Colonization of the vertebrate host niche by pathogenic fungi is an ongoing process and recent expansions of host ranges are leading to an increasing global threat to animal and human health1. Amphibian chytridiomycosis is emblematic of how the emergence of fungal diseases contributes to major biodiversity loss during the current sixth mass extinction2. Within the primitive and diverse fungal phylum of Chytridiomycota, the two causative agents of chytridiomycosis Batrachochytrium dendrobatidis (Bd) and Batrachochytrium salamandrivorans (Bsal) diverged an estimated 67 million years ago to become the only taxa known to have adapted to colonize vertebrates3,4. Yet, these pathogens demonstrate markedly different host species range, with Bsal mostly infecting a single order of hosts, the caudates (salamanders), while Bd infects over 700 species across all three orders of Amphibia5,6. These species therefore offer a unique opportunity to elucidate the acquisition of fungal pathogenicity that allowed infection of vertebrates followed by evolution of host specificity.

Host infection by both pathogens is restricted to a similar niche, the amphibian epidermis, but results in markedly different outcomes (focal necrosis and ulceration in Bsal versus hyperplasia and hyperkeratosis in Bd)4. We therefore predict that the jump of Chytridiomycota to invade amphibian hosts has been facilitated by the acquisition of common ancestral traits, whereas subsequent differentiation of infection strategies has been the result of lineage-specific adaptations. To assess these predictions, we here report the sequencing of the genomes of Bd and Bsal and comparison to those of two related saprobic chytrids; Homolaphlyctis polyrhiza (Hp) is in the same order (Rhizophydiales) as Batrachochytrium and is the closest, so far known, relative to Bd, while Spizellomyces punctatus (Sp) is in a different, primarily terrestrial, order (Spizellomycetales). Differences in protease gene content for the two pathogens are then measured experimentally, revealing stage specific activity. To more broadly characterize the host–pathogen interplay during infection, we compare the in vivo transcriptomes of Bd and Bsal in a susceptible model host species (Tylototriton wenxianensis, Tw) at late stage of infection against transcription in vitro; this reveals fundamental differences between these pathogens related to their differing infection strategies and the attendant host response.


Genome content of Batrachochytrium species

We find the evolutionary adaptation to infect amphibians to be correlated with the acquisition of genes, encoding secreted proteins that are unique either to the genus Batrachochytrium, or to Bd or Bsal. By sequencing both Bd and Bsal (Supplementary Table 1), we find that genome size of the host-restricted Bsal is larger (32.6 Mb) and more complex than that of the broad host range Bd (23.7 Mb) as well as those of Hp (16.7 Mb) and Sp (24.1 Mb), two-related free-living chytrid saprobes (Fig. 1). This variation in genome size is reflected in the complexity of the Bsal genome, with 10,138 protein-coding genes predicted compared to a range of 6,254–8,952 for the other chytrids (Supplementary Table 2, Supplementary Fig. 1c,d). Bd and Bsal share a core set of 5,706 gene clusters (6,403 or 6,344 genes, respectively, including paralogs), of which 542 clusters are not found in the two saprobic chytrids and include specific functions related to cell wall modification and candidate secreted effectors (discussed below) (Supplementary Fig. 1c, Supplementary Tables 3 and 4). The two Batrachochytrium species are most closely related and share large regions of synteny; both species are more closely related to Hp than to Sp, and Batrachochytrium and Hp share a larger proportion of syntenic orthologs than either species shares with Sp (Fig. 1).

Figure 1: Relationship and genomic organization of four chytrid species.
figure 1

A phylogenetic tree inferred using RAxML indicates the relationships of the four chytrids (branch lengths indicate the mean number of nucleotide substitutions per site). To the right is a synteny plot, visualizing regions that span two or more orthologs between any two species as a connected grey line. Scaffold numbers are shown above each genome axis if longer than 100 kb, and the location of Batra. Group 1 M36s (G1M36), Bsal Group 2 M36s (G2M36), Crinklers (CRN) and the secreted upregulated Tribes 1 & 4 are depicted with coloured bars.

Similar to Bd, heterozygous positions were abundant in Bsal and found throughout the genome (Supplementary Fig. 2a, Methods). This level of heterozygosity (161,831 total; 4.96 kb) is similar to those found in the non-GPL Bd isolates using the same methods (for example, BdCH ACON 141,620=6.05 kb, BdCAPE TF5a1 122,352=5.23 kb), while BdGPL strains have less heterozygosity (for example, BdGPL JEL423 50,711=2.16 kb)7. Similar to Bd, the Bsal genome appears to be diploid, with potential examples of trisomy, based on depth of coverage, allele balance and SNP phasing (Methods).

Protease family expansion and activity

Several of the expanded and lineage-specific protein families are highly expressed during in vivo infection of the salamander T. wenxianensis (Tw). Using RNA-Seq, we compared gene expression for parallel infections by Bsal and Bd or growth of each pathogen in culture. Of the chytrid genes that were significantly upregulated in vivo (n=550), a large proportion was unique to Bsal (n=327; 60%), unique to Bd (n=43; 8%) or unique to the genus Batrachochytrium (n=44; 8%). Furthermore, about half of the Batrachochytrium, Bsal and Bd upregulated genes were secreted (55% and 47%, respectively). The fact that these secreted proteins are both largely not present in the saprobic chytrids based on ortholog identification, and that they show increased transcription during host colonization, suggests that the transcriptional response is focused on a unique host-interaction strategy in each species. Further, these upregulated genes likely include key virulence factors, acquired for colonization of a specific host species group for each pathogen within a vertebrate host class. Indeed, these include the M36 metalloproteases implicated in pathogenicity in chytrids7,8 as well as at least two large families of secreted proteins (Tribes 1 and 4) with no recognizable functional domains, which are very highly expressed and may represent novel virulence factors unique to Bsal (Fig. 1, Supplementary Figs 3 and 4).

The M36 metalloprotease family known to mediate host invasion in other systems9,10 is markedly expanded in Bsal (Supplementary Fig. 5), concordant with the aggressive necrotic pathology that this pathogen causes. Both Bsal (n=110) and Bd (n=35) have expanded M36 families compared to lower counts in the free-living saprobic chytrids Sp and Hp (n=2 and 3, respectively). Genus and species-specific expansions in the M36 metalloproteinase family suggest both ancestral gene-family expansions underpinning adaptation to vertebrates, and species-specific expansions that are potentially contributing to the delineation of the host species group and pathogenesis. Phylogenetic analysis revealed a subclass of closely related M36 metalloproteases that are shared across both pathogens that we term the Batra Group 1 M36s (G1M36) (Fig. 2a). Species-specific gene-family expansion is illustrated by the presence of a novel secreted clade of M36 genes (n=57) unique to Bsal, which we have termed the Bsal Group 2 M36s (G2M36) (Supplementary Table 5). These G2M36s are entirely encoded by non-syntenic regions of the Bsal genome (Fig. 1), supporting a recent species-specific expansion. Although most G1M36s and G2M36s are strongly upregulated in salamander skin, eight Bsal G1M36s (19%) appear more highly expressed in vitro (Fig. 2b), suggesting complex regulatory circuits underlie this subclass of protease in Bsal. Regulation and activity of the expanded proteases is complex and life stage specific (Fig. 2c,d, Supplementary Table 6). The upregulation of secreted G1M36s and the associated protease activity in Bd zoospores compared to Bd sporangia points to a crucial role of these proteases during early host colonization in Bd, for example, during insertion of their germ tube into the epidermal cells11. In contrast, the low protease activity in Bsal zoospores, but high activity in the maturing Bsal sporangia suggests a role during later stages of pathogenesis, for example, in breaching the sporangial wall of developing sporangia and subsequent spread to neighbouring host cells4.

