- Open Access
Grazing livestock are exposed to terrestrial cyanobacteria
Veterinary Research volume 46, Article number: 16 (2015)
While toxins from aquatic cyanobacteria are a well-recognised cause of disease in birds and animals, exposure of grazing livestock to terrestrial cyanobacteria has not been described. This study identified terrestrial cyanobacteria, predominantly Phormidium spp., in the biofilm of plants from most livestock fields investigated. Lower numbers of other cyanobacteria, microalgae and fungi were present on many plants. Cyanobacterial 16S rDNA, predominantly from Phormidium spp., was detected in all samples tested, including 6 plant washings, 1 soil sample and ileal contents from 2 grazing horses. Further work was performed to test the hypothesis that ingestion of cyanotoxins contributes to the pathogenesis of some currently unexplained diseases of grazing horses, including equine grass sickness (EGS), equine motor neuron disease (EMND) and hepatopathy. Phormidium population density was significantly higher on EGS fields than on control fields. The cyanobacterial neurotoxic amino acid 2,4-diaminobutyric acid (DAB) was detected in plant washings from EGS fields, but worst case scenario estimations suggested the dose would be insufficient to cause disease. Neither DAB nor the cyanobacterial neurotoxins β-N-methylamino-L-alanine and N-(2-aminoethyl) glycine were detected in neural tissue from 6 EGS horses, 2 EMND horses and 7 control horses. Phormidium was present in low numbers on plants where horses had unexplained hepatopathy. This study did not yield evidence linking known cyanotoxins with disease in grazing horses. However, further study is warranted to identify and quantify toxins produced by cyanobacteria on livestock fields, and determine whether, under appropriate conditions, known or unknown cyanotoxins contribute to currently unexplained diseases in grazing livestock.
Cyanobacteria are a diverse group of ubiquitous environmental bacteria which can produce a wide array of toxins (cyanotoxins). While exposure to cyanotoxins from aquatic cyanobacterial blooms, scums and mats is a well-recognised cause of neurologic and hepatic disease in birds and animals , exposure of grazing livestock to terrestrial, as opposed to aquatic, cyanobacteria has not been previously described. We hypothesised that grazing livestock are exposed to Phormidium spp. since this cyanobacterial genus can grow on turf grasses and golf courses, particularly in favourable weather conditions and following fertiliser application [2-6]. Cyanobacteria including Phormidium spp. can produce a wide range of hepato-, neuro- and dermotoxins which cause disease in animals exposed to aquatic cyanobacterial blooms [7-10]. While exposure to anatoxin-a from the benthic cyanobacterium Phormidium favosum has been associated with canine neurotoxicosis , toxins from terrestrial Phormidium spp. have not been previously definitively associated with disease. We hypothesised that cyanotoxins from terrestrial Phormidium spp. may trigger or cause currently unexplained diseases of grazing livestock such as equine grass sickness (EGS), a frequently fatal multi-system neuropathy affecting grazing horses, equine motor neuron disease (EMND) and idiopathic hepatopathy. The aims of this study were to: (a) identify and enumerate Phormidium filaments in washings of the biofilm on plants collected from livestock-grazing fields; (b) evaluate spatial and temporal variation in the density of Phormidium filaments; (c) determine whether Phormidium filaments can be detected by microscopy in gastrointestinal contents from grazing horses; and (d) use a genomic approach to identify cyanobacteria in plant washings, equine ileal contents and soil. Additionally, a preliminary investigation of the potential association of cyanotoxins and EGS, EMND and hepatopathy was performed by: (a) comparing the density of Phormidium filaments on plants from horse fields immediately after an occurrence of EGS with that of plants from control horse fields; (b) quantifying the cyanobacterial neurotoxins 2,4-diaminobutyric acid [DAB], β-N-methylamino-L-alanine [BMAA] and N-(2-aminoethyl) glycine [AEG] in washings from plants collected from EGS fields; (c) quantifying DAB, BMAA and AEG in archived neural tissue from EGS and EMND horses; and (d) enumerating Phormidium spp. in washings of the biofilm on plants collected from fields grazed by horses which had idiopathic hepatopathy.
Materials and methods
Collection of plants
Most plants were collected from livestock-grazing fields (n = 88) in Scotland and North England. Most fields were grazed by horses (40 fields; termed horse control fields), cattle (13 fields) or sheep (14 fields) that had no apparent clinical neurological or hepatic disease, although detailed veterinary examinations were not performed. The remaining samples were collected from 21 “EGS” fields as soon as possible (always <96 h) after a horse grazing that field had developed acute EGS. EGS was confirmed by histopathology of autonomic and enteric ganglia . Plants were collected by carefully cutting leaves/petioles with scissors approximately 1 cm above soil level, avoiding sampling of roots and adherent soil. To ensure that plant samples were representative of the entire field, samples comprised a mixture of ≥10 aliquots collected from points situated along an imaginary “W” transect, and comprised plants that were representative of the distribution of species present on the field. The varied mixtures of plants were typical of those growing on livestock grazing fields in Northern Britain. In horse fields, plants were collected only from grazed areas and not from non-grazed “roughs”. Samples were analysed within 4 h of collection, or were rapidly frozen within 30 min of collection by mixing with dry ice pellets and then stored in airtight polythene bags at −20 °C or −80 °C pending analysis.
To determine whether there was spatial variation in the density of Phormidium filaments within individual fields, samples were collected separately from 10 individual sites along the “W” transect in 2 fields, comprising one EGS field which had high overall Phormidium filament population density and one horse control field which had low overall density.
