Technology for detecting biothreat agents requires accurate identification of a broad array of bacterial and viral organisms that can cause severe disease and/or death, whether they occur as a result of a biological attack or from a natural source in the environment. The National Institute of Allergy and Infectious Diseases (NIAID) has compiled a list of priority pathogens for biodefense (http://www.niaid.nih.gov) and several of these are also defined as select agents (http://www.selectagents.gov/) by various agencies such as Health and Human Services (HHS) and the United States Department of Agriculture (USDA) (some of the vaccine and live attenuated strains are, however, excluded from the select agents list: http://www.selectagents.gov/Select%20Agents%20and%20Toxins%20Exclusions.html). These bioagents are often virtually indistinguishable from a group of phylogenetically related species or subspecies often referred to as “near neighbors”. Near neighbors to biothreat agents may be human pathogens or harmless environmental organisms. The biothreat agent along with its near neighbors can be thought of as a biothreat cluster or biocluster for short. When monitoring for biothreat agents, it is important to determine whether any organisms from the biothreat clusters are present and to precisely identify the organism as a biothreat agent or a near neighbor. In some cases, the near neighbors are commonly found in the environment, and it is possible that a pathogenic near neighbor of a biothreat agent might deliberately be chosen for use in a biological attack. Thus, effective biosensor technology must be capable of identifying a broad array of biothreat agents and distinguishing these threats from their near neighbors unambiguously.
This requirement presents a problem for conventional molecular methods where specific PCR is used in conjunction with probes to detect specific bioagents. Not only are potentially pathogenic near neighbors present in a specimen often not distinguished, but the near neighbors sometimes react to produce false positives for the biothreat agent. To overcome these limitations, we have developed a new strategy for biothreat identification that couples biothreat cluster-specific PCR amplification to electrospray ionization/mass spectrometry (PCR/ESI-MS)–. The biothreat assay is performed on a hardware platform with prototypes known as TIGER and as the Ibis T5000, that is now marketed commercially as the Abbott PLEX-ID. In the PCR/ESI-MS approach, PCR primers are designed to amplify regions of the genomes of all species from the entire biothreat cluster, encompassing groups of organisms that include the biothreat and the associated near-neighbor organisms. The primers are designed to target genomic regions sufficiently conserved such that amplification occurs comprehensively within a biothreat cluster, but not outside of the cluster. The amplification products are then analyzed by mass spectrometry, which weighs the amplicons with sufficient mass accuracy that the base composition of A, G, C, and T nucleotides that make up the amplicon can be accurately counted. The base composition serves as a signature of each organism and enables identification and discrimination of the biothreat agents and their near neighbors with equal facility. In addition, previously undiscovered or newly emerging organisms from within these biothreat clusters are also detected. The database of signatures against which multiple additional pathogens could be identified increases over time as newer strain variants are archived and tested. An example of this was the discovery of the 2009 H1N1 virus by the Naval Health Research Center,; this offered the first characterization of a previously unrecognized influenza strain, demonstrating the capability of the PLEX-ID in identification of a real-world case of novel pathogen emergence. Because the mass spectrometer weighs all amplicons presented to it, the amplicons from unexpected or new organisms are detected and identified,,,.
Using this strategy, we designed a comprehensive assay to detect ten bacterial and four viral biothreat clusters. The assay identified the major biothreat organisms and differentiated these from their near neighbors and from thousands of other bacteria and viruses, providing a seamless net of biosurveillance for these clusters in a comprehensive biothreat assay (Figure 1). In this manuscript, we provide a detailed description of the methodology and the results of formal validation experiments with a variety of biothreats, near neighbors, and specimen types. We also describe several examples of how the assay has been used in real-world biothreat scenarios.
Bacillus anthracis, which causes anthrax in animals and humans, is closely related to B. cereus (which causes human food poisoning), B. thuringiensis (an insect pathogen and a biological insecticide), and B. mycoides (considered a harmless saprophyte). Members of the this group, known as the Bacillus cereus clade, are environmentally ubiquitous. Classical microbiological methods can only differentiate B. anthracis from other near-neighbor species when the unknown isolate is shown to cause anthrax in laboratory animal models. Classical molecular phylogenetic tools, such as the analysis of rRNA gene sequences, cannot distinguish among members of the B. cereus clade.
We demonstrate here that two primer pairs, BCT352 targeting the translation initiation factor IF-4 (infB) gene and BCT355 targeting the small acid-soluble spore protein (sspE) gene, provide signatures that can distinguish B. anthracis from all of the near-neighbor species within the B. cereus clade. Full virulence of B. anthracis requires the presence of two plasmids, pXO1 and pXO2, containing three toxin components (protective antigen, lethal factor, and edema factor) and an anti-phagocytic capsule. The primers used for the detection of these two plasmids (BCT2379 and BCT2381) were chosen to capture a previously described single-nucleotide polymorphism (SNP). This region in each of the plasmids provides two different alleles that can be used to distinguish B. anthracis Ames and other Ames-like strains from non-Ames strains. Thus, the positive identification of the B. anthracis chromosome using the infB and sspE targets, combined with detection of the virulence plasmid signatures, can be used to differentiate non-pathogenic, vaccine, fully virulent, and genetically modified strains of B. anthracis.
To demonstrate the resolving capabilities of these genomic signatures, we obtained a collection of 34 bacilli from the United States Army Medical Research Institute for Infectious Diseases (USAMRIID). These include fully virulent, partially virulent, and avirulent B. anthracis strains and an assortment of near-neighbor bacilli (Table S1). Each isolate was correctly identified by comparison of base composition signatures obtained in the biothreat assay with genomic sequence data obtained from GenBank (Table 2). The infB locus provided identical signatures across all B. anthracis strains tested, whereas the sspE locus provided two different allelic signatures. The majority of the B. anthracis strains tested had a base composition signature of “A42G23C23T21,” whereas the B. anthracis strains from the western North American region showed a SNP at this locus and had the signature of “A41G24C23T21.” As predicted, the Ames-like strains were different from the rest of the B. anthracis strains in the pXO1 and pXO2 loci. An additional 89 strains of B. anthracis were obtained from the Keim Genetics Lab; these strains have various phylogenetic variations (Table S2). The diverse strains in this collection were correctly identified in our assay. The A1.a clade showed the SNP pattern at the sspE locus previously associated with the western North American lineage (Table S3). These strains were previously reported to be distinct from other Clade A strains as they contain a 153-bp allele in the CG3 locus.
