Transuterine infection by Baylisascaris transfuga: Neurological migration and fatal debilitation in sibling moose calves (Alces alces gigas) from Alaska

Larval Baylisascaris nematodes (L3), resulting from transuterine infection and neural migration, were discovered in the cerebrum of sibling moose calves (Alces alces gigas) near 1–3 days in age from Alaska. We provide the first definitive identification, linking morphology, biogeography, and molecular phylogenetics, of Baylisascaris transfuga in naturally infected ungulates. Life history and involvement of paratenic hosts across a broader assemblage of mammals, from rodents to ungulates, in the transmission of B. transfuga remains undefined. Neural infections, debilitating young moose, may seasonally predispose calves to predation by brown bears, facilitating transmission to definitive hosts. Discovery of fatal neurological infections by L3 of B. transfuga in mammalian hosts serves to demonstrate the potential for zoonotic infection, as widely established for B. procyonis, in other regions and where raccoon definitive hosts are abundant. In zones of sympatry for multi-species assemblages of Baylisascaris across the Holarctic region presumptive identification of B. procyonis in cases of neurological larval migrans must be considered with caution. Diagnostics in neural and somatic larval migrans involving species of Baylisascaris in mammalian and other vertebrate hosts should include molecular-based and authoritative identification established in a phylogenetic context.


Introduction
The significance of infections attributed to ascaridoid nematodes among potential intermediate or paratenic hosts is in a propensity for somatic, visceral and neural migration by infective third stage larvae (L3) leading to significant disease and mortality (e.g., Sprent, 1952;Tiner, 1953;Kazacos, 1997Kazacos, , 20012016;Papini et al., 1996;Gavin et al., 2005). Among this assemblage of nematodes neural migration is perhaps best exemplified by L3 among species of Baylisascaris Sprent, 1968 andespecially Baylisascaris procyonis (Stefanski andZarnowski, 1951). A large nematode of raccoon [Procyon lotor (Linnaeus)] endemic in temperate latitudes of North America, B. procyonis has also been introduced and established in central Europe and Japan (Okulewicz and Buńkowska, 2009;Beltran-Beck et al., 2012;Robertson et al., 2013;Kazacos, 2016). Although primarily seen in raccoon definitive hosts as adult parasites, the L3 of B. procyonis have a broad range of paratenic hosts involved in transmission. Larvae have been documented among a remarkably diverse assemblage of mammals and birds, including reports of significant and devastating zoonotic infections in people (e.g., Kazacos, 1986Kazacos, , 20012016;Anderson, 2000;Gavin et al., 2005;Bauer, 2013;Sapp et al., 2017). In the temperate/boreal zone of North America and areas where Baylisascaris has been introduced in Europe or Asia, presumptive diagnosis in cases of neural larval migrans among paratenic hosts has been B. procyonis or less often B. columnaris (Leidy, 1856). These diagnoses, in the absence of verified vouchers, have been common even in zones of expected sympatry with other congeneric species (reviewed in Kazacos, 2001). The role of true intermediate or paratenic hosts in development and transmission among species of these ascaridoid nematodes in mammalian hosts remains to be clearly defined (Sapp et al., 2017); we adopt the usage of paratenic host in the https://doi.org/10.1016/j.ijppaw.2018.07.005 Received 11 May 2018; Received in revised form 12 July 2018; Accepted 14 July 2018 context of our observations and the following report.
We document and report the occurrence of fatal larval infections involving neural migration by a species of Baylisascaris in sibling moose calves (Alces alces gigas Miller) from Alaska. Definitive morphological and molecular identification confirmed infection by Baylisascaris and in conjunction with recent phylogenetic analyses among species of the genus provided a species level diagnosis (Camp et al. submitted). Neural infections by L3 of Baylisascaris in ungulates have been rarely reported and none have been definitively identified at the species level (Anderson, 1999;Kazacos, 2016;Sapp et al., 2017). Further, the current infections clearly represent the outcome of transuterine migration and intrauterine infection. We explore the pathology involved in these cases and the implications for life history patterns and transmission of Baylisascaris among bears and moose in Alaska.