Figure 2: M36 gene-family relationship and expression at differing life stages.
figure 2

(a) A phylogenetic tree inferred using RAxML from protein alignments of all identified M36 proteins in the four chytrids (branch lengths indicate the mean number of nucleotide substitutions per site). Bd genes are shown in green, Bsal genes in red, Sp genes in blue and Hp genes in black. (b) M36 expression was calculated (TMM normalized fragments per kilobase mapped; FPKM) across three in vitro replicates and three in vivo replicates (shown as 1, 2 and 3). Only M36 transcripts that are significantly differentially expressed in Tw are shown. A greater number are significantly differentially expressed in Bsal compared with Bd, which also include eight Bsal G1M36s that are downregulated. Trees indicate hierarchical clustering between data sets (above) and genes (left of heatmap). (c) Protease activity in Bd and Bsal. The protease concentration was determined in mature cultures (above) and spores (below) that were incubated with unsupplemented distilled water (control) or distilled water supplemented with different protease inhibitors. The results are presented as means+s.e.m. using a non-parametric Mann–Whitney U-analysis. Significant changes compared to the control group are signed with an asterisk (of P<0.05). (d) G1M36 and G2M36 mean fold changes in mRNA expression profiles in Bd (above) and Bsal (below). The data shows the normalized target gene quantities in spores that were incubated with skin tissue of Tw for 2 h, 3-day-old sporangia grown in TGhL and skin tissue from chytrid-infected Tw animals relative to freshly collected spores. The results are presented as means+s.d. Significant differences in expression between each experimental group are shown in Supplementary Table 6.

Variation of cell-surface proteins in Bd and Bsal

Another notable family of proteins markedly expanded in both Bd12 and Bsal compared to the free-living chytrids is characterized by multiple copies of the CBM18 domain (Fig. 3a). This domain is predicted to bind chitin and most copies of these proteins contain secretion signals that will target them to the cell surface or extracellular space. Species-specific differences are notable in the pronounced truncation of the lectin-like CBM18s of Bsal, suggesting a fundamental difference in capacity to bind some chitin-like molecules. In comparison, CBM18 genes in Bd are three-fold longer and harbour on average eight CBM18 domains compared with only 2.6 for Bsal. The lack of any significant changes in regulation of CBM18 upon exposure of sporangia to chitinases renders their role in protecting the fungi from host chitinase activity by fencing off the fungal chitin unlikely (Fig. 3b, Supplementary Table 6). Rather, we hypothesize that the CBM18s play a role in fungal adhesion to the host skin or in dampening the chitin-recognition host response.

Figure 3: CBM18 sequence similarity and expression at different life stages.
figure 3

(a) A phylogenetic tree of all chytrid CBM18 proteins inferred using RAxML with the per cent of 1,000 bootstrap replicates indicated for each node (branch lengths indicate the mean number of nucleotide substitutions per site). To the right of gene names are a diagram of the domain structure (black boxes indicate CBM18 domain, colours indicate larger domains shown in legend). (b) CBM18 mean fold changes in mRNA expression profile in Bd (above) and Bsal (below). The data represent the normalized target gene amount in spores that were incubated with skin tissue of Tylototriton wenxianensis (Tw) for 2 h, 3-day-old sporangia grown in TGhL, 3-day-old sporangia treated with TGhL broth supplemented with chitinase for 2 h and skin tissue from chytrid-infected Tw animals relative to freshly collected spores which is considered 1. The results are presented as means+s.d. Significant differences in expression between each experimental group are shown in Supplementary Table 6. DRDE, down-regulated deacetylase-like; UPDE, up-regulated deacetylase-like.

Expanded content of repetitive elements

Expansions of the M36 metalloprotease and CBM18 gene-family expansions coincide with an increased occurrence of repeat-rich regions in both pathogens. The fraction of the genome classified as repetitive sequence is 17% and 16% for Bd and Bsal compared to 3.7% and 4.5% for Sp and Hp, respectively (Supplementary Fig. 2). However, the dramatic differences in composition of repetitive regions between Bd and Bsal suggest independent acquisition of repeat-rich regions by both pathogens. While Bsal is rich in Alu elements (1.8 Mb; 5.6% of the genome), these are completely absent in Bd, Hp and Sp. Conversely, Bd is rich in DNA elements and long tandem repeats (LTR) (2.5 Mb; 10.9% of the genome), which are massively reduced or even absent in the other three chytrids. These differences suggest independent acquisition and diversification of repeat-rich regions contributing to genomic diversification of these species. The lack of the RNA-dependent RNA polymerase involved in RNAi defence may contribute to proliferation of repetitive elements in Bd and Bsal, though this gene is also missing from Hp.

The known association of gene-sparse, repeat-rich regions of the genome with high densities of virulence effectors in well-studied eukaryotic plant pathogens13 led us to examine gene-sparse regions of Bd and Bsal. Notably we found regions of low-gene density include homologues of a class of virulence effectors termed Crinkler and Necrosis (CRN) genes, previously found in the Phytophthora and Lagenidium genera of Oomycetes14,15. CRN-like genes in Bd had long intergenic regions consistent with a gene-poor repeat-rich environment (averaging 1.4 kb; Supplementary Fig. 6, Supplementary Table 7)—a trait shared with Phytophthora infestans T30-4 (ref. 16). While previously noted in Bd7,17, we find the CRN-like family is more widely distributed among the Chytridiomycota than previously realised. We identified 162 CRN-like genes in Bd, 10 in Bsal, 11 in Hp and 6 in Sp (Fig. 4a), many of which (n=55) belong to a single subfamily (known as DXX); genes in Bd contain one of two N-terminal motifs (Supplementary Fig. 7). As CRN-like genes did not appear highly expressed during advanced Tw infection (Fig. 4b), we next examined expression during additional life cycle stages. In both Bd and Bsal, some CRN-like genes were more highly expressed in the zoospore life stage compared to the sporangia life stage (Fig. 4c, Supplementary Table 6). However, incubation of Bd zoospores with Tw tissue for 2 h showed an increased expression of CRN genes, whereas Bsal zoospores were associated with decreased expression, indicating that CRN genes are of interest in the early infection stage of Bd, but not Bsal; the notable expansion of CRN-like genes in Bd suggests that they are of importance, however their function remains unknown. These data corroborate recent findings showing that the CRN-like family occur broadly though patchily throughout microbial eukaryotes as effectors in inter-organismal conflicts18.

