Correction
10 Feb 2015: The PLOS ONE Staff (2015) Correction: Reproductive Strategies of the Insidious Fish Ectoparasite, Neobenedenia sp. (Capsalidae: Monogenea). PLOS ONE 10(2): e0117881. https://doi.org/10.1371/journal.pone.0117881 View correction
Figures
Abstract
Fish monogeneans are lethal parasites in aquaculture. We provide the first experimental evidence that a notorious fish monogenean, Neobenedenia sp., can produce viable eggs in isolation for three consecutive generations. We infected individual, isolated, farmed barramundi, Lates calcarifer (Bloch) with a single oncomiracidium (larva) of the hermaphroditic monogenean Neobenedenia sp. Isolated parasites reached sexual maturity at day 10 post-hatch (24°C, 35‰) and laid ∼3,300 embryonated eggs over 17 days. Egg production rapidly increased following sexually maturity on day 10 (58±15 eggs) and peaked on day 15 (496±68 eggs) before gradually decreasing. Neobenedenia sp. exhibited egg laying and egg hatching rhythms. Parasites laid eggs continuously, but egg production increased in periods of darkness (64.3%), while the majority of oncomiracidia (81%) emerged from eggs in the first three hours of light. Eggs laid by isolated ‘parent’ parasites hatched and individual emerging oncomiracidia were used to infect more individual, isolated fish, with three consecutive, isolated, parasite generations (F1, F2 and F3) raised in the laboratory. Infection success and egg hatching success did not differ between generations. Our data show that one parasite, in the absence of a mate, presents a severe threat to captive fish populations.
Citation: Dinh Hoai T, Hutson KS (2014) Reproductive Strategies of the Insidious Fish Ectoparasite, Neobenedenia sp. (Capsalidae: Monogenea). PLoS ONE 9(9): e108801. https://doi.org/10.1371/journal.pone.0108801
Editor: László Orbán, Temasek Life Sciences Laboratory, Singapore
Received: March 18, 2014; Accepted: August 31, 2014; Published: September 29, 2014
Copyright: © 2014 Dinh Hoai, Hutson. This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
Data Availability: The authors confirm that all data underlying the findings are fully available without restriction. Data are available from the James Cook University Research Database: https://research.jcu.edu.au/researchdata/published/detail/d9eda2a2d49ef0b1ab4de74a2c77c826/.
Funding: This work was funded by an AusAID Scholarship (www.ausaid.gov.au) awarded to TDH. The Australian Society for Parasitology (http://parasite.org.au/) provided a Student Travel Award for TDH to present this research at the annual conference in Launceston, Tasmania, Australia in 2012. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.
Competing interests: The authors have declared that no competing interests exist.
Introduction
Monogeneans exhibit sophisticated life history strategies in order to ensure their survival in contrasting and unpredictable environments. Evolutionary strategies include multiple reproductive mechanisms, predator avoidance and behavioural responses to host and environmental cues that favour enhanced infection success. In wild populations these strategies ensure some parasites survive to the next generation, whereas in captive populations, where host organisms are confined in high densities, it can lead to parasite epizootics.
Various reproductive mechanisms have been observed in monogeneans including oviparity [1], viviparity [2] and self-fertilisation [3]. Most oviparous monogeneans deposit fewer than 100 eggs/parasite/day [4]–[7], although some species can produce more than 550 eggs/parasite/day [8]. In viviparous monogeneans, up to three consecutive generations can develop inside the mother parasite. For example, a single individual Gyrodactylus salaris bears the first daughter within 24 hours of the birth of the parent [9] and thus has the capacity to produce six million offspring in four weeks [1]. Self-fertilisation is known to occur in monogenean species that infect the bladder of amphibians [3], [10] and ensures reproductive potential when a parasite finds itself alone on a host. Monogeneans also exhibit egg laying and egg hatching rhythms, which can reduce the risk of predation and coincide with host behaviours to ensure infection success. Monogeneans maximise their chances of finding a host by releasing eggs into the environment during certain times of the day or night [7], extending the hatching period [11], responding to hatching cues such as shadows [12], chemicals [11], [13], mechanical disturbance [14]–[16] and osmotic changes [17], most of which are generated by the host.
