http://orcid.org/0000-0002-7250-908X
Figures
Abstract
Introduction
The prevalence of bacteremia caused by Gram negative non-fermentative (GNNF) bacteria has been increasing globally over the past decade. Many studies have investigated their epidemiology but focus on the common GNNF including Pseudomonas aeruginosa and Acinetobacter baumannii. Knowledge of the uncommon GNNF bacteremias is very limited. This study explores invasive bloodstream infection GNNF isolates that were initially unidentified after testing with standard microbiological techniques. All isolations were made during laboratory-based surveillance activities in two rural provinces of Thailand between 2006 and 2014.
Methods
A subset of GNNF clinical isolates (204/947), not identified by standard manual biochemical methodologies were run on the BD Phoenix automated identification and susceptibility testing system. If an organism was not identified (12/204) DNA was extracted for whole genome sequencing (WGS) on a MiSeq platform and data analysis performed using 3 web-based platforms: Taxonomer, CGE KmerFinder and One Codex.
Results
The BD Phoenix automated identification system recognized 92% (187/204) of the GNNF isolates, and because of their taxonomic complexity and high phenotypic similarity 37% (69/187) were only identified to the genus level. Five isolates grew too slowly for identification. Antimicrobial sensitivity (AST) data was not obtained for 93/187 (50%) identified isolates either because of their slow growth or their taxa were not in the AST database associated with the instrument. WGS identified the 12 remaining unknowns, four to genus level only.
Conclusion
The GNNF bacteria are of increasing concern in the clinical setting, and our inability to identify these organisms and determine their AST profiles will impede treatment. Databases for automated identification systems and sequencing annotation need to be improved so that opportunistic organisms are better covered.
Author summary
Infections caused by Gram negative non fermentative bacteria (GNNF), other than the more commonly described Pseudomonas aeruginosa and Acinetobacter baumannii, constitute an emerging problem. They are not only isolated in nosocomial settings, mainly affecting immunocomprised hosts, but also are opportunistic infections causing invasive disease in rural communities. GNNF bacteria are ubiquitously distributed in the environment and have a high propensity for antimicrobial resistance. Thus, their accurate identification to the species level is important for appropriate patient management. These bacteria are taxonomically heterogeneous, and many isolates are not satisfactorily identified by the standard biochemical assays because of overlapping phenotypic characteristics. In this study we explored using the BD Phoenix automated identification system to improve the identification of GNNF isolates and recognized 92% (187/204) of the previously unidentified isolates; 117 of which were to the species level. Antimicrobial resistance profiles were identified for 50% (94/187) of the isolates identified by the BD Phoenix system. For the remaining 12 unidentified organisms whole genome sequencing was performed. Three web-based programs were used for organism identification and results varied because of differences in the underlying databases used.
Citation: Whistler T, Sangwichian O, Jorakate P, Sawatwong P, Surin U, Piralam B, et al. (2019) Identification of Gram negative non-fermentative bacteria: How hard can it be? PLoS Negl Trop Dis 13(9): e0007729. https://doi.org/10.1371/journal.pntd.0007729
Editor: Alfredo G. Torres, University of Texas Medical Branch, UNITED STATES
Received: May 20, 2019; Accepted: August 25, 2019; Published: September 30, 2019
This is an open access article, free of all copyright, and may be freely reproduced, distributed, transmitted, modified, built upon, or otherwise used by anyone for any lawful purpose. The work is made available under the Creative Commons CC0 public domain dedication.
Data Availability: Sequences have been deposited in the NCBI Sequence Read Archive and can be accessed through Biosample identifiers SAMN11784141-52. All relevant data are within the manuscript and its Supporting Information files.
Funding: Support for this project was provided by the Global Disease Detection program of the U.S. Centers for Disease Control and Prevention, and the Pneumococcal Vaccines Accelerated Development and Introduction Plan (PneumoADIP) funded by the GAVI Alliance based at the Johns Hopkins Bloomberg School of Public Health. 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
The non-fermentative Gram-negative bacteria are widely distributed in the environment and have become increasingly common isolates in the clinical laboratory. Being ubiquitous in nature, they are often disregarded as contaminants. Medically, their pathogenic potential has been proved beyond doubt by their frequent isolation from clinical material and their association with disease. This group of bacteria has emerged as opportunistic pathogens, particularly in immunocompromised hosts, and are difficult to treat because of widespread antibiotic resistance. Due to their taxonomic complexity and phenotypic similarity accurate identification represents a challenge for conventional microbiology.