Two experiments were performed to determine whether there was temporal variation in the density of Phormidium filaments. To assess short-term variation, Phormidium filament population density was determined in samples collected from 9 fields (3 EGS, 6 horse control fields) at both 0700 and 1900 h. To assess longer term variation, Phormidium filament density was determined in samples collected from 8 fields at approximately weekly intervals from April to July 2006, including the period of highest incidence of EGS which is typically May in the UK . One of these fields was a control horse field, while 7 were fields where at least one EGS case had occurred in the preceding 2 years; none of the fields had EGS cases during the sampling year. To determine if Phormidium filament density was influenced by weather, densities for the 8 individual fields were correlated with average daily air temperature, rainfall and sunshine hours, using data from a Meteorological Office weather station located within 48 km of all fields.
Unfortunately it was not possible to assess the population density of Phormidium filaments on fields grazed by EMND horses due to the rarity and sporadic occurrence of this disease . Plants were also collected from 22 fields in France where the grazing horses had idiopathic subclinical hepatopathy, as evidenced by elevated serum activities of gamma glutamyltransferase and glutamate dehydrogenase. Despite extensive investigation, no aetiology had been identified. Samples were collected as described previously, but were kept on ice for 24 h before analysis.
Enumeration of Phormidium filaments on plants
To suspend cyanobacteria that were adherent to plants, 20 mL sterile 0.9% saline was added to 10 g wet weight plants in a 50 mL plastic tube which was shaken vigorously by hand for 1 min. As a pilot study indicated that vigorous vortexing (Shaker VX-2500 Multi-Tube Vortexer, VWR International, Lutterworth, UK) of the plant suspension for 0, 1, 2 and 18 h had no significant effect on the yield of free filaments (data not presented), this method was not further employed. A 20 μL aliquot of the suspension was removed immediately after shaking, placed on a microscope slide, a cover-slip added and the total number of Phormidium filaments enumerated. The remaining suspension was frozen at −80 °C for future analysis.
Detection of cyanobacterial 16S rDNA in plant washings, soil and equine ileal contents
To confirm identify of cyanobacteria within samples, 16S rDNA amplicons were prepared from plant washings from 6 EGS fields, soil from 1 EGS field and ileal contents from 2 EGS horses and sequenced using an Illumina MiSeq. Ileal contents were harvested within 2 h of death and stored at −80 °C pending analysis. Soil was collected from an EGS field, at a depth of 2–10 cm, and stored at −80 °C pending analysis. The MO-BIO Powersoil DNA Isolation Kit was used to extract total sample DNA following manufacturer’s instructions. Before bead beating, samples were heated at 65 °C for 10 min to increase cell lysis. 100 ng DNA was used in a two-round nested PCR protocol to amplify the V2-V3 region of the 16S gene. All PCR steps used the Q5 High-Fidelity 2X Master Mix (New England Biolabs). The first round of PCR consisted of 20 cycles using the primers 28 F (5’ GAGTTTGATCNTGGCTCAG 3’) and 805R (5’ GACTACCAGGGTATCTAATC 3’) in a total reaction volume of 50 μL. The reaction ran at 94 °C for 2 min, 20 cycles of 94 °C for 1 min, 55 °C for 45 s, 72 °C for 1.5 min followed by 72 °C for 20 min. After each PCR round, AMPure XP PCR Purification (Agencourt) was used to purify amplified DNA from other components of the reaction mixture. Purified PCR product (20 μL) was added into the second round of PCR along with the mastermix and barcoded primers 104 F (5’ GGCGVACGGGTGAGTAA 3’) and 519R (5’ GTNTTACNGCGGCKGCTG 3’) to a total volume of 50 μL. Primers include adapter sequences required for binding to the Illumina flow cell and barcodes for multiplexing. The reaction conditions were 98 °C for 30 s followed by 20 cycles of 98 °C for 10 s, 67 °C for 30 s, 72 °C for 10 s, and 72 °C for 2 min. 250 bp paired-end sequencing was performed using an Illumina Miseq.
Primers were removed using CUTADAPT  (allowing 1 bp error per 10 bp). MOTHUR  was used for quality control and for taxonomic assignment of reads, following a protocol developed for MiSeq by MOTHUR creators . Sequences were removed from analysis if they were of length <350 bp, contained homopolymers of >9 bp or ambiguous base calls, did not align to the SILVA reference alignment , were identified as chimeric using UCHIME  or were classified as other than bacterial. Taxonomic classification was done using MOTHUR’s Bayesian classifier against the Greengenes database  trimmed to the V2-V3 16S region . Sequences were assigned taxonomy if there was a >80% chance of correct assignment.
Microscopic examination for cyanobacteria in equine gastrointestinal tract samples
To determine whether cyanobacteria were detectable microscopically in gastrointestinal contents of grazing horses, conventional light and fluorescence microscopy was performed on saline suspensions of freshly collected luminal contents from the stomach (n = 2), jejunum (n = 2), ileum (n = 4), caecum (n = 2) and colon (n = 2) of horses with acute EGS, and of faeces from 2 horses with chronic EGS and 2 healthy control horses.