Brief history
Twin moose calves from Kincaid Park, a municipal park in Anchorage, Alaska (ca., 61.1541°N and 150.0167°W), estimated to be 1-3 days in age, were orphaned on 23 May 2011 when their dam was shot for aggressive behavior. The calves were subsequently transported to a permitted holding facility maintained by the Alaska Moose Federation, at Palmer, AK. On arrival both calves were wobbly and with wet umbilical cords, indicative of recent birth. The male calf (Alaska Department of Fish and Game, necropsy ID 2011-067 Pathology ID VII-126) was consistently weak and apparently could not suckle or swallow properly, was euthanized on 30 May 2011 and necropsied 24 h later. The female sibling was more vigorous, but later broke her leg, and was euthanized and necropsied on 19 August 2011(Pathology ID VII-201-ADFG OMC ID Tag 56). At necropsy, a panel of tissues was collected for histological evaluation from each calf with specimens fixed in 10% neutral buffered formalin. Intact tissue from the cerebellum and cerebrum of the female calf was also cryo-archived at minus 20 C.

Histology of the nervous system
A suite of tissues including brains were collected for histology and preserved in 10% neutral buffered formalin, processed at Histology Consulting Services (Pullman, Washington), and slides analyzed by a pathologist (KBH). Briefly, paraffin-embedded sections were cut to 5 μm, stained with hematoxylin and eosin and permanently mounted.

Recovery of intact L3 from brain specimen
A frozen, unfixed, tissue sample of several grams from the cerebellum of the infected female calf was received at the US National Parasite Collection in April 2012 (EPH). Tissue was examined in detail initially by compression and transmitted illumination at magnifications to 60×, and secondarily by physical maceration in saline and sieving through a 200 mesh (75 μm) screen. A single larva was recovered from macerated tissue, preserved in 95% ethanol and held at minus 80C for later molecular characterization. Further microscopy of this larval specimen was not conducted given the potential for damage or loss which would have jeopardized attempts for a definitive species-level identification based on DNA sequence comparisons.

DNA extraction and PCR
A presumptive L3 of Baylisascaris recovered from the brain tissue was received in the Department of Entomology and Nematology at the University of California, Davis (SN and LEC). This larval specimen was destructively sampled. DNA from a single Baylisascaris L3 was prepared using the Epicentre MasterPure Complete DNA Purification Kit (Epicentre Biotechnologies, Madison, Wisconsin). Regions of two mitochondrial genes (12S ribosomal DNA, cytochrome c oxidase subunit 2 [cox2]), and two nuclear rDNA genes (large-subunit [28S] and the internal transcribed spacers/5.8S gene [ITS-1, 5.8S, ITS-2, abbreviated ITS]) were amplified by PCR. Primers 505 and 506 were used to amplify the 12S region; primers 210 and 211 were used to amplify the cox2 region. Primers 391 and 501 were used to amplify the 5' end of the 28S rDNA; and primers 521 and 94 were used to amplify the ITS region. Primer sequences for all genes used for PCR or sequencing are described in Table 1. Other species of Baylisascaris and individuals used in the phylogenetic analyses (sequences obtained from GenBank), DNA extraction methods and other procedures are provided in Camp et al. (submitted).
For the Baylisascaris larva, 25 μl polymerase chain reactions contained 200 μM deoxynucleoside triphosphates, 0.5 units of KOD XL polymerase (EMD Millipore, Billerica, MA), 0.5 μM of each primer, and 2.5 μl of DNA template. For 12S and LSU amplifications, cycling parameters followed Nadler et al. (2006). For cox2, cycling parameters followed Nadler and Hudspeth (2000). For ITS, cycling parameters included a 4 min denaturation at 94°C, then 35 cycles of 94°C for 30 s, 56°C for 30 s, 72°C for 1 min, and a final extension of 7 min at 72°C. PCR products were enzymatically treated for sequencing with exonuclease I and shrimp alkaline phosphatase (USB Affymetrix Pre-sequencing kit, USA) and directly sequenced using an ABI 3730 DNA Sequencer (Applied Biosystems, Thermo Fisher Scientific) with the PCR primers (12S, cox2), or both PCR primers and internal primers (ITS, 28S, Table 1).
Sequence contigs were assembled using CodonCode Aligner (version 5.1.5, CodonCode Corporation, Centerville, Massachusetts) and Phred base calling. All sequences were double-stranded for verification. Site polymorphisms were recorded only when both alternative nucleotide peaks were present in all sequencing reactions representing both DNA strands. If the heights of the alternative nucleotide peaks at polymorphic sites were not equal, the height of the minor peak was required to significantly exceed background terminations and comprise ≥25% of the major peak to be scored as a polymorphism. GenBank accession numbers for all analyzed sequences are provided in Table 2.