Automated systems that perform organism identification and antimicrobial susceptibility testing are now the mainstay of clinical microbiology laboratories. The recent implementation of the BD Phoenix and a MiSeq next generation sequencing (NGS) instrument in our laboratory-based surveillance activities has allowed us to re-examine a subset of previously unidentified Gram negative bacilli and determine which genera are contributing to bloodstream infections in rural, agrarian populations in Thailand. An understanding of the uncommon Gram negative non-fermentative (GNNF) bacteria causing invasive disease in these communities should assist in diagnosis and treatment and possibly impact patient outcomes.
Methods
Ethical statement
The CDC Human Subjects Review Office determined this protocol to be a routine public health activity not involving human subject research (CGH Determination and Approval number 2014–273).
Isolate collection
Unidentified Gram negative bacterial isolates used in this study (Fig 1) were collected during 2006–2014 as part of a previously published surveillance system [1]. Organisms were taken from the isolate culture collections of the Sa Kaeo and Nakhon Phanom Provincial Health Laboratories that had been previously been characterized using standard biochemical testing methods [2]. A random subset of approximately 20% (n = 204) of the 947 unidentified organisms were used in this study.
*WGS–whole genome sequencing.
BD Phoenix system procedures
Upon removal from the freezer, isolates were grown on tryptic soy agar with 5% sheep blood. The inoculum for the Phoenix Gram-negative identification and susceptibility combination panel NMIC/ID 55 was prepared according to the manufacturer’s instructions and panels were sealed, logged, and loaded into the instrument for incubation at 35°C (http://legacy.bd.com/ds/technicalCenter/clsi/clsi-Phoenix_GramNegative_V5.15_V4.31.pdf). Kinetic, colorimetric, and fluorescent signals were automatically collected by the instrument every 20 minutes until results were completed. The Phoenix system leads to an identification result when a species or group of species is identified with a ≥90% confidence level [3]. Antimicrobial susceptibility testing (AST) breakpoints were interpreted using the Clinical and Laboratory Standards Institute (CLSI) guidelines from 2016 [4].
Whole genome sequencing
DNA was extracted from bacterial colonies using the manual Qiagen DNA Mini Kit. Libraries were prepared employing the Illumina Nextera XT DNA Library Prep Kit according to the manufacturer's instructions. Whole genome sequencing was performed on the Illumina MiSeq sequencer (Illumina, San Diego, CA) using Illumina MiSeq Reagent Kit version 2.0 and 300 cycles paired-end runs.
Sequences have been deposited in the NCBI Sequence Read Archive and can be accessed through Biosample identifiers SAMN11784141–52.
Downstream genome analysis
The whole genome data were analyzed using open access tools through web-based servers that accept raw fastq files. Organism identification for the study isolates were determined using: 1) Center for Genomic Epidemiology (CGE) KmerFinder 3.0 (https://cge.cbs.dtu.dk/services/KmerFinder/) [5] with the selected database bacteria organisms (K: 16, P: ATG) updated July 2018. Run 10/16/2018. This method finds the unique 16-mers (k-mers) in the input sequence and predicts species based on the number of overlapping k-mers between the query genome and genomes in a reference database. The prediction is made at which it has the highest number of 16-mers in common despite of position. 2) Taxonomer (https://www.taxonomer.com/) run in full analysis mode which analyzes the incoming read data in two steps: (a) binning, which classifies reads into top categories, such as Human, Bacteria, Virus, etc. and (b) classification, which further categorizes each read into a particular phylum or species, if sufficiently unique. Bacterial reads are classified against 16S rRNA and bacterial transcriptomes compiled from Greengenes and UniRef50 databases [6]. 3) One Codex (https://onecodex.com/) [7] using the free research account that allows for analysis of 25 samples. One Codex classifies the input files against three databases of microbial genomes and genes a) the RefSeq Complete Genomes, b) the extended One Codex database and c) a targeted loci database.
Results are presented as absolute percentages regardless of phylogeny level so are presented as the percent of total bacterial reads classified.
