An investigation of conventional microbial culture for the Naja atra bite wound, and the comparison between culture-based 16S Sanger sequencing and 16S metagenomics of the snake oropharyngeal bacterial microbiota.

Naja atra is a major venomous snake found in Taiwan. The bite of this snake causes extensive wound necrosis or necrotizing soft tissue infection. Conventional microbial culture-based techniques may fail to identify potential human pathogens and render antibiotics ineffective in the management of wound infection. Therefore, we evaluated 16S Sanger sequencing and next-generation sequencing (NGS) to identify bacterial species in the oropharynx of N. atra. Using conventional microbial culture methods and the VITEK 2 system, we isolated nine species from snakebite wounds. On the basis of the 16S Sanger sequencing of bacterial clones from agar plates, we identified 18 bacterial species in the oropharynx of N. atra, including Morganella morganii, Proteus vulgaris, and Proteus mirabilis, which were also present in the infected bite wound. Using NGS of 16S metagenomics, we uncovered more than 286 bacterial species in the oropharynx of N. atra. In addition, the bacterial species identified using 16S Sanger sequencing accounted for only 2% of those identified through NGS of 16S metagenomics. The bacterial microbiota of the oropharynx of N. atra were modeled better using NGS of 16S metagenomics compared to microbial culture-based techniques. Stenotrophomonas maltophilia, Acinetobacter baumannii, and Proteus penneri were also identified in the NGS of 16S metagenomics. Understanding the bacterial microbiota that are native to the oropharynx of N. atra, in addition to the bite wound, may have additional therapeutic implications regarding empiric antibiotic selection for managing N. atra bites.

Introduction

Snakebites are one of the most neglected tropical diseases [1, 2]. Worldwide, more than five million people are bitten and up to 2.7 million are envenomed every year [1]. Wound infection is a severe complication after a snakebite and is associated with considerable mortality and morbidity [3-6]. Among common venomous snakes in Asian regions, Naja species with cytotoxic venoms carry the highest risk of wound infection [7]. N. atra is the only Naja species distributed in Taiwan. This snake accounts for only 6% of all snake bite incidents but causes the most severe infectious complications among the major venomous snakes [7, 8]. Furthermore, wound necrosis or necrotizing soft tissue infections are frequently reported [5, 9, 10]. Using conventional culturing techniques [11], Enterococcus spp. and Morganella morganii were the most commonly isolated pathogens in infected N. atra bite wounds, which is similar to the snake’s oral cavity [5, 7, 12, 13]. However, in spite of the aggressive administration of specific antivenom, antibiotics, or both, more than 50% of patients underwent surgery because of wound infection following a bite [5]. The high surgical proportion may be due to the poor efficacy of the antivenom against the cytotoxic components of the venom, failure of conventional culture-based techniques to report less significant or nonculturable microorganisms, including potential human pathogens, or improperly chosen empiric antibiotics [14-16].

Patients with snakebites receive several forms of treatment (e.g., wound cleansing, topical herb application, or prophylactic antibiotic administration) that might change the bacterial composition and loads recovered from cultures [7]. Although empiric antibiotic administration in patients with snake bites is a common practice [17], it may be ineffective in preventing secondary infection if the microbiology of the bite wound and oropharynx of the culprit snake is not comprehensively determined [10]. Therefore, we first glance at the features of infected N. atra bite patients and the bacteria recovered from the bite wound based on a conventional microbial culture method in clinical settings. We then compare the capacity of conventional microbial culture-based 16S Sanger sequencing and next-generation sequencing (NGS) methods to evaluate the bacterial microbiota of the oropharynx of N. atra and to better appraise microbial diversity and therapeutic implications.

Materials and methods

Ethics statement

The human study was approved by the Institutional Review Board (CE16225A) and the snake study was conformed to the National Law.

Patient information

All N. atra bite cases were admitted to Taichung Veterans General Hospital between January 2001 and July 2006. Patients with suspected wound infections who received a deep tissue or biopsy microbial culture were carefully examined. The following data were collected: age, sex, bitten body part, clinical manifestations, and management (including the dosage and timing of specific antivenom administration, indication and timing for surgery, and types of surgery). We used the same criteria as Mao et al. [5, 7] to define wound infection and other complications. Some study participants overlapped with previous studies that had different reference periods [5,7].

