Infectivity of chordodes nobilii larvae (gordiida: nematomorpha).
In spite of the obvious ecologic significance of the Gordiida, an essential detail is still lacking regarding certain key aspects of their biology--namely their infective capacity. This property, in turn, would permit inferences regarding other aspects of the gordiid biology, such as their reproductive success. The infective capacity accordingly can be evaluated by means of the quantitative descriptor of parasite populations "infection index mean abundance" or IIMA (Bush, Lafferty, Lotsg, & Shotsak, 1997). That index has been used to evaluate the susceptibility of the gordiid species Chordodes nobilii Camerano, 1901 (Gordiida, Nematomorpha) to environmental contamination (Achiorno, de Villalobos, & Ferrari, 2008a, 2009, 2010, 2015) and to variations in temperature (Achiorno, de Villalobos, & Ferrari, 2008b), for which purpose assay protocols specific for this group have been developed. The ecotoxicologic assays devised up to the present have demonstrated that the preparasitic stages of C. nobilii are susceptible to different toxic agents--i. e., the three pesticides glyphosate, malathion, and carbendazim; the two metals, chromium ([Cr.sup.6+]) and cadmium ([Cd.sup.2+]) and the detergent sodium dodecyl sulfate. Mean abundance has also been used by Bolek et al. (2013) in order to determine if after being exposed to a freezing temperature, the larvae and/or cysts could successfully infect. Those studies provided evidence in favor of the possibility that the gordiids could be utilized as bioindicators of contamination.
For this reason, a knowledge of the intrinsic variability in the infective capacity of the species under investigation here--as a measurement of gordiid viability--would warrant priority in order to establish the range of acceptable responses for normal or standard conditions in the laboratory, and to compare the criteria among different ecotoxicologic assays.
The objective of the present study was therefore to establish a baseline for the infective capacity of the South-American species C. nobilii under controlled laboratory conditions through the use of the IIMA as the parameter of evaluation.
MATERIALS AND METHODS
Collection of gordiids and generation of larvae in the laboratory: For conducting this study, adults from both sexes of Chordodes nobilii were collected from streams within the Sauce Grande basin in the locality of Sierra de La Ventana, Buenos Aires, Argentina (38[grados]09" S --61[grados]48" W). Samplings were made in various field trips during the spring and summer seasons from 2006 through 2009, those being the reproductive seasons of the species. Once in the laboratory, individuals were kept in containers with aerated natural freshwater at a controlled room temperature of 23[+ o -] 1 [grados]C. This water was gradually replaced with reconstituted hard water (pH 7.6-8.0, hardness 160-180 mg/L as C03Ca), which was exchanged each week. Because adults do not feed, providing food was unnecessary. After mating, all the females identified--in this study a total of 12--were placed in individual containers for oviposition. Subsequently, the egg strings obtained in the laboratory--those being ca. 0.5 mm widthwere separated and thereafter maintained in running dechlorinated water under the same temperature conditions and in the ambient photoperiod until reaching the free-larva stage. Egg maturity was judged by the color of the egg strings, which shade became darker as the larvae developed (Hanelt & Janovy, 1999). At that stage the egg-string samples were scrutinized microscopically. If in the sample 50 % of the individuals appeared to be free larvae, we proceeded to evaluate the infectivity. The taxonomic determination of the C. nobilii adults was made according to de Villalobos and Zanca (2001). The females were identified after the completion of oviposition and before the eggs developed into free larvae.
Determination of viability of Chordodes nobilii individuals under study: Figure 1 is a schematic diagram of the methodology used. For evaluation of the gordiids' infective capacity-and therefore their survival--Aedes aegypti larvae, reared in the laboratory, were used as hosts. These larvae were placed in containers (N = 30 J. aegvptii larvae per container, with 12 mL of dechlorinated tap water and wheat germ as food) along with 3-mm-long C. nobilii eggstring segments containing ca. 4000 C. nobilii individuals. Those egg-string segments first had been checked to confirm that [mayor que o igual a] 50 % were in the free-larval stage. In this way, we could assume a similar exposure rate for each sample. For the entire study, a total of 90 egg-string segments were used. After a 72 h exposure to the C. nobilii larvae, the A. aegypti larvae were fixed in 70 % (v/v) aqueous ethanol. The mosquito larvae were then dissected under the light microscope in order to quantify the C. nobilii larvae in the body cavities. The IIMAs were calculated as the total number of C. nobilii larvae present divided by the total number of A. aegypti larvae examined (Bush et al., 1997).