Results
Approximately 7% (947/14,507) of all clinical isolates could not be identified by standard biochemical methods. A proportion of these, denoted as “unknown” (204/947 (21.5%); Fig 1), were randomly selected and examined using the BD Phoenix automated identification and susceptibility testing system. Identification to at least the genus level was achieved for 187/204 (91.7%) (Fig 2; S1 Tables). The largest number of isolates identified as Achromobacter species (46/204; 22.5%), with nearly 70% of cases being in adults ≥50 years of age (32/46, Table 1). One case appeared to be hospital onset (defined as positive blood cultures obtained >2 days after hospital admission), with blood obtained for blood culture 5 days after admission. All others were community-acquired infections. AST data was available for 36 isolates (78.3%) and all showed resistance to ampicillin, amoxicillin-clavulanate, aztreonam, and cefazolin. Cefepime resistance was determined in 14/36 isolates with the remaining 18 isolates scoring as intermediate (Fig 3; S1 Tables). Ten Achromobacter isolates identified by Phoenix had no associated AST data as isolate growth was too slow, preventing the control from reaching the required cutoff value and terminating that portion of the panel. On re-test a similar result was obtained.
Antibiotic abbreviation by drug class: Aminoglycosides: AMK–Amikacin, GEN—Gentamicin; Beta-lactam: PIP–Piperacillin, ATM–Aztreonam, TZP–Piperacillin-Tazobactam; Carbapenem: IPM–Imipenem, MEM–Meroenem; Cephalosporin: CAZ–Ceftazidime, CTX–Cefotaxime, FEP–Cefepime; CHL–Chloramphenicol; Fluoroquinolone: CIP–Ciprofloxacin, LVX–Levofloxacin; TET- Tetracycline; Folate Antagonist: SXT—Trimethoprim-Sulfamethoxazole. In the figure legend n = number of isolates for which BD Phoenix antimicrobial sensitivity test (AST) data was available/total number of species specific isolates in this study. For several isolates where AST data was not recorded the isolate grew too slowly to meet the growth control criteria cutoff. Clinical and Laboratory Standards Institute (CLSI) 2016 minimum inhibitory concentration break points were applied. Moraxella (n = 14) and Pasteurella (n = 12) species are not included in the BD Phoenix AST database and therefore this data is not available.
Pseudomonas species were identified in 35/204 isolates (17.2%) of which the most common were P. putida (11; 31.4%), and P. pseudoalcaligenes 8 (22.9%). P. oryzihabitans and P. aeruginosa had 5 and 4 isolates respectively, and one isolation each of P. luteola, P. mendocina and P. stutzeri. Three Pseudomonas isolates were not speciated. The majority of isolates were not able to meet the growth criteria required in the AST control, even upon re-testing, and susceptibility profiles were only available for 9/35 (25.7%) isolates. These were 100% resistant to ampicillin, amoxicillin/clavulanate (augmentin), cefazolin, and cefoxitin, as expected with intrinsic resistance to these antibiotics. All 9 were sensitive to amikacin, cefepime, imipenem and piperacillin/tazobactam (Fig 3; S1 Tables). Twenty percent of cases (7/35) were in children <5 years old (Table 1); and 3/4 likely hospital onset were in children <5 years old.
The third most common isolates were Moraxella species (14/204 cases (6.9%)), with 5 being hospital onset infections, and most cases occurring in adults ≥50 years old (9/14; 64.3%). AST profiles were not available as Moraxella species are not included in the Phoenix AST database [8].
Other genera identified are Sphingomonas paucimobilis (13/204 isolates), twelve isolations of Pasteurella species (7 P. multocida, 2 P. aerogenes, and 3 P. pneumotropica), and 9 isolations of Ochrobactrum anthropi.
Clinical outcome data was available for 126/204 (61.8%) of case-patients (Table 1), ninety patients (71.4%) had a complete recovery, or their condition was improving at the time of discharge. Twenty-three patients (18.3%) showed no improvement (13 were transferred to another hospital and two discharged against medical advice). Thirteen patients died (10.3%).
AST profiles were not determined for 93/187 (50%) isolates: 44/187 isolates (23.5%) as they were not included in the Phoenix AST taxa (15 different species; S1 Tables). A further 50 (26.7%) isolates grew too slowly so the cutoff value required in the AST growth control was not reached.