Neobenedenia are marine capsalid monogeneans of critical concern to aquaculture because they exhibit several life history traits that aid their survival. Neobenedenia spp. have direct life cycles with short generation times [18], [19] and low host specificity [20], [21] which has resulted in major stock losses in several aquaculture fish species (see [18], [22]–[24]). Furthermore, attached parasite stages are transparent, which can reduce predation by cleaner organisms [21]. Eggs are encapsulated by a proteinaceous shell which confers protection to the developing embryo from digestion [25], most chemicals [26]–[29] and bacteria [1]. Capsalid monogeneans are hermaphrodites, displaying several types of reproduction including mutual cross-insemination [30], attachment of spermatophores to other individuals [31] and self-insemination (as observed by the copulatory organ lodged in the parasite's own uterus; see [30], [32]). However, no studies have experimentally examined whether fish monogeneans can successfully reproduce in isolation and produce viable eggs and larvae.
The aim of this research was to experimentally examine the reproductive strategies of Neobenedenia. Specifically we sought to determine: 1) whether Neobenedenia can reproduce in isolation; 2) Neobenedenia fecundity over time; 3) whether Neobenedenia exhibit egg laying rhythms and/or hatching rhythms. We used a barramundi, or Asian seabass, Lates calcarifer – Neobenedenia sp. model system for our experiments. Barramundi (Perciformes: Latidae) are distributed in estuaries and coastal seas from south-western India to north-eastern Australia, with approximate latitudes of ±25° [33]. This species is among the most important food fishes in tropical Australasia and is farmed throughout eastern and western Asia (China, India, Israel, Indonesia, Malaysia, Philippines, Singapore, Tahiti, Taiwan, Thailand) and Australia [34]. High intensities of Neobenedenia on farmed fish damage host epidermis through attachment and feeding [19], [23], [35] and increase secondary infections [36], [37].
Materials and Methods
Ethics Statement
This work was conducted using a barramundi, Lates calcarifer – Neobenedenia sp. model system with all procedures approved by the James Cook University Animal Ethics Committee (A1579). Neobenedenia sp. used in experiments were collected from private land in north Queensland, Australia. Future permissions should be directed to Coral Coast Barramundi Pty Ltd.
Source of Animals
Hatchery reared freshwater L. calcarifer; mean size 125±23 mm) were purchased from Good Fortune Bay Hatchery, Queensland, Australia for use in experiments 1–4. Fish were not previously exposed to Neobenedenia. Fish were transported to the laboratory in 50 L tanks with air supplied through battery powered aerators and held in fresh water in 100 L aquaria until required. Fish were acclimated to sea water 48 h prior to experiments by increasing salinity to 5, 10, 20, 30 and 35‰ over 6 h intervals. Sea water used in experiments was UV treated, 10 µm filtered, 35‰, unless stated otherwise.
Neobenedenia sp. used in experiments were collected from a land-based marine L. calcarifer farm (Coral Coast Barramundi Pty Ltd) in north Queensland, Australia. An infection was maintained on L. calcarifer (size range 110–220 mm) held in 100 L marine aquaria to provide a continuous source of parasites. Neobenedenia sp. (hereafter as Neobenedenia) investigated in this study is presently unidentified given the absence of diagnostic criteria to differentiate between geographical/host isolates and species [20], [21], [38] [20], [21], [33]. Representative parasites were accessioned in the Australian Helminth Collection (AHC) at the South Australian Museum (SAMA AHC 35461; see [39]).