Representative strains of the B. cereus clade, including 24 B. cereus strains and 12 B. thuringiensis strains were also tested (Table S2). None of these carried the virulence plasmids pXO1 or pXO2 (data not shown). Futher, the base compositions observed for the two genomic markers showed distinct signatures compared to B. anthracis. The amplicon for sspE showed a 6-bp deletion compared to the B. anthracis signatures, whereas the infB signature was the same length but had a different base composition. Based on the combined compositions of these two primer regions, the B. cereus/B. thuringiensis biocluster could be divided into 29 distinct genotypes. Some of the B. thuringiensis species have individual clusters but most are related to B. cereus species. Several studies over the past two decades have looked at the fine structure of the B. cereus clade and have reported similar findings. Nucleic acids from species outside the B. cereus clade, such as B. subtilis and B. megaterium, were not amplified with the sspE primer pair. The advantage of measuring multiple signatures across the genome and in associated plasmids is that this provides sufficient information to characterize the biothreat agent (i.e., vaccine vs. virulent strains of B. anthracis) as well as distinguish it from its near-neighbors.
The bubonic plague caused by Yersinia pestis is a highly contagious disease that persists endemically in many countries in the world with unpredictable resurgences. Y. pestis is classified as a biothreat agent. It is a nonmotile, capsulated, Gram-negative bacterium transmitted to humans and susceptible animals through flea bites or aerosols. Other species in this biocluster include Y. enterocolitica (a diarrheagenic pathogen), Y. frederiksenii, Y. ruckeri, and Y. pseudotuberculosis (an enteric pathogen). Y. pseudotuberculosis exhibits more than 90% genomic homology with Y. pestis, making much of the Y. pestis genome unsuitable for amplification as base composition signatures do not resolve Y. pestis and Y. pseudotuberculosis
,. Two specific markers within the Y. pestis genome were identified that provide differentiation from Y. pseudotuberculosis. One of these is located in the valyl-tRNA synthetase gene (valS). This region (Table 1) has a SNP that is retained in all the Y. pestis genomes studied to date and that is distinct from the Y. pseudotuberculosis signature for this region (Table S4). A second primer pair was designed to target the invasin gene invA, a surface-expressed protein that is reponsible for cellular penetration and invasion. Although both Y. pseudotuberculosis and Y. enterocolitica contain intact invasin genes, the central region of the Y. pestis inv gene is disrupted by a 708-bp IS200-like element. Primers targeting this region allow for the unambiguous detection of Y. pestis (Table S4). In addition, Y. pestis harbors plasmids that are required for the expression of virulence–. Primer pairs targeted against the pla gene from the pPCP1 plasmid of Y. pestis and the caf1 gene from the pMT1 plasmid of Y. pestis were included in the assay to provide specific detection of virulence plasmid-carrying Y. pestis.
Genomic data from the completely sequenced Y. pestis genomes were used to verify the expected signatures for these primer pairs (Table S4). All Y. pestis strains for which relevant sequence was available in GenBank showed identical base composition signatures. Partially virulent Y. pestis strains such as Y. pestis Angola (PLA+/CAF−) and pestoides F (PLA−/CAF+) were correctly identified. These results were further confirmed by experimental testing a collection of seven Y. pestis strains with known phenotypes obtained from the USAMRIID culture collection (Table S5). In addition to the four virulent phenotypes containing PLA+/CAF+, two strains (Nairobi and Java 9) lacking the caf gene and pestoides F lacking the pla gene were analyzed. All of the results showed data consistent with the expected molecular signatures. Finally, a set of 15 near neighbors of Y. pestis were tested using the assay; each was correctly identified and differentiated from the Y. pestis signatures (Table S6). In particular, this assay clearly distinguished the Y. pestis signatures from those of Y. pseudotuberculosis, which is often the confounder in molecular assays.
The Francisella tularensis biothreat cluster is comprised of the select agent F. tularensis and the near-neighbor species F. philomiragia and F. novicida. F. tularensis is the causative agent of tularemia, a disease that affects humans and other mammals; the natural reservoir is thought to be lagamorphs and rodents with ticks as the primary vector,. F. tularensis has been divided into three subspecies: F. tularensis subsp. tularensis (type A), which is divided into subtypes A.I and A.II., is the most virulent and is found primarily in North America and Europe. F. tularensis subsp. holarctica (type B) is less virulent and found in Europe and in Asia, F. tularensis subsp. mediaasiatica has been isolated only in Central Asia and is considered to be of lower virulence. The latter two subspecies can cause an incapacitating infection, however. The near-neighbor species F. novicida (considered by some investigators to be another subspecies of F. tularensis) and F. philomiragia are reportedly of of low pathogenicity and cause disease only in immunocompromised humans. Because of the potential of each of these species and subspecies to cause disease of varying severity, it is important to both detect and distinguish these species and subspecies.
In the biothreat assay, the Francisella biocluster is identified by two genus-specific primer pairs targeting the asd (BCT2328) and galE (BCT2332) genes (Table 1). Use of galE for identification of Francisella genus has been previously described. Based on inspection of the sequence alignments for these genes of all available Francisella sequences, both of these primer pairs are expected to generate amplicons from all known members of the Francisella genus. Base composition analysis of the expected amplicons shows that Francisella species and subspecies are distinguishable from each other (Table S7). F. tularensis base counts are characterized by a homogenous signature for all type A.I strains. Schu S4 is the type strain, and the rest of the Francisella signatures are defined here as variations compared to this reference strain. F. tularensis subsp. tularensis str. WY96-3128 (type A.II) had a T to C SNP in the galE primer pair region. The same signature was observed for F. tularensis subsp. mediaasiatica FSC217 strain. This is in agreement with genome-wide SNP analysis, which indicates that differentiation of these particular strains likely predated the acquisition of the asd or galE mutations that characterize the subspecies. Further, the subspecies mediaasiatica is reported to be closer to the Type A.II lineage, even though its pathogenicity is characteristic of the Type B strains. F. tularensis subspecies novicida was distinguished by a G to A mutation from the consensus seen in F. tularensis signature from primer pair BCT2332.