Phylogenetic analysis
Multiple Alignment: For non-coding genes (12S, 28S, ITS) sequences for each species or geographic isolate were aligned using ProAlign v0.5a0 (Löytynoja and Milinkovitch, 2003). Nucleotide sequences of the protein-coding gene cox2 were translated using CodonCode Aligner and the longest open reading frame was selected for each sequence and verified by BLAST comparison. The inferred amino acid sequences for each gene were aligned using default options in CLUSTAL X (Larkin et al., 2007), and the cox2 nucleotide sequences were aligned to their respective aligned amino acids using the RevTrans Server (v1.4; Wernersson and Pedersen, 2003).
Parsimony analyses: Maximum parsimony (MP) analyses were done for each gene and the combined data using the branch-and-bound option of PAUP* version 4.0a150 (Swofford, 2003). To assess clade support values, bootstrap parsimony searches were done using branch-andbound with 1000 replicates. PAUP* was also used to obtain distance matrices for each aligned gene.
Bayesian analyses: Bayesian inference (BI) was done for each gene and the combined data using MrBayes v3.2.6 (Ronquist et al., 2012) executed on the Cyberinfrastructure for Phylogenetic Research (CIPRES) web portal (Miller et al., 2010; http://www.phylo.org). For non-coding genes, best-fit evolutionary models (Table 3) were chosen prior to Bayesian analyses using MrModelTest v2.3 (Nylander, 2004) and the Akaike Information Criterion (AIC). For cox2, partitioning schemes and evolutionary models were selected using PartitionFinder v1.1.1 and the AIC (Lanfear et al., 2012). These models were applied to each gene or partition, including the combined analysis. Two independent Bayesian runs were conducted for each analysis with 4 Markov Chain Monte Carlo chains and 4 million generations. Chains were sampled every 4000 generations, and the first 25% of trees were discarded as burn-in. In the post burn-in samples, stationarity was assessed based on: an average standard deviation of split frequencies below 0.01; an average potential scale reduction factor of 1.000; and mean marginal likelihoods that were similar for both runs. Trees remaining after burn-in were used to create 50% majority-rule consensus trees with posterior probabilities for each clade.

Morphological identification and histology
A full set of tissues were examined microscopically from each calf. Only the pertinent tissue findings are reported respectively for each calf.
VII-126: Spinal cord, forebrain, pituitary, hippocampus, cerebellum, pons, Circle of Willis and maxillary ganglion were within normal limits. The cerebral cortex contained scattered foci of lymphocytes and gitter cells. In one of these foci, there were also multinucleated giant cells as well as cross sections of parasites. These parasites had a coelom, coelomyarian polymyarian musculature primarily in the dorsal and ventral fields, a bacillary body and prominent lateral alae and a well developed intestinal tract (Figs. 1 and 2). The histopathologic diagnosis was moderate, multifocal random, lymphohistiocytic to granulomatous encephalitis with intralesional nematodes. V11-201: The eye, spinal cord, pituitary, cerebellum, right anterior hypothalamus, left anterior hypothalamus, and left posterior hippocampus were within normal limits. The right frontal lobe and right   posterior hippocampus contained focal pyogranulomatous inflammation around nematode cross sections with features identical to those described above (Figs. 1 and 2). The right posterior hippocampus had a glial nodule with lymphoplasmacytic surrounding inflammation but no foreign body evident. The morphologic diagnoses in both was moderate, multifocal random, lymphohistiocytic to granulomatous encephalitis with intralesional nematodes. The initial diagnosis in both sibling calves was verminous encephalitis attributed to larval (third stage) ascaridoid nematodes present in the hippocampus and cerebrum. Characteristic third-stage larvae, demonstrated in histology from both calves, were consistent morphologically with a species of Baylisascaris (Figs. 1 and 2). In transverse section diameter ranged from 65 to 85 μm. Morphometric data and observations of morphology of the intact L3 from brain tissue were not determined at the time of collection, nor prior to molecular analyses. Voucher histological slides from respective sibling hosts were originally deposited in the US National Parasite Collection (USNPC 105409, single slide from male calf; and USNPC 108284, 2 slides from female calf) which had been curated at the Beltsville Area Research Center of USDA, Agricultural Research Service. Materials are now held in the National Museum of Natural History, Smithsonian Institution, Washington, D.C.

