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Jenkins, C.L.; Bean, H.D. Diagnosing Staph Infections with VOC Biomarkers. Encyclopedia. Available online: https://encyclopedia.pub/entry/42086 (accessed on 17 November 2024).
Jenkins CL, Bean HD. Diagnosing Staph Infections with VOC Biomarkers. Encyclopedia. Available at: https://encyclopedia.pub/entry/42086. Accessed November 17, 2024.
Jenkins, Carrie L., Heather D. Bean. "Diagnosing Staph Infections with VOC Biomarkers" Encyclopedia, https://encyclopedia.pub/entry/42086 (accessed November 17, 2024).
Jenkins, C.L., & Bean, H.D. (2023, March 10). Diagnosing Staph Infections with VOC Biomarkers. In Encyclopedia. https://encyclopedia.pub/entry/42086
Jenkins, Carrie L. and Heather D. Bean. "Diagnosing Staph Infections with VOC Biomarkers." Encyclopedia. Web. 10 March, 2023.
Diagnosing Staph Infections with VOC Biomarkers
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This entry is adapted from the peer-reviewed paper 10.3390/pathogens12020181

Staphylococci are broadly adaptable and their ability to grow in unique environments has been widely established, but the most common and clinically relevant staphylococcal niche is the skin and mucous membranes of mammals and birds. S. aureus causes severe infections in mammalian tissues and organs, with high morbidities, mortalities, and treatment costs. S. epidermidis is an important human commensal but is also capable of deadly infections. The development of volatile organic compound (VOC) profiles for the detection and identification of pathogens is an area of intensive research, with significant efforts toward establishing breath tests for infections.

Metabolomics Volatile Organic Compounds Breathprint Breath-based Diagnostics Staphylococcus aureus Staphylococcus epidermidis Coagulase Negative Staphylococci Diagnosis GC×GC-TOFMS Bovine Mastitis

