Diapause in the pea aphid (Acyrthosiphon pisum) is a slowing but not a cessation of development
© Shingleton et al; licensee BioMed Central Ltd. 2003
Received: 07 May 2003
Accepted: 08 August 2003
Published: 08 August 2003
Many insects undergo a period of arrested development, called diapause, to avoid seasonally recurring adverse conditions. Whilst the phenology and endocrinology of insect diapause have been well studied, there has been comparatively little research into the developmental details of diapause. We investigated developmental aspects of diapause in sexually-produced embryos of the pea aphid, Acyrthosiphon pisum.
We found that early stages of embryogenesis progressed at a temperature-independent rate, characteristic of diapause, whereas later stages of embryogenesis progressed at a temperature-dependent rate. However, embryos maintained at very high temperatures during the temperature-independent stage showed severe developmental abnormalities. Under no temperature regime did embryos display a distinct resting stage. Rather, morphological development progressed slowly but continuously throughout embryogenesis.
Diapause in the pea aphid, and perhaps in many other insects, is a temperature-independent slowing but not a cessation of morphological development. This suggests that the mechanisms limiting developmental rate during diapause may be the same as those controlling developmental rate at other stages of growth.
Many animals have evolved to survive seasonally recurring adverse conditions by entering a diapause stage. Diapause is generally characterized by a slowing of metabolism, a reduction or elimination of cell division and a cessation of morphological development, evident as a 'resting stage' . Diapause occurs in response to stimuli that predict adverse environmental conditions, not in response to the conditions themselves. Once in diapause, development is not resumed even if conditions return to those amenable to growth. It is this lack of responsiveness that is a distinguishing characteristic of diapause . In most animals diapause can occur only at a specific developmental stage, be it as an embryo, juvenile, or adult. Diapause, therefore, represents a discrete developmental process that should be controlled, at least in part, by stereotyped gene expression.
Until recently diapause was generally considered a physiological phenomenon, and much research had concerned the conditions that induce diapause and the endocrinology of its regulation [2, 3]. Nevertheless, diapause is also a developmental process, and these previous studies did not address fundamental questions concerning development before, during and after diapause. More recent research has begun to focus on the molecular aspects of diapause, with studies of Bombyx morii, Sarcophaga crassipalis, and Lymantria dispar identifying genes up- and down-regulated during diapause [1, 4–7]. In order to complete this picture, however, detailed descriptions of the morphological aspects of development spanning diapause are also necessary.
Certain aspects of aphid egg development have been elucidated in other species. The conditions required to induce the production of sexual males and females has been established [8, 9]. There has also been work on the influence of genetic background and the environment on the duration of egg development in different species and strains [10, 11]. The most comprehensive study of aphid egg development, by Behrandt , suggests that it constitutes three stages: (i) a temperature dependent period of initial development, (ii) a temperature independent 'diapause' followed by (iii) temperature dependent development. Additionally, development is only completed successfully if the eggs are chilled for at least a short period of time during early development. The embryonic stage upon which diapause is supposed to impinge is, however, unclear. According to Behrandt, diapause occurs at the end of anatrepsis (germband immersion) in Aphis fabae. This has been corroborated by the observation that in Sitobioum graminum the majority of embryos also pass winter at the end of anatrepsis , and the same may be true of Aphis pomi in Virginia USA . Other aphids, however, including German clones of Aphis pomi, appear to develop constantly throughout the winter, with no definite resting stage . A resting stage is a widely reported characteristic of diapause [1, 2, 16–18] and so the extent to which diapause occurs generally in aphids is therefore in some doubt.
Here we present a description of the development of sexually-produced pea aphid embryos. We maintained embryos under conditions that mimic those experienced naturally (0–4°C), and tracked their development through sampling and dissection. In aphids, and most other insects, however, there is a strong relationship between temperature and developmental rate . In order, therefore, to determine whether any resting stage we observed at 0–4°C was truly diapause and not a consequence of low rearing temperatures, we also tracked the development of embryos maintained under warmer conditions (10°C and 16°C). Any putative diapause observed at 0–4°C should also be observed at higher temperatures. Further, to determine whether there was a cessation of cell division at any point during development, we immunostained the embryos with anti-Histone H3, which identifies cells undergoing mitosis. Finally, we tested whether putatively diapausing embryos could resume development and hatch earlier than the reported 100 days  by transferring embryos from 0–4°C to 16°C at day 49 and tracking their development. We show that under winter-like conditions, development is continuous but slow, and progresses in a temperature independent manner for part of the time. The data indicate that A. pisum undergoes a type of diapause, but one that is different from the 'cessation of development' presented as diapause in many other insects.