Figure 4: Crinkler gene-family relationship and expression patterns.
figure 4

(a) A phylogenetic tree inferred using RAxML from the N-terminal region (first 50 amino acids) of all identified CRNs, showing Bd genes in green, Bsal genes in red, Sp genes in blue and Hp genes in black (branch lengths indicate the mean number of nucleotide substitutions per site). Two motifs were identified from these sequences. (b) Most CRNs were downregulated in Tw, and all those that were significantly differentially expressed (shown) were downregulated, including three Bsal genes (indicated by asterisk). Trees indicate hierarchical clustering between data sets (above) and genes (left of heatmap). (c) CRN mean fold changes in mRNA expression profile in Bd (above) and Bsal (below). The data show the normalized target gene amount in spores that were incubated with skin tissue of Tw for 2 h, 3-day-old sporangia grown in TGhL and skin tissue from chytrid-infected Tw animals relative to freshly collected spores which is considered 1. Significant differences in expression between each experimental group are shown in Supplementary Table 6.

Differences in host immune response

Despite Bsal and Bd being their own closest known relatives and causing a similar lethal skin disease, both vertebrate chytrids deploy strikingly different strategies during pathogenesis, reflecting their individual infection strategies in salamander hosts. The relatively mild skin pathology caused by Bd19 nevertheless induces a massive host response resulting in epidermal hyperplasia and hyperkeratosis coinciding with marked expression changes in genes involved in epidermal cornification, electrolyte and fluid homeostasis and immunity (Fig. 5). To examine host gene expression, we generated a de novo assembly of Tw transcripts based on RNA-Seq data (Supplementary Table 8). Bd infection induces marked upregulation of Tw host genes involved in innate (that is, inflammatory, antimicrobial peptides) and adaptive (that is, immunoglobulin, MHC) immune responses, a feature of infection that has previously been noted in some species for Bd20. Simultaneously, mucins are downregulated, and an absence of infiltration by immune cells in the infected skin was found. These responses suggest the host immune defences are dysregulated, which combined with loss of homeostasis, explains the lethality of the infection. In contrast, salamanders remain basically unresponsive towards the Bsal-induced necrosis and massive tissue destruction4 that results in erosion of the skin barrier leading to subsequent, overwhelming septicaemia and death. Unlike the significant upregulation of immune genes in response to Bd infection, we detected very little increased transcription linked to an immune response to Bsal (Fig. 5c). The lack of a substantial host immune response to Bsal suggests that it has immune-dampening properties in caudates, which could be attributed to one of its unique gene families.

Figure 5: Transcriptomes and skin histology for Tw post infection from Bsal or Bd.
figure 5

(a) Skin of Tw at 10 days after exposure to Bsal (left) or Bd (right). Bsal thalli are abundantly present across the entire thickness of the epidermis (}) resulting in extensive loss of keratinocytes, whereas Bd thalli are associated with the superficial epidermal layers and hyperkeratotic foci (*). For both infections, histological evidence of an inflammatory response is lacking (Hematoxylin and eosin stain, × 400). (b) MA plots (showing Log2 fold change in the trimmed mean of M-values (TMM) normalized Fragments Per Kilobase of transcript per Million mapped reads (FPKM) vs average Log2 counts per million) of Tw transcripts during Bsal infection (left) and Bd infection (right) compared with non-infected. Significant differential expression is highlighted in blue (Bsal) and red (Bd), where FDR P value<0.001 and >fourfold change of TMM normalized FPKM. (c) Multiple classes of immune genes (x-axis) were found differentially expressed during Bd infection, while few were found during Bsal infection. The y-axis shows the number of genes either upregulated (positive count) or downregulated during infection (negative count).


Our study shows that the differential expansion of putative virulence factors by at least two chytrid fungi is associated with an expanded host range of chytridiomycete fungi to include vertebrate hosts. Despite being closely related and both causing a lethal skin disease, the pathogenesis of these vertebrate-adapted fungal pathogens is strikingly different with the more host-restricted pathogen deploying a notably expanded arsenal of putative virulence factors and yet not triggering a strong host immune response. The evolutionary plasticity that has resulted in this remarkable, and thus-far uncharacterised, arsenal of fungal virulence factors within the genus Batrachochytrium underscores the urgent need to uncover and describe the global phylogenomic diversity of these fungi.

Pressing challenges include an understanding of the population genetic structure of Bsal, and variation in virulence that may exist. In this experiment, we have used a widely used isolate of Bd (JEL423) belonging to the Global Panzootic Lineage (BdGPL), which is responsible for major amphibian die-offs21. However, other Bd lineages and other hosts may yield variation in induced immune responses alongside life stage or infection-specific transcriptional responses. Furthermore, the experimental validation of many of the putative pathogenicity factors in these lineages and species of chytrids remain to be demonstrated. In particular, the newly discovered tribes in both Bd and Bsal, as well as the enigmatic chytrid Crinkler genes, currently have no ascribed function and further research on these putative virulence effectors is urgently needed. Finally, the difficulty we faced in generating a contiguous Bsal assembly could be improved through longer sequencing reads, or techniques that were used to ensure the high quality Bd genome. Indeed, an improved Bsal assembly may further resolve repeat families, syntenic divergence from Bd, and aneuploidies that may be present, which in turn may affect expression, life-stage and infection dynamics.

Understanding the amphibian-destroying armamentarium that chytrids harbour is crucial to making informed predictions of the risk that novel chytrid lineages pose to naïve and thus-far uninfected regions of the world. This research is a vital step towards correctly informing policy makers of the risk that specific lineages pose, enabling legislation to be enacted to stop the further advance of these pathogens into disease-free regions through biosecurity mechanisms such as restricting animal trade22.


Genome sequencing and assembly

B. salamandrivorans (Bsal) was sequenced using 29,503,468 paired-end reads (101 nt long) with insert sizes of 441 bp, and an additional 5,895,159 reads with insert sizes ranging from 500 bp to 2.5 kb, with a mean of 900 bp (totalling 262.9 × depth; Supplementary Table 1). The genome was assembled with Allpaths version R48559 (ref. 23) using 140 × fragment coverage. We detected high levels of heterozygosity, so included the ‘haploidify’ setting. The completeness, contiguity and correctness of the assembly were analysed using the GAEMR genome analysis package ( We also assessed the ability of Platanus v1.2.1 (ref. 24), which is designed for the assembly of highly heterozygous genomes. However, this tool did not surpass the Allpaths assembly. Additionally, we attempted a number of kmer-normalized assemblies, and splitting MiSeq reads to make pseudo-jump-paired reads. In general, these assemblies had fewer contigs but also less total sequence (dropping 2–5 Mb of sequence). We therefore chose to use the Allpaths assembly that was 32,636,440 nt in length, divided among 5,358 contigs (N50 10.5 kb).

B. dendrobatidis (Bd) strain JEL423 was sequenced using Sanger technology and paired-end reads were generated from 4 kb plasmid, 10 kb plasmid and 40 kb Fosmid genomic clones. A total of 12.5 × sequence coverage was generated and assembled using Arachne25. A 175 kb scaffold corresponding to the mitochondrial genome was removed from this assembly for annotation and analysis. Nearly all of the sequence is in large scaffolds; 98% of the sequence is present in 17 scaffolds; 97% of the bases of Q40 quality are higher (one error every 10−4 bases).

