The Life Cycle of Huffmanela Huffmani Moravec, 1987 (Nematoda: Trichosomoididae), an Endemic Marine-Relict Parasite of Centrarchidae from a Central Texas Spring
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© Institute of Parasitology, Biology Centre CAS Folia Parasitologica 2016, 63: 020 doi: 10.14411/fp.2016.020 http://folia.paru.cas.cz Research Article The life cycle of Huffmanela huffmani Moravec, 1987 (Nematoda: Trichosomoididae), an endemic marine-relict parasite of Centrarchidae from a Central Texas spring McLean L. D. Worsham1, David G. Huffman1, František Moravec2 and J. Randy Gibson3 1 Freeman Aquatic Biology, Texas State University, San Marcos, TX, USA; 2!"#$%& 3'**+<"=#>?G' Abstract: The life cycle of the swim bladder nematode Huffmanela huffmani Moravec, 1987 (Trichinelloidea: Trichosomoididae), $[$$$>#"J?K'NK$- mentally completed. The amphipods Hyalella cf. azteca (Saussure), Hyalella sp. and Gammarus sp. were successfully infected with larvated eggs of Huffmanela huffmani. After ingestion of eggs of H. huffmani%K$$$[Q" from their eggshells and penetrate through the digestive tract to the hemocoel of the amphipod. Within about 5 days in the hemocoel of the experimental amphipods at 22 °C, the larvae presumably attained the second larval stage and were infective for the experimen- ["Lepomis spp. The minimum incubation period before adult nematodes began laying eggs in the swim %["N%%R*VYY*?[K$$N J* Keywords: swim bladder nematode, Trichinelloidea, development, intermediate host, Amphipoda, Hyalella, Gammarus[' Adult trichinelloid nematodes occur in a wide range has been studied in detail (e.g. Löwenstein 1910, Thomas "% * ? " ! $ [\Y]<$[\^RJN epithelial surfaces, although a few species infect spleen 1980). The eggs of this nematode were directly infective to or liver tissues, or are found in other tissues (Anderson ["*?"%$ 2000, Anderson et al. 2009). Although the development about the life cycles of representatives of the trichosomoi- and transmission of some species with medical importance did genus Trichuroides # [\]\ _T. chiropteri # $ [ $ 1949 from the urinary bladder of bats), or of the numerous animal hosts have been extensively studied (for reviews species of Huffmanela>"[\`R$[* see Moravec et al. 1987, Anderson 2000, Moravec 2001), Huffmanela huffmani Moravec, 1987 (Trichinelloidea: the biology of trichinelloids as a whole still remains little ?j J{ $ - known. Aside from well-studied trichinelloid taxa, little tode known only from the swim bladders of centrarchid else is known about the morphogenesis of larvae during [$$$>#" "$$"! _>#{J?K_Y\V|}|^}}~&\RVV}VY}}<{* of trichinelloid species. This is particularly true regarding ?[$H. huffmani was in 1979, whether or not an intermediate host is required (Moravec when Underwood and Dronen (1984) reported eggs from 2001). N%"># Most of the data available on the life cycles of [$[$ trichinelloids pertains to representatives of the species-rich of Capillaria Zeder, 1800. The species was later formal- $ # [\[V N ly described as Huffmanela huffmani based on eggs alone on the life cycles of representative of other trichinelloid (Moravec 1987) and the new genus Huffmanela was erect- families is rather scarce or absent (Anderson 2000). Within ed to accommodate it. Adults of the species were subse- the Trichosomoididae (apparently closely related to Cap- =%%J>"_[\``{*? illariidae), only the life cycle of Trichosomoides crassi- description of H. huffmani preceded the reassignment of cauda (Bellingham, 1840) from the urinary tract of rats several species from Capillaria into the genus Huffmanela, Address for correspondence: M.L.D. Worsham, Freeman Aquatic Biology, Texas State University – San Marcos, San Marcos, TX 78666-4616, USA. Phone: (406) 600-5515; Fax:(512) 245-7919; E-mail: [email protected] This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. doi: 10.14411/fp.2016.020 Worsham et al.: Life cycle of Huffmanela huffmani Table 1. [ Q $ > $%%"%"*?[\"[% expected to encouter and consume benthic, spring-related, detritivorous invertebrates. [ [ Example taxon 0 ~Q Herichthys cyanoguttatus Baird et Girard 1 Limnetic/zooplanktivorous Lepomis macrochirus#[= 2 Littoral/invertivorous Lepomis miniatus 3 Benthic/invertivorous Lepomis microlophus Günther 4 Spring-dominant benthic/invertivorous Lepomis auritus Linnaeus NJ>"Y[% so, to identify that host and use it to experimentally com- Moravec (2001). plete the life cycle. Presented herein is the experimentally Some twenty other species of Huffmanela are now doc- completed life cycle of H. huffmani; the [% N[ %YN$J* coastal and blue-water habitats of diverse geographic re- NR_#*Y[| MATERIALS AND METHODS and Iwaki 2014). Since all species of Huffmanela other than H. huffmani are marine, it is likely that H. huffmani is a ma- [ rine relict. This assertion is consistent with the presence of intermediate hosts numerous other marine-relict invertebrates unique to the Initially, centrarchids foraging around spring openings in >$_>{_J[\`{* $_$$>#{N$- Furthermore, even though many invertebrate taxa that are riodically observed, photographed and videographed by divers !