Analysis for DAB, BMAA and AEG in plant washings and equine neural tissue
DAB, BMAA and AEG were assayed using UPLC-MS/MS as previously described [21,22] in plant washing pellets from 3 EGS fields after 6 M HCl hydrolysis. The hydrolysate was centrifuge filtered, dried and derivatised with AQC for UPLC-MS/MS analysis, in comparison with synthetic standards . Plant washing pellets were prepared by adding plants (5 g wet mass for sample 1, 6 g for samples 2 and 3) to 10 mL saline, shaking vigorously for 1 min, decanting the fluid, then ultracentrifugation at 13 000 rpm for 10 min before discarding the supernatant. These data were used to calculate the estimated daily DAB intake by a horse grazing for 24 h on each of these EGS fields.
DAB, BMAA and AEG were also assayed in archived formalin-fixed, wax-embedded, neural tissue from EGS and EMND-affected horses and from control horses. Sample 1 (EGS) comprised a pool of cranial cervical (superior) ganglia (CCG) from 6 different EGS-affected horses (mix breed and gender, median age 6 years, range 3–20). EGS was confirmed by histopathology of autonomic and enteric ganglia in all cases . Sample 2 (control) comprised a pool of CCG from 6 different control horses (mix breed and gender; 14, 6–30 years) which were euthanased because of non-neurological disorders. Sample 3 (EMND) comprised pooled neural tissues from a 9 year-old Thoroughbred cross mare that had EMND confirmed at necropsy, including CCG, transverse segments of spinal cord at C1-2, C4-5, C7, C8, T1, T5, L6, S1 and rostral medulla oblongata. Sample 4 (EMND) was a sample of sacrococcygeus dorsalis muscle from a 6 year-old Cob gelding which had EMND. Sample 5 (control) was a wax-embedded formalin-fixed sample of medulla from a 20 year-old Thoroughbred cross mare that had no apparent neurologic disease. Neural samples were excised from formalin-fixed blocks, deparaffinised, washed with xylenes and hydrated using an alcohol series . The subsequent material was hydrolysed with 6 M HCl for 16 h, the supernatant centrifuge filtered and dried in a speedvac. Once dry, the residue was resuspended with 20 mM HCl and derivatised with AQC for UPLC-MS/MS analysis of BMAA and its isomers.
Data were not normally distributed. Inter- and within- group comparisons were made using the Mann Whitney and Wilcoxon Rank Sum tests, respectively. Correlations were done using Spearman’s Rank correlation. The spatial variability in Phormidium filament population density within a field was determined by calculating the coefficient of variance for 10 individual samples collected from that field.
Identification of cyanobacteria in plant samples
During sample collection it was noted that some plants, particularly at the base and branching points, had a slimy coating of mucilage consistent with that produced by cyanobacteria and algae . Light and fluorescence microscopy revealed that these areas had a biofilm containing numerous cyanobacterial filaments. Microscopic examination of plant washings indicated that cyanobacteria were predominantly Phormidium spp. (Figure 1), with filaments in washings from many fresh samples exhibiting typical spontaneous oscillatory motion . The numbers of cells per Phormidium filament on horse (median 16, range 3–67; n = 281), cattle (14, 6–56; n = 36) and sheep (18, range 4–76; n = 85) fields were not significantly different. Some plant samples also had low numbers of a second, very narrow filamentous cyanobacterium of the Leptolyngbya or Leptothrix genera, and low numbers of unicellular cyanobacteria of the Aphanocapsa genus. Many samples also had filamentous green algae, unicellular green algae, and low numbers of diatoms, motile algal flagellates and desmids (Closterium sp.): these were not enumerated.
Density of Phormidium filaments in plant samples
Phormidium filaments were present in samples from all EGS (n = 21) fields and most horse control (29/40), cattle (11/13) and sheep (13/14) fields. Phormidium filament population density was significantly higher in EGS fields (median 2400, range 100–68 900 filaments g wet mass plants−1) than in horse control (250, 0–4200; p < 0.0001), cattle (300, 0–1400; p = 0.0002) and sheep (700, 0–3300; p = 0.0012) fields (Figure 2). There were no significant differences in density among horse control, cattle and sheep fields. There was marked spatial variation in Phormidium filament population density across transects in an EGS field (coefficient of variance 126%) and a horse control field (143%) (Figure 3). There was marked variation, but no significant difference, in Phormidium filament population density in samples collected from 9 horse control fields at 0700 h and 1900 h, with density at 1900 h increased in 5 fields and reduced in 3 fields (Figure 4). There was no apparent consistent pattern to the weekly changes in population density in samples collected from 8 horse fields between April and July (Figure 5), and Phormidium filament population density in these samples was not significantly correlated with average air temperature, rainfall or sunshine hours. A low density (50, 50, 100 filaments g wet mass plants−1) of Phormidium filaments was present in only 3/22 samples from the French fields.
Genomic identification of cyanobacteria in EGS plant washings, soil and equine ileal contents
Cyanobacterial 16S rDNA sequences were detected in all samples tested (see Additional file 1). Most sequences were attributable to unclassified Phormidium. The following sequences were identified; Anabaena cylindrica (1 plant washing), 1 unclassified Nostoc sp. (2 plant washings), 1 unclassified Nostocaceae fam. (2 plant washings), Phormidium animale (4 plant washings), 1 unclassified Phormidium sp. (6 plant washings, 2 ileal contents), 1 unclassified Phormidium sp. (2 plant washings), 1 unclassified Phormidiaceae fam. (2 plant washings), 1 unclassified Oscillatoriales ord. (1 plant washing), 1 unclassified Oscillatoriophycideae class (2 plant washings), Leptolyngbya frigida (1 plant washing), 1 unclassified Leptolyngbya sp. (1 plant washing), 1 unclassified Pseudanabaenaceae fam. (1 plant washing), 1 unclassified Cyanobacteria phylum (4 plant washings) and 1 unclassified Cyanobacteria phylum (3 plant washings). rDNA from 3 lines of Melainabacteria were identified; YS2/4C0d-2 (1 soil sample), mle1-12 (5 plant washings, 1 ileal contents, 1 soil sample) and ML635J-21 (5 plant washings, 1 soil sample). Additionally, rDNA from DAB-producing actinomycetes, including Clavibacter spp. and Rathayibacter spp., was detected in 6 plant washings and soil.