Heterozygosity and ploidy of Bsal in relation to other chytrids

Genome-sequencing reads from Bsal were aligned back to the Bsal genome using Burrows Wheeler Aligner (BWA) v0.7.4-r385 mem26, providing an average 169 × deep alignment. Binomial-SNP Caller from Pileup format (BiSCaP) v0.11 (ref. 27) with default settings was used to call variants. Bd strains harbouring trisomic and tetrasomic chromosomes had a high number of bi-allelic heterozygous positions with tri-allelic binomial probabilities (33:66 ratios) (between 1,944 and 6,654 per isolate7) and very few tri-alleles (between 2 and 145 per isolate7) possibly suggesting transient chromosome loss and gain as seen by in vitro passages of Bd. Even more pronounced were the 65,642 heterozygous positions in 33:66 ratios (40.56% of all heterozygous calls) across the Bsal genome. However, only 38 bases had three separate alleles, 24 of which included insertion/deletion variants.

The majority of Bsal heterozygous positions (136,501; 84%) were phased into two distinct haplotypes of two or more positions, all of which had 100% of the reads in accordance (using a minimal depth of 4 for each haplotype). These values are consistent with a polyploid genome arising from recent or transient duplications of one (or both) sets of the homologous chromosomes. Ploidy of the Bsal genome was further analysed using depth of coverage and allele balance (tallies of bases with differing per cent of reads agreeing with the reference: 47–53% for bi- or tetra-alleles, 30–36% and 63–69% for tri-alleles, and 22–28% and 72–78% for tetra-alleles). Due to large number of contigs, they were ordered according to mean depth of coverage. Contigs with the lowest and highest mean coverage were over represented by the smallest contigs. All contigs smaller than 5 kb were therefore excluded from representation (Supplementary Fig. 2b).

Approximately 1/8th of the genome with the lowest coverage had the greatest proportion of tri-allelic positions. The remaining 7/8th of the genome had predominantly bi-allelic heterozygous positions, consistent with a tetraploidy. This pattern of tetraploidy with trisomy is similar to those identified in Bd JEL423 (ref. 7). However, due to the low contiguous nature of the assembly, the 1/8th assembly that has evidence for triploidy could be enriched for assembly issues, which may suggest an overall diploid genome. Indeed, mapping synteny and ploidy together did not suggest whole chromosome copy number variation, and instead that tri-alleles may derive from repetitive elements (such as centromeres), or otherwise problematic regions of the assembly (Supplementary Fig. 2b). To examine this, we performed two-tailed Fisher’s exact test with q-value FDR28 of PFAM domains contained in tri-allelic compared with bi-allelic regions. We identified 13 significantly enriched terms, four of which were Glutamine amidotransferases (GATases 2, 4, 6, 7). Other likely multi-copy family members included HSP90, ABC transporters and a peptidase S41.

Repetitive content of Bsal in relation to other chytrids

To characterize the repetitive content of each of the four chytrids, we ran RepeatModeler v1.0.7 ( to identify de novo repeats from the assemblies. The proportion of repetitive elements between the two Batrachochytrium species was relatively consistent (Bd=17.1%, Bsal=16.2%). However, the total repetitive sequence in Bsal amounted to an additional 1.3 Mb, and both Batrachochytrium genomes were repeat rich compared with Sp (3.7%) or Hp (4.5%). Furthermore, the composition was markedly different between the two species (Supplementary Fig. 2c,d). Specially, Bsal has about 1% (263 kb) of its genome comprised of short interspersed nuclear elements, all of which were Alu elements, which is entirely absent in Bd and Hp, and comprises <0.01% of the Sp genome. Bsal also had >10 × the number of low complexity repeats (192 kb:13 kb) and nearly 20 × the genomic occupancy of simple repeats compared with Bd (404 kb:36 kb). Conversely, Bd had 2 × the occupancy of long interspersed nuclear elements 2 in its genome compared with that found in Bsal (195 kb:122 kb). Even more pronounced was the difference in LTR (Bd=411 kb, Bsal=153 kb) and DNA elements (Bd=1.3 Mb, Bsal=0.5 Mb). DNA elements were not identified in either of the non-amphibian-infecting chytrids. That Batrachochytrium should harbour such repeat-rich genomes compared with its closest chytrid relatives may indicate a conserved functional role, such as gene duplication, or an ancestral reduced ability to purge repetitive elements.

The largest difference in repetitive content was in the number of unclassified repeats identified in Bsal (4.2 Mb; 13%) compared with Bd (2.2 Mb; 9.24%). To characterize these repeats, we first ran an all vs all BLASTn with e−50 to avoid spurious hits. OrthoMCL and manually checking both confirmed a number of unknown families that could be merged with either other unknown families or annotated families. One repeat family in Bd had sequence similarity with LTR Copia at the start, and DNA elements on the other-end (unknown families were therefore placed into an LTR/DNA category). We next took all remaining unknown families that comprised >0.3% of each genome, identified ORFs using ORFFinder, and BLASTp the largest ORF to the nr protein database. A number of unknown families were categorized including Sp repeat-family 6, which contained five domains belonging to LTR copia-type transposons. Similarly, Sp family 71 had four domains belonging to Gypsy transposons. This process gave categories for 92% of Sp repeats, 90% Hp repeats, 75% of Bd repeats and 62% of Bsal repeats (Supplementary Fig. 2c). Those that were not categorized included 51 Bsal repeat families, 16 Bd families, 6 Sp families and 11 Hp families.

Gene prediction, improvement and annotation for chytrids

Gene prediction and annotation for B. salamandrivorans (Bsal), B. dendrobatidis (Bd), S. punctatus (Sp) and H. polyrhiza (Hp) was achieved using a de novo Eukaryotic Annotation Pipeline (Supplementary Table 2). The genome of Hp was downloaded from Genbank (accession AFSM00000000)8 prior to annotation; as a gene set was not available in Genbank for this assembly, this assembly was annotated in parallel and that data is available on FigShare (,, and For Sp, the available assembly and annotation was used (Genbank BioProject PRJNA37881)29. RNA-Seq data was generated for Bsal and Bd and used to inform and update gene prediction, respectively. For Bsal, 78,103,411 paired-end reads (15.7 Terabases) of RNA was sequenced on three lanes of Illumina HiSeq from in vitro cultures (Supplementary Table 1). For Bd, initial gene calls were predicted using a combination of FGENESH30, GENEID31, EST-based genes and manual annotation; this initial set (previously made available on the Broad Institute website at was improved using 50,374,154 paired-end reads (10.1 Tb) from RNA sequenced on three lanes of Illumina HiSeq from in vitro cultures (Supplementary Table 1), as well as 1,390 transcripts (800 kb) from Bd infection (described in detail below). Updated Bd genes were given new locus ids starting with BDEG_20001. Trinity version r20140413p1 (ref. 32) was used to assemble the RNA-Seq with the genome-guided mode, minimum kmer=2, and a max intron size of 10 kb. The programme to assemble spliced alignments33 was then used to align these transcripts to the genome, which were subsequently filtered for repetitive sequence using Repbase34, PFAM35, TransposonPSI (TPSI)36 and multiple similar mappings by BLAT37.

