Figures
Abstract
Background
Melioidosis, caused by the Gram-negative bacterium Burkholderia pseudomallei, is an emerging cause of pneumonia-derived sepsis in the tropics. The gut microbiota supports local mucosal immunity and is increasingly recognized as a protective mediator in host defenses against systemic infection. Here, we aimed to characterize the composition and function of the intestinal microbiota during experimental melioidosis.
Methodology/Principal findings
C57BL/6 mice were infected intranasally with B. pseudomallei and sacrificed at different time points to assess bacterial loads and inflammation. In selected experiments, the gut microbiota was disrupted with broad-spectrum antibiotics prior to inoculation. Fecal bacterial composition was analyzed by means of IS-pro, a 16S-23S interspacer region-based profiling method. A marked shift in fecal bacterial composition was seen in all mice during systemic B. pseudomallei infection with a strong increase in Proteobacteria and decrease in Actinobacteria, with an increase in bacterial diversity. We found enhanced early dissemination of B. pseudomallei and systemic inflammation during experimental melioidosis in microbiota-disrupted mice compared with controls. Whole-genome transcriptional profiling of the lung identified several genes that were differentially expressed between mice with a normal or disrupted intestinal microbiota. Genes involved in acute phase signaling, including macrophage-related signaling pathways were significantly elevated in microbiota disrupted mice. Compared with controls, alveolar macrophages derived from antibiotic pretreated mice showed a diminished capacity to phagocytose B. pseudomallei. This might in part explain the observed protective effect of the gut microbiota in the host defense against pneumonia-derived melioidosis.
Author summary
Melioidosis is a common cause of community-acquired pneumonia and sepsis in Asia. The causative agent, Burkholderia pseudomallei, is listed as a potential bioterror weapon. The intestinal microbiota has been suggested to be a modulator of innate immune defenses against bacterial infections. Here we investigated in mice whether the intestinal microbiota affects the clinical course of melioidosis and vice versa. The composition of the gut microbiota changed strongly during melioidosis. Mice with a disrupted gut microbiota showed increased bacterial dissemination when compared with controls following intranasal infection with B. pseudomallei, indicating that the intestinal microbiota acts as a protective factor in host defense against melioidosis. Macrophages in microbiota-disrupted mice showed a diminished capacity to phagocytose B. pseudomallei. Further research is needed to explore whether this knowledge could be used to the advantage of patients.
Citation: Lankelma JM, Birnie E, Weehuizen TAF, Scicluna BP, Belzer C, Houtkooper RH, et al. (2017) The gut microbiota as a modulator of innate immunity during melioidosis. PLoS Negl Trop Dis 11(4): e0005548. https://doi.org/10.1371/journal.pntd.0005548
Editor: Pamela L. C. Small, University of Tennessee, UNITED STATES
Received: October 29, 2016; Accepted: April 4, 2017; Published: April 19, 2017
Copyright: © 2017 Lankelma et al. 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 credited.
Data Availability: All relevant data are within the paper and its Supporting Information files.
Funding: This work was financially supported by the Netherlands Organization for Scientific Research (NWO; VIDI grant to WJW, grant number: 91716475). The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Melioidosis is a frequent cause of community-acquired sepsis in Southeast Asia and northern Australia [1, 2]. Pneumonia is the presenting symptom in most adult patients [3] and results in a rapidly progressive illness with a high mortality up to 40% [1, 3]. The disease is caused by Burkholderia pseudomallei, a facultative intracellular Gram-negative bacterium that is commonly found in the soil from countries located between 20° north latitude and 20° south latitude [1, 2, 4]. Due to its high lethality, poor sensitivity to antibiotics, wide availability and easy dissemination, it has been classified as a Tier 1 biological threat agent. The global burden of melioidosis is probably much larger than previously anticipated: it was recently estimated that each year 165,000 (95% credible interval 68,000–412,000) people suffer from this debilitating disease resulting in 89,000 (36,000–227,000) fatalities [5]. Melioidosis is probably underreported in as many as 45 countries due to a lack of adequate diagnostic facilities [5]. In the near future, the management of patients may be compromised by emergence of resistance due to increased use of antibiotics in endemic regions [6]. Thus, there is an urgent need to better understand the pathogenesis of melioidosis.