Embryonic development at 0–4°C
The sexually-produced A. pisum embryo lacked a distinct resting stage when maintained at 0–4°C. Although there was no significant change in the length of the embryo from day 21 to 56 (figure 3), there was continued growth of the legs and further differentiation of the organs, most obviously of the gut (not shown). Figure 2 illustrates the development of an embryo maintained at 4°C days and 0°C nights from day 15 – 85. Staining with anti-Histone H3 revealed cell division in most, but not all, of the embryos collected throughout this period (figures 2B,2C &2D). Cell division was detected in a number of embryos from every sample, indicating there was no uniform resting stage at a particular age. After day 56 the embryo increased in body length and between day 63 and 77 it began to undergo katatrepsis (figures 2G,2H,2I,2J), the process by which the embryo re-orientates in the egg. By the beginning of katatrepsis (day 63) the embryos had moved to the posterior of the egg such that the amnion and serosa lie in contact (figure 2G). Subsequent embryological movements suggest that these membranes fuse, and the head of the embryo emerges from the opening to move up the ventral side of the egg as the serosa shrinks. At day 70 the embryo has curled at the posterior of the egg with its heads against the ventral side of the egg (figure 2H). It was not possible to distinguish between the amnion and the serosa once they had fused so we will collectively refer to them as the amnioserosa. By day 77 the embryo had completed katatrepsis and was positioned with its anterior lying at the anterior of the egg and its posterior lying at the posterior of the egg (figures 2I &2J). At this stage the embryo had a cap-like structure at the front of its head, which appears to be the remains of the amnioserosa. Either during or after this process of embryonic reorientation the embryo underwent dorsal closure. It is unclear how this was achieved, but by day 84 it had been completed, as the embryo had deposited an embryonic cuticle (figure 2K). This cuticle was shed upon hatching and possessed a serrated egg burster at the anterior end. Hatching was almost immediate upon transfer to 16°C at day 98. Sixty nine percent (n= 62) of the transferred eggs hatched, and all within 4 days of transfer (mean = 1.29 days, S.D. = 0.67).
Embryonic development at 10°C
Embryonic development at 10°C suggests that early development of the sexually-produced A. pisum embryo, particularly before katatrepsis, is temperature independent. Figure 3 shows the growth of aphid embryos maintained at 10°C. The rate of body and leg growth in embryos prior to katatrepsis was not significantly higher in embryos maintained at 10°C than embryos maintained at 0–4°C (GLM: body or leg length = time + temperature + time*temperature: Body; Ftime*temperature(1, 130) = 0.1357, p = 0.7132: Leg; Ftime*temperature(1, 130) = 3.1184, p = 0.0798). Staining with anti-Histone H3 revealed cell division at all ages.
Hatching success in embryos maintained at 10°C was lower than at 0–4°C. Three embryos hatched after 58 days at 10°C, and one more hatched a day later (n = 80). Upon transfer to 16°C on day 78, only 26% of the eggs hatched (n = 31) over a period of 8 days (mean = 3.6 days, S.D. = 3.6).
Embryonic development at 16°C
Embryonic development at 16°C again suggests that early development of the sexually-produced A. pisum embryo is temperature independent. Figure 3 shows the developmental progress of aphids maintained at 16°C. Statistical analysis revealed that for those embryos that apparently developed normally, the rate of growth prior to katatrepsis was not significantly higher at 16°C than at 0–4°C for both overall body length and leg length (GLM: body or leg length = time + temperature + time*temperature: Body; Ftime*temperature(1, 122) = 0.3706, p = 0.5438: Leg; Ftime*temperature(1, 122) = 0.1657, p < 0.6847). Embryos maintained at 16°C underwent katatrepsis earlier than those maintained at 0–4°C and 10°C (figure 4). Embryos again appeared to undertake katatrepsis at a less developed stage at 16°C than at 0–4°C; that is embryos just prior to katatrepsis had significantly shorter bodies at 16°C than at 0–4°C (figure 5). Nevertheless, embryos that had just completed katatrepsis were the same size at 16°C as at 0–4°C (figure 5).