All four genomes were annotated using TBLASTn, Genewise38, tRNA, rfam, rnammer (rnaGenes)39, GenemarkHmmEs, TPSI and Repbase34. We generated a training set using Genewise38 and Genemark38. Next, GlimmerHmm40, Snap41 and Augustus42 were used to generate ab initio gene models. The best gene model at a given locus was selected from these data sets using evidence modeller (EM)43; conserved genes missing in gene sets were identified with OrthoMCL44 and combined with the EVM set. Genes were then filtered if >30% coding sequence overlapped TPSI36 hits (e-value 1e−10), overlapped repeat Pfam/TigrFam hits, or RepeatRunner45 proteins.

For the updated Bd gene calls, the total number predicted remained similar to the previous non-RNA-Seq-guided set (150 dropped, no new genes added). However, the number of predicted transcripts was greatly increased (8,819→9,893), resulting from a large increase in those that are spliced (7,801→8,940), and only a modest decrease in those that are not spliced (1,018→953). Subsequently, there was a large increase in the total number of predicted exons (38,552→47,046) and introns (29,733→37,153), and >5% more of the genome was covered with genic and exonic regions. In addition, untranslated regions of transcripts that previously took up 1.16% of the Bd genome now covered 6.9% of the genome.

In total, 10,138 genes were identified for Bsal (5,291 on+strand, 4,847 on−strand), encoding 12,474 transcripts (9,875 spliced and 2,599 unspliced), encompassing 58,251 exons and 45,777 introns. Bsal has a lower proportion of spliced transcripts (79%), compared with Hp (85%), Sp (88%) and Bd (90%). For Hp we identified a total of 6,254 genes encoding 6,254 transcripts. For Sp we identified 8,952 genes encoding 9,424 transcripts. Sp had an average of 6 exons per gene (56,727/8,952), which is greater than the average of 5 exons per gene in Hp, and 4.7 exons per gene in Bd and Bsal. All gene sets had high coverage of a set of 248 core eukaryotic genes, indicating that our annotation is highly complete; the updated RNA-Seq gene set was substantially improved for Bd (Supplementary Fig. 1a–c).

Genes were functionally annotated by assigning PFAM domains35, GO terms, KEGG assignment and ortholog mapping to genes of known function. HMMER3 (ref. 46) was used to identify PFAM (release 27) and TIGRFam (release 12) domains, and BLASTx used against the KEGG v65 database (e-value<1 × 10−10). GO terms were assigned using Blast2GO version2.3.5 (ref. 47), with a minimum e-value of 1 × 10−10. SignalP 4.0 (ref. 48) and TMHMM49 were used to identify secreted proteins and trans-membrane proteins respectively (Supplementary Fig. 1d).

The protease composition of each chytrid was determined using top high scoring pairs from BLASTp searches (e-value<1 × 10−5) made to the file ‘pepunit.lib’, which is a non-redundant library of 447,156 protein sequences of all the peptidases and peptidase inhibitors that are included in the MEROPS database (downloaded 2nd September 2014 from Bd had 586 top hits, Bsal had 589 total, Sp had 538 total and Hp had 416 total. M36 metalloproteases were aligned using MUSCLE v3.8.31 (ref. 50) and trimmed of excess gaps using trimAl 1.2rev59 (ref. 51) gappyout. We constructed the gene trees with RAxML v7.7.8 (ref. 52) and 1,000 bootstrap replicates, using the best-fitting amino acid transition model (WAG) according to Bayesian information criterion implemented by Prottest v3.4 (ref. 53).

To explore CRN-like genes among the four chytrids, we downloaded the protein sequences from the P. infestans T30-4 genome (PRJNA17665), extracted the 437 annotated as Crinklers and ran BLASTp searches (e-values<1e−5) using that as our database. This identified 162 candidate CRNs for Bd, 10 for Bsal, 11 for Hp and 6 for Sp (162 in total). Of these, only 2 had signal peptides (Hp gene Hp_03611 and Sp gene SPPG_05862), suggesting few are secreted. Notably, 25 had Protein Kinase domains. Each of these genes were trimmed to 50 aa, and aligned using MUSCLE v3.8.31 (ref. 50). To identify subfamilies, we also BLASTp searched (e-values<1e−5) all of the proteins against the Crinkler protein domains13. In total, 141 predicted chytrid CRNs were assigned a known subfamily (119 for Bd, 9 for Bsal, 7 for Hp, 6 for Sp). CRN subfamilies did not clearly overlap with N-terminal domains.

We tested a variety of methods to optimize clustering of CRNs and to identify domains, including cd-hit v4.6-2012-04-25 (ref. 54) under a number of sequence similarity identities, as well as trimming the more divergent C-terminal to 35, 40, 45 and 50 aa, followed by, or proceeded by, a MUSCLE v3.8.31 alignment50 with or without removing excess gaps using trimAl 1.2rev59 (ref. 51) gappyout. Motif searching was performed using GLAM2 (-Q –O. –M –z 20 –a 3 –b 15 –w 5 –r 30 –n 10000 –D 0.1 –E 2.0 –I 0.02 –J 1.0)55. Searching all of the sequences together after trimming to 50 aa did not yield a convincing single domain (Supplementary Fig. 7). Instead, we found that manually separating genes with two over-represented sequences obtained the highest confidence alignments spanning the most number of CRNs. The first domain (MPKR[YF]LNVEY) had a bit score of 1,576 and was present in 31 genes spanning most of the DAB subfamily (5/8), and half of the DXX subfamily (14/28) as well as 8/25 DXX-DHA, 2/5 DXX-newDXV. The second domain (YI[QK]YL) had a bit score of 1,191 and was present in 27 genes spanning all of the DFA-DDC subfamily and most of the DFB subfamily (12/13), as well as 1/2 DBE, 5/17 DX8, 1/28 DXX and 3/5 DXX-newDXV. The remaining 96 included a number of whole subfamilies such DN17 and newD2, and importantly, all of the Bsal, Sp and Hp predicted CRNs, but could not be subdivided into any convincing motifs (Supplementary Fig. 7).

To check if any novel chytrid CRNs were present, we constructed a Hidden Markov Model (HMM) using the two N-terminus sequences with HMMER 3.1b1 (ref. 46), and searched the protein sequences for the four chytrids with a e-value<1 × 10−5 cutoff. The HMM from the first domain identified one new gene that had not previously been identified from Bd (BDEG_28597) and five DXX-DHA genes that had not been included in either of the domains. By now including them, we were able to obtain a higher bit score (1,576→1,772) for the new domain starting with R[YF]LNVEY (Supplementary Fig. 7). An updated HMM did not yield any further gene matches. Conversely, the HMM from the second domain identified 34 new genes that had not previously been identified from Bd and only one that had been identified and not included in the two domains (also not identified as in a CRN subfamily). Including these genes provided a large increase to the bit score (1,191→2,671) for a new domain starting with ME?[TN].{0,1}[KR].{0,1}FYI. Similarly, an updated HMM did not yield any further gene matches. The remaining 90 CRN’s in neither domain 1 or 2 had a slightly reduced bit score (699→584) and only a low confidence motif: M.{0,39}[LV][EQ][ST]. A tree of all identified CRN 50aa N-termini was made using RAxML v7.7.8 (ref. 52) with 1,000 bootstrap replicates with the amino acid transition model WAG (Fig. 4a). Finally, intergenic distances (5′ and 3′) for each CRN were plotted (Supplementary Fig. 6), and distances were compared to full gene sets, secreted genes, and proteases for each species using t-tests (Supplementary Table 7).