Experiment 1: Reproduction of Isolated Neobenedenia
To determine whether hermaphroditic Neobenedenia can reproduce in isolation, individual, isolated fish were infected with a single oncomiracidium (larva). Oncomiracidia were sourced from embryonated Neobenedenia eggs collected from the laboratory infection. Eggs were incubated in glass cavity blocks in sea water at 25°C in culture chambers on a 12∶12 h LD cycle (Sanyo: ML-351 Versatile Environmental Incubation Chamber). A third of the solution (2 mL) was exchanged every 24 h and eggs were monitored daily under a stereomicroscope using both transmitted and incident light. When eye spots were observed in the eggs, monitoring was increased to every 2 h in order to obtain newly hatched oncomiracidia. Individual oncomiracidia <4 h old were gently aspirated using a fine-tip glass pipette under a stereomicroscope and introduced to a 10 L aquarium containing an individual L. calcarifer in 6 L of sea water. Each oncomiracidium was released at the bottom of the aquarium to avoid the effects of surface tension and currents which can trap and kill oncomiracidia [1]. When the oncomiracidia were introduced, air supply to the fish was stopped for 1 h in order to reduce water currents and thereby increase infection success [19]. Thirty replicates were made at room temperature (24.3±0.2°C). Salinity in each aquarium was checked using a refractometer every 24 h and adjusted by adding distilled water to maintain 35±1‰.
To determine the onset of egg production, a piece of 5 cm2 fine gauge (0.5×0.5 mm) netting was immersed in each aquarium and checked daily under a stereomicroscope. Eggs have filamentous strings which easily entangle on netting [40]. The day that eggs were observed on the netting was recorded as time to sexual maturity. Eggs always entangle on netting on the day of sexual maturity (AK Brazenor, unpublished data). Netting was renewed daily and any suspended eggs remaining in the sea water were collected daily by filtering the solution through a 60 µm mesh.
In order to confirm isolated fish were infected by a single, individual parasite, fish were immersed in fresh water at the end of the experiment, which kills Neobenedenia [see 35]. Fish were bathed in 1 L of fresh water containing a mild sedative (Aqui-S 1∶1000) for 5 min. The fresh water solution and the body surface of the fish were examined twice under a stereomicroscope to collect detached and attached parasites, respectively.
We sought to determine the reproductive viability of consecutive generations of reproductively isolated parasites for a single parasite lineage. Eggs laid by a randomly selected isolated ‘parent’ parasite were incubated in culture chambers (25°C, 35‰). A single oncomiracidium from these eggs was used to infect each of 15 replicate, isolated L. calcarifer. This process was repeated to infect 10 and 30 fish using oncomiracidia from generation F1 and F2, respectively (Table 1). Infection success was recorded as the number of oncomiracidia that attained sexual maturity from the number of fish challenged.
Experiment 2: Egg Hatching Success
In order to assess the viability of eggs laid by isolated parasites, egg hatching success was determined for a single parasite lineage for three consecutive, reproductively isolated, Neobenedenia generations. A total of 30 fish (ten for each generation) were infected as per the methods in Experiment 1. Infection success was recorded as the number of oncomiracidia that attained sexual maturity from the number of fish challenged. Neobenedenia eggs were collected by filtering the aquarium sea water through a 60 µm filter three days following sexual maturity. Following egg collection, individual fish were bathed in fresh water to confirm infection by an individual parasite (see Experiment 1). Clusters of eggs (containing 8–46 individual eggs) were incubated in sea water in cavity blocks in laboratory conditions (natural light, 24.3±0.1°C) with six replicate egg clusters made for each infected fish. Cavity blocks were filled with sea water to the brim and covered with a glass cover. Blocks were monitored for egg hatching every 24 h, when one third of the solution was changed with minimal disturbance to the eggs. When hatching was observed, oncomiracidia were removed with a pipette. Hatching experiments were continued until 48 h passed without hatching in any treatment. Hatching success of Neobenedenia eggs was measured as the number of oncomiracidia removed divided by the total number of eggs.
Experiment 3: Fecundity of Isolated and Cross-fertile Neobenedenia
To determine the fecundity of isolated parasites, egg production was monitored every 24 h. Twenty-five fish were infected with an individual oncomiracidium sourced from the laboratory infection (see Experiment 1). All aquaria (10 L with 6 L sea water) were maintained in laboratory conditions (24.3±0.1°C, 35±1‰). Ten fish (40%) were successfully infected. Daily egg production was determined by filtering the aquarium sea water through a 60 µm filter at 1800 each day. Immediately prior to filtering, fish were gently removed by hand and placed into a new aquarium containing fresh sea water. Eggs were counted under a stereomicroscope using a hand held counter to determine egg production/parasite/day. The filtered sea water was also examined carefully following death and detachment of a parasite. The experiment was terminated when mean egg production was <50 eggs/day for two consecutive days. At the termination of the experiment, individual fish were bathed in fresh water to confirm infection by an individual parasite (see Experiment 1).
