Vitamin D induces the expression of antimicrobial peptides with activity against Staphylococcus aureus. Thus, we studied the association between serum 25-hydroxyvitamin D (25(OH)D) and S. aureus nasal colonization and carriage. Nasal swabs, blood samples and clinical data from 2,115 women and 1,674 men, aged 30–87 years, were collected in the Tromsø Staph and Skin Study 2007–08, as part of the population-based sixth Tromsø Study. Multivariate logistic regression analyses were stratified by recognized risk factors for S. aureus carriage: sex, age and smoking. In non-smoking men, we observed a 6.6% and 6.7% decrease in the probability of S. aureus colonization and carriage, respectively, by each 5 nmol/l increase in serum 25(OH)D concentration (P < 0.001 and P = 0.001), and serum 25(OH)D > 59 nmol/l and ≥75 nmol/l as thresholds for ~30% and ~50% reduction in S. aureus colonization and carriage. In non-smoking men aged 44–60 years, the odds ratio for S. aureus colonization was 0.44 (95% confidence interval, 0.28−0.69) in the top tertile of serum 25(OH)D versus the bottom tertile. In women and smokers there were no such associations. Our study supports that serum vitamin D is a determinant of S. aureus colonization and carriage.
The burden of disease from Staphylococcus aureus is high and worrying due to widespread antimicrobial resistance . Nasal carriage of S. aureus is a major risk factor for infections with the bacterium [2–4]. Since about 20% of healthy adults are persistent nasal carriers , prevention or elimination of the carrier state may contribute substantially in reducing the S. aureus disease burden. However, there is still limited evidence in relation to modifiable risk factors for the carrier state . Smoking is so far the only protective factor observed across different studies [6, 7], while serum glucose levels  and oral contraceptives use  have been positively associated with S. aureus nasal carriage. Interestingly, an inverse dose-dependent association was recently observed between serum vitamin D levels and risk of methicillin resistant S. aureus (MRSA) nasal carriage, while no association was found for methicillin sensitive S. aureus (MSSA) .
Vitamin D has direct effects on immunity modulated by the vitamin D receptor (VDR) present in immune cells. Binding of VDR to its responsive element induces expression of antimicrobial peptides (i.e. cathelicidin and β-defensin) with activity against S. aureus in vitro [10–12].
Serum 25-hydroxyvitamin D (25(OH)D) provides an overall estimate of vitamin D status and integrates vitamin D derived from endogenous production from sun exposure, and from dietary intake . Importantly, populations living at higher latitudes with periodic lack of photosynthesis show larger proportions of vitamin D insufficiency and increased risk of several chronic and some infectious diseases [13–18]. In the present Norwegian study population, the Tromsø Study, we observed variation in serum 25(OH)D levels by season, age, body weight, intake of vitamin D, physical activity and smoking [19, 20], and variation in S. aureus carriage rates by sex and age .
Further studies of the role of vitamin D in the host-microbe interplay may give novel clues to targets for prevention of S. aureus carriage and infection as well as underlying biological mechanisms. We therefore examined the cross-sectional relationship between serum 25(OH)D concentration and S. aureus nasal colonization and carriage in 4,000 men and women participating in the Tromsø Staph and Skin Study (TSSS), a sub-study of the sixth Tromsø Study, evaluating both possible dose-response and thresholds for adequate immune response against S. aureus.
Subjects and methods
Population and study design: The Tromsø Staph and Skin Study (TSSS)
The Tromsø Study is a longitudinal, multipurpose, population-based study in the municipality of Tromsø, Norway, 69°N. In the sixth Tromsø Study (October 2007–December 2008), a total of 12,984 subjects (65.7%) attended . TSSS took place during October 2007 till July 2008 and nasal swab cultures were collected from all attendees aged 30–49 years and random samples of older attendees (relative distribution of birth cohorts as in the municipality). The 4,026 participants who had a first nasal swab culture were invited to a repeated sample within a few weeks (Fig. 1). Participants with missing data on serum 25(OH)D (n = 60) or smoking status (n = 48) and those taking antibiotics, either systemic or eye drops/ointments, within 24 h before nasal swabbing (first swab n = 27, second swab n = 14) were excluded. We included 3,789 participants with minimum one valid nasal swab culture for analysis of S. aureus nasal colonization, and 2,780 participants with two valid nasal swab cultures for the analysis of S. aureus carriage (Fig. 1).