For analysis of the IIMAs obtained, the data were grouped according to the female who made the ovoposition. Descriptive statistical analyses were performed, as well as analyses of frequency along with the Kruskal-Wallis test, at a significance level of < 0.05 (Zar, 2010). According to Hanelt (2009), the length of the female gordiid worm is an accurate indicator of the egg output over a lifetime and moreover the variation in reproductive success is extremely low in this population; in order to discard the possibility that the size of the egg string influenced the infective capacity of the C. nobilii progeny, we analyzed the correlation between those two parameters by means of the coefficient of Spearman. All of the statistical analyses were performed by the Infostat statistical program (www.infostat.com.ar).
The present study--undertaken in order to determine the viability of C. nobilii larvae through their ability to infect A. aegypti larvae indicated a great inconsistency in their infectivity. The first IIMA analysis (N= 90) indicated that a wide range and variability existed among the values, with a minimum of 1.56, a maximum of 21.4, a mean [+ o -] SD of 6.84 [+ o -] 4.67, and a variance of 21.5. Nevertheless, the analysis of frequency indicated that almost 50 % of the values fell in the class between 1.56 and 4.87 at a mean of 3.21, while the remaining 50 % was divided among five classes (Table 1).
The grouping of the IIMA values according to the female progenitor (Fig. 2) demonstrated that the infective capacity of the larvae originating from females J, K, and L was significantly greater than those from the rest of the females (H= 71; P <0.0001), and the females A and B were those individuals whose larvae were the least infective. This differential infective capability among members of the cohort originating from the different females, would infer that the variability in the infectivity of C. nobilii larvae could result from differing characteristics of the progenitors.
The analysis by the Spearman coefficient (at -0.04) indicated that no correlation existed between the IIMA values and the total lengths of the egg strings. Therefore, under the experimental conditions used here, the length of the egg string bears no relationship to the infectivity of the resulting larvae.
The results presented here are the first providing information on the infective variability of a South-American species of Gordiida, Chordodes nobilii, on the basis of laboratory experiments. These findings enable the wide range in that infective capacity of C. nobilii to be attributed to the particular progenitors of those larvae. Thus, the evaluation of infectivity on the basis of the IIMA assay, demonstrated that the progeny of certain specific females were more successful in infecting Aedes aegypti larvae than others. A very relevant and crucial result that stems from the analysis of infective capacity, as evaluated by the IIMA, is related to the potentiality of the gordiids to be used as bioindicators of contamination. In such an application of C. nobilii, comparisons among different assays would be required to establish a baseline set of IIMA values. The infectivity of these larvae, however, proved to be extremely variable; moreover, according to the findings presented here, that capacity was attributable to the progenitors. This characteristic of the species results in a considerable and highly significant variability in the baseline level of infectivity. These findings therefore constitute a warning to investigators alerting them to the necessity of normalizing comparisons among assays conducted with different populations of C. nobilii. As a consequence, in order to make comparisons among different bioassays with these gordiid larvae through the use of the IIMA as the form of measurement, the data obtained would always need to be referred to the respective control values for each assay.
If we consider the difference in successful infection among the larvae originating from different progenitors, a significant point that results from the analysis of our findings is that the data enable us to make inferences on the reproductive success of the group. If we consider that "reproductive success can be defined as the passing of genes on to the next generation in a way that they too can pass those genes on" (Pagel, 2009)--that is, we must not only consider the reproductive success of an individual or population but also the probability passing on that capacity to the progeny--then "the genetic contribution of a subpopulation to the next generation depends not only on the number of propagules produced but also critically on the fitness of these propagules" (Therese & Bashey, 2012). In this regard, only certain fraction of a female's eggs hatch into larvae, and only a portion of those larvae will have an adequate infective capacity, in order to pass on those genes to the next generation. Therefore, we must consider the possibility that the reproductive success of a species of parasite such as the gordiid C. nobilii is related to both the numbers of offspring and the latter's individual and collective infective capacity.