To determine the fecundity of parasites given an opportunity to cross-inseminate, egg production was monitored every 12 h for fish infected with multiple oncomiracidia. Groups of ten oncomiracidia were used to challenge three fish, maintained in three separate aquaria in laboratory conditions. Egg production was monitored every 12 h (at 0600 and 1800). The experiment was terminated when mean egg production was <50 eggs/day for two consecutive days. On the day the experiment was terminated, fish were bathed in fresh water and parasites were counted. Egg production in each replicate was divided by the total number of parasites recovered to determine mean number of eggs laid per parasite.
Experiment 4: Egg Laying Rhythm
To determine whether Neobenedenia exhibit an egg laying rhythm, egg production was monitored every 3 h for three days. Four fish infected with an individual, isolated Neobenedenia, were monitored between day 12 and 15 post-infection. Ten litre aquaria containing individual infected fish were placed in culture chambers on day 10 post-infection on a 12∶12 h LD cycle at 25°C. Aquaria were aerated with battery operated aerators and salinity was maintained at 35±1‰. Egg production was determined every 3 h for three days (72 h) by filtering the aquarium sea water through a 60 µm filter, commencing at the first period following the onset of darkness (1800–2100) on day 12. Immediately prior to filtering, fish were gently removed by hand and placed into a new aquarium with fresh sea water. Eggs were counted under a stereomicroscope using a hand held counter to determine egg production/parasite/3 h. At the termination of the experiment, individual fish were bathed in fresh water to confirm infection by an individual Neobenedenia (see Experiment 1).
Experiment 5: Hatching Rhythm
To determine whether Neobenedenia exhibit an egg hatching rhythm, hatching was observed every 3 h throughout the day and night until all eggs had hatched. Eggs were sourced from parasites infecting fish held in the laboratory infection. Individual infected fish were removed from 100 L tanks to a 10 L aquarium with fresh sea water containing pieces of 5 cm2 fine gauge netting for 2 h. Netting was removed and immediately placed in a Petri dish containing fresh sea water. Pieces of netting were randomly chosen and cut with dissecting scissors to obtain pieces with ∼20 to 25 entangled eggs. A piece of netting was placed in each of 10 replicate glass cavity blocks and filled with fresh sea water to the brim and sealed with a glass lid.
Cavity blocks were exposed to natural light from a window in the laboratory. Temperature (24.1±0.1°C) was measured using a Hach Temperature Meter (HQ30d/LDO101). Approximate official times of sunrise and sunset during the experiment were 0645 and 1755, respectively. Eggs were monitored daily and a third of the sea water (2 mL) was exchanged daily. When eye spots were detected on developing embryos, monitoring was increased to every 3 h. When oncomiracidia began hatching, each piece of netting was transferred to a new cavity block containing fresh sea water at 3 h intervals, throughout the day and night. During the night, netting was transferred using dim light directed away from the cavity blocks. After each transfer, a few drops of formaldehyde were added to the cavity blocks from which the netting had been removed. Formaldehyde rapidly killed any oncomiracidia that had hatched in the block in the previous 3 h period [41]. Oncomiracidia were counted under a stereomicroscope using a hand held counter. The experiment was terminated when all embryonated eggs had hatched. Non-embryonated eggs (n = 7) were excluded from the analyses.
Data collected for each of the five experiments described was made publically available in the James Cook University research data repository: https://research.jcu.edu.au/researchdata/default/detail/d9eda2a2d49ef0b1ab4de74a2c77c826/
Statistical Analysis
A chi-square distribution was used to examine proportional infection success between consecutive isolated generations. Egg hatching data were analysed by permutational analysis of variance in the PERMANOVA function of PRIMER 6.0. PERMANOVA compares the observed value of a test statistic (F-ratio) against a recalculated test statistic generated from random permutation of the data. PERMANOVAs with 999 permutations based on Euclidean distance were used to test the effect of generation on hatching success with fish as a nested factor in the design.
