protective function for NO in resistance of C57BL/6 mice in a respiratory infection model or in controlling intracellular B. pseudomallei in macrophages . However, we could neither exclude whether NO might play a role when bacteria were administered systemically, or a protective function in innate susceptible BALB/c mice.
The present study aimed to further elucidate the role of NO for resistance against B. pseudomallei in a systemic model of murine melioidosis. We compared the outcome of susceptible BALB/c and relatively resistant C57BL/6 mice lacking NO expression after intravenous infection with B. pseudomallei. To examine the impact of NO in controlling intracellular B. pseudomallei growth in macrophages, we analyzed the intracellular survival kinetics in primary bone marrow derived macrophages from BALB/c and C57BL/6 mice that lack NO release.
Lack of iNOS renders C57BL/6 mice more resistant against systemic B. pseudomallei infection
NO contributes to resistance against B. pseudomallei infection in BALB/c mice
Macrophages from C57BL/6 and BALB/c mice lacking NO differ in their ability to control intracellular growth of B. pseudomallei
The IFN-γ effector molecule NO is known to contribute to resistance against a variety of pathogens such as Mycobacterium tuberculosis, Salmonella, Chlamydia, Toxoplasma gondii, and others [1–5]. Our present data indicate that NO seems to have a two-sided role in murine B. pseudomallei infection, dependent on the background mouse strain. In a respiratory infection model of melioidosis we recently reported that NO did not play a role for resistance in innate relatively resistant C57BL/6 mice, but iNOS-/- mice tend to be more protected from infection . Similar observations were obtained in mice that were challenged intravenously with B. pseudomallei in the present study. Similar phenomena have also been observed in a murine Toxoplasma gondii and HSV-1 infection model [6, 17] where inhibition of NO led to prolonged survival of infected mice. Since at the same time lack of NO expression was associated with an increased load of the respective pathogen in tissues, it was suggested that NO has both, a microbicidal function as well as a detrimental role that led to immunopathologic changes and finally caused death [6, 17]. However, the bacterial load in internal organs of C57BL/6 iNOS-/- mice was neither enhanced in a respiratory nor in an intravenous B. pseudomallei infection model. In contrast, the number of live bacteria was significantly lower compared to control animals ( and present study). This is in clear contrast to results obtained in Toxoplasma and HSV-1 infection studies where NO - despite its damaging effect - had a role in restricting growth of the pathogens [6, 17]. However, after infection with B. pseudomallei, dispensable NO production in wild type mice is likely to cause damage to host cells. This might eventually led to a reduced ability to control bacterial growth and finally contribute for a higher mortality compared to animals that lack NO expression. Thus, in contrast to other murine infection models in that NO beside its detrimental effects still exhibit detectable killing activity against pathogens [6, 7], we did not found NO to contribute for the elimination or even reduction of the bacterial load after B. pseudomallei infection in innate relatively resistant C57BL/6 mice.
In contrast to the phenotype observed in C57BL/6 mice, we found NO to contribute to in vivo resistance in innate susceptible BALB/c mice. Also the in vitro killing activities of primary BALB/c macrophages were significantly decreased when NO was inhibited. Since our previous finding revealed that macrophages are absolutely essential for resistance in both susceptible and resistant mice , we assume that NO-mediated killing activity of macrophages is likely to contribute to resistance in BALB/c mice. This assumption is supported by our finding that enhanced mortality was associated with enhanced bacterial burden in spleens and livers of AG treated BALB/c mice. The fact that NO was dispensable for controlling B. pseudomallei growth in C57BL/6 mice indicates that IFN-γ dependent but NO-independent bactericidal mechanisms are crucial for resistance in this mouse strain. In contrast, bactericidal mechanisms that are present in C57BL/6 mice obviously lack to work efficiently in BALB/c mice. Thus, beneficial effects of NO seem to outweigh damaging effects in susceptible mice after B. pseudomallei challenge. Differences in the role of NO for resistance in susceptible and resistant mice have so far been described in a Toxoplasma gondii infection model, where - similar to our findings - NO contributed to resistance in innate susceptible but not resistant mice [7, 9].
The function of NO in resistance against a pathogen can differ among susceptible and resistant mouse strains. We here report that NO has rather damaging effects in innate resistant C57BL/6 mice in a murine model of melioidosis and did not play any role in the killing activity of C57BL/6 macrophages. In contrast, NO contributed to full resistance in innate susceptible BALB/c mice and was also involved in restricting the intracellular growth of macrophages from susceptible mice. The ambiguous role for NO to either protect or affect the host is likely to serve as one component that determines susceptibility against B. pseudomallei infection.
Burkholderia pseudomallei strain E8 was used throughout the study . Bacteria were grown on Columbia agar at 37°C for 24 h. Colonies were harvested using LB broth containing 20% glycerol and frozen in 50 μl aliquots at -70°C.