The intestinal microbiota not only provides direct colonization resistance against invading pathogens, but is increasingly recognized as an important modulator of systemic immunity [7–9]. It was first suggested by Clarke and colleagues that bacterial cell wall components such as peptidoglycan are translocated into the bloodstream and at distant sites ‘prime’ immune effector cells [10]. This way, the effectiveness of bone-marrow derived neutrophils in killing pathogens such as Streptococcus pneumoniae and Staphylococcus aureus is increased [10]. Subsequent studies could demonstrate a protective effect of a healthy microbiota in a variety of in vivo murine models of infection: S. aureus, Pseudomonas aeruginosa or Klebsiella pneumoniae pneumonia [11–13] and Listeria monocytogenes or Escherichia coli induced sepsis [14, 15]. In line, we recently demonstrated that the gut microbiota plays a protective role in pathogenesis of pneumococcal pneumonia by enhancing primary alveolar macrophage function [16].
To the best of our knowledge, the role of the gut microbiota in the host defense against melioidosis has never been investigated. The importance of this subject is underscored by the notion that melioidosis has a notoriously protracted course for which cure can only be achieved through long-term antibiotic therapy. The minimum of two weeks of intravenous antibiotics followed by three months of oral antibiotics [1, 2] will have a profound effect on the microbiota. We hypothesized that a healthy microbiota supports the host defense against B. pseudomallei infection. In order to address this question, we made use of our well-established murine model of pneumonia-derived melioidosis [17, 18] and in selected experiments disrupted the gut microbiota with oral antibiotics before infection following a standard protocol [10, 16]. We show that the intestinal microbiota changes significantly during melioidosis, independent of antibiotic treatment. Secondly, we show that antibiotic disruption of the intestinal microbiota is associated with a less effective innate immune defense against experimental B. pseudomallei infection.
Results
Profound changes in gut microbiota composition during murine pneumonia-derived melioidosis
To first obtain insight into the composition of the intestinal microbiota during melioidosis, we inoculated mice intranasally with live B. pseudomallei to induce pneumonia-derived melioidosis and collected fecal pellets at baseline (t = 0) and after 72 hours, when all mice had symptoms of systemic infection. The gut microbiota was analysed by IS-pro technique, using the number of nucleotides between the genes for the 16S and 23S ribosomal subunits in bacterial DNA as a unique classification characteristic [19, 20]. Infection with B. pseudomallei was associated with profound changes in the composition of the intestinal microbiota (Fig 1). Clustering analysis, by unweighted pair group method with arithmetic mean (UPGMA) on cosine distances of all samples, resulted in separation of all pre- and post-infection samples (t = 0 vs t = 72), indicating that pre- and post-infection samples from each mouse were highly dissimilar. In all mice, a strong increase in Proteobacteria was seen as well as a decrease in Actinobacteria. The composition of Bacteroides and Firmicutes also changed in strikingly similar patterns. Of note, B. pseudomallei was not detected in any fecal sample. Total microbial diversity was significantly increased (p = 0.006), mostly due to increased diversity of Bacteroides (p = 0.055) and Proteobacteria (p = 0.007) (Fig 1).
Fecal pellets were sampled from eight mice before (t = 0) they were infected intranasally with 150 CFU of B. pseudomallei and 72 hours after (t = 72). Microbial composition was analysed by IS-pro, using the number of nucleotides between the genes for ribosomal subunit 16 and 23 in the DNA (interspacer region) of the bacterium as a unique classification characteristic. (A) Clustering analysis, by unweighted pair group method with arithmetic mean (UPGMA) on cosine distances, shows the similarity of samples; individual mice are indicated by a number. Colors represent the most important bacterial phyla (purple, Actinobacteria; red, Bacteroidetes; blue, Firmicutes, Actinobacteria, Fusobacteria, and Verrucomicrobia (FAFV); yellow, Proteobacteria). Length of the interspacer regions in basepairs is indicated on the y-axis; lines indicate the presence of PCR products. Color intensity increases with the presence of PCR product. (B) Diversity of microbial communities before and 72 hours after induction of melioidosis, expressed as Shannon index (green: total bacteria; red: Bacteroidetes; Blue: Firmicutes, Actinobacteria, Fusobacteria, and Verrucomicrobia (FAFV); yellow: Proteobacteria). Data are presented as box- and whisker plots showing the smallest observation, lower quartile, median, upper quartile and largest observation. ** p<0.01 pre- versus post-infection.