Deep tissue or biopsy microbial cultures (aerobic and anaerobic) were performed during surgical debridement. Bacteria were identified using the VITEK 2 system (BioMérieux Inc., Durham, NC, USA). Culture sampling was performed as previously described [11].

Sample collection and identification of isolated bacteria in the N. atra oropharynx

All cobras in this study were collected in 2020 from various locations in central Taiwan by a snake rescue team. The cobras’ mouths were opened using a sterile mouth gag. Two oropharyngeal swabs were collected using commercial sterile cotton-tipped swab sticks. We used the same conditions for the cultivation and isolation of these bacteria from both the wound and oropharynx [16]. Briefly, swabs were taken by rotating the cotton tip on the floor of the oral cavity and then inoculated on cetrimide agar, eosin methylene blue agar, and thiosulfate-citrate-bile salts-sucrose agar. The spread plates were incubated aerobically for 24–48 h at 37°C. Isolated pre-treatments before sampling strains were initially identified by colony morphology and gram characteristics. Subsequently, Sanger sequencing of the 16S ribosomal RNA gene was performed to confirm the identification of species.

DNA extraction and construction of a 16S rDNA metagenomic library for N. atra oropharynx samples

Genomic DNA was extracted from each sample using the QIAamp DNA mini kit based on the manufacturer’s instructions. The Illumina 16S library preparation protocol and two-step polymerase chain reaction (PCR) were followed. The V3–V4 hypervariable region (500–600 bp) of the 16S rDNA gene segment was amplified using barcoded PCR: 16s_illumina_V3F 5′-CCTACGGGNGGCWGCAG-3′ and 16s_illumina_V4R 5′-GACTACHVGGGTATCTAATCC-3′. PCR products were purified on 0.8% agarose gel at 80 V for 40 min. Then they were quantified using the Qubit dsDNA HS assay kit (Invitrogen, Carlsbad, CA, USA) according to the manufacturer’s protocol.

Illumina MiSeq sequencing

Purified amplicons were pooled together and paired-end sequenced at 2 × 300 bp on an Illumina MiSeq platform (Illumina, San Diego, CA, USA).

Analysis of 16S metagenomics

Taxonomic classification was performed using the Illumina BaseSpace (v1.0.1) 16S metagenomics workflow. The Illumina-curated version of Greengenes released in May 2013 was used as the reference database. The algorithm is an implementation of the Naïve Bayesian Classifier (The Ribosomal Database Project) described by Wang Q [18].

Results

Clinical characteristics of N. atra bite patients

Positive deep tissue or biopsy microbial cultures were identified in 15 (nine men (60%) and six women (40%)) of 86 total cobra bite patients. The patients’ median age was 54 years (interquartile range, IQR: 38–66 years). The bite site occurred on the upper limb in six cases (40%) and the lower limb in eight cases (53.3%). The other case was bitten on the right side of the neck while in bed. Local effects such as suspected acute compartment syndrome, skin necrosis, bullae or blisters, local numbness, necrotizing adiposities, and necrotizing fasciitis were observed in 2, 15, 5, 5, 3, and 12 patients, respectively. Systemic effects such as fever (≥38°C), rhabdomyolysis, and gastrointestinal issues were observed in 12, 2, and 7 patients, respectively. The median dose of bivalent antivenom for N. atra and B. multicinctus administration was 15 vials (IQR: 12–16). The elapsed times between the bite and the first dose of antivenom administration were <6, 6–12, and >12 h in 11, 1, and 3 patients, respectively. The surgical indication was wound necrosis with secondary infection for all 15 patients. Cleansing procedures included fasciotomy or fasciectomy, debridement, and finger or toe amputation in 9, 12, and 1 patient, respectively. Reconstructive procedures comprised a split-thickness skin graft or full-thickness skin graft and flap surgery in 12 and 7 patients, respectively. The median elapsed time between the bite and the first operation was 3 days (IQR, 1–4 days). The median elapsed time between the bite and obtaining deep tissue or a biopsy culture was 4 days (IQR, 2–8 days). Antibiotics were administered to all patients upon arrival at the emergency department before obtaining a deep tissue or biopsy culture, and they included penicillin, oxacillin, amoxicillin/clavulanic acid, ampicillin/sulbactam, cefazolin, gentamicin, and metronidazole in 1, 3, 2, 6, 12, 8, and 2 patients, respectively (Table 1).