To ascertain if the four chytrids secreted proteins included any large families (in addition to metalloproteases for example), we clustered all predicted secreted genes using MCL ( with recommended settings ‘-I 1.4’. We clustered both the entire length of the protein (initially) and after cleaving the secreted peptide (Supplementary Fig. 3). Associated PFAM domains were found in all or nearly all members of some tribes, including the 2nd largest, which contained protease M36 domains, or the 6th largest which contained the peptidase S41 domain. The largest tribe had 105 proteins, and belonged entirely to Bsal, as did the 4th largest tribe. Many of the members of these secreted tribes were significantly differentially expressed between in vivo and in vitro conditions, including Tribe 1 (48%). Furthermore, these tribes are located almost exclusively in non-syntenic, unique regions of the Bsal genome (Fig. 1).

Carbohydrate-binding module 18-containing genes

Carbohydrate-binding proteins were identified with BLASTp searches to the Carbohydrate-Active enZYmes Database ( using the stringent e-value cutoff of e−50 to avoid spurious hits. Looking at only the top high scoring pair, we identified very similar numbers between Hp, Bsal, Bd (n=75, 87 and 93 respectively), and a greater number for Sp (n=129). To examine carbohydrate binding modules (CBM), including CBM18, which is expanded in Bd and has been previously implicated in host–pathogen interactions56, we downloaded the CBM18 protein domain family (Chitin_bind_1) HMM representation from the Sanger Pfam24.0 database35, and used the HMMER3 application hmmsearch to search the four chytrid genomes with the same e-value cutoff of 0.01. In addition to the 18 previously identified CBM18 harbouring genes56, we found three additional CBM18 genes for Bd. We also increased the number of CBM18 domains found in Bd from 67 to 90. For Sp, we found just 5 genes with 8 domains. For Bsal, we found 15 genes with 30 domains. For Hp we found only 1 gene with 6 domains. None of the chytrid CBM18 genes were identified as a 1:1 ortholog. Each gene was aligned using muscle, and a tree was constructed with RAxML v7.7.8 (ref. 52) with 1,000 bootstrap replicates with the amino acid transition model WAG (Fig. 3).

Genes containing carbohydrate esterase 4 (CE4) superfamily mainly includes chitin deacetylases (EC clustered together, and had been previously described as deacetylase-like (DE)56. Bd had 10 (previously 9 were reported56) although one lacked a DE domain. Bsal had 6 DE CBM18s, 1 of which lacked the DE domain. Sp had 3 DE CBM18s, and Hp had none. Another group of CBM18s contained a common central domain of tyrosinase, and previously described as tyrosinase-like (TL). Bd had 5 (previously 3 were reported56), Bsal had 3, Hp had 1 and Sp had none. The third group consisted of genes with no secondary domains and was previously described as lectin-like (LL). We recovered the same 6 genes in Bd as previously reported, and similarly found 6 in Bsal, 1 in Sp and none in Hp. However, the 6 Bd LL CBM18 had 48 CBM18 modules (averaging 8 per gene), while the 6 Bsal LL CBM18s had only 16 CBM18 modules (averaging 2.6 per gene). Bsal LL CBM18s are also considerably truncated compared with those of Bd, (mean Bsal protein length=606, mean Bd protein length=206). Finally, one of the CBM18 genes in Sp was drastically divergent from each of the others, and in addition to the CBM18 domain, also contained a glycoside hydrolase family 64 (GH64), a glycosyl hydrolase, family 18 (GH18), a Hormone receptor domain (HRM) and a Carbohydrate-binding (CB) domain. This gene is unlikely to be related in function to the other three groups, but could be used to root the tree.

Most Bd CBM18s are upregulated in vivo, 17/21 (81%), although largely nonsignificantly (Fig. 3). The four Bd CBM18s that are downregulated in vivo include three DE proteins (BDEG_23687, BDEG_23733 and BDEG_28751) and one TL protein (BDEG_26083). BDEG_23733 and BDEG_26083 are significantly downregulated in vivo. Three genes were significantly upregulated in vivo, including two DE proteins (BDEG_25495 and BDEG_25497) and one TL protein (BDEG_26084). Therefore, only the Bd LL are all upregulated in vivo, albeit nonsignificantly. Conversely, the Bsal truncated LL include three upregulated, one significantly (CBM18 07447) and three downregulated. Therefore, CBM18 genes differ among the chytrids both structurally and in expression. Only 7/15 (47%) Bsal CBM18s are upregulated in vivo. However, 5 of these are significantly upregulated including 2 TL, 2 DE and 1 LL (mentioned above). Interestingly, there is a phylogenetic signal to the regulation, whereby 1 of the 2 DE clusters is Batrachochytrium specific, and all genes contained are downregulated: 3 significantly (2/2 sig. downregulated Bsal genes+1 Bd gene) and 2 nonsignificantly (termed downregulated DE; DRDE). The other DE cluster had Sp genes and Batrachochytrium genes: 2 of which were nonsignificantly downregulated, 3 were nonsignificantly upregulated and 4 were significantly upregulated.

Ortholog-based phylogenetic and functional analysis of chytrids

To reconstruct the evolutionary relationships between the four chytrid species, we identified 1:1 orthologs with OrthoMCL44. We aligned orthologs with MUSCLE v3.8.31 (ref. 50), extracted the CDS sequences in a codon context, and trimmed to the smallest contiguous sequence, and then concatenated alignments. In total, we aligned 4.1 Mb of transcripts for each chytrid. From greatest to smallest in nucleotide similarity of core orthologs, Bsal and Bd were 66% identical, Bsal and Bd were each 59% identical to Hp and Sp was 53% identical with Bd, Bsal and Hp. Prottest v3.4 (ref. 53) was used to determine the best-fitting amino acid transition model (DCMut) according to Bayesian information criterion. The final tree was produced using RAxML v7.7.8 (ref. 52) with 1,000 bootstrap replicates. DAGchainer57 was used to identify maximally scoring syntenic blocks of two or more ordered gene pairs, which covered most of Bd, Bsal and Hp (72%, 50% and 87%, respectively), but only 14% of Sp, owing to its greater divergence.

We identified 3,378 genes (33% Bsal genes, 38% Sp genes, 39% Bd genes and 54% Hp genes) that were in 1:1 orthology between the four species (Supplementary Fig. 1c, Supplementary Table 3). Each chytrid had a large proportion of unique genes (Hp=1,028 genes; 16%, Bd=1,989 genes; 23%, Bsal=3,300 genes; 33%, Sp=3,343 genes; 37%). Unique Hp genes (1,028) belonged to 983 individual clusters (1.05:1), indicating a wide range of functions. Similarly, unique Sp genes (3,343) belonged to 2,884 clusters (1.16:1). Unique Bd and Bsal genes (1,989 and 3,300) belonged to far fewer clusters (935; 2.13:1 and 1,866; 1.77:1) indicating unique genes among the Batrachochytrium species are from larger expanded gene families. We found 3.58 × the number of Batrachochytrium-specific genes (in Bd and Bsal) compared with those not found in Bd and Bsal.