Antibiotic gut microbiota disruption is associated with increased growth and dissemination of B. pseudomallei
To investigate whether gut microbiota composition impacts on host defense during melioidosis, we pre-treated mice with broad-spectrum antibiotics in drinking water in order disrupt the intestinal microbiota (Fig 2A) [10, 16]. We then inoculated mice intranasally with live B. pseudomallei (150 colony forming units (CFU), LD50) [17, 18] and sacrificed them after 24 or 72 hours. The antibiotic treatment caused dramatic changes in the intestinal microbiota compared to untreated control mice, with a marked reduction in the number of species (Fig 2B). Relative to control mice, antibiotic pre-treated mice displayed significantly increased bacterial loads in lung and liver 24 hours after infection (Fig 2C–2E). Bacterial loads in blood and broncho-alveolar lavage fluid (BALF) were not affected (Fig 2D and S1 Fig). To determine whether the effect of gut microbiota disruption on bacterial growth was dependent on the infectious dose, we next infected mice with 500 CFU B. pseudomallei (LD100). Using this higher infectious dose, the observed increase in bacterial dissemination in antibiotic treated mice was also present at the early time-point following infection (Fig 2F–2H). In addition, we tested whether the observed effects were specific for this combination of antibiotics by performing the same experiment, using only metronidazole and ampicillin in drinking water (S2 Fig). Similar to the previous experiments, we again observed increased bacterial loads after 24 hours in lungs of antibiotic pre-treated mice compared to controls—indicating that the intestinal bacteria targeted by these two antibiotics are involved in the observed effects.
(A) Study design. (B) Before infection, the fecal microbiota of control- and antibiotic treated mice was analysed by IS-pro. Colors represent the most important bacterial phyla (purple, Actinobacteria; red, Bacteroidetes; blue, Firmicutes, Actinobacteria, Fusobacteria, and Verrucomicrobia (FAFV); yellow, Proteobacteria). Length of the interspacer regions in basepairs is indicated on the x-axis; height of the peaks indicates the presence of PCR products. Samples are pooled from eight mice per group; representative of two experiments. Control and antibiotic pre-treated mice were inoculated intranasally with 150 CFU (C-E) or 500 CFU (F-H) B. pseudomallei and sacrificed at the indicated time points. Bacterial loads in lung homogenate (C, F), blood (D, G) and liver homogenate (E, H) are depicted as scatter dot plots with a line at the median. Numbers in the boxes below (D) and (G) indicate the number of positive blood cultures for the total number of mice. White dots represent control mice, grey dots antibiotic treated mice. N = 6–8 mice per group. * p<0.05, ** p<0.01, *** p<0.001 control versus antibiotic treated.
Gut microbiota disruption is associated with increased proinflammatory cytokine release during experimental melioidosis
Having found an inoculum-dependent effect of antibiotic pre-treatment on bacterial growth both at the primary site of infection and at distant sites, we next studied the impact of antibiotic pre-treatment on local and systemic cytokine release in mice infected with 500 CFU B. pseudomallei. In lung homogenate, cytokine levels were similar between groups at all time-points (Table 1). Plasma levels of tumor necrosis factor (TNF)-α and interferon (IFN)-γ however were significantly increased in mice with a disrupted gut microbiota, 72 hours after infection (Table 1).
Limited impact of antibiotic induced gut microbiota disruption on survival and organ injury
To evaluate whether the above findings would lead to impaired survival in the experimental group, we followed groups of 20 mice for 14 days after intranasal inoculation with 150 CFU B. pseudomallei. The lower dose was chosen since this LD50 [17, 18] would allow to demonstrate a potential detrimental effect of gut microbiota depletion. Mice in the antibiotic pre-treated group showed a trend toward increased mortality but this did not reach statistical significance (Fig 3A). Likewise, a clinical observation score reflected a trend towards increased morbidity in the experimental group (Fig 3B). The marked organ injury in this model of melioidosis is reflected by elevated plasma markers of hepatocellular damage (aspartate aminotranspherase, AST and alanine aminotranspherase, ALT), renal failure (urea) and general cellular damage (lactate dehydrogenase, LDH), especially shortly before mortality occurs [17, 18] (Fig 3C–3F). However, in line with survival, no significant differences in these parameters were observed, indicating a limited influence of gut microbiota disruption on the extent of organ damage.
Survival (A) and clinical observation score (B) of control (white dots) and antibiotic treated mice (grey dots) after intranasal inoculation with 150 CFU B. pseudomallei (n = 20 mice per group, depicted is the mean). No statistically significant differences were detected. Aspartate aminotranspherase (AST, C), alanine aminotranspherase (ALT, D), urea (E) and lactate dehydrogenase (LDH, F) were measured in plasma after inoculation with 500 CFU B. pseudomallei as markers for liver-, renal- and general damage. Data are presented as box- and whisker plots showing the smallest observation, lower quartile, median, upper quartile and largest observation. White bars represent control mice, grey bars antibiotic treated mice. N = 5–6 samples per group. ND = not detectable.