Once egg production started in Experiment 3, fecundity increased rapidly to a peak approximately six days later, and then declined more slowly over subsequent days. This is a relatively common pattern of fecundity in invertebrate species (see [42]) and can be modelled in a variety of ways. We chose to use a model of the following form y = a xbe −cx (where y is the number of eggs produced, x is the reproductive age in days). The model was fitted using the nls function in SPlus/R. An ANOVA was used to determine significant difference in average fecundity between model groups. Levene's test was used to compare model fit between groups. Day 25 and 26, where mean egg production was <50 eggs/parasite/day, were excluded because less than three replicate fish remained in the isolated group. A chi-square test was used to examine the egg hatching rhythm using the proportion of eggs hatched during 3 h intervals. Significance was accepted at p<0.05.
Results
Multiple Generations from Isolated Neobenedenia
Single Neobenedenia infecting an individual, isolated fish, laid embryonated eggs that hatched into viable oncomiracidia. A further two consecutive, isolated, generations were reared in the laboratory (Table 1). There was no significant difference in infection success (p = 0.277) or hatching success (p = 0.723) between consecutive generations (Table 1), however, fish host had a significant effect on hatching success (p = 0.001). Following fresh water bathing, all experimental fish were confirmed to be infected with a single, individual Neobenedenia.
Fecundity
Individual, isolated Neobenedenia were fecund and produced 3,229±37 eggs/parasite over the course of the experiment (17 days of egg-laying; or 8±2 eggs/parasite/hour (e/p/h) or 190±11 eggs/parasite/day (e/p/d)). All parasites reached sexual maturity on day 10 post-infection (at 24.2±0.1°C). Egg production rapidly increased from the day of sexual maturity (58±15 on day 10) and peaked on day 15 (496±68) post-infection (Fig. 1). Following day 16, egg production gradually decreased, to almost negligible egg production on day 25 and 26. A total of eight fish mortalities occurred over the course of the experiment with 9, 8, 6, 3 and 2 fish remaining on days 12, 13, 20, 24 and 26, respectively. No dead, detached parasites were observed in filtered sea water for the duration of the experiment. Following fresh water bathing, all experimental fish (including mortalities) were confirmed to be infected with a single, individual Neobenedenia.
Parasites reached sexual maturity on day 10. Error bars indicate standard error.
There was no significant difference between fecundity of isolated parasites and fish infected with multiple parasites (p = 0.44). Three fish challenged with multiple oncomiracidia (n = 0) were successfully infected with three, three and four parasites, respectively. Neobenedenia with the opportunity to cross-inseminate produced 8±1 e/p/h or 191±22 e/p/d or 2,865±77 eggs/parasite over the course of the experiment (15 days), with 64.3% of eggs produced during periods of darkness (Fig. 2). Parasites reached sexual maturity on day 10 post-infection (Fig. 2). Egg production rapidly increased from 66±5 on day 10 to 489±43 on day 15. On day 16, egg production began to gradually decrease, prior to almost negligible egg production on day 23 and 24 (Fig. 2). No fish mortalities occurred during the experiment, and there were no dead, detached parasites observed in filtered sea water for the duration of the experiment. Parameter estimates for isolated and cross-fertile individuals modelled separately are shown in Table 2. Although there was no significant difference in average fecundity between groups, the model better described the cross-fertile group (R2 = 0.93) than the isolated group (R2 = 0.585). Comparing the residuals of each model with a Levene's test indicated that the residual variance was significantly higher in the isolated group than the cross-fertile group (p = 0.0048).
Parasites reached sexual maturity on day 10 and had the opportunity to cross-fertilise. Error bars indicate standard error.
Egg Laying Rhythm
Neobenedenia laid eggs continuously, but exhibited a distinct egg-laying rhythm with more eggs laid during periods of darkness. Egg production began gradually increasing in the 3 h period prior to darkness and during periods of darkness, peaking between midnight and 0300 (Fig. 3). Production decreased in the 3 h period prior to illumination and the lowest egg production was between midday and 1500 (Fig. 3). Each parasite laid an average of 22±4 eggs/h in periods of darkness and 12±2 eggs/h in periods of light between day 12 and 15 post-infection.