Each chytrid was also uniquely missing a smaller proportion of gene orthogroups (Hp=730; 12%, Bd=160; 2%, Bsal=95; 1%, Sp=549; 6%). Hp had 1.3 × more uniquely absent genes compared with unique genes. Bd and Sp both had >5 × more unique genes than uniquely absent genes. Most strikingly, Bsal has 20 × more unique genes compared with uniquely absent genes. This indicates that gene families among these four species are expanding overall, and the biggest expansions have occurred in the Bsal lineage.

The immense variation in genome size and gene content reflects both the selection and evolutionary differences between the species, but also the paucity of available chytrid genomes for comparison and the evolutionary history masked by that absence. Despite this sample-size limitation, the conservation of large gene sets between the amphibian-infecting chytrids may harbour some of the more conserved pathogenicity-enabling genes. To explore this further, we performed two-tailed Fisher’s exact test with q-value FDR for PFAM and GO terms in each of the orthogroups (Supplementary Table 3, Supplementary Fig. 1c) against the remaining orthogroups. Out of the 22,837 PFAM domains, we found 2,007 significantly enriched. Out of the 5,541 genes with GO terms, we found 959 were significantly enriched by comparing each orthogroup subset against the remaining gene sets. For Bsal specific genes, we found 14 enriched PFAM terms, the most significant of which are Protein kinase domain (5.87e−44), Fungalysin metallopeptidase (M36) (3.71e−42) and Protein tyrosine kinase (3.27e−20). We found nine Bd specific enriched PFAM domains, the most significant of which are Eukaryotic aspartyl protease (4.73e−86), Xylanase inhibitor C-terminal (2.5e−66), Peptidase family S41 (3.55e−12) and Fungalysin metallopeptidase (M36) (3.01e−05). Batrachochytrium-specific genes (Bd+Bsal) included Polysaccharide deacetylase (3.12e−15) and Chitin-recognition protein (7.22e−07) enriched terms. Polysaccharide deacetylases such as chitin deacetylase act as virulence factors in other species such as Cryptococcus neoformans58, as do chitin-recognition proteins59.

Similar numbers of proteases were identified between Sp, Bd and Bsal (n=538–589), and slightly fewer were found in Hp (n=416). The protease profiles were, however, markedly different (Supplementary Fig. 5), with substantial increases of Aspartic peptidases A01 and A11 in Bd, and a large expansion (>3 × ) of M36 metalloproteases in Bsal (n=110) compared with Bd (n=35)—which is itself vastly expanded compared with Hp or Sp (n=2 and 3, respectively) (Fig. 2). To test for non-classical secretion of proteins, including CRNs, we used SecretomeP60 (NN-score≥0.5) on each of the protein sequences of the four chytrids. However, most of the proteins were flagged as potentially being non-classically secreted (6,523 Bsal genes, 4,478 Bd genes, 4,581 Sp genes, 2,991 Hp genes), suggesting low-specificity. Cell wall genes were identified using OrthoMCL44-identified orthologs between Bsal, Bd, Sp, Hp and Aspergillus nidulans FGSC A4 (for which cell wall genes are well documented and more complete than those in Saccharomyces cerevisiae). For meiotic genes, we compared the chytrid orthologs to those of S. cerevisiae using OrthoMCL44.

Host–pathogen transcriptomes

The animal experiment was performed with the approval of the ethical committee of the Faculty of Veterinary Medicine (Ghent University, EC2014/77) under strict BSL2 conditions.

First, the transcriptomal program of Bd and Bsal during in vitro cultures was determined. The fungi were cultured in PmTG broth and RNA from 5-day-old growing cultures was extracted with the RNeasy Plant kit (Qiagen), according to the manufacturer’s instructions. Second, we sequenced the transcriptome of the salamander T. wenxianensis (Tw) during infection by Bd or Bsal or an uninfected control (Supplementary Table 1). Nine captive bred Tw were housed individually at 15±1 °C on moist tissue, with access to a hiding place. All animals were clinically healthy and free of Bd and Bsal as assessed by sampling the skin using cotton-tipped swabs and subsequent performing qPCR. After 1 week of acclimatization, six animals were exposed to 1 ml of 104 Bd (three animals) or Bsal (ther animals) spores per ml water for 24 h6. Three additional animals were used as negative controls and were sham treated with 1 ml water for 24 h. Animals were fed twice weekly with crickets and followed up by clinical examination. At 10 days post infection (Bd infection load 1,100 GE per PCR reaction; Bsal infection load 1,900 GE per PCR reaction) the animals were killed and the skin was removed immediately. A part of the skin (10 mg) was stored in RNA later for 24 h and RNA then extracted with TRI Reagent combined with the RNeasy Plant kit (Qiagen). Skin samples for histopathology were stored in formalin. Histopathology confirmed the Bd or Bsal infection in all inoculated salamanders. Strand-specific libraries were constructed for each of the three replicates for each condition, using TruSeq RNA sample preparation with poly-A selection, and paired-end reads were generated on an Illumina HiSeq2000.

As no salamander gene set was available for comparison, we generated a new reference transcriptome assembly for analysis (Supplementary Table 8). We assembled Tw reads both from uninfected and infected samples with Trinity version r20140413p1 (ref. 32) using the strand-specific option (--SS_lib_type RF) and a minimum kmer coverage of 2 (--min_kmer_cov). We then aligned the resulting transcripts to the Bsal and Bd gene sets to remove fungal transcripts. Transdecoder was used to identify coding regions in these transcripts. After a final removal of Batrachochytrium transcripts, this Transcriptome Shotgun Assembly project was deposited at DDBJ/EMBL/GenBank under the accession GESS00000000. The version described in this paper is the first version, GESS01000000.

For each sample, we aligned reads to the transcripts of host or pathogen using Bowtie61. For Bd and Bsal, we aligned the reads to the RNA-Seq updated gene sets, and for Tw we aligned to the transdecoder coding regions. The RNA-Seq counts for biological replicate samples showed a high degree of correlation (Supplementary Fig. 8). We identified differential expression with our replicates using EdgeR62, with significance set at FDR P value<0.001 and >fourfold change of TMM normalized FPKM for the following five comparisons: (1) Bd in vitroBd in vivo, (2) Bsal in vitroBsal in vivo, (3) TwTw with Bd, (4) TwTw with Bsal and (5) Tw with BdTw with Bsal. Two-tailed Fisher’s exact test with q-value FDR for PFAM and GO terms in each of the differentially expressed subsets were compared against the remaining set. For the enrichment tests, and identification of differentially expressed immune genes, we joined those genes that were significantly up or downregulated in Bd relative to Bsal with those up or downregulated in Bd relative to control, and did the same for Bsal (that is, merged up or down in Bsal relative to Bd with up or down in Bsal relative to control).

Overall, Bd genes appear downregulated in vivo (5,532/8,249; 67%; Supplementary Fig. 8d, Supplementary Data 1); however, this is probably affected by the lower sensitivity of the in vivo samples compared to in vitro. The majority of Bd G1M36s are upregulated in vivo (16/25; 64%) (Fig. 2b, five of which (20%) were significantly upregulated—while none were significantly downregulated in vivo. Surprisingly, 92% of the Bd CRNs were downregulated in vivo, with only 12 upregulated (2 DXX, 2 DX8, 1 DN17, 1 DX8, 1 newD2 and 5 belonging to no subfamily). Ten of these belonged to Bd CRN1, one of them to Bd CRN2 and the final one was in the remaining set.