Table 1

Demographic data and management of patients with positive deep tissue or biopsy culture.

Demographic data	Case number, n = 15
Age (median, IQR)	54 (38–66)
Male (%)	9 (60)
Body part of bitten
Upper limb	6
Lower limb	8
Trunk/Others	1 (neck)
Local complications
Tissue swellinga
Minimal	0
Mild	1
Moderate	8
Severe	5
Acute compartment syndrome, suspected	2
Skin necrosis	15
Bullae/blister	5
Local numbness	5
Lymphangitis/lymphadenitis	0
Necrotizing soft tissue infection
Necrotizing adiposities	3
Necrotizing fasciitis	12
Finger or toe gangrene	0
Systemic complications
Fever (≥38°C)	12
Rhabdomyolysisb	2
Gastrointestinal effectc	7
Ptosis or muscle weakness	0
Management
Time elapsed between bite and first dose of antivenomd in h
<6 h	11
6–12 h	1
>12 h	3
Total antivenom dose in vial (median, IQR)	15 (12–16)
Operation case
Fasciotomy/fasciectomy	9
Debridement	12
STSG/FTSGe	12
Flap	7
Finger or toe amputation	1
Time elapsed between bite and first operation in days (median, IQR)	3 (1–4)
Time elapsed between bite and obtaining deep tissue or biopsy culture in days (median, IQR)	4 (2–8)
Antibiotics administered prior to obtaining deep tissue or biopsy culture 15
Penicillin	1
Oxacillin	3
Amoxicillin/clavulanic acid	2
Ampicillin/sulbactam	6
Cefazolin	12
Gentamicin	8
Metronidazole	2

a: minimal: local swelling at the bite site; mild: swelling involving a whole hand or foot; moderate: swelling from the hand to the forearm, or from the foot to the leg; severe: swelling extending to the arm, thigh, or the above area, from a hand or foot bite. Because Blaylock’s classification cannot be applied to bites on the body or trunk, the patient bitten on the neck was not included in the swelling grade analysis despite serious tissue swelling;

b: creatine kinase level of 2599 and 4306 U/L, respectively;

c: including nausea, vomiting, abdominal upset, or diarrhea;

d: bivalent specific antivenom for Naja atra and Bungarus multicinctus;

e: split-thickness skin graft and full-thickness skin graft.

Identification of bacteria from infected N. atra bite wounds based on the VITEK 2 system

Nine bacteria were isolated from infected cobra bite wounds (Table 2). Enterococcus sp. (aerobic gram-positive bacteria) was present in seven cases and was the most common gram-positive pathogen. The most common aerobic gram-negative bacterial species was Morganella morganii (10 cases). Proteus vulgaris and Serratia marcescens were isolated from two cases. P. mirabilis, P. penneri, Providencia rettgeri, Pseudomonas aeruginosa, and Shewanella sp. were found in one case each. In addition, 10 patients had wounds with at least two bacterial pathogens. Simultaneously, an anaerobic culture was performed in 11 of the 15 patients, but no anaerobic bacteria were found in the study.

Table 2

Bacteria isolated from infected cobra bite wound culture.

Species	Case number
Aerobic gram-positive bacteria
Enterococcus sp.	7
Aerobic gram-negative bacteria
Morganella morganii	10
Proteus mirabilis	1
Proteus penneri	1
Proteus vulgaris	2
Providentia rettgeri	1
Pseudomonas aeruginosa	1
Serratia marcescens	2
Shewanella sp.	1
polymicrobial: ≥ 2 pathogens	10

Identification of bacteria from the N. atra oropharynx through conventional microbial culture-based 16S Sanger sequencing

Because N. atra is rarely found, we collected five adult snakes for the experiment. After obtaining swabs from their oropharynx, 54 single colonies were recovered on a culture plate. We then identified 18 bacterial species using the 16S Sanger sequencing method (S1 Table). The colonies consisted of M. morganii in 17 clones (31.5%), followed by Bordetella petrii in 6 clones (11.1%) and Corynebacterium freneyi in 5 clones (9.3%). Therefore, M. morganii was the principal bacterium isolated from both cobra bite wounds and the cobra oropharynx (Tables 2 and S1).