Molecular characterization
Phylogenetic analyses: Parsimony analysis of the 12S rDNA sequences yielded two equally parsimonious trees of length 139 (CI 0.87). The strict consensus of these trees was identical in topology to the Bayesian consensus tree (Fig. 3A). The sequence of the larval Baylisascaris specimen from the moose was strongly supported (> 99% bootstrap parsimony and Bayesian posterior probability, BPP) as part of an unresolved trichotomy including B. transfuga.
Parsimony analysis of the cox2 sequences yielded four equally parsimonious trees of length 126 (CI 0.86). The strict consensus of these trees was less resolved that the Bayesian consensus tree (Fig. 3B), specifically the parsimony consensus tree was a polytomy for the clade consisting of B. procyonis and B. columnaris. The sequence from the larval Baylisascaris specimen received 100% support (bootstrap parsimony and BPP) as belonging to the clade containing B. transfuga and was weakly supported as sister to B. transfuga from a Canadian Grizzly bear.
Parsimony analysis of the 28S rDNA sequences yielded one most parsimonious tree of length 108 (CI 0.97). The topology of this tree was identical to the Bayesian consensus tree (Fig. 3C). The sequence from the larval Baylisascaris specimen received 100% support (bootstrap parsimony and BPP) as part of an unresolved trichotomy representing B. transfuga.
Parsimony analysis of the ITS rDNA sequences yielded one most parsimonious tree of length 314 (CI 0.97). The topology of this tree was identical to the Bayesian consensus tree (Fig. 3D). The sequence from the larval Baylisascaris specimen received 100% support (bootstrap parsimony and BPP) as part of an unresolved trichotomy representing B. transfuga.
Parsimony analysis of the combined dataset yielded four equally parsimonious trees of length 690 (CI 0.93). The strict consensus of these trees was less resolved than the Bayesian consensus tree (Fig. 4), specifically the parsimony consensus tree was a polytomy for the clade consisting of B. procyonis and B. columnaris. The sequence from the larval Baylisascaris specimen received 100% support (bootstrap parsimony and BPP) as part of the clade containing B. transfuga and was weakly supported as sister to B. transfuga from a Canadian grizzly bear.
Distance comparisons: Uncorrected pairwise percent sequence divergence for 12S rDNA and cox2 showed no difference between the Baylisacaris larva from the moose and B. transfuga from a grizzly bear (Table 4). For these two genes, the next lowest pairwise divergence values for the larval specimen was to B. transfuga from a black bear. Uncorrected pairwise percent sequence divergence for 28S rDNA and ITS rDNA showed no differences between the Baylisacaris larva from the moose and B. transfuga from both grizzly and black bears (Table 5).

Discussion
Correct or complete identification is important in revealing the potential routes of exposure and transmission along with the array of definitive and intermediate/paratenic hosts that may be involved in circulation for species of Baylisascaris at different geographic localities (e.g., Sapp et al., 2017). Risk for zoonotic infection would also be reflected based on the geographic distribution and transmission patterns for different species of Baylisascaris. Most prior reports and discussion of larval migrans (ocular, neural, visceral) attributable to species of Baylisascaris have suggested presumptive diagnoses of B. procyonis. Such diagnoses have often been presented in the absence of definitive evidence and absence of archived vouchers, even in regions where multiple species may be known to occur (e.g., reviewed in Kazacos, 2001;Gavin et al., 2005;Kazacos, 2016). Presumptive identification was most often linked to putative exposure and epidemiological observations consistent with the local occurrence of raccoons or less often skunks in the case of B. columnaris (Kazacos, 2001). This also parallels reports in Europe in regions where B. procyonis has been inadvertently introduced and established with the translocation of raccoons (e.g., Okulewicz and Buńkowska, 2009;Beltran-Beck et al., 2012).