In order to evaluate the reproductive successfulness of a given population of these gordiids, the influence of the progenitors must be taken into account. Hanelt (2009) proposed that "within gordiid populations the offspring of the next generation are contributed nearly equally by females"--in other words, the variation in reproductive success is low for the group. The findings of our study strengthen the point of view that these populations of gordiids exhibit a high variation in reproductive success that has been described as a normal characteristic of the helminths (Hanelt, 2009), such that certain progenitors contribute more greatly to the next generation than others.
These results accordingly argue for the necessity of performing new studies, since the gordiids have a low variation in reproductive success, upon consideration of the numbers of offspring produced (Hanelt, 2009), but exhibit a significant variability in infective capacity among different ovopositions. Such variation can be thought not to be a property definitively influenced by the females, consistent with the asseveration of Levitan (1991) that "estimates of reproductive output based on body size or gamete production alone can be misleading. The assumption that large body size and high gamete production translate into high reproductive success may be not right when the influence of fertilization success is ignored." Thus, the fecundation modality of the group needs to receive attention because, when fertilization occurs, the females and males form Gordian knots that are fraught, with the possibility that a given female may be inseminated by various males at the same time (Bolek et al., 2015; Schmidt-Rhaesa, 1997). Such multiple fecundations could result in a major degree of genetic variability in the progeny and as a consequence affect the reproductive success. Furthermore, in the example of the gordiids, what must also be kept in mind is "the importance of the host environment to the fitness of parasites and the potential for trans-hosts [sic] effects to alter the ecological and evolutionary dynamics of parasite populations" (Therese & Bashey, 2012).
To conclude, we wish to emphasize that the data from the present study not only contributed with information on the gordiids of South America, but also enabled inferences to be made that clarified doubts regarding different aspects of the biology of this group. Moreover, the conclusions drawn from the results of these experiments will be highly useful when performing ecotoxicological studies with the gordiids. Furthermore, these findings would be relevant to the standardization of bioassays involving a species from any given parasitic group. Finally, these results would indicate as well the necessity to use the parameter IIMA as a benchmark for consideration in different studies on the biology of the Gordiida in particular. A highly relevant point stemming from the present investigation concerns the conclusions drawn regarding the evaluation of reproductive success. Although an analysis of reproductive success was not the principal objective of these experiments, the data we obtained reinforce the notion previously proposed by other investigators that to determine the reproductive success of a given species one must take into account the significance of fertilization and the fitness of the progeny. In the C. nobilii under investigation here, the progeny's fitness is tantamount to that generation's infective capacity. From this conclusion arises the necessity of studying parasites utilizing, whenever possible, the property of infectivity for the evaluation of different parameters.
Received 08-IV-2016. Corrected 26-VIII-2016. Accepted 29-IX-2016.
This work was supported by Grants from National University of Lujan, and CIC-Buenos Aires, Argentina. We thank Juan Garcia (CEPAVE, CONICET) for providing us with A. aegypti (Diptera) larvae. Donald F. Haggerty, a retired academic career investigator and native English speaker, translated the manuscript from the original Spanish and edited the final version of the text.