A comparison between bacterial microbiota in N. atra bite wounds and the cobra oropharynx

To understand the microbial diversity of snakebite wounds and identify the relative proportion and types of species in the wound, we compared cultured bacteria between cobra bite wounds and the cobra oropharynx. Among bacterial strains, 18 species were isolated from the cobra oropharynx using 16S Sanger sequencing, and 9 species were isolated from cobra bite wounds using the VITEK 2 system (Fig 1A). Overall, the microbial culture method identified only three bacterial species (i.e., M. morganii, P. vulgaris, and P. mirabilis) in both cobra bite wounds and the oropharynx of cobras (Fig 1A), and these three bacterial species accounted for 31.5%, 3.7%, and 3.7% of those in the cobra oropharynx, respectively (Fig 1B, right vertical bar), and appeared in the bite wounds of 10, 2, and 1 patients, respectively (Fig 1B, left vertical bar).

Fig 1

Bacteria in N. atra bite wounds and cobra oropharyngeal swabs.

(A) Venn diagram indicates that 18 bacterial species strains (yellow) were detected in the oropharynx of N. atra by culture-based method, and 9 species were detected from bite wounds (blue) by using the VITEK 2 system. Three bacteria were both present in the oropharynx of snake and the bite wounds. (B) The most commonly species were Morganella morganii, Proteus vulgaris, and Proteus mirabilis.

Identification of bacterial microbiota in the cobra oropharynx through next-generation sequencing

To better understand the bacterial microbiota in the cobra oropharynx, oropharynx swabs from five cobras were collected, and 16S metagenomic sequencing was performed. To model oropharynx bacterial microbiota, we calculated the number of identified species using operational taxonomic units (OTUs) and the abundance of species using the Shannon species diversity index. The OTU range and the Shannon species diversity index were 286–416 and 1.907–2.224 in the cobra oropharynx, respectively (Table 3). Taxonomic classification was conducted using the Ribosomal Database Project Classifier and Greengenes Database. The five most abundant bacterial species accounted for 84% ± 2.9% of those in the oropharynx bacterial microbiota. The 16S metagenomic sequencing data revealed that the most common bacterial species in the oropharynx of all five cobras were P. azotoformans, P. lundensis, Delftia tsuruhatensis, and Methylobacterium goesingense. These species accounted for 27.7% ± 8.7%, 22.3% ± 11.6%, 20.3% ± 1.9%, and 9.0% ± 1.7% of the oropharynx bacterial microbiota, respectively. In addition, through the NGS method, we found that the only four bacteria present in both N. atra bite wounds and the oropharynx were Enterococcus sp., Morganella morganii, Proteus mirabilis, and Proteus penneri (Table 4).

Table 3

Bacteria identified in the oropharynx of N. atra based on the 16S metagenomics method.

Sample ID	Shannon Species Diversity	Number of Species Identified (OTU)	Top 5 species
			1	2	3	4	5
MS18121-1	1.907	404	Pseudomonas azotoformans	Pseudomonas lundensis	Delftia tsuruhatensis	Methylobacterium goesingense	Delftia lacustris
			29.82%	22.44%	20.73%	9.21%	2.78%
MS18121-2	2.224	362	Pseudomonas azotoformans	Pseudomonas lundensis	Delftia tsuruhatensis	Methylobacterium goesingense	Kushneria indalinina
			25.55%	20.65%	18.65%	8.71%	6.46%
MS18121-3	2.065	411	Pseudomonas lundensis	Delftia tsuruhatensis	Pseudomonas azotoformans	Methylobacterium goesingense	Dysgonomonas wimpennyi
			39.58%	18.09%	14.52%	6.36%	2.59%
MS18121-4	2.015	286	Pseudomonas azotoformans	Delftia tsuruhatensis	Methylobacterium goesingense	Pseudomonas fluorescens	Pseudomonas lundensis
			38.12%	22.33%	11.06%	8.84%	7.06%
MS18121-5	1.998	416	Pseudomonas azotoformans	Delftia tsuruhatensis	Pseudomonas lundensis	Methylobacterium goesingense	Delftia lacustris
			30.52%	21.67%	21.52%	9.75%	2.99%

Table 4

Identification of the bacterial species in N. atra oropharynx and bit wounds.