Examination of cyanobacteria in equine gastrointestinal tract samples
No intact cyanobacteria were apparent. Gastric contents from 2 EGS horses appeared to contain occasional highly degraded and apparently non-viable Phormidium filaments.
Analysis for DAB, BMAA and AEG
DAB was detected in all 3 plant washing pellets. Mean free and bound DAB concentrations (pg filament−1), respectively were: pellet 1, 43.5, 355.2; pellet 2, 121.6, 2131.4; pellet 3, 0.4, 8.2. BMAA and AEG were not detected in plant washings. BMAA, AEG and DAB were not detected in neural tissues at minimum detection limits 0.0065 picomoles per injection for L-BMAA and AEG and 0.0013 picomoles per injection for DAB.
Estimation of the worst case scenario daily intake of Phormidium filaments and DAB for horses grazing EGS fields
Worst case scenario estimation of daily intake of Phormidium filaments for a horse grazing fulltime on the field with the highest Phormidium filament population density (68 900 filaments g wet weight plants−1) is 7.6 × 106 filaments kg−1. This estimation assumes that an average 500 kg horse consumes 11.5 kg of herbage dry matter daily, with a typical mean dry matter of 21% , equating to 55 kg wet herbage daily. The estimated daily intakes of DAB (mg kg−1) for horses grazing the 3 EGS fields are: Field 1 (free 0.017; bound 0.14; total 0.16); Field 2 (free 0.007; bound 0.12; total 0.12); Field 3 (free 0.004; bound 0.08; total 0.09). Plant-washing pellets 1, 2 and 3 contained, respectively, 2700, 450 and 82 050 Phormidium filaments.
This is the first study to demonstrate that grazing livestock are exposed to pasture-derived terrestrial cyanobacteria, −microalgae (diatoms, Closterium) and their toxins. Indeed, the most commonly identified cyanobacteria, Phormidium spp., were identified within the biofilm of plants growing in most of the fields examined.
There was marked spatial variation in the population density of Phormidium on plants, both within and between fields, with counts ranging from 0–68 900 filaments g wet plants−1. Repeat sampling at 12 h and weekly intervals suggested there was also apparent marked temporal variation in Phormidium population density, although some of this variability could have reflected spatial variation. Phormidium density did not appear to follow a consistent diurnal or weekly pattern and was not apparently correlated with average daily air temperature, rainfall or sunshine hours. However these latter findings should be interpreted with caution since these relationships were assessed under limited circumstances and further detailed investigation is required to clarify the influence of weather on Phormidium density. Variation in Phormidium population density presumably reflects the suitability of the local biofilm microenvironment for cyanobacterial growth and survival. Factors reported to influence cyanobacterial growth and survival include light duration and irradiance, temperature, availability of water, phosphate-, iron- and nitrate concentrations, and numbers of invertebrate prey species [27,28]. We hypothesise that high exposure levels may be encountered when environmental conditions are optimal, as occurs on turf grasses [2-6], a situation akin to the occurrence of cyanobacterial blooms in aquatic environments during eutrophication [29,30]. Indeed the highest Phormidium population density recorded in the study (68 900 filaments g wet plants−1) was a clear statistical outlier suggesting that it could be considered to represent such a “bloom” occurrence. Variation in apparent Phormidium density also likely reflects the organism’s motility, with filaments moving up and down plant leaves/petioles at up to 11 μm s−1 , presumably to seek favourable light conditions. As Phormidium spp. are more likely to be present at the tips of short plants than long plants , Phormidium population density within plant washings may also reflect plant length and the proportion of lower and upper leaves/petioles sampled. This study may have underestimated Phormidium density because an indeterminate number of cyanobacteria may have remained adherent within the plant biofilm despite vigorous shaking. While the Phormidium spp. were readily enumerated in plant washings, many of the aforementioned factors which influence Phormidium population density will compromise accurate estimation of the number of Phormidium filaments ingested by grazing animals. For example, since there was considerable spatial and temporal variation in cyanobacterial density, the number of cyanobacteria ingested may be markedly higher in an animal grazing a cyanobacterium-rich area of grassland. In a worst-case scenario estimation, a 500 kg horse grazing fulltime on the EGS field with the highest Phormidium population density (68 900 filaments g wet mass plants−1) and a median number of 16 cells filament−1, would ingest 7.6 × 106 Phormidium filaments kg−1 day−1or 121 × 106 Phormidium cells kg−1 day−1.