1. In Vitro and Animal Model Feasibility Studies

Volatile organic compound (VOC) biomarkers for S. aureus infections have been studied at all stages of biological and chemical translational development [1][2][3][4][5][6], demonstrating feasibility for diagnosing and characterizing staph infections in clinical and field settings. Based on the published analyses of S. aureus VOCs, ten analytes comprise a common S. aureus volatile suite (Table 1) [4][6][7][8][9][10][11][12][13][14][15]. All of these metabolites are produced by a broad diversity of fungi and bacteria, including coagulase-negative staphylococci, suggesting they may be produced by universal metabolic pathways [16]. However, combining the differences in the relative abundances of these common metabolites with suites of accessory metabolites yields VOC profiles that differentiate staph from other microbial taxa. In in vitro cultures, S. aureus has been successfully differentiated from Acinetobacter spp., Candida spp., Clostridium perfringens, Enterobacter spp., Enterococcus spp., Proteus mirabilis, Klebsiella spp., P. aeruginosa, Streptococcus spp., E. coli, Burkholderia cepacia complex, H. influenzae, H. pylori, Citrobacter spp., S. maltophilia, Salmonella enterica, Serratia marcescens, Moraxella catarrhalis, Neisseria meningitidis, S. epidermidis, and S. lugdunensis based on their volatile profiles measured using GC, direct injection MS, and sensor array technologies (Table 2) [4][5][6][7][12][14][15][17][18][19][20][21][22][23][24][25][26]. The unique and shared VOC profiles of each taxon form the foundation of in vitro detection and identification technologies being developed for clinical use [27]. Differences in the volatile profiles have been extended to in vitro models of skin wound infection biofilms, where it has been shown that S. aureus can be differentiated from Gram-negative bacteria, such as P. aeruginosa, and also Gram-positive pathogens such as Streptococcus pyogenes [28][29][30]. S. aureus and S. epidermidis also have unique volatile profiles in vitro under a variety of growth conditions, indicating that infections caused by the former will be differentiable from non-infectious colonization by the latter [5][6][12][31][32].
Table 1. The canonical VOCs of the S. aureus volatilome.
IUPAC Name Common Name Molecular Formula MW * CAS * KEGG * References
acetaldehyde ethanal CH3CHO 44 75-07-0 C00084 [4][6][9]
ethanol ethyl alcohol C2H6O 46 64-17-5 C00469 [4][6][9][11][15]
methanethiol methyl mercaptan CH4S 48 74-93-1 C00409 [4][13]
propan-2-one acetone C3H6O 58 67-64-1 C00207 [4][6]
acetic acid acetic acid C2H4O2 60 64-19-7 C00033 [4][6][12][14]
3-methylbutanal isovaleraldehyde C5H10O 86 590-86-3 C07329 [4][6][9]
3-hydroxybutan-2-one acetoin C4H8O2 88 513-86-0 C00466 [7][8][11][12][14]
3-methylbutan-1-ol isoamyl alcohol C5H12O 88 123-51-3 C07328 [4][6][7][11][12][13][14][15]
(methyldisulfanyl)methane dimethyl disulfide C2H6S2 94 624-92-0 C08371 [4][6][7][13]
3-methylbutanoic acid isovaleric acid C5H10O2 102 503-74-2 C08262 [4][6][12][13][14]
* MW: Molecular weight; CAS: Chemical Abstracts Service; KEGG: Kyoto Encyclopedia of Genes and Genomes.
Table 2. Analyses of the in vitro volatilomes of S. aureus in comparison to other pathogens.
Ref. VOC
Detection
Method		 Acinetobacter spp. Acinetobacter baumannii Burkholderia cepacia complex Candida spp. Candida albicans Citrobacter spp. Clostridium perfringens Enterobacter spp. Enterobacter cloacae Enterococcus spp. Escherichia coli Haemophilus influenzae Helicobacter pylori Klebsiella spp. Klebsiella pneumoniae Moraxella catarrhalis Neisseria meningitidis Proteus mirabilis Pseudomonas aeruginosa Staphylococcus epidermidis Stenotrophomonas maltophilia Streptococcus spp. Streptococcus pyogenes
[17] PRT-MS           x         x   x x         x        
[18] E-Nose   x     x       x   x x     x       x   x    
[4] GC-MS                                     x        
[5] GC×GC-MS                                       x      
[6] GC×GC-MS                                       x      
[7] GC-MS                             x     x x        
[12] GC-MS                     x               x x      
[14] GC-MS                     x               x x      
[15] GC-IMS                     x               x        
[19] SIFT-MS                     x           x   x     x  
[20] SIFT-MS     x                               x   x    
[21] GC×GC-MS x     x       x   x x     x       x x        
[22] E-Nose                     x x       x     x     x  
[23] E-Nose             x       x               x       x
[24] SESI-HRMS                     x x             x   x x  
[25] GC-MS                     x       x       x        
[26] GC-MS         x           x                        
[28] GC-MS                                     x        
[29] GC-MS                                     x       x
[30] SIFT-MS                                     x       x
[31] IMR-MS *                   x                   x      
[32] CSA **   x     x     x   x x     x       x x x   x  
* IMR-MS: ion-molecule reaction mass spectrometry ** CSA: Colorimetric Sensor Array.
While only a subset (25–34%) of in vitro VOCs reliably translate to in vivo detection [2], animal model studies have shown that breath VOCs can identify infection etiology, even down to the strain level for the bacterial pathogen. Zhou and colleagues developed an in vivo rabbit pneumonia model and an ex vivo human lung paracancerous model to differentiate lung infections caused by E. coli, P. aeruginosa, and S. aureus [33]. They observed that within six hours post-inoculation of the lung tissue cultures, significant differences were detected in the VOCs produced by each of the three infection etiologies and the uninfected controls when analyzed by SPME-GC-MS. The breath volatiles from the rabbit infection models also showed significant differences when analyzed at 24 h post-inoculation, with six discriminatory VOCs translating from the in vitro to in vivo models. Mouse model studies by Zhu, Hill, and colleagues determined that SESI-MS breathprinting distinguished between seven of the most common causes of human bacterial lung infections: S. aureus, H. influenzae, K. pneumoniae, Legionella pneumophila, M. catarrhalis, P. aeruginosa, and S. pneumoniae [34]. They also demonstrated that breath VOCs could discriminate between infections caused by P. aeruginosa strains PAO1 vs. FRD1, and S. aureus RN450 [2] and that the etiology of bacterial lung infections can be correctly classified from early infection to clearance (from 6–120 h post-infection) [35]. In studies that exposed mice to live S. aureus and P. aeruginosa, non-infectious but immunogenic lysates of the bacteria, or saline controls, they found that breathprints of infections are the combination of bacterial metabolites, host metabolites that are correlated to immune response, and novel biomarkers that are created by the feedback between pathogen and host during active infection [3]. The involvement of the host immune system in generating VOC biomarkers during staph infections lends further support for the feasibility of differentiating between infections vs. asymptomatic colonization in humans and animals.
VOC biomarkers are also being developed to identify clinically important staph strains, such as MRSA and toxigenic isolates. In 2010, Jia and colleagues performed a proof-of-concept study of methicillin-sensitive S. aureus ATCC 29213 (MSSA) and methicillin-resistant S. aureus NRS 382 (MRSA) cultivated in vitro and analyzed via SPME-GC-MS [9], concluding that VOC analysis by GC-MS was suitable for differentiating MRSA and MSSA and that it may form the basis for an innovative and non-invasive diagnostic platform. These initial findings were strengthened by a SESI-MS/MS analysis of VOCs produced by isogenic MRSA and MSSA S. aureus strains-RN450 and 450M, respectively–that genetically differ only by the presence/absence of the SCCmec genes that confer methicillin resistance [36]. In this study, Li and colleagues evaluated the in vitro bacterial metabolic perturbations caused by antibiotic treatment with ampicillin. They showed that the MRSA and MSSA strains exhibited discriminately different metabolic profiles under the same growth conditions both before and after exposure to antibiotics. Further, Bean and colleagues showed that the volatilome differences between S. aureus RN450 and 450M are also detectable in the breathprints of mouse lung infection models caused by these strains, even without antibiotic exposure [37]. Combined, these studies suggest that VOCs may be used to both detect MRSA infections in situ prior to antibiotic treatment failure, and to subsequently monitor antibiotic treatment efficacy. VOCs have also shown promise for the detection and differentiation of enterotoxic and non-enterotoxic S. aureus strains [13] –an important issue for food safety–broadening the potential utility of VOC-based diagnostics for staph.