Information was obtained from questionnaires, interview, clinical examinations and blood samples performed by specially-trained healthcare workers according to standardised procedures. The study was approved by the Regional Committee of Medical and Health Research Ethics, North Norway.
Detection of S. aureus nasal colonization and carriage
Both anterior nares were sampled with a NaCl-moistened sterile rayon-tipped swab that was placed in Amies charcoal transport medium (Copan, Brescia, Italy). All specimens were cultured within 3 days at the Department of Microbiology and Infection Control, University Hospital of North Norway (UNN), Tromsø. The swabs were plated on chromID S. aureus and chromID™ MRSA agars (bioMérieux, Marcy I’Etoile, France) and incubated for 48 hours at 35°C. Colony morphology on the agar plates was the basis for S. aureus and MRSA identification. Suspected positive colonies were confirmed as S. aureus by the Staphaurex Plus agglutination test (Murex Diagnostic Ltd, Dartford, UK). No MRSA was registered.
S. aureus colonization state was defined as positive or negative for S. aureus in the first sample. Carrier state was based on the culturing results of two consecutive samples; carrier = two positive samples and non-carrier = one or no positive sample .
Assessment of serum 25-hydroxyvitamin D concentrations
Non-fasting blood samples were drawn from an antecubital vein, and sera were consecutively analysed for 25(OH)D by immunometry (electrochemiluminescence immunoassay), using an automated clinical chemistry analyser (Modular E170; Roche Diagnostics [20, 24]). The total analytical coefficient of variation was 7.3%. We recently showed that smokers had 15–20% higher serum 25(OH)D than non-smokers. However, this was not observed when using other immunological and liquid-chromatography mass spectrometry methods . To this discrepancy, presently, we have no explanation. Thus, non-smokers and smokers are analysed separately.
Assessment of characteristics of the study population
Two self-administered structured questionnaires covered a broad range of issues related to health and lifestyle. Body height and weight were measured, and body mass index was calculated (BMI kg/m2) . Use of antibiotics in the last 24 hours was registered by interview.
Logistic regression models were used to study the association between serum 25(OH)D and S. aureus colonization and carriage; odds ratios (ORs) and 95% confidence intervals (CIs) were determined. Due to lack of prior knowledge of serum 25(OH)D thresholds for adequate immune response, serum 25(OH)D tertiles were selected as suitable for the samples; non-smokers were subdivided as: <44.9 nmol/l, 44.9–58.6 nmol/l, >58.6 nmol/l; and smokers: <59.6 nmol/l, 59.6–75.3 nmol/l, >75.3 nmol/l. Also, proposed cut-points for vitamin D deficiency/insufficiency were examined (i.e. < 50.0, 50.0–<75.0, ≥75.0 nmol/l)  among non-smokers. Selected characteristics of men and women in the different serum 25(OH)D tertiles were compared by one-way ANOVA and Kruskal-Wallis test for continuous variables and two-sided Pearson chi-squared test for categorical variables.
We evaluated model fit and biological plausibility of several covariates and the final multivariate models included age, BMI, diabetes mellitus (yes/no), and calendar month (2 months categories), and in smokers also number of cigarettes smoked per day and total years smoked. Further adjustment for education (< or ≥ college/university degree), last hospitalization in 12 months (yes/no), recreational physical activity (3 levels), and alcohol intake (< or ≥2 times a week) did not alter the multivariate risk estimates.
We studied whether age modified the association in stratified logistic regression models using tertiles of age for non-smokers grouped as: <44 years, 44–60 years, >60 years.
Tests of reliability of the final analyses were done by the Hosmer-Lemeshow goodness of fit test. Tests for linear trend were performed by assigning consecutive integers to each tertile of serum 25(OH)D, and testing whether the slope coefficient differed from zero using the Wald chi-square test. Test for interaction was done by inclusion of the multiplicative term of the two predictor variables in the model. Two-sided P values < 0.05 were considered statistically significant. STATA version 11.0 (StataCorp) was used.