Table 2 summarizes the time-to-positivity ((TTP) defined as the time from the start of blood culture bottle incubation to a positive signal) and the patient self-reported antibiotic use within 72 hours of hospital admission. Antibiotic use was extremely high among cases with only 16.9% (31/183) reporting that no antibiotics were used. Blood culture TTP shows that 111/176 (63.1%) of cultures were called within 48 hours (Table 2), despite the high levels of antibiotic usage.
A total of 17/204 (5.9%) isolates could not be identified by the Phoenix system, five because of no growth. Characterization of the remaining 12 isolates was undertaken through WGS on an Illumina MiSeq platform.
Isolate NA66303 was identified as Laribacter hongkongensis by all 3 programs (Table 3; S2 Tables). The One Codex software identified the sample as a low-complexity/isolate and a high confidence identification with 88.8% of reads (n = 960,230) being specific to L. hongkongensis. CGE KmerFinder mapped 68.4% of Kmers to the strains HLHK9 and LHGZ1. The Taxonomer software classified 977,524/1,081,322 (90.4%) reads as bacterial, with 252,896 (34.1%) being classified to L. hongkongensis HLHK9.
The One Codex database was the only program to call isolate SA27898 with high confidence. It classified 81.4% of reads (n = 548,861) of which 79.6% (n = 436,853) were specific to Moraxella atlantae, with an estimated depth of coverage at 45X. CGE KmerFinder identified M. osloensis strain CCUG 350 with a query coverage of 3.1% to this template of 91,679 k-mers. No other significant results were obtained. Taxonomer was able to classify 275,794/548,852 reads (50.2%) as bacterial, but of these only 16,909 (6.1% bacterial or 3.1% of the total number of reads) were assigned to Enhydrobacter aerosaccus SK60. A further 8,505 reads were assigned to other Moraxella species (S2 Tables). Of note 267,145 reads (48.7%) were unclassified in Taxonomer.
NA45737 was identified by both One Codex and CGE KmerFinder as M. osloensis. In One Codex the isolate was characterized as having no single dominant species and M. osloensis was a medium abundant species (defined as 5–25% of classified reads) with 13.3% (n = 236,195) of classified reads. Table 4 shows greater detail of the read classifications for NA45737 by phylogeny. At the genus level, even though Enhydrobacter has approximately 2.6X more reads than the Moraxella, it was classified as the latter because no species was identified to the Enhydrobacter. Taxonomer binned 46.6% of reads as bacterial (1,773,485) and a larger proportion as unclassified (2,003,568; (52.7%)), with 29.0% of the bacterial reads assigned to E. aerosaccus SK60 (Fig 4).
Reads are classified against 16S sequences and protein sequences from Uniref50. The size of a given sector represents the relative abundance at the read level. Taxonomic ranks are hierarchical with the highest level placed in the center. Reads not classified at the species level, either because they are shared between taxa or represent novel microorganisms, are collapsed to the lowest common ancestor and shown as part of slices that terminate at higher taxonomic ranks (e.g. genus).
SC13199 was an Acinetobacter species isolate as corroborated by all 3 programs. One Codex counted 69.5% (1,386,621/ 1,994,443) classified reads as belonging to the Acinetobacter genus. The two highest abundance species were Acinetobacter sp. CIP 53.82 (365,836 reads (25.3%)) and A. indicus (349,113 (24.1%)). Taxonomer classified 61.7% of reads (n = 1,230,514) as bacterial with 15% (190,138/1,230,514) categorize as Acinetobacter with no dominant species. CGE KmerFinder identified A. indicus with 58.8% query coverage. A second isolate, NA45230, was identified as Acinetobacter with no speciation. One Codex classified 83.5% of reads of which 97.8% were Acinetobacter. Taxonomer mapped 49% of reads and 51.4% were Acinetobacter species; CGE KmerFinder had 24.7% of reads mapped to 6 Acinetobacter species.