Female BALB/c mice were obtained from Charles River (Wiga Sulzfeld, Germany). iNOS-/- and respective C57BL/6J control mice were obtained from The Jackson Laboratory (Bar Harbor, Maine). Animals were provided with food and water ad libitum. Generally, naturally occurring death of infected animals was documented as survival end points. However, approx. 20 percent of mice that were observed to be severely ill were euthanized. All mouse experiments were performed in full compliance with the relevant laws and approved by the Landesamt für Landwirtschaft, Lebensmittelsicherheit und Fischerei, Western Pommerania, Germany (Az: LALLF M-V/TSD/7221.3-1.1-044/05).
Infection of mice and determination of organ bacterial burden
Frozen bacteria were thawed from the stock, plated on Colombia Agar, and grown overnight. Prior to infection, bacteria were harvested from Colombia Agar and diluted in phosphate buffered saline (PBS) to the appropriate concentration. For intravenous (i.v.) infection, a bacterial suspension of 200 μl was injected into the lateral tail vein. The mortality of the animals was monitored daily. To enumerate bacteria in internal organs, organs were aseptically removed and homogenized in 0.5 to 1 ml sterile PBS containing 0.5% Tergitol and 1% bovine serum albumin. Organ suspensions were plated on Ashdown agar and number of CFU was determined.
NO inhibition in vivo
To selectively inhibit NO production in vivo, we treated mice with aminoguanidin (AG) as reported by others . Mice continuously received AG via drinking water (2% w/v) at least six days prior to and during infection and were additionally treated i.p. 6 h prior and 18 h after B. pseudomallei challenge with AG (1.5 mg AG per animal in 200 μl PBS). Control animals received sham injections with PBS.
Culture and infection of bone marrow derived macrophages (BMM)
Murine bone marrow derived macrophages (BMM) were generated under serum-free conditions from BALB/c mice as previously described . Briefly, tibias and femurs were aseptically removed, and bone marrow cells were flushed with sterile PBS and then centrifuged at 150 × g for 10 min. Cells were resuspended in RPMI medium containing 5% Panexin BMM (PAN Biotech, Aidenbach, Germany), 2 ng/ml of recombinant murine granulocyte-macrophage colony-stimulating factor (PAN Biotech), and 50 μM mercaptoethanol and cultivated for at least 10 days at 37°C and 5% CO2. Twenty-four hours prior to infection experiments, cells were seeded in 48 well plates (1.5 × 105 cells per well) and infected with B. pseudomallei at a MOI as indicated for each experiment for 30 min. Cells were then washed twice with PBS and medium containing 100 μg/ml kanamycin was added to each well. At the indicated time points (time zero was taken 20 min after incubation under antibiotic-containing medium) the number of intracellular colony forming units (CFU) was determined. IFN-γ stimulation was performed using 100 U/ml IFN-γ. For in vitro NO inhibition of BALB/c BMM, cells were treated by adding 2 mM AG into the medium 16-20 h prior to infection, during the 30 min infection time with B. pseudomallei and subsequent incubation under kanamycin-containing medium.
Measurement of NO was performed as recently described . To measure NO in cell culture supernantant, cells were seeded in 96 well plates 24 h prior to infection and IFN-γ at a concentration of 100 ng/ml was added. Cells were infected with B. pseudomallei und incubated under kanamycin-containing medium as described above. At indicated time point cell culture supernatant was collected and NO production was determined by the Griess reagent system. To determine NO concentration in the serum, 100 μl serum samples were rigorously mixed with 100 μl acetonitril and centrifuged for 10 minutes at 10 000 × g to remove serum proteins. Serum supernatant was taken and measured as described above.
Kaplan-Meier survival curves and the log rank test were used to compare the mortality of different groups of mice. To compare statistical significances of bacterial loads in internal organs or macrophages, either the Student's t-test or Mann-Whitney test was used as indicated for each experiment. Statistical significances were determined as follows: *p = 0.1, ** p = 0.01, *** p = 0.001.
PW was supported by the Royal Golden Jubilee Ph.D. Program (RGJ) under the Thailand Research Fund. We thank Claudia Cordt and Helga Schalimow for excellent technical assistance.