2. Diagnosing Human Infections

VOC signatures detected in human biospecimens can differentiate infected vs. non-infected individuals in conditions where S. aureus is a prevalent etiology, with new diagnostics for Ventilator-Associated Pneumonia (VAP) being a common target for volatile biomarkers. An investigation by Schnabel and colleagues of 100 patients with a clinical suspicion of VAP sampled exhaled breath from the expiratory limb of the ventilators and analyzed the VOCs using GC-TOFMS [38]. Bronchoalveolar lavage (BAL) diagnostic criteria confirmed VAP in 32 patients and ruled out VAP in 68. Subsequent multivariate statistical analysis of the breath VOC profiles enabled the identification of 12 compounds that discriminate against VAP+ and VAP- patients with sensitivity and specificity of approximately 76% and 73%, respectively [38]. The BreathDx Consortium recently published results from a study of 93 breath samples from ventilated patients who were enrolled upon clinical suspicion of VAP [39]. They identified a panel of 10 VOCs that had a 96% negative predictive value for differentiating subjects with VAP (diagnosed via positive BAL cultures) versus those who are culture negative, with potentially important implications for reducing the overprescription of antibiotics in ventilated patients. Staph-specific biomarkers for VAP are also under development. In a pilot study of 22 mechanically ventilated patients diagnosed with VAP, 17 of which were confirmed by positive cultures, Filipiak and colleagues found important overlaps between the in vitro VOCs produced by S. aureus, E. coli, Candida spp., and hemolytic Streptococcus and the VOCs detected in patients infected by those pathogens [40]. As observed in mouse model studies, they found that roughly a third of S. aureus VOCs they had previously detected in vitro were found in the breath of S. aureus-infected patients. The ventilated patients were sampled longitudinally over three to eight days, and several patients transitioned between infected and uninfected states during the analysis. Promisingly, several of the potential breath biomarkers for S. aureus were detected more frequently during periods of infection vs. resolution. Similar encouraging overlaps between S. aureus VOCs from in vitro bacterial cultures and ex vivo specimens were seen in the analysis of mucus from sinus infections [41]. However, neither study contained sufficient numbers of S. aureus-positive subjects and samples to confirm these correlations.
The most significant progress in the development of S. aureus VOC biomarkers has come from studies of persons with cystic fibrosis (CF) lung infections. In an analysis of the VOCs detected in 154 BAL fluid samples from CF patients with a variety of lung infections, Nasir et al. built models to discriminate samples from S. aureus vs. P. aeruginosa infections (n = 59), as well as models that discriminate S. aureus positive vs. negative samples (n = 133) [1]. The former model included 11 VOC biomarkers that had an area under the receiver operator curve (AUROC) of 0.79, and the latter model was 8 VOCs that could discriminate staph infected vs. uninfected patients with an AUROC of 0.88. Neerincx and colleagues analyzed the breath of 18 CF patients, 13 of whom had S. aureus infections, and identified nine VOCs that differentiate infected and uninfected CF patients with sensitivity and specificity of 1.00 and 0.80, respectively [42]. In both studies, the S. aureus-infected cohort included some subjects who had co-infections with other pathogens, such as S. maltophilia, H. influenzae, fungi/yeast, and nontuberculous mycobacteria, and the S. aureus-negative cohort included a mix of subjects who had no detected pathogens and subjects who had other infections. The predictive ability of VOCs to differentiate S. aureus infected versus uninfected patients in such a complex infection landscape as CF lung disease is notable.
Several studies have demonstrated the feasibility of detecting and characterizing non-respiratory infections by VOC analysis of ex vivo specimens or in vitro cultures. In a pilot study by Rogosch and colleagues, laboratory-confirmed bloodstream infections (n = 8) were detected with 100% diagnostic accuracy via E-Nose analysis of tracheal aspirates of 28 intubated preterm neonates [43]. The preclinical detection of late-onset sepsis caused by S. aureus and CoNS in preterm infants is possible up to three days prior to the onset of symptoms by the analysis of fecal VOCs using high-field asymmetric waveform ion mobility spectrometry [44]. Colorimetric sensor arrays (CSAs) have been developed to detect patterns of specific VOCs from in vitro cultures, enabling the direct identification of bacteria and yeast that cause bloodstream infections during blood culture enrichment [32][45]. Lim et al. showed that a blood culture cap modified to contain 73 VOC color indicators could differentiate S. aureus, S. epidermidis, and S. lugdunensis from 15 other bacterial taxa after 9 h of culturing with an overall sensitivity and specificity of 95.3% and 99.7%, respectively, using a CSA library based on more than a thousand blood culture analyses [32]. CSAs can also be used to perform rapid antibiotic susceptibility testing directly from blood cultures by growing aliquots of the cultures in an antibiotic array and monitoring for bacterial growth via VOC production. Kuil and colleagues analyzed the performance of the SPECIFIC REVEAL® CSA system for antibiotic susceptibility testing of 96 positive blood cultures [46]. They observed perfect agreement with the categorical results (susceptible, intermediate, or resistant) provided by the bioMérieux VITEK®2 system for infections caused by Gram-negative bacteria and 91% agreement for the Gram-positives, including S. aureus. The errors in the susceptibility results for the Gram-positive infections were due to the misclassification of CoNS, with five S. epidermidis and four other CoNS showing discrepancies for oxacillin, cefoxitin, or vancomycin.
Few research studies utilizing GC-MS analysis focus on identifying S. epidermidis volatiles [5][6][12][47], but as a skin commensal, there has been interest in how S. epidermidis VOCs contribute to the attraction of mosquitoes. Verhulst and colleagues demonstrate a profile of eight S. epidermidis VOCs, produced in the context of human skin, comprising a suite of semiochemicals that attract Anopheles gambiae, a mosquito known to carry malaria [47]. These compounds include dimethyl disulfide, butyl acetate, butyl 2-methylbutanoate, 2-pentadecanone, dimethyl tetrasulfide, dimethyl pentasulfide, hexathiepane, and the inorganic compound octasulfur. With the universality of S. epidermidis as a human colonizer but the paucity of information on S. epidermidis VOCs, much work remains to characterize this bacterium (including strain-to-strain variations) and to determine the similarities and differences of its volatilome compared to its aggressively pathogenic relative, S. aureus.