To demonstrate the specificity of the assay for the Francisella biocluster, we tested a collection of 57 reference isolates obtained from the USAMRIID (Table S7). Included were members of all phylogenetic lineages within the Francisella biocluster. Francisella species were correctly identified and grouped into phylogenetic clades. All 34 Type A.I subspecies yielded identical base compositions for both primer pairs consistent with the predicted amplicons from the Schu S4 genome. Twelve of the type B, subspecies holarctica strains had signatures that differed from the Type A.I subspecies in both the primer pairs, clearly differentiating the two major groups of the Francisella genus. Type A.II strain signatures were different from the Type A.I signatures by a single T to C SNP in the galE primer amplicon, consistent with the genome sequence of Francisella subsp. tularensis strain WY96-3128. However, two of the Type B strains tested, FRAN041 (Strain JAP-Cincinnati) and FRAN011 (Strain LR) could not be distinguished from the Type A.II subspecies using these two primer pairs. As described above, this signature appears to be consistent with subsp. mediaasiatica strains as well. Sequence similarities between the Type B Japanese strains, F. tularensis mediaasiatica and Type A.II lineages were previously noted (, Duncan, manuscript in preparation). The F. novicida strain (FRAN003) differed from Type A.I by a single SNP in the galE region, whereas the species outlier, F. philomiragia, was clearly different from the rest of the F. tularensis biocluster in both primer regions. The asd primer pair produced the expected amplicon for all strains of F. philomiragia. In contrast, the galE locus primer pair did not yield an amplicon for all strains. This region in a recently sequenced F. philomiragia strain (ATCC 25017) has mismatches to the primer regions (Genbank Accession Number NC_010336). Even without data from the asd primer pair, the differentiation of this species from other F. tularensis was unambiguous. Based on the two primer analysis done here, Francisella strains could be categorized into five groups: Types “A.I,” “B,” “novicida,” “philomiragia,” and a fifth group that contains strains within the Type A.II/mediaasiatica/holarctica/Japanese lineages that might have diverged before the acquisition of the asd and galE mutations.
The genus Vibrio, within the family Vibrionaceae, represents a diverse group of Gram-negative bacteria that contain at least 65 described species, most of which are found exclusively in aquatic environments. Of these, at least 12 species are known human pathogens, and several other species are known to be pathogenic to marine mammals and fish. Members of this genus include Vibrio cholerae, the causative agent of cholera. Although large outbreaks of cholera are caused by toxigenic strains of the serogroups O1 and O139, non-toxigenic strains cause sporadic cases of disease. Other important pathogens in this group include V. parahaemolyticus and V. vulnificus, which cause significant morbidity worldwide.
We previously described a high-throughput pan-Vibrio assay for simultaneous identification of all known pathogenic Vibrio species. The assay included broad-range PCR primers that targeted conserved sites in several housekeeping genes and the V. cholerae-specific toxin genes ctxA and ctxB. Base compositions from these regions were able to distinguish the various species tested and provided sub-species differentiation within the V. cholerae isolates. For the biothreat assay, three of the primer pairs from the pan-Vibrio assay were used (Table 1). One of these primer pairs was exclusive to V. cholerae species detection (ompU). One amplifies the toxin gene ctxA. The third primer pair, targeted to gapA gene, was designed to amplify most of the known species in this family and the resulting base compositions provide species-level resolution (Table S8). Genomic data analysis and experimental analysis of 42 well-characterized strains representing the phylogeny of this biocluster was used to demonstrate assay specificity.
To demonstrate the ability to detect and identify Vibrio spp. from natural aquatic samples, a subset of samples collected in 2006 from freshwater lakes and sites along the Georgian coast of the Black Sea were tested. Six different Vibrio species were detected and identified in 13 of the 19 natural water samples collected from both freshwater and seawater sites spanning the seasons summer to winter in this study. More than one Vibrio species were also detected in some samples. These detections were confirmed by 16S rRNA clone library analysis.
The Burkholderia biocluster is identified in the biothreat assay by two primer pairs, BCT1070 and BCT1071 (Table 1). The primer sets amplify conserved regions of the RNA component of ribonuclease P (RNAse P) and regions CR-IV and CR-V that bracket the highly variable extension P19. These primer pairs have homology to this gene from other proteobacteria; however, the length and base composition of the resulting amplicons are highly discriminating. The information content within amplicons from BCT1070 and BCT1071 is basically the same, and this feature is meant as a built-in redundancy check for speciation calls. Some B. pseudomallei strains provide the same signature as B. mallei (Table S9), but the next closest relative, B. thailandensis, is clearly segregated. Analysis of known sequences indicates that the assay will resolve most known Burkholderia species (with members of the B. cepacia biocluster being further distinguished through their distinct amplicon lengths. A notable exception is the polychlorinated biphenyl reducer B. xenovorans, which shows the same mass signature as B. pseudomallei str. 668. While this is a source of potential false positive reporting of B. pseudomallei, the occurrence of B. xenovorans, which occupies a distinct ecological niche and is not pathogenic, is quite rare.
Several extremely dangerous pathogens that can infect humans and animals are found in the Brucella biocluster. These bacteria are easily transmitted by ingestion of unsterilized milk or meat from infected animals or close contact with their secretions or by inhalation of aerosols. Brucella species have slightly different preferred host specificities: B. melitensis infects goats and sheep, B. abortus infects cattle, B. suis infects pigs, B. ovis infects sheep, B. canis infects dogs, and B. neotomae infects wood rats. Taxonomists have alternated between individual species naming and naming as a single species B. melitensis, containing B. melitensis 16M and five other biovars: abortus, canis, neotomae, ovis, and suis. Recently, four additional species of Brucella have been described, including two that infect marine mammals. The current convention adopted by the International Committee on Systematics of Prokaryotes, subcommittee on Brucella (http://www.the-icsp.org/subcoms/Brucella.htm) recommends re-approval of the classical Brucella species with their recognized biovars.
In the biothreat assay, members of the Brucella biocluster are identified by two primer pairs, BCT1111 and BCT1112, that amplify two non-overlapping regions of the RNA component of ribonuclease P gene (Table 1). These two regions were chosen for their ability to amplify all Brucella species and to distinguish these from other near-neighbor Alphaproteobacteria species. Table S10 shows the base compositions expected from the two Brucella primer pairs used in the assay; signatures were derived from GenBank data for the sequenced Brucella species.