Species	16S Metagenomics NGS (oropharynx)	Sanger sequencing of bacterial culture (oropharynx)	Vitek2 system of bacterial culture (bite wounds)
Stenotrophomonas maltophilia	O	X	X
Acinetobacter baumannii	O	X	X
Morganella morganii	O	O	O
Proteus mirabilis	O	O	O
Proteus penneri	O	X	O
Enterococcus spp.	O	O	O

Comparison of bacterial microbiota in N. atra oropharynx identified through 16S Sanger sequencing of bacterial culture and 16S metagenomic sequencing

We grouped the bacteria by genus to compare the bacterial microbiota of the cobra oropharynx identified through 16S Sanger and metagenomic sequencing. The 16S metagenomic sequencing data indicated that the most representative bacterial genera were Pseudomonas (62%), Delftia (19%), and Methylobacterium (9%), but none of these genera were detected in the bacterial culture (Fig 2A, left). By contrast, the most representative genera, as obtained from the cultured clones, were Morganella in 31.5% of the clones, Corynebacterium in 22.2%, Proteus in 7.4%, and Enterococcus in 7.4% (Fig 2B). Only 2% of the bacteria identified through 16S metagenomic sequencing were found by Sanger sequencing of the bacterial culture (Fig 2A, right). The proportions of each genus in 2% of the bacteria were identical in these two methods, i.e., 0.83%, 0.3%, and 0.32% for the genera Corynebacterium, Morganella, and Proteus, respectively (Fig 2A, right). Notably, the pathogenic bacteria Stenotrophomonas maltophilia and Acinetobacter baumannii were identified by 16S metagenomic sequencing, which were undetected in both wounds using the VITEK 2 system and the cobra oropharynx using 16S Sanger sequencing of the microbial culture (Table 4).

Fig 2

Pie charts of the abundance of 16S bacteria from the oropharynx of N. atra identified through next-generation sequencing (NGS) and culturing (genus level).

(A) Bacterial abundance identified through the swabs of the oropharynx of N. atra and 16S rDNA through NGS (left). The culture-based method only detected 2% of all bacteria uncovering by NGS method (right). (B) The proportion of detected bacteria at the genus level through culturing.

Discussion

N. atra belongs to the family Elapidae, but its bite causes minimal or insignificant neurotoxicity. Furthermore, necrotizing soft tissue infection was the principal manifestation of its bite [5, 19]. We demonstrated that the use of empiric antibiotics in N. atra bite management was probably widespread but may not have been directly effective on pathogens. The most common pathogen recovered from deep tissue or biopsy culture after wound debridement was M. morganii. This bacterium is naturally resistant to various antibiotics, including penicillin, amoxicillin, ampicillin, oxacillin, cefazolin, and sulfamethoxazole [20]. In Taiwan, Chen et al. suggested that amoxicillin/clavulanate with ciprofloxacin or piperacillin/tazobactam is the antibiotics of choice in the management of snakebites because Enterococcus spp. and M. morganii are frequently present in the infected bite wound [21]. Mao et al. and Chiang et al. suggested that first-generation cephalosporin with aminoglycoside or sulfamethoxazole/trimethoprim is the preferable antibiotics in the management of infected Protobothrops mucrosquamatus and Trimeresurus stejnegeri stejnegeri bites [22, 23]. These suggestions are based on conventional wound microbial culture without prior determination of antibiotic administration before obtaining cultures, thus rendering these suggestions biased.

In Thailand, Theakston et al. recommended benzylpenicillin with gentamicin as a prophylactic antibiotic regimen after Calloselasma rhodostoma envenomation because Enterobacter, Pseudomonas, Staphylococcus, and Clostridium spp. were cultured from the venom and mouth of this snake [24]. In Brazil, Jorge et al. suggested the use of chloramphenicol as the antibiotic of choice for managing Bothrops envenomation because the most frequently isolated pathogens from these wounds include M. morganii, Providencia rettgeri, Enterobacter sp., Escherichia coli, Enterococcus sp., and Bacteroides sp. [25]. However, in Ecuador, a controlled study suggests that chloramphenicol and gentamicin were ineffective in preventing abscess formation (9 cases among 114 snake bites) given that they are administered for 24 h and less than half of the patients are identified as Bothrops bites [26]. In the United States, prophylactic antibiotic administration is not recommended for treating rattlesnake bites given the low incidence of wound infection (0.98%) [27]. Although the administration of specific antivenom remains the standard of care in the management of snakebites, administration of prophylactic, empiric antibiotics, or both is controversial. This is not only because the diagnosis of secondary infection is confounded by the venom’s effects but also because the microbiology of the infected wound and oropharynx of the culprit snake is not well established [7]. In addition, a recent study demonstrated that the bivalent antivenom for N. atra and B. multicinctus is ineffective against the necrotic effect of the venom [15]. Because most N. atra bite patients underwent surgery for secondary wound infections, this seems to be a role for empiric antibiotics in the management of severe local or systemic septic complications following a bite.