Intestinal microbiota does not influence neutrophils during melioidosis
As the microbiota has been reported to be an important regulator of neutrophil homeostasis [10, 14, 15, 21] and neutrophils play an essential role in the host defense against melioidosis [22, 23], we hypothesized that these might play a role in the observed differences. 72 hours after infection, all mice showed extensive lung infiltrates characterized by neutrophil influx, necrosis, bronchitis, endothelialitis and oedema (Fig 4A and 4B). However, when we analysed HE-stained lung tissue sections using a semi-quantitative pathology scoring system, no differences were found between control and antibiotic pre-treated mice (Fig 4C). Quantification of a Ly-6GC staining demonstrated a similar pulmonary influx of neutrophils in both groups (Fig 4D–4F). In line, a similar pulmonary influx of cells was observed in BALF during melioidosis (Fig 4G). Equal neutrophil degranulation was confirmed by lung myeloperoxidase levels in control and antibiotic treated mice after infection with B. pseudomallei (Fig 4H). Similar results were obtained for mice inoculated with 150 or 500 CFU; only the latter are shown. Lastly, since a healthy microbiota is proposed to stimulate granulopoiesis [10, 14, 15, 21], we studied neutrophil numbers in bone marrow and blood of naïve control and antibiotic treated mice; however, we did not find any differences (Fig 4I).
Lungs were obtained at the indicated time points after intranasal inoculation with 500 CFU B. pseudomallei. Paraffin-embedded lung tissue sections were stained with haematoxylin/eosin to score different parameters for pathology (A-B, 2x magnification, representative images). The combined score, given by a blinded pathologist, was not different between the two groups (C). Sections from the same samples were stained for Ly-6GC as a neutrophil marker (representative microphotographs, 2x magnification) (D-E). The percentage Ly-6GC-positive surface of the total lung surface was calculated using ImageJ (F). The number of cells per mL BALF was counted using a Coulter counter (G). Myeloperoxidase was quantified in lung homogenates as a measure for neutrophil degranulation (H). Bone marrow and blood was obtained from naïve control and antibiotic pre-treated mice and using FACS analysis the percentage of Ly6GC+, CD11b+ cells within the viable CD45+ population was determined (I). Data are presented as box- and whisker plots showing the smallest observation, lower quartile, median, upper quartile and largest observation. White bars represent control mice, grey bars antibiotic treated mice. No statistically significant differences were found.
Altered lung transcriptome and impaired phagocytosis of B. pseudomallei by alveolar macrophages in gut microbiota disrupted mice
To obtain insight into the mechanism by which the gut microbiota exerts its effects during pneumonia-induced melioidosis, we investigated the effect of antibiotic microbiota disruption on lung transcriptomes. Comparing lung transcriptomes of uninfected intestinal microbiota disrupted mice to control mice revealed 40 significantly altered genes (Fig 5A, 21 genes under-expressed and 19 genes over-expressed in antibiotic pre-treated mice). Ingenuity pathway analysis revealed that genes with elevated expression in antibiotic treated mice significantly enriched several cellular biological pathways, including acute phase response signaling, coagulation system and, notably, IL-12 signaling and production in macrophages as well as production of nitric oxide (NO) and reactive oxygen species (ROS) in macrophages (Fig 5B). Of note, these gene expression differences were not biased by altered neutrophil infiltration (S3 Fig). However, since the analysis was performed on whole lung tissue, it is possible that the genes in these pathways were upregulated in other cell types than macrophages. Altogether, these data suggest that disruption of the intestinal microbiota by antibiotic treatment may impact on lung homeostasis, with macrophages more likely influenced.