$Q- %>Y[Y \'$$>#># inclusively. After determining the preferred feeding habitats of %$Q[- the centrarchid species known to be susceptible to H. huffmani %_%*Y`{*>>#- (Moravec et al. 1987, O’Docharty 2007), each species was as- "%K[$ signed to one of four feeding-niche categories. Because the pre- previous surveys have indicated that H. huffmani is also sumptive intermediate host was suspected of being a benthic, !$Q\'$$>#_> spring-dependent, detritivorous invertebrate, we were able to [\`]K*Y]RYR{*?[ use these category assignments to rank the centrarchid species are consistent with the hypothesis that H. huffmani is a ma- by how frequently they would be expected to encounter and con- rine relict with a spring-associated distribution. sume such invertebrates. These species are listed in Table 1 along ?!$Huffmanela are described with their feeding-niche categories and respective contrast coef- from eggs alone, with adults having been described thus far [* from only six species (Bullard et al. 2012). Each species Following the feeding preferendum analysis, centrarchids of Huffmanela$$Q$[ were collected from Spring Lake and necropsied in order to de- ["*JN" termine if the actual levels of parasitism for each species corre- egg deposition, little else is known about any of the life cy- sponded to the expectations that emerged from the feeding pref- cles of Huffmanela spp. The location of egg deposition by *?"[N% H. huffmani (and many other Huffmanela spp. that are his- N[$%% ["{- least 10 l of spring water. Because it was not known if eggs of %%%"[- H. huffmani are environmentally sensitive, and one of the goals tive host to infect the next host. Previous research has been [N%"% $[% unable to get ingested eggs of H. huffmani to hatch inside to the laboratory was expedited in order to ensure that dissolved ["_K[\\`>"Y[K* oxygen and temperature did not deviate substantially from op- Y]RYR{&[" timal conditions potentially required by H. huffmani. Fish were host laden with eggs of H. huffmani must be decomposed $$N\N- or digested in order for the eggs to become available to the sian well water physicochemically similar to SMS water in most presumptive intermediate host. %$*?[NYY Eggs of H. huffmani are appreciably denser than water, [Y[Y!%$* and once liberated from the host, they ultimately come to Fish were killed by pithing and the swim bladder was excised. rest on the benthic sediments. Because eggs cannot infect A small portion of the epithelium of the ventral wall of the swim [% bladder was separated from the remainder of the swim bladder %["%- and was used to roughly estimate the intensity of infection us- ed that a benthic detritivore must be serving as the interme- $ $ ]& Y& [* diate host (Cox et al. 2004, O’Docharty 2007). Therefore, Because a single swim bladder might contain a million or more [$"H. huffmani was to eggs (Cox 1998), intensity was not determined by counts, but was determine if there is, in fact, an intermediate host, and if %$$K$"[N Folia Parasitologica 2016, 63: 020 Page 2 of 15 doi: 10.14411/fp.2016.020 Worsham et al.: Life cycle of Huffmanela huffmani Table 2. Descriptions of infection-intensity categories used to es- at least 16 species of oligochaetes, 2 aphanoneurans and 3 leeches timate the intensity of infection with eggs of Huffmanela huffm- (Worsham et al. 2016). ani Moravec, 1987 in the ventral wall of the swim bladders of Benthic invertebrates were collected from near spring open- wild-caught centrarchids. ings using a Ponar grab sampler. Individual collections were Infection- transported back to the laboratory in separate containers of 22 °C intensity Description spring water and maintained alive until sorted. The organisms category were examined under a dissecting microscope and sorted into 0 no eggs detected containers representing the lowest discernable taxon. From these 1 trace infection; only a few eggs observed collections, live cultures of candidate intermediate hosts were es- 2 up to 25% of swim bladder infected with eggs 3 greater than 25% and up to 50% of swim bladder infected tablished and maintained in the laboratory in labelled 1200 ml 4 greater than 50% of swim bladder infected plastic food containers with windows cut in the sides and cov- NY3*?N\ \NQN$- eggs had been deposited. These intensity estimates were broken icochemical conditions similar to the SMS. ["Q[?%Y* Selection of candidate