The snake oral cavity contains various aerobic and anaerobic bacteria, particularly fecal gram-negative rods because their prey (e.g., mammals, reptiles, and fish) usually defecate while being ingested [3, 28, 29]. The bacterial composition varies across snake species and may be influenced by venom properties [24, 30, 31] and the fecal flora of the prey in different geographic regions [29]. On the basis of conventional microbial culture methods, Enterobacter, Proteus, and Pseudomonas were the most frequently isolated gram-negative rods, Enterococcus and Micrococcus were the most common gram-positive cocci, and Clostridium was the most common anaerobic bacteria found in the fangs or venom of Crotalus atrox [32]. P. aeruginosa, coagulase-negative Staphylococcus sp., Alcaligenes sp., and Enterobacter cloacae were all isolated from the venom of C. viridis helleri, and Bacillus sp., Proteus rettgeri, and coagulase-negative Staphylococcus sp. were observed in C. scutulatus [29]. Furthermore, Stenotrophomonas maltophilia, P. aeruginosa, and Diphtheroid bacillus were obtained from Trimeresurus albolabris [13]. In contrast to crotaline snakes, the oral cavity of N. atra harbors more complex pathogenic bacteria, including gram-negative bacterial species M. morganii, Aeromonas hydrophila, and Proteus, and gram-positive bacteria, like Enterococcus faecalis, coagulase-negative Staphylococcus sp., and anaerobic species (Clostridium), which may be associated with higher incidences of bite wound infection (i.e., 76%–81%) [12, 13]. However, in N. mossambica bites, patients had serious wound necrosis or necrotizing soft tissue infection even with the use of specific antibiotics or third-generation cephalosporin [10]. This can be caused by additional wound necrosis-inducing bacteria that were undetected, unreported, or both in conventional microbial culture in addition to venom-induced cytotoxicity and local tissue damage.

Currently, microbial culture remains the principal method to detect bacteria in clinical practice. Meanwhile, the accuracy and reliability of NGS of 16S metagenomics have rapidly improved [33]. We used NGS to examine the bacterial microbiota of the oropharynx of N. atra and to construct a better model of a snake oropharynx microbial profile, which may have therapeutic implications. Our NGS data indicated that the bacterial microbiota, as identified using OTUs, included more than 286 species. However, using the culture-based method, only 18 bacterial species could be identified in the same sample from the cobra oropharynx and only 9 species in infected wounds. The lower number of bacterial species identified in deep tissue or biopsy culture in this study compared with the Mao et al. study is probably due to the lower number of bacteria in deep tissue or from biopsy compared with wound swab sampling, fastidious or uncultivable bacteria, antibiotic therapy, or several of these aspects initiated before sampling [7, 34]. Only three bacterial species recovered from deep tissue or biopsy cultures were also present in the oropharynx swab culture of N. atra, which suggests the requirement of simultaneous determination of both the bite wound and snake oropharynx bacterial microbiota. Given the considerable variability in the incidence of infection in snake bite wounds (1%–81%) [35, 36], the causative organisms, and the methods used to isolate a pathogen in variable clinical settings [5, 10, 27, 37–39], an institutional protocol for antibiotic selection during snake bite wound management should be adapted based on the regional microbiology data of both snake bite wounds and snakes.