Establishing identity
In the current Alaskan cases, the possibility of B. procyonis infection was eliminated based on the contemporary and historical distribution of raccoons as the primary definitive hosts for this ascaridoid (see Gehrt, 2003). The northern limit of natural range for raccoons in western North America extends to south coastal British Columbia (about 51°N) in the west and into southeast Alberta in the east (about 54°N) (e.g., MacDonald and Cook, 2009). The northern limits for distribution in western Canada have been expanding since the 1970's, but the core range remains over 1000 km to the south of localities in southcentral Alaska (e.g., Gehrt, 2003); a pertinent extralimital record is from Wood Buffalo National Park in northeastern Alberta (Soper, 1942). Although raccoons were released for possible introduction in areas around SE Alaska (Haida Gwaii and Alexander Archipelago) and adjacent to Kodiak Island at various times since the 1930's, none were translocated to central Alaska. Further, species of skunks, similar to raccoons, are not present in Alaska, and the range for striped skunk, Mephitis mephitis (Schreber), extends into southeastern Yukon and northern British Columbia, only approaching within 500 km. This geographic distribution effectively establishes the current absence of the largely host specific B. columnaris at higher boreal and subarctic latitudes (Rosatte and Larivière, 2003). Badgers as hosts of B. melis, are also well outside of the geographic range. Ursids as the hosts for B. transfuga, and mustelids as the hosts for B. devosi would appear to represent the sole endemic assemblages for circulation of these species of ascaridoids that are historically recognized and expected to have broad distributions in Alaska.

Morphological diagnostics
Based on the diameter of L3 in histological sections (maximum near 85 μm, Fig. 1), it was evident that larvae in moose differed substantially in diameter (width) at the midbody from those identified as B. columnaris, B. devosi or B. procyonis in prior studies (range about 45-65; or 55-70 μm in fully developed L3) (Sprent, 1953(Sprent, , 1955Kazacos, 1986Kazacos, , 1997Bowman, 1987); ranges for the diameter of L3 B. transfuga have apparently not been published. Despite these apparent differences, definitive diagnosis based solely on dimensions or structural attributes of the L3 among species of Baylisascaris remains elusive (e.g., Sapp et al., 2017). Through a rough process of elimination, however, L3 in moose may be attributable to B. transfuga. Further the greater diameter at the midbody, as demonstrated in our observations, clearly differentiates the L3 in moose from those of Toxascaris leonina (von Linstow, 1902) and Toxocara canis (Werner, 1782) (e.g., Bowman, 1987), common ascaridoids of canid hosts in Alaska which may also be involved in cases of visceral larva migrans (Sprent, 1955;Jenkins et al., 2013;Rausch and Fay, 2011).

Molecular identification
Diagnosis of somatic and neurological infection by third-stage larvae among species of Baylisascaris continues to be challenging (Gavin Fig. 4. Parsimony analysis of the combined nuclear and mitochondrial genes yielded four equally parsimonious trees (CI 0.93). Strict consensus supported monophyly of B. transfuga and identity of the L3 recovered from moose.  Bauer, 2013;Franssen et al., 2013;Kazacos, 2016;Sapp et al., 2017). The possibility of definitive molecular diagnosis for L3 in cases of larval migrans has not been universally available for species of Baylisascaris and serological tests have been non-specific (e.g., Boyce et al., 1988;Testini et al., 2011). Consequently, addressing or identifying the potential risk to public health posed by those species of Baylisascaris in circulation in North America (and globally) remains problematic (Franssen et al., 2013). Authoritative molecular identification and phylogenetic diagnosis including broad comparisons among congeners clearly established B. transfuga as the cause of neural infections in the sibling moose calves (Figures 3 and 4). There are apparently no prior records in ungulates for this species of Baylisascaris. Further explorations are necessary to refine the understanding of host and geographic range for B. transfuga. Broadening evidence indicates that the single nominal species as currently recognized encompasses a complex of distinct nematode taxa in North American bears (Sapp et al., 2017;Camp et al., submitted).