Naïve antibiotic treated- and control mice were sacrificed after the two-day antibiotic washout period and lungs or alveolar macrophages were harvested. (A) Volcano plot depicting significant (multiple comparison adjusted p<0.05) differentially expressed genes in lungs from naïve control and antibiotic pre-treated mice (microbiota disrupted). Red indicates increased expression; blue indicates decreased expression. (B) Significantly enriched canonical signalling pathways in antibiotic treated mice, represented as a bar plot (Ingenuity pathway analysis). (C-D) Alveolar macrophages from naïve control- and antibiotic treated mice were stimulated for 20 hours with medium, LPS 10 ng/mL, PAM3CSK4 1 ug/mL or heat-killed B. pseudomallei 4x106 CFU/mL and TNFα and IL-6 were measured in supernatant. (E) Alveolar macrophages from naïve control- and antibiotic treated mice (each well pooled from two mice) were incubated with 2,5x107 CFU/mL FITC-labeled heat killed B. pseudomallei and their phagocytic index determined via flowcytometry as described in the Methods. (F) Control and antibiotic microbiota disrupted mice were given 5x106 heat killed FITC-labeled B. pseudomallei intranasally and sacrificed after three hours. Cytospins of BALF were stained with PerCP Cy5.5-CD45 and DAPI to assess whether bacteria were located intracellularly (F, representative image). Alveolar macrophages in BALF were analysed by flowcytometry and phagocytic indexes were calculated (G). Data are presented as box- and whisker plots showing the smallest observation, lower quartile, median, upper quartile and largest observation. White bars represent control mice, grey bars antibiotic treated mice. N = 8 mice per group. ** p<0.01 control versus antibiotic treated.
As alveolar macrophages are crucial in the first line of defense during pneumonia and are important in the innate immune response in melioidosis [24], we further studied the influence of gut microbiota disruption on the function of alveolar macrophages. Responsiveness of alveolar macrophages derived from gut microbiota-disrupted mice towards PAM3CSK4, LPS or heat-killed B. pseudomallei was not different from controls in terms of proinflammatory cytokine production (Fig 5C and 5D). In line, no differences in metabolic profiles of alveolar macrophages derived from naïve control and antibiotic pre-treated mice were observed; for this we used extracellular flux technology, which enables assessment of mitochondrial function in live cells, simultaneously measuring oxygen consumption and glycolysis (S4 Fig). In a last set of experiments, we investigated the influence of gut microbiota disruption on the capacity of alveolar macrophages to phagocytose B. pseudomallei, since an effect of the gut microbiota hereon has been described previously in a setting of S. pneumoniae, S. aureus and K. pneumoniae infection [10, 12, 16]. Cells from BALF were plated and adhering cells were incubated with heat-killed, FITC-labeled B. pseudomallei, after which the phagocytosis index was determined by flow cytometry (Fig 5E). To confirm this finding, we inoculated mice with heat-killed, FITC-labeled B. pseudomallei and performed broncho-alveolar lavage three hours later, followed by flowcytometry. Again, we found that alveolar macrophages derived from antibiotic pre-treated mice had a diminished capacity to phagocytose B. pseudomallei when compared with controls (Fig 5F and 5G). These data suggest that an unperturbed gut microbiota enhances the capacity of alveolar macrophages to phagocytose B. pseudomallei in vivo. The observed effect was compartment specific; in contrast to alveolar macrophages, ex vivo phagocytosis capacity of blood neutrophils, peritoneal macrophages and bone-marrow derived macrophages derived from gut microbiota-disrupted mice was equal compared with controls, as well as cytokine production (S5 Fig). Of note, we did not observe any differences in pulmonary microbiota composition between control- and antibiotic treated mice (S6 Fig).
Discussion
To the best of our knowledge, this study is the first to investigate the role of the intestinal microbiota during melioidosis. Our data suggest a bidirectional interplay between intestinal microbiota and innate host defenses against B. pseudomallei. Firstly, we observed significant changes in fecal microbiota composition during melioidosis, independent of antibiotic treatment. A strikingly similar pattern of increased Proteobacteria, decreased Actinobacteria and increased diversity was observed in all mice. Secondly, a well-balanced gut microbiota appears to have a protective effect during melioidosis, especially when B. pseudomallei has its first encounter with alveolar macrophages in the lung. Antibiotic disruption of the intestinal microbiota affects the capacity of these cells to internalize the pathogen, which was associated with increased bacterial proliferation and dissemination after 24 hours. In this model, the subsequent effects of a disturbed gut microbiota on distant organ injury and survival were limited.