The genus Clostridium consists of relatively large, Gram-positive, rod-shaped bacteria in the phylum Firmicutes. Most clostridia are opportunistic pathogens that are anaerobic, but spores are able to survive long periods of exposure to air. Most of the clostridia are saprophytes, but a few are pathogenic in humans, primarily Clostridium botulinum, C. perfringens, C. difficile, and C. tetani. Botulism is an acute neurological disease caused by a neurotoxin produced by C. botulinum. Eight C. botulinum neurotoxin types have been identified: types A, B, C1, C2, D, E, F, and G,. Types A, B, E, and F cause human botulism. Types C and D cause most cases of botulism in animals. C. perfringens is classified into five types on the basis of its ability to produce one or more of the major lethal toxins, alpha, beta, epsilon, and iota. C. tetani is another clostridium that can be highly toxigenic to humans. Other clostridia can be highly invasive under certain circumstances.
In the biothreat assay, the clostridia are identified using two primer pairs, BCT1075 and BCT1076, targeting RNase P. These two primer pairs are capable of amplifying all members of the genus Clostridium and differentiate the major species (Table S11). The C. botulinum strains form three base composition clusters, differing from each other by one or more SNPs in each of the two amplified regions. Types A, B1, and F form a unique group and are distinguishable from all other clostridia. The second group consists of types A2, A3, and Ba4 have base compositions that overlap with C. sporogenes. The third C. botulinum group comprises types B and E and some strains of C. perfringens as well as the recently sequenced C. ljungdahlii. Most strains of C. tetani and the opportunistic clinical pathogen C. difficile form unique groups. Other clostridia that are rarely human pathogens are clearly differentiated from all the above, thus providing a rapid means of detection of the pathogenic clostridia.
Q fever is a zoonosis caused by Coxiella burnetii, an obligate Gram-negative intracellular bacterium. C. burnetii infects various hosts, including humans, ruminants, and pets. Because of its highly infectious nature, C. burnetii is recognized as a biothreat agent. The bacterium can exist in a spore-like life cycle and remain viable and virulent for many months. Phylogenetically it occupies a unique niche, with very few near neighbors. The closest known organism based on genomic and 16S rRNA analysis is Legionella pneumophila
In the biothreat assay, we use primers targeting isocitrate dehydrogenase (icd) and insertion sequence IS1111A transposase for unambiguous detection of C. burnetii (BCT1079 and BCT1080, respectively). The latter occurs in multiple copies in the bacterium (from 5 to 31 copies),. Base composition analysis of the expected products showed that all sequenced Coxiella genomes (NM, Dugway, K, and Q) share identical signatures in both amplified regions (Table S12). These primer pairs do not amplify Legionella (data not shown) and should not amplify nucleic acids from any of the other proteobacteria. The C. burnetii G (Q212) sequenced genome showed two different base counts at the IS111A locus, suggesting a SNP variant in this region, similar to operonic diversities often seen in 16S rRNA sequences for other bacteria.
The Rickettsiaceae are a family of obligate intracellular small Gram-negative coccobacilli that infect humans chiefly through insect vectors, mostly from animal hosts. The rickettsial fevers are acute bacteremic illnesses characterized by headache, mental confusion, and, in severe cases, meningoencephalitis. The genus Rickettsia is divided into three main groups: R. prowazekii, the agent of classical epidemic typhus; R. typhi, the causal agent of endemic typhus; and the “spotted fever” group of rickettsiae, which contains a large number of species transmitted from rodents, dogs, and wild animals by ticks. The latter group includes R. rickettsii, the agent of Rocky Mountain spotted fever; R. conorii, the cause of tick typhus in the Mediterranean area and in India; R. africae, which is found in the African veld; R. japonica, R. australis, and a variety of other similar organisms that are widely distributed in Asia and Australia.
Organisms in the Rickettsia biocluster are identified by two primer pairs, BCT1083 and BCT1084, which prime different regions of the RNA component of the RNase P. Since the primers target Rickettsia-specific sequences, no amplification is expected outside the Rickettsiaceae family. Using these two primer pairs, members of the Rickettsia biocluster can be distinguished from each other. In particular, R. prowazekii, R. typhi, and R. rickettsii species yield distinct PLEX-ID base composition clusters (Table S13).
Enterobacteriaceae (Escherichia coli O157:H7, Shigella, Salmonella enterica)
Diarrheagenic enterobacteria, such as E. coli, Salmonella, and Shigella species, are closely related organisms that are ubiquitous food and water-borne pathogens. These agents have the potential to cause significant damage to the food supply and are high-risk clinical pathogens. There are over 3,500 Salmonella subtypes, and all are human pathogens. The majority of these serotypes belong to a single Salmonella species, Salmonella enterica, which includes six subspecies (subsp. enterica, subsp. salamae, subsp. arizonae, subsp. diarizonae, subsp. houtenae, and subspecies indica). For Shigella, there are four species (Shigella dysenteriae, S. flexneri, S. boydii, and S. sonnei); all can cause enteric illnesses. There are at least five pathotypes of E. coli: enteroinvasive E. coli (EIEC), enterotoxigenic E. coli (ETEC), enteropathogenic E. coli (EPEC), enterohemorrhagic E. coli (EHEC), and enteroaggregative E. coli (EAEC). Symptoms caused by these organisms are often similar, and these organisms are difficult to differentiate by genomic analysis.
In the biothreat assay, a primer pair targeting the valine synthetase (BCT358) gene provides identification of all of the above species in the Enterobacteriaceae family. In addition, this primer pair also provides species resolution of Yersinia as discussed previously. The base count clusters shown in Table S14 demonstrate the ability of this primer pair to amplify members of the family Enterobacteriaceae and to provide species-level differentiation of Salmonella from E. coli and Shigella, although the Shigella species base counts are indistinguishable from a group of the E. coli strains using this primer pair (PLEX-ID cluster 5, Table S14). This is consistent with the previously described phylogenetic relationship of these bacteria. Importantly, the pathogenic E.
coli O157:H7 species is clearly differentiated from all other Enterobacteriaceae except enteropathogenic E. coli O55:H7, strain 5905 (BC cluster 1). This strain is considered the immediate ancestor of the E. coli O157:H7 lineage and contains the shiga toxin, which is atypical for other E. coli O55:H7 strains. The Salmonella species are divided into several clusters, but cannot be grouped according to the subspecies nomenclature based on data from this assay. These pathogens can be resolved in a more targeted food-borne bacteria assay (manuscript in preparation).
In order to provide additional separation between E. coli and Shigella species, we added two more primer pairs targeting two different regions of invasion plasmid antigen H (ipaH). As shown in Table S15, these two primer pairs amplify all Shigella species but do not amplify E. coli or Salmonella (data not shown). Thus, the four major Shigella species can be clearly identified as a group distinct from E. coli using information from the three primer pairs. This assay, however, does not distinguish among the various Shigella species.