Non-smokers constituted 80.7% (1,351 of 1,674) men and 78.3% (1,655 of 2,115) women. Mean serum 25(OH)D concentration was 53.3 nmol/l in non-smoking men and 52.4 nmol/l in non-smoking women. For both sexes, high serum 25(OH)D was associated with higher age, physical activity level and alcohol intake, and in women, there was a negative association with BMI (all P-values < 0.05) (Table 1). The prevalence of S. aureus nasal colonization and carriage was 37.5% (506 of 1,351) and 34.1% (338 of 992) in men, and 24.4% (403 of 1,655) and 21.3% (264 of 1,239) in women, respectively.
There was an inverse dose-response relationship between serum 25(OH)D and S. aureus nasal colonization and carriage in non-smoking men (Fig. 2). The estimated beta coefficient equals a 6.6% and a 6.7% decrease in the probability of S. aureus colonization and carriage, respectively, by each 5 nmol/l increase in serum 25(OH)D concentration (P < 0.001 and P = 0.001; unadjusted). Furthermore, in the multivariate logistic regression analysis we observed a 35% and 33% reduction in colonization and carriage risk in upper versus bottom tertiles of serum 25(OH)D in men (OR 0.65, 95%CI 0.49–0.87, P for trend 0.004; and OR 0.67, 95%CI 0.48–0.95, P for trend 0.03, respectively) (Table 3). Also, those with serum 25(OH)D concentration ≥ 75 nmol/l versus below 50 nmol/l had almost half the risk of S. aureus colonization and carriage (OR 0.54, 95%CI 0.35–0.84, P for trend 0.004; and OR 0.52, 95%CI 0.31–0.90, P for trend 0.02, respectively) (Table 3). As S. aureus carriage rate in men is inversely related to age , we stratified by age tertiles in the multivariate logistic regression analysis. In the middle-age tertile, age 44–60 years, OR for colonization and carriage in top versus bottom tertile of serum 25(OH)D was 0.44 and 0.51 (95% CI 0.28–0.69, P for trend <0.001; and 95%CI 0.30–0.88, P for trend 0.02, respectively), while in younger and older adult men no association was observed (P for interaction 0.10 and 0.45, respectively) (results not shown in figures or tables).
In non-smoking women, there was a pattern of an inverse trend of the linear regression line in the serum 25(OH)D–S. aureus colonization and carriage plots (P = 0.25, and P = 0.22, respectively; unadjusted) (Fig. 2), but there was no difference in S. aureus nasal colonization and carriage risk between tertiles or categories (i.e. cut-off values 50 and 75 nmol/l) of serum 25(OH)D (Table 3).
As general recommendations on vitamin D status in adults do not differ by sex, we examined the total population of non-smokers and observed a 3.8% and 4.4% decrease in S. aureus colonization and carriage risk by each 5 nmol/l increase in serum 25(OH)D concentration, respectively (P = 0.001 and P = 0.002; unadjusted) (Fig. 2).
In the smoking population, average vitamin D concentration was higher than in non-smokers; mean serum 25(OH)D concentration was 66.8 nmol/l in men and 71.3 nmol/l in women. In women, serum 25(OH)D was positively associated with number of cigarettes smoked per day and years of smoking (both P-values < 0.05) (Table 2). The prevalence of S. aureus nasal colonization and carriage was 29.1% (94 of 323) and 24.5% (57 of 233) in men, and 18.3% (84 of 460) and 15.2% (48 of 316) in women, respectively. All prevalence rates were significantly lower than in non-smokers (all P-values < 0.05). We did not observe any association between serum 25(OH)D concentration and S. aureus nasal colonization or carriage rates in top versus bottom tertile of serum 25(OH)D in either male (multivariate model; colonization: OR 1.19; 95%CI 0.62–2.29, P for trend 0.66; and carriage: OR 1.33, 95%CI 0.53–3.33, P for trend 0.47) or female smokers (multivariate model; colonization: OR 0.96, 95% CI 0.50–1.86, P for trend 0.83; and carriage OR 1.49, 95%CI 0.59–3.77, P for trend 0.48) (results not shown in figures or tables).