Ingestion of terrestrial cyanobacteria provides one explanation for the presence of cyanobacterial 16S rDNA in the 2 equine ileal samples in this study. It also provides a more plausible explanation for the previous report of cyanobacterial 16S rDNA in faeces from forage-fed horses than them being homologous sequences from dietary plant chloroplasts . Alternative explanations include ingestion of aquatic cyanobacteria from contaminated water sources and ingestion of foods containing cyanobacterial supplements. Cyanobacterial 16S rDNA sequences detected in ileal contents was attributable to unclassified Phormidium spp. (2 horses) and a bacterium of the Order mle1-12 (1 horse). The latter has recently been proposed as a member of a candidate class  or sister phylum  of non-photosynthetic, filamentous bacteria termed Melainabacteria, distinct from extant cyanobacteria, but with ancestral affiliations. The fate of ingested cyanobacteria is currently receiving increasing attention. The ability of ingested cyanobacteria to colonise the gastrointestinal tract has so far received little attention. Indeed cyanobacterial species in aquatic environments do not typically thrive below about pH 6.7 and cell degradation can occur under acid conditions (Codd, personal observations). Intact cyanobacteria were not identified microscopically in the equine gastrointestinal contents, although gastric contents of 2 EGS horses appeared to contain occasional highly degraded and apparently non-viable Phormidium filaments. Similarly cyanobacteria in the rumen and abomasum of cattle dying from acute cyanobacterial poisoning are markedly degraded (Codd, personal observations). While spores (akinetes) produced by some cyanobacteria could potentially survive in the gut, akinete production is not widespread among cyanobacteria and does not occur in Phormidium which predominated in this study. Further, it is not known whether akinete germination and outgrowth could occur in the aphotic, anaerobic gut. However, it is known that some species of Phormidium (P. uncinatum) can grow chemoheterotrophically (aphotic growth on glucose, fructose and acetate at a reduced rate) . Furthermore, recent work indicates that the unicellular aquatic cyanobacterium Microcystis PCC7806 can survive and potentially produce cyanotoxins for up to 17 days in an in vitro environment mimicking the human gastrointestinal tract . The possibility of gut colonisation by cyanobacteria is further supported by accumulating evidence that Melainabacteria, including the mle1-12 present in 1 horse ileum, have differentiated from extant cyanobacteria by niche adaptation, including for symbiosis in the mammalian gut [34,37-39]. Indeed, Melainabacteria is considered to have an obligate fermenter role in the gut, and its enrichment in herbivores may reflect a prominent role in plant fibre digestion . Further work, utilising larger numbers of horses, is required to characterise the populations of cyanobacteria within the equine gastrointestinal tract, and to determine whether they are capable of colonisation and in vivo cyanotoxin production. If so, it would add support to the hypothesis that cyanobacteria, while being typically a minor component of the intestinal microflora, may proliferate and produce neurotoxins in vivo, resulting in neurodegenerative diseases .
Further study is warranted to identify and quantify the toxins produced by Phormidium from livestock fields and to determine whether under appropriate environmental conditions, grazing livestock can ingest sufficient quantities of cyanotoxins from terrestrial cyanobacteria to cause disease. While the range of toxins produced by Phormidium is currently unknown, production of BMAA, LPS, microcystins and anatoxin-a is reported [8,9,41-43]. Extrapolation of data from the related cyanobacterial genus Oscillatoria suggests that Phormidium may also produce, apslysiatoxins, cylindrospermopsin and homoanatoxin-a. These toxins cause hepatotoxicity, neurotoxicity and dermatitis in animals exposed to aquatic cyanobacterial blooms [7-10]. BMAA has been linked with human motor neuron disease, Alzheimer’s disease and Parkinson’s disease [44-48] and proposed as a potential cause of equine motor neuron disease . The design of this study precluded definitive examination of potential associations between ingested cyanotoxins and disease in grazing animals. Since livestock grazing the horse control-, cattle- and sheep fields had no overt evidence of hepatic or neurological disease (although veterinary examinations were not performed), cyanotoxin exposure in these fields must have been insufficient to cause clinical disease. Additional experiments were performed to test the hypothesis that, under appropriate circumstances, ingestion of cyanobacterial hepato- and neurotoxins contributes to the pathogenesis of some currently unexplained diseases of grazing horses, including EGS, EMND of grazing horses  and hepatopathy.
Phormidium population density was significantly higher on EGS fields than on control fields, indicating that horses grazing EGS fields likely ingest higher numbers of Phormidium spp. than horses grazing control fields. This brings into question conclusions of a previous study  that cyanotoxins can be excluded as a causative factor for EGS. While the present study assessed exposure of horses to terrestrial cyanobacteria, the previous study  investigated only exposure to aquatic cyanobacteria, finding no detectable microcystins and no microscopic evidence of cyanobacteria in water samples from 16 premises on which EGS had occurred. While the cause of EGS is unknown, increasing evidence suggests it is a toxico-infectious form of botulism, whereby a dietary trigger induces intestinal overgrowth of Clostridium botulinum C and/or D, with resultant in vivo production of botulinum neurotoxins (reviewed in ). Potential involvement of cyanotoxins in EGS could therefore reflect their proposed action as triggers for botulism [50-52] or reflect direct neurotoxic effects of cyanotoxins including microcystins, anatoxin-a, DAB and BMAA [1,8,53]. Alternatively the increased Phormidium density on EGS fields may be unrelated to EGS pathogenesis, perhaps simply reflecting the elevated total nitrogen and ammonium nitrogen content of soils on EGS fields [26,54], since nitrate promotes growth of some cyanobacteria .