Neonatal or transuterine infections among ungulates
There has been limited evidence for neonatal infection linked to transuterine migration in potential ungulate paratenic hosts for species of Baylisascaris (Kazacos, 2016). The single prior report of natural neonatal infection in a lamb (Ovis aries L.) from Idaho lacked definitive species-level identification (Anderson, 1999).
Our current description and report of L3 B. transfuga clearly demonstrates a pattern of transuterine/in utero migration in the 1-3 day old moose siblings. Migration time to the brain is within 3-4 days post infection for B. procyonis, B. columnaris and B. devosi; 6-14 days to somatic sites for B. transfuga. A caveat in interpreting these observations is apparent as these time frames were based on experimental infection in mice and may not be representative (Sprent, 1952(Sprent, , 1953. Clinical onset of disease should mirror migration time to a considerable extent. The latter can vary substantially, however, with respect to host and parasite species along with patterns of exposure and dosage of infection (e.g., Sheppard and Kazacos, 1997;Sato et al., 2004;Sapp et al., 2016). Weaning time in moose is several months post parturition, although exploratory foraging may ensue within weeks of birth. These circumstances unequivocally indicate that infections were established in these neonates prior to birth. Vertical transmission would represent mobilization of larvae previously acquired and sequestered in the cow prior to or during pregnancy.
Among other ascaridoids, trans-placental migration was initially indicated for Toxocara canis, although this involved neonatal infection of canid definitive hosts (Sprent, 1954;Anderson, 2000). Further at the time of these initial studies during the 1950's it was known that L3 of ascaridoid species could be sequestered in somatic and other tissues as demonstrated for B. devosi, B. columnaris, B. transfuga, Toxocara canis and Toxascaris leonina. Neonatal infection in rodent and other mammalian paratenic hosts has also been documented experimentally for species of Toxocara Stiles, 1905(e.g., Schnieder et al., 2011Strube et al., 2013).
As established in experimental life cycle studies, one or two vertebrate paratenic (or intermediate?) hosts are required for completion of transmission among species of Baylisascaris in mammals (Sprent, 1952(Sprent, , 1953Tiner, 1953;Anderson, 2000;Kazacos, 2001Kazacos, , 2016Sapp et al., 2017). For B. columnaris, B. procyonis and B. devosi, migration in paratenic hosts (experimental mice) is rapid leading to widespread dissemination in the systemic circulation including sites in the somatic tissues and central nervous system within 3-4 days post infection (Sprent, 1952(Sprent, , 1953Tiner, 1953). Maximum length and diameter of L3 are attained between 14 days and several months post infection and viable infective larvae may persist for extended periods of several months. Among these, B. procyonis and B. columnaris are more commonly associated with sites in the central nervous system of rodent paratenic hosts (Sprent, 1952(Sprent, , 1953Tiner, 1953;Kazacos, 2001).
In infections of B. transfuga, similar migration rates were observed in experimental infections in rodent hosts, leading to permanent somatic infection by encysted L3 beginning near 8 days post infection (Sprent, 1952). Although viable larvae are encapsulated in various tissues, apparently this most often is associated with the wall of the intestine (Sprent, 1952(Sprent, , 1953. During extensive tissue migration, larvae of B. transfuga in experimental infections involving oral exposure had not been demonstrated uniformly in the central nervous system (Sprent, 1953(Sprent, , 1955Anderson, 2000;Sato et al., 2004); L3 also may be involved in ocular infections (Papini et al., 1996). The time frames established for migration and development of L3 among species of Baylisascaris and the age of these sibling moose (at 1-3 days) is clearly consistent with a pattern of transuterine infection from the cow prior to parturition (the cow was not necropsied following death). This is the first instance of definitive species-level identification of neonatal infection attributed to B. transfuga, or any species of Baylisascaris, in a naturally infected putative ungulate paratenic host (e.g., Kazacos, 2001Kazacos, , 2016. In the current cases verminous encephalitis attributed to B. transfuga, contributed directly to the debilitated condition of these sibling moose and in the absence of euthanasia, these calves are unlikely to have survived in the wild. Anderson (1999) reported a fatal neurological infection attributed to a species of Baylisascaris in a 2-3 day old domestic lamb from Idaho, however, the causative agent could not be determined. Possible involvement of B. procyonis, B. melis or B. columinaris was suggested, but B. transfuga was not included in this discussion. Baylisascaris L3 are known from a considerable array of mammalian hosts either from natural infections or experimentally (e.g., Kazacos, 2001Kazacos, , 2016, however, infections in ungulates are virtually unknown. Demonstrating that infections are determined by opportunity, exposure and biological capacity of parasites Sato et al. (2005) reported multiple cases of fatal neurological disease among Japanese macaques (Macaca fuscata Blythe) under open zoo- park conditions. The primate colony was maintained in proximity to 11 North American black bears known to be infected with B. transfuga.
Raccoons also adjacent to the colony were not known to be infected with B. procyonis. Species-level identification was not possible, although the nematodes were attributed tentatively to B. transfuga.