One Codex classified NA69389 as a mixed sample with 2 high abundance species from 69.7% of classified reads: Flavobacteriales bacterium (56.8% of classified reads, split between strains UBA896 and UBA3891 (S2 Tables)) and Chryseobacterium hominis (18.1%). Taxonomer binned fewer reads as bacterial (56.8%) with 38.5% aligned to the family Flavobacteriaceae and 17.0% associated with the genus Chrysobacterium. The dominant species being C. oranimense (2.2%) and C. gleum (1.1%). CGE KmerFinder identified C. indologenes and C. taklimakanense, each with very low template coverages (3.0% and 1.7% respectively; S2 Tables).
Wohlfahrtiimonas chitiniclastica was the dominant species identified in NA45072 by both Taxonomer and One Codex. The former classified 59% of reads as bacterial and 65.1% of those as W. chitiniclastica. One Codex classified 77.2% of classified reads as W. chitiniclastica. CGE KmerFinder was unable to identify a dominant organism.
Isolates NA48754, NA55273 and NA64181 showed consensus across the 3 programs at the genus level: Delftia, Burkholderia (most likely B. cenocepacia) and Pseudomonas respectively (S2 Tables).
The organism associated with isolates NA62451 and NA62784 was clearly identified as Roseomonas gilardii by One Codex, with >80% of classified reads linked to R. gilardii (S2 Tables). In both isolates approximately 16% of reads mapped to R. mucosa. KmerFinder also identified R. gilardii as the dominant species with high coverage of chromosome 1 and 2, however Taxonomer was not able to provide a confident identification– 33% of reads were classified to the class Alphaproteobacteria and 10% to the family Acetobacteraceae. Only about 2% or reads were assigned to any particular species.
One Codex was the only program to identify high confidence calls–where the sample had >50% of unique genomic content of that organism (Table 3), and 5/12 (42%) unknowns were such.
Discussion
The correct and rapid identification of bacteria in a clinical microbiology laboratory, along with antimicrobial sensitivity testing, is an essential step towards the correct treatment of patients. Our analysis of 9 years of blood culture surveillance data shows that traditional diagnostic methodologies resulted in a positive identification in 93.5% of isolates (13,506/14,507). A fair proportion of the unidentified isolates were GNNF bacteria which often present as colorless/pale colonies that lack key metabolic characteristics, which impairs their identification by conventional methods. In 2015, the BD Phoenix automated identification and susceptibility testing system was installed in our laboratory and we retrospectively ran 204 previously unidentified GNNF isolates through the system. This allowed us to identify a further 91.7% (187/204) of isolates to at least the genus level. Due to their taxonomic complexity and high phenotypic similarity, identification to the species level represents a challenge even for the automated systems. In the majority of cases isolates were ubiquitous environmental organisms such as Achromobacter and Sphingomonas that are likely opportunistic pathogens [9–11]. There are an increasing number of case reports and reviews published suggesting a global increase in achromobacterial disease [10, 12], even so most clinicians remain unclear to their significance (and that of other environmental organisms) when clinically isolated. Additionally, effective treatment can be challenging due to these organism’s intrinsic and acquired multidrug resistance patterns. Our surveillance populations were from rural, agrarian provinces so infections with environmental organisms is not surprising in people who are occupationally exposed. Organisms from over 30 genera were identified. Moraxella (14/204) and Pasteurella (12/204) species are considered zoonotic pathogens and infection in humans is commonly associated with animal bite, scratch or lick, but infection without epidemiologic evidence of animal contact may occur [13].
Common skin and environmental organisms are often considered likely contaminants [14], however it is difficult to decide if their presence represents a clinically important infection or a false-positive result of no clinical consequence. In our study the contamination rate was around 4.7% (Table 1) and throughout our study efforts were made to reduce contamination through on-going training for nurses on percutaneous blood collection, use of chlorhexidine and alcohol for sterilization of the venipuncture site in adults [15] and tincture of iodine in children [16] using appropriate contact times, disinfection of culture bottle tops and single needle use for bottle inoculation. TTP has been suggested as a marker of bacterial load and used to distinguish bacteremia from contamination. Some studies suggest that cultures positive 3 to 5 days after incubation are more likely to represent contaminants [17, 18]. In our study 63% of cultures were positive within 48 hours and 81.3% (143/176) within 72 hours; and several other factors should be considered i.e. blood volume inoculated and antibiotic presence which make TTP difficult to interpret. It is critical to recognize that these isolates may represent true bacteremias and if untreated due to misinterpretation as contaminants could result in devastating consequences. Isolations of GNNF bacteria have long been disregarded as probable contaminants, but have recently emerged as important healthcare associated pathogens [19]. Our data however, suggests that few of these were nosocomial infections, but likely community-acquired, with many occurring in adults > 50 years old possibly associated with weakened immune systems. Lack of data on the disease epidemiology is a great obstacle to improve patient quality of care, which is further compounded by the lack of antimicrobial resistance data. For example both Moraxella and Pasteurella species are not included in the Phoenix AST database [8], either because of the low probability of occurrence or special growth requirements. With the significant increase in the incidence of multidrug-resistant pathogens in recent years, the high resistance rates seen in several of the GNNF organisms is concerning.