Since DAB, BMAA and AEG were not detected in neural tissues from 6 EGS, 2 EMND horses and 7 control horses, a causal role for these neurotoxins in EGS and EMND could not be demonstrated. DAB was however detected in all washing pellets of plants from 3 EGS fields. While DAB is produced by cyanobacteria, additional sources include plant associated actinomycetes and some leguminous plants [56,57]. Indeed the apparent lack of correlation between DAB concentrations and the concentration of Phormidium filaments in the 3 plant washing pellets suggests that DAB was derived from a source other than, or in addition to, Phormidium. One further potential source of DAB in grass washings is actinomycetes, including the plant pathogenic Clavivibacter spp. and Rathayibacter spp., since 16S rDNA sequences from these bacteria were detected in 6 plant washings and soil. While the effect of ingested DAB on horses is unknown, the estimated worse-case scenario daily intake of DAB (free 0.017; bound 0.14; total 0.16 mg kg−1) is lower than doses used experimentally to induce neurolathyrism in laboratory animals (from 0.7 to approximately 500 mg kg−1 [58-60]).
Phormidium was present only in low numbers in plants collected from fields in France where horses had unexplained hepatopathy, indicating that a role in disease aetiology was unlikely.
This is the first study to demonstrate that grazing livestock are exposed to terrestrial cyanobacteria. While it did not yield evidence linking terrestrial cyanotoxins with neurologic or hepatic disease in grazing horses, further study is required to identify and quantify cyanotoxin exposure in grazing livestock, and to determine whether, under appropriate conditions, terrestrial cyanotoxins contribute to currently unexplained diseases. Additional study is also warranted to further identify cyanobacteria within the gastrointestinal tract of herbivores and determine whether some are capable of intestinal colonisation and in vivo toxin production.
Cervical [superior] ganglia
Equine grass sickness
Equine motor neuron disease
Codd GA, Lindsay J, Young FM, Morrison LF, Metcalf JS (2005) Cyanobacterial Toxins. In: Huisman J, Matthijs HCP, Visser PM (ed) Harmful Cyanobacteria. Springer-Verlag, London, pp 1–23
Baldwin NA, Whitton BA (1992) Cyanobacteria and eukaryotic algae in sports turf and amenity grasslands: a review. J App Phycol 4:39–47
Hodges CF, Campbell DA (1997) Nutrient salts and the toxicity of black-layer induced by cyanobacteria and Desulfovibrio desulfuricans to Agrostis palustris. Plant Soil 195:53–60
Elliott ML (1998) Use of fungicides to control blue-green algae on Bermuda grass putting-green surfaces. Crop Protection 11:631–637
Gelernter W, Stowell LJ (2000) Cyanobacteria (A.K.A. blue-green algae): wanted for causing serious damage to turf. PACE Insights 6:1–4
Tredway LP, Stowell LJ, Gelertner WD (2006) Yellow spot and the potential role of cyanobacteria as turf grass pathogens. Golf course management. PACE Turfgrass Research Institute, San Diego, pp 83–86
Skulberg OM, Carmichael WW, Andersen RA, Matsunaga S, Moore RE, Skulberg R (1992) Investigations of a neurotoxic Oscillatorialean strain (cyanophyceae) and its toxin. Isolation and characterization of homoanatoxin-a. Environ Toxicol Chem 11:321–329
Cox PA, Banack SA, Murch SJ, Rasmussen U, Tien G, Bidigare RR, Metcalf J, Morrison LF, Codd JA, Bergman B (2005) Diverse taxa of cyanobacteria produce-N-methylamino-L-alanine, a neurotoxic amino acid. Proc Natl Acad Sci U S A 102:5074–5078
Gugger M, Lenoir S, Berger C, Ledreux A, Druart JC, Humbert JF, Guette C, Bernard C (2005) First report in a river in France of the benthic cyanobacterium Phormidium favosum producing anatoxin-a associated with dog neurotoxicosis. Toxicon 45:919–928
van Apeldoorn ME, van Egmond HP, Speijers GJA, Bakker GJI (2007) Toxins of cyanobacteria. Mol Nutr Food Res 51:7–60
Doxey DL, Pogson DM, Milne EM, Gilmour JS, Chisholm HK (1992) Clinical equine dysautonomia and autonomic neuron damage. Res Vet Sci 53:106–109
Doxey DL, Gilmour JS, Milne EM (1991) A comparative study of normal equine populations and those with grass sickness (dysautonomia) in eastern Scotland. Equine Vet J 253:365–369
McGorum BC, Mayhew IG, Amory H, Deprez P, Gillies L, Green K, Mair TS, Nollet N, Wijnberg I, Hahn C (2006) Horses on pasture may be affected by equine motor neuron disease. Equine Vet J 38:47–51
Martin M (2011) Cutadapt removes adapter sequences from high-throughput sequencing reads. EMBnet J 17:10–12
Schloss PD, Westcott SL, Ryabin T, Hall JR, Hartmann M, Hollister EB, Lesniewski RA, Oakley BB, Parks DH, Robinson CJ, Sahl JW, Stres B, Thallinger GG, Van Horn DJ, Weber CF (2009) Introducing mothur: open-source, platform-independent, community-supported software for describing and comparing microbial communities. Appl Environ Microbiol 75:7537–7541