3. Diagnosing Animal Infections

Several research groups have been exploring the use of VOCs to detect S. aureus in symptomatic and sub-clinical mastitis in cattle [48][49][50][51][52], as well as the antibiotic resistance status of the infections. By adapting the VOC detection to E-Nose and other field-deployable detection devices [53][54], livestock can be routinely monitored to reduce the transmission of unnoticed infections and to advance antibiotic stewardship activities through an enhanced empirical selection of appropriate medications for MRSA. In response to the urgent need to proactively monitor livestock for antimicrobial-resistant pathogens, Yuan and colleagues propose the implementation of high-resolution visual and olfactory sensing for enhanced perception of contagious disease among dairy cattle [52]. Their goal is to engineer a novel and heterogeneous digital intelligence structure that exploits the combination of visual and olfactory data of individual animals during milking. Asymptomatically infected udders potentially exhibit elevated temperatures that can be recorded by thermal imaging cameras networked to milking robots. During milking, VOC patterns can also be detected by E-Nose. By constructing high-performance machine learning models, these artificial intelligence systems may lead the way to innovative precision livestock management. With the potential to surveil and identify early infectious disease in single animals, this technology could interrupt the commonplace asymptomatic transmission of S. aureus throughout the herd. This novel approach using artificial intelligence for perception in uncovering underlying diseases enhances the One Health Antimicrobial Resistance initiative goals regarding antimicrobial stewardship while diminishing economic losses due to unanticipated infectious outbreaks.

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Subjects: Microbiology; Infectious Diseases; Agriculture, Dairy & Animal Science
Contributors MDPI registered users' name will be linked to their SciProfiles pages. To register with us, please refer to https://encyclopedia.pub/register :
Carrie L. Jenkins
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Heather D. Bean
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Update Date: 13 Mar 2023
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