As far as we know, significant changes in the intestinal microbiota within 72 hours of systemic bacterial infection have never been demonstrated before in any model of sepsis. Human studies describing microbiota perturbation during sepsis are confounded by the universal use of antibiotics [25, 26]. We here demonstrate that the systemic inflammatory response itself can lead to marked alterations in the gut microbiota. Our findings are in line with a recent report on intestinal dysbiosis, caused by influenza infection [27]. Another study associated pulmonary Mycobacterium tuberculosis infection in mice with loss of intestinal microbiota diversity after six days, with a subsequent recovery during the following weeks [28]. As virtually no M. tuberculosis was detected in feces, it was suggested that these changes in intestinal microbiota were due to alterations in the adaptive immune system, which in the tuberculosis model becomes effective at controlling the infection around the same time [28]. We therefore expected to find lower microbial diversity three days after infection with B. pseudomallei, but observed the opposite. A possible explanation could be the elimination of several “big players” of the gut microbiota by the host immune system during severe systemic bacterial infection, giving way to other bacteria to proliferate.
The amount of data that demonstrates a beneficial effect of the intestinal microbiota on the systemic innate immune system in infection is rapidly expanding. Previous studies described a protective effect of the intestinal microbiota during E. coli and L. monocytogenes sepsis via stimulation of granulopoiesis in the bone marrow [14, 15]. Crosstalk between microbiota and bone marrow has been suggested to happen via interleukin-17, -22 and granulocyte colony-stimulating factor (G-CSF) [14, 15]. In addition, neutrophil function is affected in both germ free and antibiotic pre-treated mice, resulting in decreased killing of S. pneumoniae and S. aureus [10]. In contrast, we did not find any indications for a central role for neutrophils in the antibacterial effect of the microbiota that we observed during melioidosis. The so-called microbiota-bone marrow axis could be more important in younger mice, as were used in above mentioned studies. Also, many studies use germ free mice, which could display more pronounced phenotypes than antibiotic treated mice. Our findings are in line with earlier reports that suggest a positive effect of healthy intestinal microbiota on alveolar macrophages [11, 12, 16, 29]. As alveolar macrophages constantly adapt to their environment, one can imagine them being affected by the level of circulating compounds derived from the intestinal microbiota (e.g. cell wall components or metabolites). Microbial disturbances may induce an altered phenotype of these cells, leading to decreased phagocytosis of B. pseudomallei, which in turn may lead to decreased intracellular killing. This is in line with our previous findings in a mouse model of pneumococcal pneumonia, in which we found that phagocytic capacities of alveolar macrophages are affected by antibiotic gut microbiota disruption [16]. We found changes in a cholesterol synthesis pathway in the transcriptome of these alveolar macrophages, which could be important as cholesterol-rich membrane rafts are involved in phagocytosis [30].
This study has a number of limitations. The antibiotics were chosen based on similar experiments in the literature [10, 12, 16]; however, other antibiotic regimens may have different effects. Also, mice from different suppliers could have a different intestinal microbiota and as a result elicit different immune responses, as was recently demonstrated in a mouse model for malaria [31]. In addition, we cannot exclude a direct effect of antibiotics on the host response; however, our data are in line with previous reports on the effect of the gut microbiota on the innate immune response during infection [10, 12, 16]. Alterations in the respiratory tract microbiota could be another contributing factor to the observed phenotype [32]. We did however not find any differences in pulmonary microbiota between control- and antibiotic treated mice, making it less likely that this is of influence. Lastly, the situation in actual melioidosis patients is very different from this experimental murine setting; comorbidities, medications and interindividual differences all may influence a possible interplay between microbiota and innate immune system.
In summary, we observed increased bacterial dissemination in mice with a disrupted gut microbiota during pneumonia-derived B. pseudomallei sepsis, indicating that the intestinal microbiota improves host defense against melioidosis. Alveolar macrophages from microbiota-disrupted mice showed a diminished capacity to phagocytose B. pseudomallei. It will be very interesting to study if disruption of the microbiota by antibiotics affects susceptibility to melioidosis. There is evidence for the incidence of severe sepsis being higher after events known to be associated with disturbance of the intestinal microbiota, such as hospitalization for Clostridium difficile infection [33]. Hopefully, further research into the interplay between intestinal microbiota and melioidosis will tell us whether and how this knowledge could be used to the advantage of patients.
Methods
A detailed description of methods is available in the online supplement.
Mice
Specific pathogen-free C57BL/6 mice were purchased from Charles River (Maastricht, The Netherlands). In selected experiments, antibiotic treatment was started at six weeks of age (see below); infection was induced in all experiments at nine weeks of age. The animals were housed in IVC cages in rooms with a controlled temperature and light cyclus. They were acclimatized for one week prior to usage, and received standard rodent chow and water ad libitum.