Kozich JJ, Westcott SL, Baxter NT, Highlander SK, Schloss PD (2013) Development of a dual-index sequencing strategy and curation pipeline for analyzing amplicon sequence data on the MiSeq illumina sequencing platform. Appl Environ Microbiol 79:5112–5120
Pruesse E, Quast C, Knittel K, Fuchs BM, Ludwig W, Peplies J, Glöckner FO (2007) SILVA: a comprehensive online resource for quality checked and aligned ribosomal RNA sequence data compatible with ARB. Nucleic Acids Res 35:188–7196
Edgar RC, Haas BJ, Clemente JC, Quince C, Knight R (2011) UCHIME improves sensitivity and speed of chimera detection. Bioinformatics 27:2194–2200
DeSantis TZ, Hugenholtz P, Larsen N, Rojas M, Brodie EL, Keller K, Huber T, Dalevi D, Hu P, Andersen GL (2006) Greengenes, a chimera-checked 16S rRNA gene database and workbench compatible with ARB. Appl Environ Microbiol 72:5069–5072
Werner JJ, Koren O, Hugenholtz P, DeSantis TZ, Walters WA, Caporaso JG, Angenent LT, Knight R, Ley RE (2012) Impact of training sets on classification of high-throughput bacterial 16 s rRNA gene surveys. ISME J 6:94–103
Banack SA, Metcalf JS, Jiang L, Craighead D, Ilag LL, Cox PA (2012) Cyanobacteria produce N-(2-Aminoethyl)Glycine, a backbone for peptide nucleic acids which may have been the first genetic molecules for life on Earth. PLoS One 7:e49043
Masseret E, Banack SA, Boumediene F, Abadie E, Brient L, Pernet F, Juntas-Morales R, Pageot N, Metcalf J, Cox P, Camu W (2013) The French network on BMAA/ALS. Detection of BMAA in the marine environment of an ALS cluster in Southern France. PLoS One 8:e83406
Scicchitano MM, Dalmas DA, Boyce RW, Thomas HC, Frazier KS (2009) Protein extraction of formalin-fixed, paraffin-embedded tissue enables robust proteomic profiles by mass spectrometry. J Histochem Cytochem 57:849–860
Sutherland IW (1996) A natural terrestrial biofilm. J Indust Microbiol 17:281–283
Richardson LL, Castenholz RW (1989) Chemokinetic motility responses of the cyanobacterium Oscillatoria terebriformis. Appl Environ Microbiol 55:261–263
Edwards SE, Martz KE, Rogge A, Heinrich M (2010) Edaphic and phytochemical factors as predictors of equine grass sickness cases in the UK. Front Pharmacol 1:122
Mur LR (1983) Some aspects of the ecophysiology of cyanobacteria. Ann Microbiol 134B:61–72
Agrawal SC, Singh V (2002) Viability of dried filaments, survivability and reproduction under water stress, and survivability following heat and UV exposure in Lyngbya martensiana, Oscillatoria agardhii, Nostoc calcicola, Hormidium fluitans, Spirogyra sp. and Vaucheria geminate. Folia Microbiol 47:61–67
Fogg GE, Stewart WDP, Fay P, Walsby AE (1972) The Blue-Green Algae. Academic Press, London
Sutcliffe DW, Jones JG (1992) Eutrophication: Research and Application to Water Supply. Windermere, Freshwater Biological Association
Staley JT (1986) Bergey’s Manual of Systematic Bacteriology, vol 3. Williams and Wilkins, Baltimore
Shepherd ML, Swecker WS, Jensen RV, Ponder MA (2012) Characterization of the fecal bacterial communities of forage-fed horses by pyrosequencing of 16S rRNA V4 gene amplicons. FEMS Microbiol Lett 326:62–68
Soo RM, Skennerton CT, Sekiguchi Y, Imelfort M, Paech SJ, Dennis PG, Steen JA, Parks DH, Tyson GW, Hugenholtz P (2014) An expanded genomic representation of the phylum Cyanobacteria. Genome Biol Evol 6:1031–1045
Di Rienzi SC, Sharon I, Wrighton KC, Koren O, Hug LA, Thomas BC, Goodrich JK, Bell JT, Spector TD, Banfield JF, Ley RE (2013) The human gut and groundwater harbor nonphotosynthetic bacteria belonging to a new candidate phylum sibling to Cyanobacteria. Elife 2:e01102
Bagchi SN, Chauhan VS, Palod A (1990) Heterotrophy and nitrate metabolism in a cyanobacterium Phormidium uncinatum. Curr Microbiol 21:53–57
Stefanelli M, Vichi S, Stipa G, Funari E, Testai E, Scardala S, Manganelli M (2014) Survival, growth and toxicity of Microcystis aeruginosa PCC 7806 in experimental conditions mimicking some features of the human gastro-intestinal environment. Chem Biol Interact 215:54–61
Backhed F, Ley RE, Sonnenburg JL, Peterson DA, Gordon JI (2005) Host-bacterial mutualism in the human intestine. Science 307:1915–1920
Eckburg PB, Bik EM, Bernstein CN, Purdom E, Dethlefsen L, Sargent M, Gill SR, Nelson KE, Relman DA (2005) Diversity of the human intestinal microflora. Science 308:1635–1638
Ley R, Backhed F, Turnbaugh P, Lozupone C, Knight R, Gordon J (2005) Obesity alters gut microbial ecology. Proc Natl Acad Sci U S A 102:11070–11075
Brenner SR (2013) Blue-green algae or cyanobacteria in the intestinal micro-flora may produce neurotoxins such as Beta-N-Methylamino-L-Alanine (BMAA) which may be related to development of amyotrophic lateral sclerosis, Alzheimer’s disease and Parkinson-Dementia-Complex in humans and Equine Motor Neuron Disease in horses. Med Hypotheses 80:103
Mikheyskaya LV, Ovodova RG, Ovodov YS (1977) Isolation and characterization of lipopolysaccharides from cell walls of blue-green algae of the genus Phormidium. J Bacteriol 130:1–3