In this large population-based study with repeated nasal swab cultures we observed an inverse dose-response association between serum 25(OH)D and S. aureus nasal colonization and carriage in non-smoking men with no such clear association among women. Based on our findings, we suggest that vitamin D can upregulate the antibacterial immune response and thereby prevent S. aureus colonization and carriage, and subsequent disease. Furthermore, we hypothesize that the relative importance of vitamin D in this context is particularly high in the male population who lack female sex hormones known to boost the immune defence [25–27]. S. aureus was significantly less frequent in smokers than in non-smokers, and interestingly, serum 25(OH)D levels did not vary by S. aureus colonization or carriage states in smokers. These findings support that the inverse association between vitamin D and S. aureus colonization and carriage may be masked by smoking, which is possibly explained by the bactericidal activity of cigarette smoke  and the increased immune activity associated with smoking-induced hypoxia.
This study is, to our knowledge, the first to report an association between vitamin D levels and MSSA carriage in a general population. However, in a recent study including single nasal swab cultures from 14,000 children and adults across the USA, an inverse association between vitamin D levels and risk of MRSA was observed . The microbe-dependent association may partly be due to the increased resistance of MRSA to natural antimicrobial peptides (i.e. cathelicidin) induced by vitamin D in host defence against S. aureus . The apparent discrepancy with our MSSA results may be explained by several factors. While in Matheson et al. more detailed subgroup analysis was not presented , we observed that gender and smoking status may modify the association between vitamin D levels and S. aureus colonization and carriage. Furthermore, our study included men and women from a well-defined arctic adult source population, 69°N, and there is minimal concern about geographical and ethnical heterogeneity that, in contrast, may have influenced the findings by Matheson et al. .
The inverse dose-response relationship between vitamin D status and S. aureus prevalence observed among non-smokers in our study is in accordance with former findings , and points to targets for reducing the reservoir of S. aureus in the population, in particular when vitamin D insufficiency is common. Carriage of S. aureus precedes infection. Thus, our findings suggest that vitamin D supplementation may reduce the incidence of MSSA and MRSA infections. Importantly, we identified serum 25(OH)D above 59 nmol/l and 75 nmol/l as thresholds for ~30% and ~50% reduction in S. aureus colonization and carriage in non-smoking men. Consensus to define a cut-point for vitamin D insufficiency based on serum 25(OH)D levels is lacking. Various cut-points have been proposed based on population-based reference limits or biological indices as parathyroid hormone, calcium absorption, or bone mineral density, but without reference to immune function and infectious diseases [29, 30]. Given the high risk of S. aureus infection in combination with malnutrition in specific patient populations (i.e. surgical, dialysis, ICU, HIV ), and the fact that most of the infections are caused by the patient’s nasal strain [3, 4], our finding suggests that vitamin D repletion reaching serum 25(OH)D above 60–75 nmol/l may be a significant alternative in the prevention of hospital infections. A recent retrospective study including 52 subjects with Clostridium difficile and S. aureus infections showed a link between low vitamin D status and adverse outcome . Larger and prospective studies are needed to determine a possible role of vitamin D supplementation and repletion in relation to S. aureus colonization, carriage and infection.
The inverse relationship between serum 25(OH)D concentration and S. aureus colonization and carriage did not reach statistical significance among women in our study. It has been proposed that women are inherently protected from infections by estrogens, which increase immune function [25, 32]. A variety of immunocompetent cells express estrogen receptors, which mediate the antimicrobial effects, i.e. regulating the expression of caspases and cytokines [25–27]. Thus, we hypothesize that the stable, low lifetime prevalence of S. aureus carriage in women is mainly explained by endogenous estrogens that may overwhelm the protective effect of vitamin D. The observed gender difference is in accordance with studies of other outcomes; type 2 diabetes and insulin resistance have been associated with low vitamin D status in men only [33, 34], but so far these gender differences lack explanation.
Recent studies suggest that higher vitamin D status is protective against upper respiratory tract infections [17, 18, 35], and that seasonal influenza might be linked to the wintertime deficiency of vitamin D . Furthermore, vitamin D deficiency has been associated with increased risk of tuberculosis (TB)  and immunomodulatory effects of vitamin D and sunlight in TB therapy continue to be revealed . Importantly, however, a U-shaped association between serum 25(OH)D concentration and risk of active TB was recently observed , indicating that vitamin D supplementation may have detrimental effects on the immune function among individuals with normal or high vitamin D status.