Embryonic development after transfer from 0–4°C to 16°C
The data suggest that sexually-produced A. pisum embryos undergo a period of diapause, although a diapause different to that commonly presented in the literature. Diapause typically involves as a period of developmental arrest during which an insect is resistant to environmental influences on developmental progression . Sexually-produced A. pisum embryos do not demonstrate developmental arrest. Whilst there is little increase in overall body size between anatrepsis and katatrepsis, there is continued growth of the legs and further differentiation of body organs. A. pisum embryos do, however, show resistance to environmental influences on developmental progression. Growth rate up to katatrepsis is the same at 0–4°C, 10°C and 16°C. This is in contrast to asexually-produced embryos where growth rate approximately doubles between 5°C and 10°C and between 10°C and 16°C . In sexually-produced embryos the period of temperature independent development, or diapause, ends around katatrepsis. After this point development becomes temperature dependent, with more rapid growth at 10°C than at 0–4°C. Katatrepsis, and the end of diapause, however, occurs earlier in embryos maintained at higher temperatures, (10°C and 16°C) and can be bought forward in embryos maintained at 0–4°C by transferring them to 16°C at day 49.
At all the temperatures tested there was no cessation of morphological development. Cell division was evident at all ages and, at 0–4°C at least, there was continued growth of the legs. This appears to be somewhat contrary to the traditional understanding of diapause, which typically involves a distinct 'resting stage' [1, 21]. Much research has revealed, however, that even during the 'resting stage' there are physiological changes in the diapausing insect, leading to the concept of 'diapause development' [22, 23]. Nevertheless, such development appears to be primarily physiological rather than morphological, and was defined as physiogenesis by Andrewartha (1952). It is possible that the morphological development observed in diapausing A. pisum is exceptional. Alternatively, diapause in many other insects may also involve a slowing but not a cessation of morphological development. It is difficult to test this notion with the current literature as timed dissections of diapausing embryos, larvae and pupae have rarely been conducted. There are, however, a few examples of continued morphological development during diapause. Diapausing embryos of the orthopteran Austroicetes cruciata undergo slow development for the first two months of diapause, before entering a resting stage . Similarly, caterpillars of Cirphus unipunctata and Laphygma exigua continue to feed and develop during diapause, albeit at a much-reduced rate , and caterpillars of the corn-stalk borer Sesamia nonagriodes undergo non-stationary moults during diapause . These examples hint that the expression of diapause-controlled dormancy may vary between species . Consequently, diapause could be considered extreme regulation of developmental rate, rather than a shutting down of morphological development. The mechanisms that control diapause in A. pisum may therefore be the same as those that control the rate of morphological development at other stages of development.
Several insects that diapause over winter are resistant to environmental conditions conducive to growth only at the beginning of winter [27–31]. This prevents premature emergence, be it from egg, larvae or pupae, just at the onset of the cold temperatures the insect is trying to avoid. Once winter has commenced, diapause ends and the insect enters post-diapause quiescence, relying on persistent low temperatures to maintain developmental arrest . This appears to be the case in A. pisum. The aphid clone used for the experiment would normally oviposit in mid-October, when the average daily temperature is 9°C with a maximum of 15°C . By day 28 the embryos would be exposed to average daily temperatures of 3°C. Consequently, whilst A. pisum maintained at 0–4°C had regained temperature-dependent growth by day 49 (figure 7), it would not normally be exposed to warmer conditions until the following spring, approximately 150 days later. By this time the aphid would be fully developed and ready to hatch. In embryos that remained at 0–4°C until day 98, there was no obvious difference in development rate during and after diapause, and this is consistent with observations in other insects [1, 27]. There must, however, be some change in condition to move development from being temperature independent to temperature dependent . This change appears to be at or around katatrepsis. Identifying what this change is, and what, if anything, it has to do with katatrepsis, will be key to understanding how the pea aphid controls development during diapause.