Rampini et al. suggested that the 16S rRNA gene sequencing method identifies many more culture-negative bacteria compared with microbial culture [40]. Pseudomonas was the most abundant genus found in the cobra oropharynx cavity. In particular, P. azotoformans is an environmental bacterium that can be isolated from soil and plants. In 2020, a bacterial isolate from rabbit meat samples was treated with blue and fluorescent pigments, and the growth of uniform bacterial colonies that were visible through fluorescent pigmentation indicated P. azotoformans, which belongs to the fluorescent group [41]. P. lundensis is a new species of the Pseudomonas genus and can produce fluorescent pigments and catalase and grow at 0°C. Furthermore, they are spoilage and pathogenic bacteria found in refrigerated meat [42]. D. tsuruhatensis, which was initially considered an environmental bacterium, was later confirmed as a human pathogen [43]. In addition, it can be misidentified as a closely related nonpathogenic species, D. acidovorans, using the VITEK 2 system with a probability level of 98% [43]. Moreover, the pathogenic bacteria Stenotrophomonas maltophilia and A. baumannii detected in the N. atra oropharynx were not found in deep tissue or biopsy cultures of infected wounds. It is worth noting that S. maltophilia is a multiple-drug-resistant pathogenic bacterium that is frequently involved in pneumonia and bacteremia in humans [44].

Several reports have presented potential advantages of molecular diagnostics over microbial culture, namely, a shorter turnaround time, detection of difficult to grow bacteria, or detection after prior administration of antibiotics that inhibit bacterial growth [34]. Although PCR amplification bias and 16S rRNA copy variation may cover up real relative abundance, numerous studies have shown that the NGS method of 16S metagenomics can achieve reasonable quantification accuracy for complex microbial communities [33]. In addition, a traditional microbiology laboratory only reports a few bacteria in the culture and clinically associates it with polymicrobial infections. The advantage of the NGS method 16S metagenomics assay is not only the identification but also the quantification of the relative abundance of all bacteria in polymicrobial infections [33]. Furthermore, 16S rRNA sequencing identifies anaerobic bacteria better than the VITEK 2 system [45].

Advances in sequencing technology in the last decades have made the molecular identification of bacteria widely available, and an increasing number of studies have focused on the clinical applications of this technology. The main advantage of NGS-based sequencing is that it permits the identification of 16S rRNA on uncultured samples and provides fast and comprehensive analysis of the microbial profile, thereby reducing the time required for clinical diagnosis and treatment. However, we are in the early stages of understanding the microbiome of snakes and snakebite wounds. Generally, bacterial isolates from the oral cavity of snakes are not all pathogenic: they may cause wound infections or abscesses in humans but so do normal environmental contaminants or soil pathogens [46]. Although bacterial pathogens can make some people critically ill, many people who asymptomatically carry these organisms are often unaware that they are infected, and it is difficult to draw a line between the asymptomatic presence of such pathogens and the normal microflora [47]. We do not know if antibiotic treatment must be directed at each isolated organism, at only presumed bacterial ringleaders, or even at organisms that were once considered probably nonpathogenic lab weeds [46]. Nevertheless, ascertaining this information should be the initial stage of any study that attempts to establish appropriate antimicrobial therapy for N. atra envenomation.

Limitations

There are several limitations in our study. First, there was usually a delay of several days between the bite and the debridement surgery (to allow demarcation of the necrosis). Empiric antibiotic administration for wound infection and before obtaining microbial cultures during debridement surgery might have changed the bacterial microbiota of the wound. However, owing to the high incidence of wound infection following an N. atra bite [5, 7], it is not possible or even ethical to postpone the antibiotic administration while waiting for the culture report. Although the clinical data in 2001–2006 were analyzed, no optimized protocol is currently established in the management of N. atra bites because the diversity of pathogens might have been underestimated in the clinical setting based on conventional culture techniques and various pretreatments before sampling. Second, we did not submit the deep or biopsy tissues for 16S Sanger sequencing or NGS evaluation because the techniques are not available during the patients’ enrollment period and N. atra bites are rare in Taiwan. Third, only five adult N. atra were analyzed, and hence, these data may not be properly representative of the wild population of this snake. In addition, the changing patterns of bacterial microbiota in snakebite wounds and the N. atra oropharynx throughout the year remain unknown, although numerous studies reported the increasing resistance of various bacteria [48, 49]. Nevertheless, this is the first study to investigate the bacterial microbiota of the oropharynx of N. atra with utilization of NGS and Sanger sequencing methods. Our study findings may have therapeutic implications for N. atra bite wound infections and shed light on the complex mechanisms of wound necrosis following a bite.

Bacteria identified by Sanger sequencing of 16S ribosomal RNA gene method.

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