Mean number of eggs laid by isolated Neobenedenia sp. (n = 4) shown in three hour intervals over 72 hours (from 1800 on day 12 to 1800 on day 15). Error bars indicate standard error. Horizontal panels indicate periods of light (white; 0600–1800) and dark (black; 1800–0600).
Egg Hatching Rhythm
Neobenedenia exhibited a distinct hatching rhythm (p<0.001) with the majority of oncomiracidia (81%) hatching in the first 3 h of light (Fig. 4). Eggs began hatching on day 5, with the majority of hatching occurring on days 7 and 8. Egg hatching ceased on day 8. A total of 216 embryonated eggs were incubated and all eggs hatched during periods of natural light (0600–1500) with no eggs hatching between 1500 and 0600 on any day/night (Fig. 4).
Percentage of eggs hatched is expressed as the sum of all oncomiracidia hatched during the same period between day 5 and 8 from the total number of oncomiracidia collected. Error bars indicate standard error. The natural period of light is indicated by the white bar and the official times of dawn and dusk (0645 and 1755) are indicated by arrows.
Discussion
This study provides unambiguous experimental evidence that the fish monogenean, Neobenedenia sp., can successfully reproduce in isolation. One isolated Neobenedenia has the capacity to produce more than three thousand eggs that hatch into infective larvae within two weeks (Fig. 1), revealing that low Neobenedenia burdens in host populations do not necessarily restrict reproductive potential. Furthermore, the progeny of isolated parasites are viable for at least two more consecutive isolated generations (Table 1). While inbreeding tends to decrease hatching and infection success and the genetic diversity of parasite populations [43], we found no significant difference in egg hatching or infection success in consecutive isolated generations (Table 1). Moreover, the nested factor of fish was significant, indicating that the relationship between parasites and their individual hosts is an important aspect in determining parasite reproductive success.
Self-fertilisation is a strategy commonly seen in parasitic platyhelminths where low parasite burdens occur in host populations or where there may be a high frequency of single parasite infection [6], [44], [45]. At least four species of monogeneans in the bladders of amphibians are capable of producing viable eggs in isolation [3], [6], [10]. It is possible that Neobenedenia examined in this study reproduced by natural parthenogenesis (a form of asexual production where growth of embryos can occur without fertilisation), however, this is unlikely considering that Neobenedenia have reproductive organs of both sexes. Kearn and Whittington [30] observed two capsalid monogenean species, Benedeniella macrocolpa and B. posterocolpa, self-inseminating in preserved specimens mounted on slides, but insemination via the vaginal route is not an option in Neobenedenia spp. as there is no vagina. Insemination in Neobenedenia spp. is most likely achieved by sperm being introduced via the common genital pore or the uterus. Indeed, Whittington and Horton [20] observed the penis of one Neobenedenia melleni lodged in its own uterus. Self-insemination has been observed in live specimens of Neobenedenia girellae (see [46]) and Heterobothrium okamotoi (Monogenea: Diclidophoridae) (see [32]). Furthermore, Ogawa et al. [46] suggested that self-insemination in N. girellae may involve passage of sperm through the tegument from externally attached spermatophores. While the specific mechanism of self-insemination was not determined, our study provides the first experimental evidence that capsalid monogeneans of fish can produce viable eggs in isolation.
Parasites that exhibit high fecundity increase the likelihood of offspring successfully locating and infecting a new host. Isolated Neobenedenia were fecund, with egg production rapidly increasing following sexual maturity, before peaking and slowly decreasing over time (Fig. 1). This trend is typical of many invertebrate species [47], [48]. Neobenedenia egg production was negligible by the time adult parasites were ∼23 days old, indicating that fecundity was captured over the reproductive life span of the parasite (Fig. 1 and 2). Egg production varied with parasite age and time of day, indicating that egg production measured on an hourly or daily rate may not accurately represent parasite fecundity ([49]; Fig. 1; Fig. 3). Egg production can also be influenced by other environmental and host variables, including temperature [50]–[52].