The finding that A. pisum embryos maintained at 16°C showed considerable malformation may be a consequence of surpassing the normal thermal limits of developmental regulation. The genetic pathways involved in the development of A. pisum embryos must build an animal under two conditions. The first is slow, temperature independent development at low ambient temperatures in sexually-produced embryos, and the second is rapid temperature dependent development at higher ambient temperatures in asexually-produced embryos. Presumably the same pathways are involved in both processes – it would be surprising if A. pisum were to have different sets of genes for the two modes of development. Diapause may therefore act to limit the speed of reactions that would otherwise occur more rapidly at higher temperatures, possibly through the action of an 'inhibitory factor' [22, 33]. According to this model, the higher the ambient temperature the greater the required activity of the inhibitory factor . When temperatures are maintained at abnormally high temperatures (16°C), regulation may be compromised with only some aspects of development slowed. This may result in embryos displaying a mosaic of developmental stages.
Alternatively, the malformed phenotypes seen at 16°C may result form differing levels of temperature independence for different developmental processes. There would be no selection on embryos to make later developmental processes temperature independent, as they normally occur during winter. At unnaturally high temperatures, for example 16°C, these later, temperature dependent processes, may occur prematurely, resulting in embryos displaying a mosaic of developmental stages. This hypothesis suggests that the timing of some developmental processes occurs independently, i.e. that the beginning of one developmental process is not contingent on the ending of another. This appears to be the case for katatrepsis, which occurs in smaller embryos at higher temperatures. Premature katatrepsis did not, in itself, cause the malformations. Embryos transferred to 16°C from 0–4°C on day 49 underwent early katatrepsis but displayed a high hatching success.
It is perhaps surprising that many embryos should develop abnormally at 16°C given that they would encounter temperatures as high, or higher, during winter in their natural environment. However, such high temperatures would be experienced only temporarily, and it may be persistent exposure to high temperatures that caused the developmental abnormalities in our experiment. Further research is therefore necessary to determine the influence of fluctuating temperatures on developmental progression, both with respect to developmental abnormalities and developmental rate.
There has been little progress towards identifying the genetic control of diapause in insects. The one system where diapause has been well elucidated, dauer formation in the nematode C. elegans, indicates that the insulin pathway plays an important role . Recent work on mutant Drosophila that mimic reproductive diapause in adults also suggests a role for insulin [35, 36]. Insulin, which regulates growth in other stages of development in Drosophila [37, 38], may therefore play a similar role during A. pisum diapause. Work on diapause in the flesh fly Sarcophaga crassipalpis has identified a second class of genes that may be involved in diapause regulation . These are the heat shock proteins, which are normally expressed during times of stress  and which provide cryptoprotection during diapause. Since heat-shock proteins are also involved in cell cycle arrest, however, they may play a more central role in the regulation of diapause . Heat-shock proteins are also typically heat inducible, and so fit with the concept of a temperature dependent 'inhibitory factor' . Additionally, high levels of heat-shock proteins may disrupt development , which could help explain the developmental defects observed in embryos maintained at 16°C. Further work on the expression of both insulin and heat shock proteins in A. pisum embryos will clarify their respective roles.
Diapause in the pea aphid involves a period of slow growth, the progression of which is temperature independent. There is no distinct resting stage, which is characteristic of diapause in many insects. Diapause in the pea aphid represents an extreme regulation of developmental rate and may be controlled by the same mechanisms that control developmental rate at other life stages.
We produced sexually reproducing male and female aphids by exposing asexual females from a single clone (LSR1, collected near Ithaca, NY) to 'autumnal' conditions (short-day illumination, 13L:11D, 16°C) for five weeks. Sexuals were collected and placed at a ratio of two males to eight females in 16 mm diameter petri dishes holding single leaves of Medicago arborea inserted into 3 ml of 2% agar with 1gL-1 of Miracle-Gro (The Scotts Company, OH). Every day we collected any eggs deposited on the leaves with a soft, moist paintbrush and transferred them to dampened filter paper placed in the lid of a 16 mm diameter petri dish. Each cohort of eggs therefore contained eggs laid over a 24-hour period. The eggs were then kept at 16°C 13L:11D for a further 14 days. On day 16 we sterilised the eggs by immersing them in 1% formaldehyde for 10 minutes and then washing them three times in double-distilled water. Sterilisation and washing took place in a Buchner funnel, with liquids being passed through the filter paper on which the eggs rested. The eggs remained on their original filter paper throughout, which, while still moist, was transferred to a fresh sterile petri dish. We then sealed the dishes with parafilm (United American Can, WI) and placed them in incubators (Model: I-30BLL, Percival Scientific, Inc., IA) for storage.