The genus Alphavirus, of the family Togaviridae, contains at least 37 species and subtypes or varieties and at least 23 have been associated with human illness. Some New World Alphavirus, such as the eastern equine encephalitis viruses (EEEV) and Venezuelan equine encephalitis virus (VEEV) complex, are considered potential bioweapons. Other important members of this virus group include the western equine encephalitis virus (WEEV) complex viruses that include Sindbis virus. The Old World cluster includes Chikungunya virus and Semiliki Forest virus complex among others. We have previously described an assay for pan-Alphavirus detection and demonstrated the utility of this with field-collected mosquito and clinical samples. This assay detects a wide variety of Alphavirus in naturally occurring biological backgrounds and was used to identify a virus that was a novel subtype IIID in the VEEV complex. Two of the three primer pairs described previously were used in the biothreat assay and have been tested against a broad panel Alphavirus isolates representing both the Old World and New World Alphavirus (Table S16). Both are targeted to the NS1 region on the 5′-end of Alphavirus genome. Primer pair VIR966 exhibited the greatest breadth of coverage. Base counts from this primer pair amplicon alone were sufficient to distinguish most of the isolates at the species and strain level. The second primer pair (VIR2499) used in the study contains inosine (I) nucleotides at selected sites in both the forward and reverse primers to enhance hybridization, but despite this, did not amplify several of the Old World Alphavirus. All the Alphavirus samples tested were detected with at least the VIR966 pair and most were identified to strain or subtype level.
The genus Orthopoxvirus contains several species of related viruses including the causative agent of smallpox (Variola virus). In addition to smallpox, several other members of the genus are capable of causing human infection, including monkeypox, cowpox, and other zoonotic rodent-borne poxviruses. We have previously described a pan-Orthopoxvirus assay for identification of all members of the genus based on four PCR reactions targeting Orthopoxvirus DNA and RNA helicase and polymerase genes. The assay can detect and identify diverse orthopoxviruses, provide sub-species information, and characterize viruses from the blood of rabbitpox virus-infected rabbits. In the biothreat assay, we used two of these four primer pairs (VIR979 and VIR985). The two provide species-level resolution of the genus Orthopoxvirus and, in particular, differentiate the Variola and monkeypox viruses from each other and from vaccinia, rabbitpox, and ectromelia viruses (Table S17).
Influenza A viruses are important respiratory pathogens that cause annual epidemics and occasional pandemics. Influenza viruses cause serious global economic and public health burdens. Emergence of new influenza A virus strains can be caused by “antigenic shift,” resulting from reassortment of gene segments (including H and/or N types), by “antigenic drift” resulting from the continuing accumulation of mutations in the H and N genes, or by species jump by a virus that acquires the ability to infect and be transmitted among humans as has happened in the influenza pandemics over the last century,. In April 2009, a previously unseen virus emerged and rapidly spread globally leading to the first influenza pandemic of the 21st century. The continuous evolution of influenza genomes together with reassortment events pose challenges to the effective monitoring of influenza viruses. We previously described an RT-PCR/ESI-MS assay for the detection and characterization of influenza viruses,,,,,. Identification of each influenza A virus is based on the summation of base composition signatures obtained from the six to eight primer pairs.
In the biothreat assay, two of the previously described sets of primer pairs (VIR2798 and VIR1266) were included for rapid detection of presence of influenza A or B virus. Base composition data from the amplified regions of over a 1000 influenza A H5N1 strains from GenBank were analyzed. The majority of these could be grouped into the six base composition clusters as shown in Table S18. These clusters were unique and distinct from other avian and non-avian signatures (data not shown), with the exception of two instances of avian H9N2 sharing base composition overlap with one or more of the avian H5N1 clusters. In both these instances, however, all the overlapping strains were from local outbreaks (Shantou 2003 and Guangxi 2006) and were not widely distributed. Similar correlations were found for pandemic 2009 H1N1, seasonal H3N2, and seasonal H1N1 viruses as previously described. In the biothreat assay, the non-avian H5N1 subtypes will be reported only at the species level as influenza A virus. Further differentiation of the sub-species may be achieved using the broader PCR/ESI-MS influenza assay previously described.
Filoviridae is a viral family of negative-strand RNA viruses that include two major genera, Ebolavirus and Marburgvirus, both of which contain highly pathogenic and potential biowarfare agents. Some of the species in these groups include Sudan, Reston, Zaire, and Cote d’Ivoire ebolavirus and several strain variants of the Lake Victoria marburgvirus species. We have developed an assay for the detection of all members of this family using two primer pairs targeting the RNA-dependent RNA polymerase region of the genome. There is significant sequence diversity among the filoviruses and in order to ensure primer hybridization to all the above viruses, we used modified nucleotides in the PCR primer pairs as previously described for the detection of the SARS coronavirus. We tested these primers with samples obtained from the CDC Special Pathogens Branch (Dr. Stuart Nichol, personal communication). In all cases, we obtained the base composition signatures expected based on sequenced genomes of these viruses (Table S19). Due to the highly pathogenic nature of these viruses, these viruses were not used in any additional analytical characterization studies described below.
Data Analysis and Reporting
The above sections describe in detail the primer pairs used in the biothreat assay and the ability of the individual groups of primer pairs to detect the targeted biothreat cluster. All of these primer pairs were assembled into a single assay kit containing groups of two to three primer pairs per well for screening for all the listed biothreat agents simultaneously. The assay layout is shown in Figure S1. Sixteen wells of a 96-well microtiter plate were utilized for analysis of each sample. Up to six samples may be screened per plate. Importantly, each PCR well included a synthetic DNA calibrant that was amplified by one of the target primer pairs. This calibrant served as a PCR positive control and allowed relative determination of the quantity of the target organism as previously described,.
Data analysis and reporting for this assay were optimized for detecting the targeted biothreat clusters, and detection of organisms outside this group are not reported. Two different types of report are currently available. The first is a summary that reports detection and lack thereof for each of the 14 groups described in the previous sections for each sample (Figure S2). The criteria for inclusion in this report are the detection of the biothreat cluster organisms in one or more primer pairs targeting the individual clusters. The primer pairs targeting the plasmid markers are reported separately. In the specific example shown, the test organism was a B. anthracis strain containing both virulence plasmids. The report indicates detection of the genome and the two plasmids. The approximate genome equivalents per well for the target organism are based on relative amplification compared to the calibrant. At higher target organism concentrations, the calibrant is often outcompeted in the PCR well; therefore, the reported levels at higher loads could be inaccurate. Another more in-depth analysis of the data is available that provides base composition details to support the calls reported in the summary (Figure S3).