Ethics statement
The Institutional Animal Care and Use Committee of the Academic Medical Center approved all experiments (permit number DIX21, sub-protocols 21BB, 21CJ and 21DJ) and ethical approval was obtained to use B. pseudomallei strain 1026b for animal experiments (08–150; see Supplemental Methods). B. pseudomallei strain 1026b strain was received by our lab in 2004 as a kind gift from the Donald E. Woods lab, University of Calgary, Alberta, Canada. Samples were anonymized if applicable. Experiments were carried out in accordance with the Dutch Experiments on Animals Act.
Induction of melioidosis
Experimental melioidosis was induced by intranasal inoculation with 150 or 500 colony forming units (CFU) of B. pseudomallei strain 1026b as described [17, 18]. At 24 or 72 hours post-infection, mice were euthanized and sacrificed by bleeding from the heart, after which organs were harvested. For survival studies, mice were observed for 14 days.
Microbiota analysis
Fresh stool pellets were obtained and stored at -80°C. DNA isolation followed by IS-pro bacterial profiling was performed as described before (IS-diagnostics, Amsterdam, The Netherlands) [19, 20]. In short, the length of the 16S-23S rDNA interspace (IS) region is used to classify bacteria by PCR, combined with phylum-specific fluorescent labelling of PCR primers. IS fragment analysis was performed on an ABI Prism 3500 Genetic Analyzer (Applied Biosystems). Data were analysed with IS-pro proprietary software (IS-diagnostics, Amsterdam, The Netherlands).
Antibiotic treatment
Mice received broad-spectrum antibiotics (ampicillin 1 g/L; neomycin 1 g/L, both from Sigma, Zwijndrecht, The Netherlands; metronidazole 1 g/L, Sanofi-Aventis, Gouda, The Netherlands and vancomycin 0.5 g/L, Xellia pharmaceuticals, Copenhagen, Denmark) in drinking water for 19 days [10, 16]. This cocktail disrupts the intestinal microbiota and significantly lowers microbial diversity [16]. In selected experiments, only ampicillin and metronidazole were used. After a washout period of two days with normal drinking water, mice were inoculated with B. pseudomallei or sacrificed naïve. Weights of control- and antibiotic treated mice were equal at the moment of inoculation.
(In vivo) Phagocytosis and stimulation experiments
Alveolar macrophages, peritoneal macrophages, blood and bone marrow derived macrophages were obtained and incubated as described previously [16, 17, 34, 35]. Briefly, cells were seeded, washed and stimulated overnight with LPS or heat-killed B. pseudomallei. For in vivo phagocytosis, mice were inoculated intranasally with 5x106 CFU heat-killed, FITC (fluoresceine isothiocyanate)-labeled B. pseudomallei. After three hours, mice were anesthetized and broncho-alveolar lavage (BAL) was performed. FITC-positivity of alveolar macrophages was determined by FACS analysis. Details are provided in the online supplement.
Whole lung RNA profiling
RNA was isolated from lung homogenates using the RNeasy mini kit (Qiagen, Venlo, The Netherlands). Biotinylated cRNA was hybridized onto the Illumina MouseRef-8v2 Expression BeadChip and an Illumina iScan array scanner (Eindhoven, The Netherlands) was used to scan samples [16, 36]. Detailed methods are available in the supplemental material.
Statistical analysis
Differences between groups were analyzed by Mann-Whitney U test. Differences in microbiota diversity over time were analysed by paired t-test. For survival, Kaplan-Meier analysis followed by log-rank test was performed and the clinical scores by matched two-way ANOVA. Analyses were performed using GraphPad Prism 5. Values of P<0.05 were considered statistically significant.
Supporting information
S1 Fig. Antibiotic pre-treatment does not affect B. pseudomallei loads in broncho-alveolar lavage fluid during experimental melioidosis.
Control and antibiotic pre-treated mice were inoculated intranasally with 150 CFU (A) or 500 CFU (B) B. pseudomallei and sacrificed at the indicated time points. Bacterial loads in broncho-alveolar lavage fluid (BALF) are depicted as scatter dot plots with a line at the median. White dots represent control mice, grey dots antibiotic treated mice. N = 6–8 mice per group.
https://doi.org/10.1371/journal.pntd.0005548.s001
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S2 Fig. Ampicillin and metronidazole pre-treatment is associated with decreased pulmonary clearance of B. pseudomallei during experimental melioidosis.