Broader implications for Baylisascaris
Assuming the cryptic nature of infections, the significance of this pattern of larval development in the life cycle of B. transfuga and potential transmission among moose (and other artiodactyls) and bears would remain to be established. The complete life cycle for B. transfuga in free-ranging wild hosts has not been elucidated and could involve direct transmission through ingestion of larvated eggs, or dissemination through infected mammalian paratenic hosts (Bauer, 2013;Sapp et al., 2017). The latter pathway would be consistent with life history patterns currently known among congeners (e.g., Sprent, 1954Sprent, , 1968Anderson, 2000). Among black bears the diet is dominated by vegetation and vegetable resources, and among these omnivores, consumption of animals usually involves carrion or is opportunistic (Pelton, 2003). In contrast, brown bears are considerably more carnivorous, and predation on ungulates may be seasonally important especially for populations in the continental interior of North America (Schwartz et al., 2003). Such was reflected in observations (EPH) of a large brown bear stalking and hunting moose calves along the Igloo Creek Canyon in Denali Park, Alaska in June 2016. Rodents, especially the prolific and abundant Arctic ground squirrels [Urocitellus parryii (Richardson)] are also important sources of food at high latitudes for brown bears.
Life history and involvement of paratenic hosts across a broader assemblage of mammals, from rodents to ungulates, in the transmission of B. transfuga remains undefined (e.g., Tiner, 1953;Sprent, 1954;Testini et al., 2011;Bauer, 2013;Sapp et al., 2017). Further, the nature of abortion or neonatal mortality in moose, involving larval B. transfuga, also remains to be revealed and although logistically challenging to demonstrate, should be considered in diagnosis. Migration by developing larvae and L3 late in gestation may result in infections of the central nervous system as demonstrated in our study. In contrast, migration early in gestation could be a contributing factor in spontaneous abortion in some cases, although, again, evidence is lacking. Infections of neonatal ungulates, however, could be a factor in completion of transmission to carnivore definitive hosts, in this case either brown bear or black bear, which are common and widespread in Alaska and south into the temperate zone of North America.
Discovery of fatal neurological infections by B. transfuga in naturally infected mammalian hosts serves to demonstrate the potential for zoonotic infection, as widely established for B. procyonis in other regions and where raccoon definitive hosts are abundant (Kazacos, 1997(Kazacos, , 20012016;Papini et al., 1996;Bauer, 2013;Testini et al., 2011;Sapp et al., 2017). More importantly in zones of sympatry for multi-species assemblages of Baylisascaris across the Holarctic region presumptive identification of B. procyonis in cases of neurological larval migrans must be considered with caution. Where possible presumptive identification of B. procyonis or other species of Baylisascaris should be confirmed and accompanied by molecular sequence comparisons established in a phylogenetic context (e.g., Camp et al., submitted).
Northward expansion, associated with habitat and environmental change linked to climate warming could lead to changing distribution for raccoons and skunks and therefore, as a consequence, increasingly broader distributions for B. procyonis and B. columnaris (e.g., Hoberg et al., 2008;Hoberg, 2010;Jenkins et al., 2013). Patterns of geographic colonization by these assemblages would also be predicted to directly influence helminth diversity. Potential lag times for invasion by parasites including B. procyonis may coincide with shifting abundance of definitive hosts on the periphery of expanding geographic ranges (Hoberg and McGee, 1982;Hoberg et al., 2017). The expectation or anticipation of range shifts (either increasing or decreasing) for potential zoonotic pathogens and an array of hosts establishes a priority for definitive documentation of diversity and species. Baselines for identification and biodiversity can lead to surveillance and targeted monitoring to explore and anticipate the outcomes of environmental perturbation over time (Brooks et al., 2014).