The limit of detection (LOD) of the biothreat assay in analysis of environmental aerosol samples, one of its intended uses, was determined by analyzing serial 10-fold dilutions of nucleic acids from a number of test agents with air filter nucleic acid extract from a biodefense monitoring program (“Dirty Air”). In parallel, samples were also tested in DNA elution buffer (TE buffer) alone. Fivefold serial dilutions of nucleic acid samples (with a high concentration of 1000 GE/well for all targets except VEEV which was 5000 GE/well) of the nucleic acid extracts from all the target organisms were prepared and 10 replicates of each dilution of each agent were analyzed. The presumptive LOD was ascribed to be the lowest concentration resulting in 10 correct identifications and detections in all primer pairs targeting each biothreat cluster (Figure S4). Additional replicates were analyzed (as many as 105) to allow for sufficient data to determine the LOD with a 95% confidence interval. These measured LODs were used for subsequent analysis. Nucleic acids from test organisms were paired to reduce overall sample numbers (for example, B. anthracis and vaccinia virus nucleic acids were spiked together and analyzed in the same sample). These LOD studies were preceded by analysis of synthetic constructs, plasmids containing DNA sequences similar to those of the biothreat agents. These constructs were carefully measured using real-time PCR assays targeting the plasmid backbone (data not shown). Using this synthetic approach, the LOD for the various target primer pairs in the biothreat assay were determined to be between 7 and 250 genome equivalents (GE) per well, with most organisms detected at between 15 and 62.5 GE/well (Figure S4). The outliers were the three RNA virus groups, which showed either 125 or 250 GE/well LOD.
The LODs and the false negative rates for all threat agents tested are summarized in Table 3. The LOD for the threat agents tested in the context of environmental air background ranged from 40 to 1000 GE/well. It was found that 37.5% (6/16) of the threat agents tested had LODs of 40 GE/well, 50% (8/16) had LODs of 200 GE/well, and 12.5% (2/16) had LODs of 1000 GE/well. At the LODs, false negative rates were less than 5% for 14 of the agents used to challenge the biothreat assay kit and less than 10% for two of the agents. Detection and identification of all the threat agents relies on more than one primer pair; in the case of B. anthracis, it relies on four primer pairs. For calculation of LOD, all targeted primer pairs were expected to amplify and produce results. However, in routine operation, any primer pair producing a result would result in an organism identification. The false negative rates were calculated based on a failure to detect the threat organism.
It is critical that an assay used for biodefense monitoring be capable of detecting threats and, perhaps as importantly, of not falsely identifying a threat. The sample preparation methods employed by environmental monitoring programs result in samples containing significant amounts of nucleic acids from a variety of species. Two methods were employed to determine the specificity of the biothreat assay. First, over 1000 samples containing environmental background without a specific target agent were analyzed and used to calculate false positive rates for each agent. Second, the ability of the biothreat assay kit to detect a threat when the sample contained both the targeted threat and a near neighbor but not when the sample contained only the near neighbor was assessed.
A total of 1,353 samples in an environmental air background were analyzed during the determination of sensitivity. Each of these samples contained only two of the agents under investigation. Because the biothreat assay simultaneously analyzes each sample for every threat agent, the results from those samples not containing a particular threat agent were used to determine the false positive rates of that agent. For example, in the LOD determination of B. anthracis, the sample contained nucleic acids extracted from the environmental collection and from B. anthracis and vaccinia virus. Because those samples did not contain any of the other 14 threat agents, the data from the analysis of those samples could be used to calculate the false positive rate. The false positive rates for each of the threat agents tested was 0%, except for Rickettsia prowazekii, which was 14% (Table 4). The matrix that was used as background had high loads of environmental bacterial signatures (data not shown), including alphaproteobacteria such as Rickettsia and Mesorhizobium species. These might account for the observed higher false positive rates for rickettsial species compared to other organisms. Higher background prevalence of some of the potential biothreat agents or their near neighbors in certain regions of the world might similarly affect other detections. For instance, Burkholderia pseudomallei, which is described as a highly distributed soil saprophyte in southeast Asia would result in higher rates of reporting of this organism.
Near-neighbor nucleic acids were added to the sample in excess (fivefold higher than the LOD) of the target biothreat nucleic acids (added at twofold the LOD). The results are presented in Table 5. For each of the threat agents tested, the threat organism was correctly identified by the PLEX-ID system even when excess near-neighbor nucleic acids were present in the sample. As expected for the Brucella melitensis cluster, the PLEX-ID biothreat assay did not discriminate between B. melitensis, B. abortus, B. suis, and B. ovis, which are all considered to be potential threat organisms. When Rickettsia canadensis was included during testing of the Rickettsial primer pairs, Coxiella burnetii was also identified as a false positive. This detection was reported by the Coxiella primer pairs, not the rickettsial primer pairs, indicating that there was a possible contamination of the R. canadensis with Coxiella burnettii. Thus, the PLEX-ID clearly demonstrated the ability to detect threat agents in the presence of both background and excess near-neighbor nucleic acids.
Breadth of coverage
To determine the ability of the biothreat assay to distinguish between threat agents and near neighbors, the biothreat assay was challenged with nucleic acids purified from a panel of organisms. These samples were diluted in Tris-EDTA (pH 8.0) to allow for analysis on the biothreat assay plate at 1000 GE/well for each organism individually. In every case, the challenge organism was correctly identified. When possible, additional strains or sub-species were also identified. However, the intended use of the biothreat assay is to alarm the end user when a threat is present. The data presented in Table 6 clearly demonstrate the ability of the assay and the instrument to discriminate between threat agents and near neighbors.
The ability of an instrument to provide measurements that are directly proportional to the concentration of the test analyte is referred to as linearity. Data obtained from experiments used to determine the LOD within an environmental matrix were analyzed for linearity. The total GE reported by the PLEX-ID was plotted against the actual concentration; linear trend lines were generated to determine linearity within the challenge concentrations. Figure 2 shows results for B. anthracis linearity test, demonstrating linearity for the entire range of concentrations tested. Other organisms were linear up to the maximum concentration tested. The data are summarized in Table 7.