Traditional diagnostic technologies are insufficient for the identification of organisms not usually considered pathogenic. This limited scope has created bias in what we know about infection and the microbes capable of causing human disease. Our study illustrates that a small, but significant portion of ubiquitous environmental bacterial species can be true pathogens. In our laboratory, these limitations were overcome through the use of an automated microbial identification system, the BD Phoenix.
There was an even smaller proportion of isolates not identified through this system, and we attempted to use WGS to fill this gap. This is possible as small, affordable instrumentation such as the Illumina iSeq or MiSeq, along with decreasing sequencing costs, make WGS an attractive option for lower throughput clinical microbiology and public health laboratories. This does not allow for comprehensive detection of pathogens from clinical samples (metagenomics analysis) but expands on conventional diagnostic testing where it fails to detect the etiologic agent. Targeted 16S rRNA NGS kits are recently available for specimen microbiome composition profiling and offer a cost-effective method for bacterial taxonomic classification, similarly viral genera can be targeted by combining VirCapSeq-VERT and unbiased NGS workflows [20, 21].
Our study illustrates the value of isolate WGS: 12 previously unidentified isolates by conventional or automated methods were classified at least to the genus level. Of note, WGS also allows for examination of antimicrobial resistance genotypes, but this was beyond the scope of this study. The biggest challenge we faced with the introduction of NGS to our laboratory was the data analyses. Laboratory scientists generally lack experience in NGS short-read sequence bioinformatics and in low- or middle- income countries, laboratory computing resources are often limited and unable to handle large data sets. Fortunately, there are rapid, user-friendly web-based tools that can be applied without large investments in trained personnel or computational infrastructure. We chose three services accessible through personal computers with no requirements for computational infrastructure on the user side. For both the Phoenix automated identification system and the NGS web-based tools, the bacterial identification is highly dependent on the reference databases used. As long as there are similar microbes in the database unknowns can be identified. We believe the differences in performance between the selected platforms is a function of the reference database used. For bacterial identification Taxonomer uses 16S rRNA gene sequences from the Greengenes database and the bacterial subset of UniRef50 [6]. The KmerFinder database is a monthly updated extraction from the National Center for Biotechnology Information of whole bacterial genomes, and only contains genomes that have registered taxonomy associated [22]. One Codex has a database collected from public and private sources that is curated through manual and automated steps to remove low quality or mislabeled records [7]. Sequence reference databases are heavily biased toward common pathogens at the expense of environmental microbes and commensals. These biases, sequence inaccuracies and incompleteness are challenges for moving the field forward. Databases should include accurate annotations and high-quality reference sequences that provide a true diversity of strains. Kirstahler et al. [23] found that 43% of bacterial reference genomes, particularly incomplete ones, contained ambiguous sequences and removing these from databases reduced the number of false positive hits. This supports the need for curated microbial genome databases. Our results illustrate that reads derived from taxa that are absent from databases can result in false-negative and false-positive classifications, especially at the genus and species level. Different measures are provided in the outputs from the three programs and no parameters have been clearly defined to qualify an identification. Consistent application of identification parameters would help move this approach forward.