Our main findings may be biased by the positive association between age and serum 25(OH)D among non-smoking men; higher consumption of traditional marine food like cod liver and fresh cod liver oil, more frequent extended stays in the south, and lower BMI in the elderly may contribute to this association (results not presented). Also, in male participants, age is inversely related to S. aureus nasal carriage . Based on this, we included age as a covariate in our regression analysis and stratified by age group (i.e. tertiles) but observed no interaction. However, in the middle-age tertile with subjects relatively evenly distributed in serum 25(OH)D levels and homogenous S. aureus frequencies across the age range, the strength of the vitamin D–S. aureus associations increased.
Thus, if there is an association between serum 25(OH)D and risk of S. aureus colonization and carriage this could be explained by the immunmodulatory effects of vitamin D. S. aureus stimulates the conversion of 25-hydroxyvitamin D (25(OH)D) to the active metabolite 1,25-dihydroxyvitamin D (1,25(OH)2D) . Vitamin D stimulates the production of antimicrobial peptides (i.e. cathelicidin and β-defensin) with activity against S. aureus , and contributes to the formation of an intact epidermal barrier preventing S. aureus invasion (i.e. regulation of keratinocytes) . Interestingly, genetic polymorphisms in VDR in combination with type 1 diabetes has been associated with the risk of S. aureus colonization and carriage [38, 39].
Detailed studies have shown that there are two carrier states that differ in the immune response to S. aureus and risk of infections; persistent carriers and others . In our study, culturing results of two repeated nasal swabs differed only in a minor proportion of the participants (8%); thus classification by colonization state almost equalled carrier state. Many other similar studies have used only one sample [7, 9]. Furthermore, the high participation rate and uniform use of standard and validated clinical and laboratory procedures increase the external validity of our findings [22, 40].
The cross-sectional study design precludes establishing temporality and thus causality of serum 25(OH)D concentrations and S. aureus colonization and carriage. Due to our former studies indicating an overestimation of serum 25(OH)D levels in smokers by the ECLIA (Roche) test , we stratified by smoking status and included smoking data as covariates in the analysis of the smoking population. This strengthens the validity of the linear trend estimates. However, estimation of externally valid cut-off values for serum 25(OH)D in smokers is hindered.
In conclusion, our study indicates an inverse association between serum 25(OH)D concentration and the risk of S. aureus nasal colonization and carriage in non-smokers, particularly in men. Prospective randomised trials are needed to assess whether increase in circulating vitamin D concentration can effectively decrease the risk of S. aureus carriage and subsequent infection.
ECDC (2009) European antimicrobial resistance surveillance system (EARSS). European Centre for Disease Prevention and Control
Bode LG, Kluytmans JA, Wertheim HF, Bogaers D, Vandenbroucke-Grauls CM, Roosendaal R, Troelstra A, Box AT, Voss A, van dT I, van Belkum A, Verbrugh HA, Vos MC (2010) Preventing surgical-site infections in nasal carriers of Staphylococcus aureus. N Engl J Med 362:9–17
von Eiff C, Becker K, Machka K, Stammer H, Peters G (2001) Nasal carriage as a source of Staphylococcus aureus bacteremia. Study Group. N Engl J Med 344:11–16
Wertheim HF, Melles DC, Vos MC, van Leeuwen W, van Belkum A, Verbrugh HA, Nouwen JL (2005) The role of nasal carriage in Staphylococcus aureus infections. Lancet Infect Dis 5:751–762
van Belkum A, Melles DC, Nouwen J, van Leeuwen WB, van Wamel W, Vos MC, Wertheim HF, Verbrugh HA (2009) Co-evolutionary aspects of human colonisation and infection by Staphylococcus aureus. Infect Genet Evol 9:32–47