To determine the influence of temperature on the progression of development we stored the eggs under three temperature regimes, all with the same 13L:11D photoperiod: (1) 4°C in the light and 0°C in the dark; (2) constant 10°C; (3) constant 16°C. The first temperature regime most closely mimics natural conditions and has been previously used to successfully rear eggs to hatching . Under each temperature regime, eggs were sampled for dissection every seven days, starting on day 21. Preliminary experiments indicated that eggs maintained at 0–4°C hatched successfully when transferred to 16°C when approximately 100 days old. Consequently, eggs kept at 0–4°C were transferred to 16°C on day 98 for hatching. Eggs kept at 10°C were transferred to 16°C on day 78 for hatching. Additionally, a subset of eggs maintained at 0–4°C were transferred to 16°C on day 49 and sampled daily from day 50 to 59.
Egg fixing, dissection, and staining
Eggs were dechorionated in 50% bleach for 2 minutes. They were then transferred to a 0.5 mL eppendorf tube containing 4% paraformaldehyde in PBS:heptane (1:1) and agitated for 45 minutes. The paraformaldehyde was then replaced with methanol and the tube was shaken to pop the vitelline membrane. The embryos were then transferred to absolute methanol and stored at -20°C until dissection. Dissection began with the removal of the black serosal cutical by sticking the eggs to a microscope slide with double-sided sticky tape, covering with PBS, piercing the serosal cuticle and pushing out the embryo and yolk with a hypodermic needle. The embryos were then separated from the yolk using pulled glass-needles, again under PBS. In order to detect cell division during putative diapause, we immunostained the embryos with anti-phospho(S10)-acetyl(K14)-Histone H3 (anti-Histone H3) (rabbit immunoaffinity purified IgG, Upstate Group, Inc., MA). This anti-body recognizes Histone H3 phosphorylated at serine 10 and acetylated at lysine 14, which occurs only during mitotic cell division. Fixed embryos were washed for 30 minutes in 0.3% Triton-X 100 in PBS (PBT), and then blocked for 30 minutes with 2% Normal Goat Serum (NGS)/0.2% Bovine Serum Albumin (BSA) in PBT (BBT/NGS). Embryos were incubated for at least 2 hours at room temperature or overnight at 4°C with the primary antibody in BBT/NGS, and then washed four times in BBT. Embryos were blocked with BBT/NGS for 30 minutes prior to incubation with the biotin-conjugated secondary antibodies in BBT/NGS for at least 2 hours at room temperature or overnight at 4°C. Embryos were washed four times before being developed using the Vectastain ABC kit Elite (Vector, CA) and diaminobenzidine (Sigma Fast DAB). The embryos were subsequently mounted in 70% glycerol in PBS and their image digitized.
Embryo size measurement
The size of embryos was determined from their digitized image using the software IPlab (Scanalytics, Inc. VA). We measured both the total length of the embryo and the length of the third leg. Where the embryo was curled, the length was estimated as the sum of several linear measurements approximating the curvature of the embryo.
To determine whether the growth rate was influenced by temperature we plotted body and leg length against age in days under each of the different temperature regimes. The gradient of the line is the rate of growth. We statistically tested whether temperature influenced the rate of growth using the model:
body or leg length = a*age + b*temperature + c*(temperature*age) + k
We treated time as a continuous variable and rearing temperature as a categorical variable. We fitted this model to the data using a generalized linear model (GLM) with the program JMP 4.04 (SAS Institute, Inc., NC). This analysis gives estimates of the coefficients a, b, c and k, and tests whether they are significantly different from zero. The coefficient a gives the slope of the relationship between length and age and is the rate of growth. The coefficient b gives the relationship between temperature and length and indicates if embryos reared at a different temperatures are longer or shorter. The coefficient c indicates whether there is an interaction between the affects of temperature and age on length. If this interaction term is significantly different from zero it indicates that the slope of the relationship between length and age (rate of development) varies with temperature. All the data were log transformed prior to analysis to uphold assumptions of normality of error and homogeneity of variance.
We thank Christian Braendle and Greg Davis for their comments on early drafts of the manuscript. We thank Princeton University for funding this work.
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