The advantages of web-based analysis for laboratories is obvious. The intensive computing happens on a server located anywhere in the world, which reduces the necessity to invest in expensive computers and bioinformatics resources, and lets scientists interact with their data immediately and directly. Results are obtained rapidly and can be presented in a user-friendly interface such as a sunburst chart (Fig 4) with a dynamic graphic view that presents corresponding species’ proportion. The choice of an appropriate analytical tool is crucial and not trivial. Results still require interpretation by a microbiologist, and an understanding of the analytical limitations is essential, as is clearly evident in our data. Even with these limitations NGS technology should be considered an essential supplement to culture-based methods, particularly where standard diagnostic tests consistently fail to identify the causative pathogen. The development of targeted sequencing kits will enable organism identification from specimens on lower throughput instruments such as the iSeq and MiSeq, a crucial step in any clinical/public health microbiology investigation.
The commonest GNNF bacteria (Acinetobacter spp. and P. aeruginosa) are widely considered common nosocomial infections [24–26], and this was evident in the two Thai rural provinces under surveillance here; Rhodes et al. [1] showed these were the second and sixth commonest hospital onset infections respectively. In this same study they were the 7th and 10th commonest pathogens causing community onset bloodstream infections. Our data also illustrates that the less commonly identified GNNF isolates are predominantly community onset (Table 1). This is a concern as the phenotypic similarity and taxonomic complexity makes these organisms frequently difficult to identify, and their clinical significance may be difficult to determine as these organisms rarely cause invasive infections. From the literature we discover that L. hongkongensis causes non-bloody acute diarrhea with cases linked to eating freshwater fish [27]. It can cause invasive [28, 29] and even fatal disease [30], and has mainly been described in East Asia [28, 31] but a worldwide distribution is suggested by case reports from Europe [32] and North America [33]. The few reported cases of W. chitiniclastica infection globally show septicemia and skin and soft tissue infections [34–36]. Numerous cases are documented in relation to maggot infestations and several affected were homeless [34, 37, 38]. Bacteremic cases have been reported from North and South America [34, 38], Europe [37], the United Kingdom [39]. As with our unidentified isolates, Roseomonas species are considered opportunistic pathogens because of their low pathogenic potential in humans, and R. gilardii is most frequently related to human infections [40–42]. It is significantly associated with septicemia and underlying immunocompromised conditions [40, 43]. Several cases have been presented of catheter-related bacteremia with immunosuppression raising [41, 43] the possibility that Roseomonas species may be a part of the normal skin flora of humans. Finally M. atlantae infections are rarely reported in the literature and the few cases of bacteremia appear to all have underlying conditions predisposing them to infection [44, 45]. These organisms are rare, difficult to identify and are easily overlooked so it is likely that their occurrence is underestimated. The clinical significance and appropriate therapy for patients with these bacteremias are not well studied. This together with the emerging challenge of multi-drug resistance, is of serious concern for treatment.
The use of WGS in public health or clinical microbiology laboratories would provide unparalleled improvements in pathogen identification, antibiotic resistance detection, and outbreak investigations, however, this capacity is severely hindered by lack of common standards. Regulatory agencies have not yet provided (or even proposed) standard guidelines, testing has not been standardized, and benchmarks have not been set. External quality assurance and proficiency testing programs are in progress. Analytical pipelines with well-curated, continually updated reference database are also important components to implementation. Once these hurdles have been achieved the incorporation of NGS into clinical and public health routine workflows is achievable.
Disclaimers
Findings and conclusions presented in this paper represent the views of the authors and do not necessarily official position of the U.S. Centers for Disease Control and Prevention or the institutions with which the authors are affiliated.
Supporting information
S1 Tables. BD Phoenix summary data.
Summary data extracted from the BD Phoenix automated identification system reports for each isolate run on the combination panel NMIC/ID 55.
https://doi.org/10.1371/journal.pntd.0007729.s001
(XLSX)
S2 Tables. WGS analysis summaries.
Collated data from results generated by the 3 web-based platforms: KmerFinder, Taxonomer and One Codex for the whole genome sequence data from 12 unidentified isolates.
https://doi.org/10.1371/journal.pntd.0007729.s002
(XLSX)
Acknowledgments
We are grateful for the contributions of the many study collaborators, including Nakhon Phanom and Sa Kaeo Provincial Health Offices, surveillance officers, and the district and provincial hospital staff. The authors would like to acknowledge the contributions of TUC staff Thantapat Akarachotpong and Apiwat Lapamnouysup for their continued support of our surveillance, data and laboratory activities.
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