Nouwen J, Ott A, Boelens H et al (2004) Smoking pattern and fasting glucose levels determine Staphylococcus aureus nasal carriage. Erasmus University Medical Centre, Rotterdam, The Netherlands. PhD thesis
Wang JT, Liao CH, Fang CT, Chie WC, Lai MS, Lauderdale TL, Lee WS, Huang JH, Chang SC (2009) Prevalence of and risk factors for colonization by methicillin-resistant Staphylococcus aureus among adults in community settings in Taiwan. J Clin Microbiol 47:2957–2963
Choi CS, Yin CS, Bakar AA, Sakewi Z, Naing NN, Jamal F, Othman N (2006) Nasal carriage of Staphylococcus aureus among healthy adults. J Microbiol Immunol Infect 39:458–464
Matheson EM, Mainous AG III, Hueston WJ, Diaz VA, Everett CJ (2010) Vitamin D and methicillin-resistant Staphylococcus aureus nasal carriage. Scand J Infect Dis 42:455–460
Schauber J, Dorschner RA, Yamasaki K, Brouha B, Gallo RL (2006) Control of the innate epithelial antimicrobial response is cell-type specific and dependent on relevant microenvironmental stimuli. Immunology 118:509–519
Schauber J, Gallo RL (2008) The vitamin D pathway: a new target for control of the skin's immune response? Exp Dermatol 17:633–639
White JH (2010) Vitamin D as an inducer of cathelicidin antimicrobial peptide expression: past, present and future. J Steroid Biochem Mol Biol 121:234–238
Pearce SH, Cheetham TD (2010) Diagnosis and management of vitamin D deficiency. BMJ 340:b5664
Bischoff-Ferrari HA, Giovannucci E, Willett WC, Dietrich T, Dawson-Hughes B (2006) Estimation of optimal serum concentrations of 25-hydroxyvitamin D for multiple health outcomes. Am J Clin Nutr 84:18–28
Cannell JJ, Vieth R, Umhau JC, Holick MF, Grant WB, Madronich S, Garland CF, Giovannucci E (2006) Epidemic influenza and vitamin D. Epidemiol Infect 134:1129–1140
Chesney RW (2010) Vitamin D and the magic mountain: the anti-infectious role of the vitamin. J Pediatr 156:698–703
Ginde AA, Mansbach JM, Camargo CA Jr (2009) Association between serum 25-hydroxyvitamin D level and upper respiratory tract infection in the Third National Health and Nutrition Examination Survey. Arch Intern Med 169:384–390
Laaksi I, Ruohola JP, Tuohimaa P, Auvinen A, Haataja R, Pihlajamaki H, Ylikomi T (2007) An association of serum vitamin D concentrations < 40 nmol/L with acute respiratory tract infection in young Finnish men. Am J Clin Nutr 86:714–717
Grimnes G, Almaas B, Eggen AE, Emaus N, Figenschau Y, Hopstock LA, Hutchinson MS, Methlie P, Mihailova A, Sneve M, Torjesen P, Wilsgaard T, Jorde R (2010) Effect of smoking on the serum levels of 25-hydroxyvitamin D depends on the assay employed. Eur J Endocrinol 163:339–348
Jorde R, Sneve M, Hutchinson M, Emaus N, Figenschau Y, Grimnes G (2010) Tracking of serum 25-hydroxyvitamin D levels during 14 years in a population-based study and during 12 months in an intervention study. Am J Epidemiol 171:903–908
Olsen K, Simonsen GS, Sundsfjord A, Haukland HH, Sollid JE, Danielsen K, Haldorsen B, Eggen AE, Furberg AS (2009) The epidemiology of Staphylococcus aureus nasal and throat carriage in a large community-based population in Northern Norway. The Tromsø Staph and Skin Study. Poster number 1678 at the 19th ECCMID (19th European conference of clinical microbiology and infectious diseases), Helsinki
Jacobsen BK, Eggen AE, Mathiesen EB, Wilsgaard T, Njølstad I (2011) Cohort profile: the Tromsø Study. Int J Epidemiol 1–7. doi:10.1093/ije/dyr049
van Belkum A, Verkaik NJ, de Vogel CP, Boelens HA, Verveer J, Nouwen JL, Verbrugh HA, Wertheim HF (2009) Reclassification of Staphylococcus aureus nasal carriage types. J Infect Dis 199:1820–1826
Leino A, Turpeinen U, Koskinen P (2008) Automated measurement of 25-OH vitamin D3 on the Roche Modular E170 analyzer. Clin Chem 54:2059–2062
Marriott I, Huet-Hudson YM (2006) Sexual dimorphism in innate immune responses to infectious organisms. Immunol Res 34:177–192
Salem ML (2004) Estrogen, a double-edged sword: modulation of TH1- and TH2-mediated inflammations by differential regulation of TH1/TH2 cytokine production. Curr Drug Targets Inflamm Allergy 3:97–104