- Nahrevanian H: Involvement of nitric oxide and its up/down stream molecules in the immunity against parasitic infections. Braz J Infect Dis. 2009, 13: 440-8.PubMedGoogle Scholar
- Yang CS, Yuk JM, Jo EK: The role of nitric oxide in mycobacterial infections. Immune Netw. 2009, 9: 46-52. 10.4110/in.2009.9.2.46.PubMedPubMed CentralView ArticleGoogle Scholar
- Costa VM, Torres KC, Mendonca RZ, Gresser I, Gollob KJ, Abrahamsohn IA: Type I IFNs stimulate nitric oxide production and resistance to Trypanosoma cruzi infection. J Immunol. 2006, 177: 3193-200.PubMedView ArticleGoogle Scholar
- Huang J, DeGraves FJ, Lenz SD, Gao D, Feng P, D Li, Schlapp T, Kaltenboeck B: The quantity of nitric oxide released by macrophages regulates Chlamydia-induced disease. Proc Natl Acad Sci USA. 2002, 99: 3914-9. 10.1073/pnas.062578399.PubMedPubMed CentralView ArticleGoogle Scholar
- Vazquez-Torres A, Jones-Carson J, Mastroeni P, Ischiropoulos H, Fang FC: Antimicrobial actions of the NADPH phagocyte oxidase and inducible nitric oxide synthase in experimental salmonellosis. I. Effects on microbial killing by activated peritoneal macrophages in vitro. J Exp Med. 2000, 192: 227-36. 10.1084/jem.192.2.227.PubMedPubMed CentralView ArticleGoogle Scholar
- Khan IA, Schwartzman JD, Matsuura T, Kasper LH: A dichotomous role for nitric oxide during acute Toxoplasma gondii infection in mice. Proc Natl Acad Sci USA. 1997, 94: 13955-60. 10.1073/pnas.94.25.13955.PubMedPubMed CentralView ArticleGoogle Scholar
- Schluter D, Deckert-Schluter M, Lorenz E, Meyer T, Rollinghoff M, Bogdan C: Inhibition of inducible nitric oxide synthase exacerbates chronic cerebral toxoplasmosis in Toxoplasma gondii-susceptible C57BL/6 mice but does not reactivate the latent disease in T. gondii-resistant BALB/c mice. J Immunol. 1999, 162: 3512-8.PubMedGoogle Scholar
- Saeftel M, Fleischer B, Hoerauf A: Stage-dependent role of nitric oxide in control of Trypanosoma cruzi infection. Infect Immun. 2001, 69: 2252-9. 10.1128/IAI.69.4.2252-2259.2001.PubMedPubMed CentralView ArticleGoogle Scholar
- Kang KM, Lee GS, Lee JH, Choi IW, Shin DW, Lee YH: Effects of iNOS inhibitor on IFN-gamma production and apoptosis of splenocytes in genetically different strains of mice infected with Toxoplasma gondii. Korean J Parasitol. 2004, 42: 175-83. 10.3347/kjp.2004.42.4.175.PubMedPubMed CentralView ArticleGoogle Scholar
- White NJ: Melioidosis. Lancet. 2003, 361: 1715-22. 10.1016/S0140-6736(03)13374-0.PubMedView ArticleGoogle Scholar
- Dance DA: Melioidosis. Curr Opin Infect Dis. 2002, 15: 127-32.PubMedView ArticleGoogle Scholar
- Leelarasamee A, Bovornkitti S: Melioidosis: review and update. Rev Infect Dis. 1989, 11: 413-25. 10.1093/clinids/11.3.413.PubMedView ArticleGoogle Scholar
- Hoppe I, Brenneke B, Rohde M, Kreft A, Haussler S, Reganzerowski A, Steinmetz I: Characterization of a murine model of melioidosis: comparison of different strains of mice. Infect Immun. 1999, 67: 2891-900.PubMedPubMed CentralGoogle Scholar
- Liu B, Koo GC, Yap EH, Chua KL, Gan YH: Model of differential susceptibility to mucosal Burkholderia pseudomallei infection. Infect Immun. 2002, 70: 504-11. 10.1128/IAI.70.2.504-511.2002.PubMedPubMed CentralView ArticleGoogle Scholar
- Leakey AK, Ulett GC, Hirst RG: BALB/c and C57Bl/6 mice infected with virulent Burkholderia pseudomallei provide contrasting animal models for the acute and chronic forms of human melioidosis. Microb Pathog. 1998, 24: 269-75. 10.1006/mpat.1997.0179.PubMedView ArticleGoogle Scholar
- Breitbach K, Klocke S, Tschernig T, van Rooijen N, Baumann U, Steinmetz I: Role of inducible nitric oxide synthase and NADPH oxidase in early control of Burkholderia pseudomallei infection in mice. Infect Immun. 2006, 74: 6300-9. 10.1128/IAI.00966-06.PubMedPubMed CentralView ArticleGoogle Scholar
- Adler H, Beland JL, Del-Pan NC, Kobzik L, Brewer JP, Martin TR, Rimm IJ: Suppression of herpes simplex virus type 1 (HSV-1)-induced pneumonia in mice by inhibition of inducible nitric oxide synthase (iNOS, NOS2). J Exp Med. 1997, 185: 1533-40. 10.1084/jem.185.9.1533.PubMedPubMed CentralView ArticleGoogle Scholar
- MacFarlane AS, Schwacha MG, Eisenstein TK: In vivo blockage of nitric oxide with aminoguanidine inhibits immunosuppression induced by an attenuated strain of Salmonella typhimurium, potentiates Salmonella infection, and inhibits macrophage and polymorphonuclear leukocyte influx into the spleen. Infect Immun. 1999, 67: 891-8.PubMedPubMed CentralGoogle Scholar
- Eske K, Breitbach K, Kohler J, Wongprompitak P, Steinmetz I: Generation of murine bone marrow derived macrophages in a standardised serum-free cell culture system. J Immunol Methods. 2009, 342: 13-9. 10.1016/j.jim.2008.11.011.PubMedView ArticleGoogle Scholar
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