Mice were pre-treated with metronidazole and ampicillin in drinking water, in exactly the same experimental setup as described in the Methods section. Control and antibiotic pre-treated mice were inoculated intranasally with 500 CFU B. pseudomallei and sacrificed 24 hours after infection. Bacterial loads in blood, liver and spleen homogenate (A) and lung homogenate (B) are depicted as scatter dot plots with a line at the median. White dots represent control mice, grey dots antibiotic treated mice. N = 8 mice per group. *p<0.05 control versus antibiotic treated.
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S3 Fig. Cellular composition of broncho-alveolar lavage fluid from naïve control and antibiotic pre-treated mice.
Bar chart depicting the median percentage of alveolar macrophages (AMs) and neutrophils in broncho-alveolar lavage fluid from naïve control and antibiotic pre-treated mice.
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S4 Fig. Cellular metabolism of alveolar macrophages from control and antibiotic pre-treated mice.
(A) Extracellular acidification rate (ECAR) and (B) oxygen consumption rate (OCR) of alveolar macrophages from control and antibiotic treated mice, as a measure for glycolytic function and mitochondrial respiration function, respectively. Arrows indicate the sequential adding of oligomycin (O, 1,5 μM), FCCP (F, 1,5 μM) and antimycin A + rotenone (A/R, 2,5 μM/ 1,25 μM). Data are normalized to DNA content. White dots represent control mice, grey antibiotic treated mice. Data are presented as median ± interquartile range (n = 6–7 per group).
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S5 Fig. Bone marrow derived macrophages, peritoneal macrophages and blood from control and antibiotic pre-treated mice do not differ in terms of cellular responsiveness or phagocytosis capacity.
Naïve antibiotic treated- and control mice were sacrificed after the two-day antibiotic washout period and bone marrow, blood and peritoneal macrophages were harvested. Bone marrow derived macrophages (BMDM), peritoneal macrophages and blood were stimulated with LPS 100 ng/mL or 3x107 CFU/mL heat-killed B. pseudomallei for 14 hours (A-B, D-E, G-H). Alternatively, whole blood or macrophages were incubated with 2,5x107 CFU/mL FITC-labeled heat killed B. pseudomallei to investigate their phagocytic capacities (C, F, I). Internalization of bacteria was assessed by flowcytometry as described in the Methods section. TNF-α and IL-6 production by BMDMs (A-B), peritoneal macrophages (D-E) and whole blood (G-H) upon stimulation with LPS or heat-killed B. pseudomallei did not differ between groups. The phagocytic capacity of BMDMs (C), peritoneal macrophages (F) and whole blood derived neutrophils was also similar (I). Data are presented as box- and whisker plots showing the smallest observation, lower quartile, median, upper quartile and largest observation. White bars represent control mice, grey bars antibiotic treated mice. N = 4–8 mice per group. All are representative of two experiments.
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S6 Fig. Composition of pulmonary microbiota in naïve control and antibiotic pre-treated mice.
To investigate the pulmonary microbiota, whole lungs were harvested from naïve control and antibiotic (ampicillin, vancomycin, metronidazole and neomycin) pre-treated mice on day 19. Total bacterial 16S rDNA was isolated and sequenced. (A) Lung microbiota composition at the Class level (second highest bacterial taxonomic rank). (B) Lung microbiota composition at the Genus level (lowest detectable bacterial taxonomic rank). Data are presented as box-and-whisker plots depicting median, interquartile range and range of the percentage of total 16S rDNA reads in each sample (n = 6 mice/group). White, control mice; grey, antibiotic pre-treated mice. Only Classes and Genera that had a median prevalence of 5% or more amongst all samples are depicted. No statistically significant differences were detected.
https://doi.org/10.1371/journal.pntd.0005548.s006
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Acknowledgments
We are very grateful to Marieke ten Brink, Joost Daalhuisen, Regina de Beer, Malieka Degen, Linda Poort and Daisy Picavet for their technical assistance. Onno de Boer greatly helped in the analysis of the neutrophil stainings.
Author Contributions
- Conceptualization: JML TvdP WJW.
- Formal analysis: JML BPS CB.
- Funding acquisition: WJW.
- Investigation: JML EB TAFW RHH CB JJTHR AEB.
- Project administration: JML TAFW.
- Resources: RHH CB AEB.
- Software: BPS CB.
- Supervision: AFdV TvdP WJW.
- Visualization: JML WJW.
- Writing – original draft: JML WJW.
- Writing – review & editing: EB TAFW BPS CB RHH JJTHR AFdV TvdP AEB.
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