Achiorno, C. L., de Villalobos, C., & Ferrari, L. (2008a). Toxicity of the herbicide glyphosate to Chordodes nobilii (Gordiida, Nematomorpha). Chemosphere, 71, 1816-1822. D0I:10.1016/j.chemosphere.2008.02.001
Achiorno, C. L., de Villalobos, C., & Ferrari, L. (2008b). Effect of extreme temperature on egg development, larval and adult survival of Chordodes nobilii Camerano, 1901 (Gordiida, Nematomorpha). Acta Parasitologica, 55(4), 392-396. DOI: 10.2478/ s11686-008-0052-5
Achiorno, C. L., de Villalobos, C., & Ferrari, L. (2009). Sensitivity of preparasitic stages of Chordodes nobilii (Gordiida, Nematomorpha) to malation. Ecotoxicology, 18, 594-599. DOI: 10.1007/s10646-009-0317-2
Achiorno, C. L., de Villalobos, C., & Ferrari, L. (2015). Susceptibility of preparasitic stages of Chordodes nobilii (Gordiida, Nematomorpha) to the fungicide carbendazim. Journal of Helminthology, 89, 748-754. D0I:10.1017/S0022149X14000728
Achiorno, C., de Villalobos, C., & Ferrari, L. (2010). Validation test with embryonic and larval stages of Chordodes nobilii (Gordiida, Nematomorpha): Sensitivity to three reference toxicants. Chemosphere, 81, 133140. D0I:10.1016/j.chemosphere.2010.06.076
Bolek, M. G., Rogers, E., Szmygiel, C., Shannon, R. P., Doerfert-Schrader, W. E., Schmidt-Rhaesa, A., & Hanelt, B. (2013). Survival of Larval and Cyst Stages of Gordiids (Nematomorpha) After Exposure to Freezing. Journal of Parasitology, 99(3), 397-402. DOI: 10.1645/12-62.1
Bolek, M. G., Schmidt-Rhaesa, A., de Villalobos, L. C., & Hanelt, B. (2015). Phylum Nematomorpha. In J. Thorp, & D. C. Rogers (Eds.), Ecology and General Biology: Thorp and Covich's Freshwater Invertebrates. Academic Press.
Bush, A. O., Lafferty, K. D., Lotsg, J. M., & Shotsak, A. W. (1997). Parasitology meets ecology on its own terms: Margolis et al., revisited. Journal of Parasitology, 83, 576-583. DOI: 10.2307/3284227
Cochran, P. A., Kinziger, A., & Poly, W. J. (1999). Predation on horsehair worms (Phylum Nematomorpha). Journal of Freshwater Ecology, 14, 211-218. DOI: 10.1080/02705060.1999.9663672
de Villalobos, C., & Zanca, F. (2001). Scanning electron microscopy and intraspecific variation of Chordodes festae Camerano, 1897 and C. peraccae (Camerano, 1894) (Nematomorpha: Gordioidea). Systematic Parasitology, 50(2), 117-125. DOI: 10.1023/A:1011921326564
de Villalobos, C., Ortiz-Sandoval, J. J., & Habit, E. (2008). Finding of Gordius austrinus (Gordiida, Nematomorpha) in the diet of Salmo trutta (Salmoniformes) in Patagonia. Gayana, 72(1), 31-35.
Hanelt, B. (2009). An anomaly against a current paradigm --extremely low rates of individual fecundity variability of the Gordian worm (Nematomorpha: Gordiida). Parasitology, 136(02), 211-218. DOI: 10.1017/ S0031182008005337
Hanelt, B., Thomas, F., & Schmidt-Rhaesa, A. (2005). Biology of the phylum Nematomorpha. Advances in Parasitology, 59, 243-305. DOI: 10.1016/ S0065-308X(05)59004-3
Hanelt, B., & Janovy, J. Jr. (1999). The Life Cycle of a Horsehair Worm, Gordius robustus (Nematomorpha: Gordioidea). The Journal of Parasitology, 85(1), 139-141. DOI: 10.2307/3285720
Infostat. (2014). GrupoInfostat. Facultad de Ciencias Agropecuarias, Universidad Nacional de Cordoba, Argentina. www.infostat.com.ar
Kinziger, A. P., Cochran, P., & Cochran, J. (2002). Additional cases of predation on horsehair worms (Phylum Nematomorpha), with a recent record for Missouri.
Transactions of the Missouri Academy of Science, 36, 11-13.
Levitan, D. R. (1991). Influence of Body Size and Population Density on Fertilization Success and Reproductive Output in a Free-Spawning Invertebrate. The
Biological Bulletin, 181, 261-268.