Parasite fecundity can vary between self-fertile and cross-fertile individuals. Wedekind et al. [53] reported that self-fertile cestodes, Schistocephalus solidus, infecting stickleback, Gasterosteus aculeatus, exhibited higher fecundity compared to parasites placed in pairs. In contrast, Tinsley and Owen [3] found that multiple infections of the monogenean Protopolystoma xenopodis infecting the toad, Bufo regularis, sometimes resulted in greater output per individual than isolated parasites. In our study, there was no significant difference in fecundity for isolated and cross-fertile Neobenedenia. It is plausible that Neobenedenia may not have cross-fertilised, despite being infected with multiple individuals and their ability to ‘crawl’ along the external surfaces of fishes in order to locate another parasite [54]. Thus, molecular methods are warranted to quantify the frequency of cross-fertilisation in Neobenedenia.
Parasite egg laying rhythms could be a predator avoidance behaviour and could also align with temporal host behaviours [25]. Neobenedenia laid eggs continuously, but significantly more eggs (64.3%) were laid at night (Fig. 3 & 4). Egg-laying rhythms are common in many invertebrates, with most releasing their gametes during periods of darkness (Fig. 3; [55], [56], [57]). The egg laying rhythm of Diplozoon homoion gracile (Monogenea: Diplozoidae), a gill parasite of southern barbel, Barbus meridionalis, is also nocturnal [7]. Similarly, Mooney et al. [51] found that Heteraxine heterocerca (Monogenea: Heteraxinidae) a gill parasite of Japanese yellowtail, Seriola quinqueradiata, laid eggs continuously, but more eggs (72.9%) were laid during periods of darkness, with the majority of eggs released during the first 3 h periods immediately after dark. Alternatively, some monogenean species store their eggs in utero to be released at a specific time of day [8], [51].
Hatching rhythms can also increase the chances of larvae contacting a specific host [58], [54]. This is crucial for infection success because free swimming oncomiracidia are typically short lived (24 to 48 h) [1], [26], [59]. Neobenedenia exhibited a distinct hatching rhythm, with 81% of the larvae emerging during the first 3 h of natural light (Fig. 4). Monogeneans can maximise their chances of finding a host by extending the hatching period [11], while some species respond to hatching cues such as shadows [12], chemicals [11], [13], mechanical disturbance [14]–[16] and osmotic changes [17], most of which are generated by the host. Hatching rhythms have been documented in other marine monogeneans in the first few hours of light (Entobdella solea [60]; Diclidophora spp. [15]) and also in the first few hours following dusk (Entobdella hippoglossi [61]; Diplozoon homoion gracile [7]). Other species exhibit more complicated rhythms [41], [58], [62], [63]. Hatching rhythms of monogeneans are often related to times when the behaviour of the host makes it more vulnerable to infection [7], [15], [59]–[62]. Eggs also hatch in response to other environmental cues such as light periodicity and intensity [60], [64], host skin secretions [65], mechanical disturbances [66] and seasonal differences [15]. In addition, rhythmic hatching may minimise predation on monogeneans by other organisms, especially filter feeders [58], [63].
In conclusion, Neobenedenia exhibits a variety of strategies to aid survival of subsequent generations. Parasites can reproduce in isolation to produce viable, infective oncomiracidia for three consecutive generations. High fecundity, egg laying and egg hatching rhythms ensure the success and persistence of this harmful parasite in wild and farmed fishes.
Acknowledgments
We thank Alexander Brazenor, Thane Militz and Alejandro Trujillo-González (JCU) for technical assistance and Good Fortune Bay Pty Ltd and Coral Coast Barramundi Pty Ltd for provision of specimens. Emeritus Professor Rhondda Jones and Dr Richard Saunders (JCU) provided statistical advice and Associate Professor Ian Whittington (South Australian Museum) provided discussion on monogenean biology.
Author Contributions
Conceived and designed the experiments: KSH. Performed the experiments: TDH. Analyzed the data: TDH KSH. Contributed reagents/materials/analysis tools: KSH. Wrote the paper: KSH TDH.
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