Yeretssian G, Doiron K, Shao W, Leavitt BR, Hayden MR, Nicholson DW, Saleh M (2009) Gender differences in expression of the human caspase-12 long variant determines susceptibility to Listeria monocytogenes infection. Proc Natl Acad Sci USA 106:9016–9020
Turner J, Cho Y, Dinh NN, Waring AJ, Lehrer RI (1998) Activities of LL-37, a cathelin-associated antimicrobial peptide of human neutrophils. Antimicrob Agents Chemother 42:2206–2214
Hollis BW (2005) Circulating 25-hydroxyvitamin D levels indicative of vitamin D sufficiency: implications for establishing a new effective dietary intake recommendation for vitamin D. J Nutr 135:317–322
Lips P (2004) Which circulating level of 25-hydroxyvitamin D is appropriate? J Steroid Biochem Mol Biol 89–90:611–614
Youssef D, Bailey B, El Abbassi A, Copeland R, Adebonojo L, Manning T, Peiris AN (2010) Healthcare costs of Staphylococcus aureus and Clostridium difficile infections in veterans: role of vitamin D deficiency. Epidemiol Infect 138:1322–1327
Beery TA (2003) Sex differences in infection and sepsis. Crit Care Nurs Clin North Am 15:55–62
Ford ES, Zhao G, Tsai J, Li C (2011) Association between concentrations of vitamin D and concentrations of insulin, glucose, and HbA1c among adolescents in the United States. Diabetes Care:1–3. doi:10.2337/dc10-1754
Knekt P, Laaksonen M, Mattila C, Harkanen T, Marniemi J, Heliovaara M, Rissanen H, Montonen J, Reunanen A (2008) Serum vitamin D and subsequent occurrence of type 2 diabetes. Epidemiology 19:666–671
Laaksi I, Ruohola JP, Mattila V, Auvinen A, Ylikomi T, Pihlajamaki H (2010) Vitamin D supplementation for the prevention of acute respiratory tract infection: a randomized, double-blinded trial among young Finnish men. J Infect Dis 202:809–814
Nnoaham KE, Clarke A (2008) Low serum vitamin D levels and tuberculosis: a systematic review and meta-analysis. Int J Epidemiol 37:113–119
Nielsen NO, Skifte T, Andersson M, Wohlfahrt J, Soborg B, Koch A, Melbye M, Ladefoged K (2010) Both high and low serum vitamin D concentrations are associated with tuberculosis: a case-control study in Greenland. Br J Nutr 104:1487–1491
Claassen M, Nouwen J, Fang Y, Ott A, Verbrugh H, Hofman A, van Belkum A, Uitterlinden A (2005) Staphylococcus aureus nasal carriage is not associated with known polymorphism in the Vitamin D receptor gene. FEMS Immunol Med Microbiol 43:173–176
Panierakis C, Goulielmos G, Mamoulakis D, Maraki S, Papavasiliou E, Galanakis E (2009) Staphylococcus aureus nasal carriage might be associated with vitamin D receptor polymorphisms in type 1 diabetes. Int J Infect Dis 13:e437–e443
Haldorsen B, Olsen K, Ericson Sollid J, Husom Haukland H, Sundsfjord A, Simonsen G, Breivik S, Larsen G, Furberg AS (2009) Nasal and throat swab cultures for the assessment of Staphylococcus aureus colonization and carriage. The Tromsø Staph and Skin Study. Poster number 1150 at the 19th ECCMID (19th European conference of clinical microbiology and infectious diseases), Helsinki
We thank Bjørg C Haldorsen for excellent technical assistance, each participant in the Tromsø Study for their collaboration, the staff at the screening centre and the laboratory at the Dept of Medical Biochemistry, University Hospital of North Norway for the serum 25(OH)D analysis. This work was supported by grants from the Research Council of Norway (grant number 191264), the Northern Norway Regional Health Authority (grant numbers SFP877-09, SFP920-10), and the Odd Berg Group Medical Research fund 2007.
Conflicts of interest
All authors had no conflicts of interest.
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Olsen, K., Falch, B.M., Danielsen, K. et al. Staphylococcus aureus nasal carriage is associated with serum 25-hydroxyvitamin D levels, gender and smoking status. The Tromsø Staph and Skin Study. Eur J Clin Microbiol Infect Dis 31, 465–473 (2012). https://doi.org/10.1007/s10096-011-1331-x
- Nasal Swab
- Nasal Carriage
- Nasal Colonization
- Adequate Immune Response
- Carriage Risk