Codd GA, Bell SG, Kaya K, Ward CJ, Beattie KA, Metcalf JS (1999) Cyanobacterial toxins, exposure routes and human health. Eur J Phycol 34:405–415
Aboal M, Puig MA, Asencio AD (2005) Production of microcystins in calcareous Mediterranean streams: the Alharabe River, Segura River basin in south-east Spain. J Appl Phycol 17:231–243
Spencer PS, Nunn PB, Hugon J, Ludolph AC, Ross SM, Roy DN, Robertson RC (1987) Guam amyotrophic lateral sclerosis-Parkinsonism-dementia linked to a plant excitant neurotoxin. Science 237:517–522
Cox PA, Banack SA, Murch SJ (2003) Biomagnification of cyanobacterial neurotoxins and neurodegenerative disease among the Chamorro people of Guam. Proc Natl Acad Sci U S A 100:13380–13383
Bradley WG, Mash DC (2009) Beyond Guam: The cyanobacteria/BMAA hypothesis of the cause of ALS and other neurodegenerative diseases. Amyotroph Lat Scler 10:7–20
Pablo J, Banack SA, Cox PA, Johnson TE, Papapetropoulos S, Bradley WG, Buck A, Mash DC (2009) Cyanobacterial neurotoxin BMAA in ALS and Alzheimer’s disease. Acta Neurol Scand 120:216–225
Chiu AS, Gehringer MM, Welch JH, Neilan BA (2011) Does α-amino-β-methylaminopropionic acid (BMAA) play a role in neurodegeneration? Int J Environ Res Public Health 8:3728–3746
Newton JR, Wylie CE, Proudman CJ, McGorum BC, Poxton IR, Overviews S (2010) Equine grass sickness: are we any nearer to answers on its cause and prevention after a century of research? Equine Vet J 42:477–481
Eriksson JE, Lindholm T. Sinilevakukintojen aiheuttamat lintu-ja kalakuolemat. Vesistojen levahaitat. Maakunnallinen vesipaiva. Lahtis Motespublikation. 1998; May 18.
Mahakhant A, Klungsugya P, Arunpairojana A, Sano T, Watanabe M, Kaya K, Atthasampunna P (1999) Toxicity of cyanobacterial blooms in Thailand. Thailand Institute of Scientific and Technological Research; Research Project No. 39–02
Murphy T, Lawson A, Nalewajko C, Murkin H, Ross L, Oguma K, McIntyre T (2000) Algal toxins - initiators of avian botulism? Inc Environ Toxicol 15:558–567
Menga G, Suna Y, Fua W, Guob Z, Lihong X (2011) Microcystin-LR induces cytoskeleton system reorganization through hyperphosphorylation of tau and HSP27 via PP2A inhibition and subsequent activation of the p38 MAPK signaling pathway in neuroendocrine (PC12) cells. Toxicol 290:218–229
McCarthy HE, French NP, Edwards GB, Miller K, Proudman CJ (2004) Why are certain premises at increased risk of equine grass sickness? A matched case–control study. Equine Vet J 36:130–134
Kumar Saha S, Uma L, Subramanian G (2003) Nitrogen stress induced changes in the marine cyanobacterium Oscillatoria willei BDU 130511. FEMS Microbiol Ecol 45:263–272
Sasaki J, Chijimatsu M, Suzuki K (1998) Taxonomic significance of 2,4-diaminobutyric acid isomers in the cell wall peptidoglycan of actinomycetes and reclassification of Clavibacter toxicus as Rathayibacter toxicus comb. nov. Int J Syst Bacteriol 48:403–410
Kruger T, Monch B, Oppenhauser S, Luckas B (2010) LC–MS/MS determination of the isomeric neurotoxins BMAA (b-N-methylamino-L-alanine) and DAB (2,4-diaminobutyric acid) in cyanobacteria and seeds of Cycas revoluta and Lathyrus latifolius. Toxicon 55:547–557
Ressler C, Redstone PA, Erenberg RH (1961) Isolation and identification of a neuroactive factor from Lathyrus latifolius. Science 134:188–190
Mushahwar IS, Koeppe RE (1963) Concerning the metabolism of D- and L-α, γ-diaminobutyric acid-2–C14 in rats. J Biol Chem 238:2460–2463
Vivanco F, Ramos F, Jimenez-Diaz C (1966) Determination of γ-aminobutyric acid and other free amino acids in whole brains of rats poisoned with β, β’iminodipropionitrile and α, γ- diaminobutyric acid with, or without, administration of thyroxine. J Neurochem 13:1461–1467
This project was funded by The Equine Grass Sickness Fund and the Charles Engelhard Foundation. Laura Glendinning was funded by the BBSRC through the EASTBIO program. We thank Bryony Waggett, Karen Wilson, Emily Price and Douglas Callaghan for assistance with sample collection and processing.
The authors declare that they have no competing interests.
BM conceived the study. BM, SP and GC acquired the samples, and identified and quantified cyanobacteria. LG and GM performed genomics. JM, SB and PC performed cyanotoxin assays. All authors contributed to preparation and approval of the manuscript.
Identity of cyanobacterial 16S rDNA sequences detected in EGS plant washings ( n = 6), equine ileal contents ( n = 2) and soil ( n = 1). Numbers in parentheses refer to numbers of plant washings (P), ileal contents (I) and soil (S) which contained each sequence.
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McGorum, B.C., Pirie, R.S., Glendinning, L. et al. Grazing livestock are exposed to terrestrial cyanobacteria. Vet Res 46, 16 (2015) doi:10.1186/s13567-015-0143-x
- Grazing Livestock
- Ileal Content
- Horse Control
- Terrestrial Cyanobacterium
- Equine Motor Neuron Disease