Pagel, T. (2009). Determinants of individual reproductive success in a natural pike (Esox lucius L.) population: a DNA-based parentage assignment approach (Master's thesis). Leibniz-Institute of Freshwater Ecology and Inland Fisheries, Berlin, 22.12.2009. Retrieved from http://www.adaptfish.rem.sfu.ca/thesesAThesis_MSc_Pagel.pdf
Ponton, F., Lebarbenchon, C., Lefebre, T., Thomas, F., Duneau, D., Marche, L., ... & Biron, D. (2006). Hairworm anti-predator strategy: a study of causes and consequences. Parasitology, 133, 631-638. DOI: 10.1017/S0031182006000904
Schmidt-Rhaesa, A. (1997). Nematomorpha. In G. Fischer (Ed.), Su[sz]wasserfauna von Mitteleuropa (pp. 1-123). Germany: Spektrum Akademischer Verlag.
Schmidt-Rhaesa, A. (2012). Nematomorpha. In A. Schmidt-Rhaesa (Ed.), Handbook of Zoology, Gastrotrichia, Cycloneuralia and Gnathifera. Nematomorpha, Priapulida, Kinorhyncha and Loricifera (Vol. 1, pp. 29-145). Berlin: De Gruyter.
Schmidt-Rhaesa, A., & Ehrmann, R. (2001). Horsehair Worms (Nematomorpha) as Parasites of Praying Mantids with a Discussion of their Life Cycle. Zoologischer Anzeiger, 240, 167-179. DOI: 10.1078/0044-5231-00014
Therese, M. O., & Bashey, F. (2012). Natal-host environmental effects on juvenile size, transmission success, and operational sex ratio in the entomopathogenic nematode Steinernema carpocapsae. The Journal of Parasitology, 98(6), 1095-1100. DOI: 10.1645/ GE-3069.1
Zar, J. H. 2010. Biostatistical analysis. N.J.: Prentice Hall.
Cecilia L. Achiorno (1,2), L. Cristina de Villalobos (2), Lucrecia Ferrari (3,4)
(1.) Centro de Estudios Parasitologicos y de Vectores (CEPAVE)--Universidad Nacional de La Plata (CCT La PlataCONICET- UNLP). Boulevard 120 S/N e/60 y 61 (B1902CHX) La Plata, Buenos Aires, Argentina; email@example.com
(2.) Facultad de Ciencias Naturales y Museo, Universidad Nacional de La Plata, La Plata, Buenos Aires, Argentina; firstname.lastname@example.org
(3.) Comision de Investigaciones Cientificas (CIC), La Plata, Buenos Aires, Argentina; email@example.com
(4.) Programa de Ecofisiologia Aplicada (PRODEA)--Instituto de Ecologia y Desarrollo Sustentable (INEDES) UNLuCONICET y Departamento de Ciencias Basicas. Universidad Nacional de Lujan, Casilla de Correo 221, B6700ZBALujan, Argentina; firstname.lastname@example.org
Leyenda: Fig. 1. Flow diagram of experimental procedure. FL: freeliving larvae.
Leyenda: Fig. 2. Infective capacity of Chordodes nobilii larvae for Aedes aegypti larvae with respect to the female that made the oviposition. In the figure, the average IIMA on the ordinate for each of the C. nobilii progenitor females indicated on the abscissa. The error bars represent the SDs.
TABLE 1 Frequency analysis for Chordodes nobilii infectivity Class LL UL M AF RF 1 1.56 4.87 3.21 49 0.52 2 4.87 8.18 6.52 22 0.23 3 8.18 11.49 9.83 7 0.07 4 11.49 14.79 13.14 7 0.07 5 14.79 18.1 16.45 8 0.08 6 18.1 21.41 19.76 2 0.02 Frequency analysis for indexes IIMA (N = 90). The table shows for each class, lower limit (LL), upper limit (UL), mean (M), absolute frequency (AF) and relative frequency (RF).
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|Author:||Achiorno, Cecilia L.; Cristina de Villalobos, L.; Ferrari, Lucrecia|
|Publication:||Revista de Biologia Tropical|
|Date:||Mar 1, 2017|
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