The biothreat assay described here identifies ten bacterial and four viral biothreat clusters included in the NIAID priority pathogen (Category A: seven agents, Category B: 18; Category C: three) and HHS/USDA select agent (18 agents) lists. The assay also identifies a broad range of near-neighbor organisms that may cause severe disease in humans or animals or that may be harmless environmental organisms. The biothreat cluster analysis strategy using PCR/ESI-MS addresses several fundamental design requirements for biothreat protection. First, biothreat agents and near-neighbor organisms are identified unambiguously and equally. Closely related organisms often cause false alarms in conventional PCR approaches to detect biothreat agents. Perhaps more importantly, it enables identification of unexpected pathogens within the biothreat clusters that might be used in a biological attack. Second, the genetic targets for amplification in the biothreat assay are universally conserved, essential to microbial life. This lowers the risk of failed detections because these targets cannot be dispensed with by the microbe and would be difficult to modify by engineering to avoid detection. Third, the comprehensive nature of the biothreat assay enables very broad surveillance of the potential biothreat landscape, including the detection of the virulence plasmids where appropriate. Fourth, the PCR/ESI-MS instrumentation enables very high-throughput sample analysis; the theoretical maximum throughput of the biothreat assay on a current-generation PLEX-ID instrument is approximately 180 specimens over 24 hours.
Some of the component primer pairs of the comprehensive biothreat assay were validated before the biothreat assay was assembled. The Orthopoxvirus primers have been shown to detect and identify a diverse collection of over 30 isolates of orthopoxviruses and to identify sub-species and characterize viruses from the blood of rabbitpox-infected rabbits. The Alphavirus primers were used to amplify a panel of 36 virus isolates representing characterized Old World and New World Alphavirus
. Base compositions from the resulting amplicons were used to unambiguously determine the species or subtypes of 35 of the isolates. In addition, the assay was used to identify Alphavirus directly in mosquitoes and detected an unanticipated Mucambo virus species.
The Francisella biocluster primers were used in an investigation to understand why the U.S. Government Biowatch sensors were triggered by an apparent false alarm on September 24–25, 2005 during a large public gathering along the Capital Mall area in Washington, DC. The sensors signaled low-level detections of F. tularensis. Uncertainty as to whether or not there was a biological attack led the CDC to issue an official national health advisory via the health alert network to alert healthcare personnel to possible tularemia exposure (CDCHAN-00238-05-09-30-ADV-N). Specimens analyzed by the primer pairs that comprise the F. tularensis biothreat cluster component of the biothreat assay were used to analyze the air specimens. The results showed that the base composition signature in the extracted air samples had the signature of F. tularensis subsp. novicida, a naturally occurring organism with significantly lower virulence than F. tularensis subsp. tularensis, the main bioagent in the cluster. Thus the detections of F. tularensis observed in these air samples most likely represented detection of a naturally occurring organism. The biothreat assay described here would immediately identify this organism as a near neighbor of a biothreat agent.
The V. cholerae biocluster primers were previously field-tested using natural water samples from both freshwater lakes and the Georgian coastal zone of the Black Sea. Of the 278 total water samples screened, nine different Vibrio species were detected, 114 samples were positive for V. cholerae, and five samples were positive for the cholera toxin A gene (ctxA). The results were confirmed with conventional PCR.
The Y. pestis primers were used to identify the first reported case of plague in Afghanistan where the illness is associated with consumption of camel meat. In late December 2007, an outbreak of acute gastroenteritis occurred in Nimroz Province of southern Afghanistan. Of the 83 patients, 17 died. Molecular testing of patient clinical samples and of tissue from the camel using PCR/ESI-MS revealed DNA signatures consistent with Y. pestis. Confirmatory testing using real-time PCR and immunological seroconversion of one of the patients confirmed that the outbreak was caused by plague with a rare gastrointestinal presentation.
Assembly of this comprehensive collection of biothreat cluster primers into a single assay on the PLEX-ID has the potential to serve a variety of biosecurity needs. First, the biothreat assay can be used for environmental surveillance − the application that was experimentally demonstrated in this manuscript. Another potential use of the assay is as a reflex test to the pan-bacterial PLEX-ID assay intended to identify all bacteria in normally sterile bodily fluids (e.g., blood, cerebral spinal fluid). In this concept of operation, the pan-bacterial assay would be used routinely in clinical diagnostics and, if potential biothreat agents were detected, the biothreat assay would be used to provide detailed analysis.
Although several of the primer pairs used in this assay were studied previously, the biothreat assay is a multiplexed version: Thirty-six primer pairs are combined into 16 PCR reactions. The multiplexed assay was tested with environmental air from Biowatch filters. Feasibility studies were performed at 1000 GE of each target organism spiked into background matrix. The environmental background did not inhibit the ability of PLEX-ID to correctly detect the target organisms. Additional studies were conducted to demonstrate the analytical performance of the assay. These included sensitivity, specificity, linearity, and breadth of coverage of the biothreat clusters. Analytical sensitivity of the target organisms varied between 40–1000 GE/well with no false positive detections, and false negative rates below 5% for most organisms tested. The matrix that was used as background had high loads of environmental bacterial signatures (data not shown), including alphaproteobacteria such as Rickettsia and Mesorhizobium species. These might account for the observed higher false positive rates for rickettsial species compared to other organisms. Breadth of coverage and specificity for detection of biothreat agents were determined with Critical Reagents Program (CRP; http://www.jpeocbd.osd.mil/packs/Default.aspx?pg=1205) reagents. There was an excellent correlation between PLEX-ID identifications and the identity of the spiked strains. Presence of two- to five- fold excess of a near-neighbor organism did not interfere with the detection of the biothreat agent. PLEX-ID assays in general are semi-quantitative at best and have a limited dynamic range for reporting genome levels of detected organisms. The levels of organisms determined using the biothreat assay indicate the approximate genome equivalents/well for the target organism based on relative amplification compared to the calibrant. At higher target organism concentrations, the calibrant is often outcompeted in the PCR reaction, therefore the reported levels at the higher loads were inaccurate. This, however, does not interfere with the ability of the assay to detect the threat agent. In contrast, a specific RT-PCR assay targeting a single organism might be able to provide a measurement over a much larger linear range.