Bsal genes were also mostly downregulated in vivo, but to a lesser extent than Bd (5,468/9,372; 56.5%; Supplementary Fig. 8b, Supplementary Data 1). Of these, 613 genes were significantly downregulated, while 447 were significantly upregulated in vivo. Much like Bd, 8/10 Bsal CRNs were downregulated, 3 of which were significantly downregulated. Similarly, the majority of Bsal G1M36’s are upregulated in vivo (22/41; 54%). However, unlike Bd, eight (19%) were significantly downregulated in vivo, while 11 (27%) were significantly upregulated. This comparison suggests a more complex regulation of this subclass of protease in Bsal. Bsal G2M36s are mostly upregulated in vivo (26/36; 72%), 4 of which are significant—while none are significantly downregulated in vivo. A small number of M36s did not cluster with G1M36s or G2M36s, and included those also found in Hp and Sp. For Bsal, 3 of the 4 were downregulated in vivo, while 4 of the 5 were downregulated in vivo for Bd. Both of those upregulated in vivo were significant, and belonged to unique orthogroups.

We found substantial differences in host transcriptional response to Bd and Bsal (Supplementary Data 2). The largest category of genes differentially expressed in Tw were found from Bd infections. Most of these genes were upregulated (n=384) compared with 96 for Bsal. Tw also had a large number of downregulated genes during Bd infection (n=106) compared with only 12 for Bsal. Only two GO terms were enriched, including Immune system processes and extracellular region (Fisher exact test with q-value multiple correction), both from Tw genes upregulated during Bd infection (q=3.89e−07 and 5.15e−06, respectively) (Supplementary Data 3). We found that a large number of immune-related genes, including Antimicrobial peptides, B-cell related protein, interferons, macrophage proteins, MHCs, NF-KB and Toll-like receptors were differentially upregulated in Bd-infected salamanders (Fig. 5c, Supplementary Data 4), but with no differential expression found in Bsal infected animals. We also found a number of immune genes that were overwhelmingly differentially expressed by Bd infected animals, but also present in low numbers during Bsal infections (Fig. 5). These included cytokines, immunoglobulins, interleukins and Tumour Necrosis Factors (Supplementary Data 4). In addition to inflammatory factors, we saw a number of metalloproteinase inhibitors. Finally, a large number of transporters were differentially expressed during Bd infection, including nine downregulated and five upregulated aquaporins, which have been described as ‘the plumbing system for cells’63. By comparison, only one (sodium/glucose cotransporter) was upregulated by animals infected by Bsal. Keratin was also differentially expressed, including three upregulated during Bd infection and 3 downregulated during Bd infection.

Detection of protease activity and mRNA expression

Per condition, 150 mg of a mature Bd and Bsal culture containing all life stages was collected, centrifuged for 3 min at 3,000 r.p.m., and resuspended in unsupplemented 200 μl distilled water or 200 μl distilled water supplemented with antipain dihydrochloride (50 μg ml−1), bestatin (40 μg ml−1), chymostatin (60 μg ml−1), E-64 (10 μg ml−1), leupeptin (0.5 μg ml−1), pepstatin (0.7 μg ml−1), phosphoramidon (330 μg ml−1), pefabloc (1 mg ml−1), EDTA (0.5 mg ml−1) or aprotinin (2 μg ml−1). The cultures were lysed via sonication and the protease activity of the lysate was analysed using the Pierce Fluorescent Protease Assay Kit (Thermo Fisher Scientific), according to the manufacturer’s instructions. Based on the results obtained, protease activity of Bd and Bsal spores (107 spores per condition) was examined in control spores and spores supplemented with antipain dihydrochloride (50 μg ml−1), chymostatin (60 μg ml−1), E-64 (10 μg ml−1), pefabloc (1 mg ml−1), EDTA (0.5 mg ml−1) or a general protease inhibitor cocktail (Sigma-Aldrich), as described above. Bd and Bsal spores were collected by putting sterile distilled water on a culture flask containing mature sporangia. Once the zoospores were released, the water containing the zoospores was collected. To reduce the percentage of mature cells, the water containing the zoospores was passed over a sterile mesh filter with pore size 10 μm (Pluristrainer, PluriSelect). The flow through was used as the zoospore fraction (>90% purity). The results were analysed in SPPS using a non-parametric Mann–Whitney U-analysis.

Using TRI Reagent combined with the RNeasy plant kit (Qiagen), total RNA was isolated from freshly collected spores (107 spores per condition), spores (107 spores per condition) that were incubated with chytrid negative skin tissue of T. wenxianensis for 2 h in distilled water, 3 day old sporangia (5 × 106 sporangia per condition) treated with unsupplemented TGhL broth or TGhL broth supplemented with chitinase (Sigma-Aldrich; 0.200 units) for 2 h and skin tissue from the chytrid-infected T. wenxianensis animals (10 mg per animal). Pure Bd and Bsal sporangia conditions (>90% purity) were obtained by seeding the zoospore fraction in a six well at a concentration of 5 × 106 zoospores per well in TGhL broth. The spores were incubated during 3 days at 20 °C or 15 °C, respectively, until they reached the sporangia life stage. The RNA concentration was measured by absorbance at 260 nm using a nanodrop spectrophotometer and the quality of the RNA samples was checked using an Experion RNA StdSens Analysis kit (Bio-Rad). Total RNA (1 μg) was reverse transcribed to cDNA with the iScript cDNA synthesis kit (Bio-Rad). The housekeeping genes α-centractin, R6046, TEF1a and GAPDH were included as reference genes. The list of genes and sequences of the primers used for quantitative PCR analysis can be found in Supplementary Table 10. Real-time quantitative PCR reactions were run in duplicate and the reactions were performed in 10 μl volumes using the iQ SYBR Green Supermix (Bio-Rad). The experimental protocol for PCR (40 cycles) was performed on a CFX384 RT-PCR cycler (Bio-Rad). The results are shown as fold changes of mRNA expression relative to the mRNA expression levels in fresh spores. Fold changes were calculated using the cycle threshold (ΔΔCT) method (Livak and Schmittgen, 2001), and they were analysed in SPPS using a non-parametric Kruskal–Wallis analysis, followed by a Dunn–Bonferroni post hoc test (Supplementary Table 6).

Data availability

The data reported in this paper are outlined in Supplementary Information files and the raw sequences are deposited at GenBank under Bioproject PRJNA326253 for B. dendrobatidis and Bioprojects PRJNA326249 and PRJNA311566 for B. salamandrivorans. The genome assemblies and annotations are deposited at GenBank under Bioprojects PRJNA13653 for B. dendrobatidis and PRJNA311566 for B. salamandrivorans. The transcriptome assembly of T. wenxianensis is deposited at GenBank under accession GESS00000000, and RNA-Seq data from T. wenxianensis is deposited at GenBank under Bioproject PRJNA300849.

Additional information

How to cite this article: Farrer, R. A. et al. Genomic innovations linked to infection strategies across emerging pathogenic chytrid fungi. Nat. Commun. 8, 14742 doi: 10.1038/ncomms14742 (2017).

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