In summary, the PLEX-ID Biothreat Assay kit was evaluated for detection of biothreat agents in environmental air samples. The data presented demonstrate the capability of the PCR/ESI-MS method to accurately detect and identify organisms from ten bacterial and four viral biothreat clusters. The assay discriminated between target agent and near neighbors with high specificity and sensitivity. The method accurately reported each organism with which it was challenged and accurately identified threat species as a threat; species and/or strains that are not considered a threat were not reported as such. The assay is capable of simultaneous detection of most NIAID Category A, B, and C priority pathogens and HHS/USDA select agents and thus provides a means for comprehensive coverage using a high-throughput assay. The validation data support use of the Ibis PLEX-ID and the biothreat assay for detection of biological warfare agents in complex environmental matrices. Additional testing of this assay with an EU validation panel is described in a companion manuscript (Grunow et al.).
The nucleic acid samples used in this study were obtained from the Critical Reagents Program (CRP), BEI Resources, ATCC, Keim Genetics Lab, or were prepared from MRI culture collections. Environmental collections were obtained on dry filter unit (DFU) filters from a variety of locations in the Washington, D.C. region. Nucleic acids were eluted from the environmental matrix by placing DFUs in 20 ml PBS/0.2% Triton X-200 and manually shaking. The eluent was then shaken in a Biospec Mini BeadBeater-96 with ATL buffer (Qiagen), Herring Sperm DNA, Proteinase K, and antifoam for 5 min. Samples were incubated for 21 min at 16°C and then centrifuged. AL buffer (Qiagen) was added to the supernatants and incubated for 1 min at 70°C. Ethanol was added to the sample, which was then loaded onto a Qiagen spin column, centrifuged, and sequentially washed with AL, AW2, and AW4 buffers (Qiagen). The sample was eluted from the spin columns in 200 µl of AE buffer (Qiagen).
The primer pairs that make up the biothreat assay (Table 1) were selected to provide the desired resolving capability for the assay as described in detail in the Results section. Thirty-six primer pairs were used in the assay; primer pairs were grouped two to three per well to occupy 16 wells of a 96-well microtiter plate. The groupings were chosen to eliminate primer interactions and target overlap. The assay layout is shown in Figure S1. Each assay plate can be used to screen up to six samples.
PCR and RT-PCR
Internal positive controls similar to the amplicon expected from one of the primer pairs in each of the multiplexed reactions were made from cloned synthetic DNA (BlueHeron Biotechnology, Bothell, WA) and were included in each PCR reaction at 100 copies per reaction. The internal controls were designed to be identical to the expected target priming regions with the exception of five-base pair deletions to enable the control to be distinguished from the target-derived amplicon. PCR was performed in a 50 µL reaction volume containing 5 µL nucleic acid extract in a reaction mix as previously described. The plate was heat-sealed with foil on a Thermo Scientific ALPS microplate heat sealer (Rockford, IL). Each sealed plate was loaded onto a Mastercycler Pro thermocycler (Eppendorf, Hauppauge, NY) and PCR-amplified under the following conditions: 95°C for 10 min; then 8 cycles of 95°C for 30 s, 48°C for 30 s, and 72°C for 30 s; then 37 cycles of 95°C for 15 s, 56°C for 20 s, and 72°C for 20 s; followed by 72°C for 2 min, and 99°C for 20 min. One-step RT-PCR was performed in wells with primers designed for viral detection. Since all reactions for a sample were run in the same 96-well plate RT-PCR cycling conditions were used for both the RT-PCR and PCR reactions as previously described.
After thermocycling, plates were stored at −40°C until the samples could be analyzed by ESI/MS on the PLEX-ID. Mass spectrometry was performed on a PLEX-ID biosensor (Abbott Molecular, Des Plaines, IL). After PCR amplification, 30 µL aliquots of each PCR reaction were desalted and analyzed by mass spectrometry as previously described,. Briefly, the PLEX-ID platform is capable of analyzing nearly 3000 PCR reactions in 24 hours and integrates a novel sample purification scheme with a high throughput fluidics/robotics platform. The PLEX-ID instrument is comprised of an input plate stacker which accommodates fifteen 96-well microtiter plates, an automated purification module which desalts and purifies amplicons with a magnetic-bead-based weak anion exchange method, and an autosampler coupled to a novel dual electrospray head which injects analytes into a Perkin Elmer ESI-TOF mass spectrometer. The platform analyzes one PCR reaction every 30 seconds in a fully automated modality. The PLEX-ID platform utilizes a novel carousel-based design for the rapid and efficient purification of PCR amplicons. The carousel is comprised of 22 identical spin cuvette modules in which the analyte solution is purified prior to ESI-MS analysis. Every 30 seconds the carousel rotates by one position facilitating the aspiration/or dispensation of the requisite reagents.
Data Analysis and Results Reporting
Data analysis and results reporting was performed in an automated fashion using on-board computer on the Ibis PLEX-ID system. For this assay, a customized reporting rule set was designed that allowed rapid and accurate detection of the biothreat targets. The biothreat assay report has 21 primer groups or threat clusters as shown in Figure S2. These groups consist of primer pairs used to identify the target biothreat organisms. Each of the threat clusters is treated independently and the results are reported for each cluster separately. Thus, the presence or absence of each of the target biothreat clusters is directly reported. Mixed detections of two or more threats or a threat with an unrelated near neighbor in another group are also reported. Further, two additional metrics (Q-score and level) are provided in the report to assess the quality of the reported detection. The Q-Score is a rating between 0 (low) and 1 (high) of the confidence in the identification of the organism. The Q-Score is based on a number of different parameters such as, the multi-primer joint log likelihood ratio, which is an indicator of how well the hypothesized organisms as a group represent the observed data; the multi-primer single log likelihood ratio, which is an indicator of how significant the contribution of a single organism is to the solution; the fraction of missed detections, which represents the percentage of primers for a detected organism that should have produced known base count compositions, but did not; and, finally, the fraction of no data, which indicates the percentage of primers for a detected organism for which no known data exists within the PLEX-ID system. For the biothreat assay described here, a Q-score ≥0.85 is considered a reportable result. The level is an indication of the amount of the amplicon present in the sample reported as genome equivalents/well. This is calculated with reference to the internal calibrant as described previously. The normal range for reporting these levels is between 0.1× and 10× the levels of internal controls in the assay, which in the case of the PLEX-ID Biothreat assay represents a working range of ∼10 GE/well to 1000 GE/well.
In addition to the summary style report shown in Figure S2, the system is capable of reporting organism/strain level matches based on the genomic sequence data in the PLEX-ID database (Figure S3). This is provided as a research utility tool in a separate analysis workstation. Additional details for each of the matches, including the detected base compositions and levels, are available using this report.