Natural variation in life history and aging phenotypes is associated with mitochondrial DNA deletion frequency in Caenorhabditis briggsae
- Suzanne Estes1Email author,
- Anna L Coleman-Hulbert†1,
- Kiley A Hicks†1,
- Gene de Haan1,
- Sarah R Martha1,
- Jeremiah B Knapp1,
- Samson W Smith1,
- Kevin C Stein1 and
- Dee R Denver2
© Estes et al; licensee BioMed Central Ltd. 2011
Received: 22 April 2010
Accepted: 12 January 2011
Published: 12 January 2011
Mutations that impair mitochondrial functioning are associated with a variety of metabolic and age-related disorders. A barrier to rigorous tests of the role of mitochondrial dysfunction in aging processes has been the lack of model systems with relevant, naturally occurring mitochondrial genetic variation. Toward the goal of developing such a model system, we studied natural variation in life history, metabolic, and aging phenotypes as it relates to levels of a naturally-occurring heteroplasmic mitochondrial ND5 deletion recently discovered to segregate among wild populations of the soil nematode, Caenorhabditis briggsae. The normal product of ND5 is a central component of the mitochondrial electron transport chain and integral to cellular energy metabolism.
We quantified significant variation among C. briggsae isolates for all phenotypes measured, only some of which was statistically associated with isolate-specific ND5 deletion frequency. We found that fecundity-related traits and pharyngeal pumping rate were strongly inversely related to ND5 deletion level and that C. briggsae isolates with high ND5 deletion levels experienced a tradeoff between early fecundity and lifespan. Conversely, oxidative stress resistance was only weakly associated with ND5 deletion level while ATP content was unrelated to deletion level. Finally, mean levels of reactive oxygen species measured in vivo showed a significant non-linear relationship with ND5 deletion level, a pattern that may be driven by among-isolate variation in antioxidant or other compensatory mechanisms.
Our findings suggest that the ND5 deletion may adversely affect fitness and mitochondrial functioning while promoting aging in natural populations, and help to further establish this species as a useful model for explicit tests of hypotheses in aging biology and mitochondrial genetics.
Caenorhabditis elegans has long been appreciated as a useful model organism for developmental, molecular, and aging biology. As molecular genetic and genomic approaches have become increasingly available, nematode biologists have also become interested in explaining and predicting natural patterns of phenotypic and genomic evolution. These interests have motivated recent efforts to quantify natural phenotypic variation and molecular population genetic structuring, and to characterize the ecology and natural history of nematode species in order to interpret such findings within robust population and ecological genetic contexts [e.g., [1–5]]. Caenorhabditis briggsae was until recently the closest known relative of C. elegans and has therefore been the subject of many different types of comparative analyses [e.g., [6–9]]. Building upon previous discoveries of mitochondrial DNA (mtDNA) variation segregating among natural populations [10, 11], we sought to further develop the C. briggsae system by quantifying the degree to which this mtDNA diversity is associated with population-level variation in life-history, physiological, and aging related phenotypes. This work will provide a foundation for generating and testing hypotheses in mitochondrial mutation biology and aging research.
Mutations that impair functioning of the mitochondrial electron transport chain (ETC) are associated with a variety of human metabolic and age-related disorders [12–14]. A barrier to in-depth studies of the inheritance, population dynamics, and effects of clinically relevant mtDNA mutations has been the lack of genetic model systems that adequately represent the features of pathogenic mtDNA mutations . Howe and Denver  discovered a naturally occurring heteroplasmic mtDNA deletion segregating among geographically distinct populations of the soil nematode, Caenorhabditis briggsae. The deletion eliminates the 5' end (first 786 bp) of the NADH dehydrogenase subunit 5 (ND5) gene, the normal protein product of which is an essential and highly conserved core subunit of mitochondrial ETC complex I . In humans, several neurodegenerative disorders including Parkinson's disease are associated with heteroplasmic ND5 mutations .
Based on other studies of ETC complex I-deficient genotypes [15–18], we hypothesized that expression of truncated ND5 protein products would be associated with mitochondrial dysfunction, increased reactive oxygen species (ROS) production, reduced fitness, and faster rates of aging. Higher rates of nuclear [6, 19] and mitochondrial  mutation in C. briggsae relative to C. elegans and a negative correlation between ND5 deletion frequency and reproductive output in C. briggsae  are consistent with this hypothesis, although it cannot yet be ruled out that nuclear-encoded genes are responsible instead.
With the dual goals of further characterizing global phenotypic variation in C. briggsae and developing a novel model system for mitochondrial mutation dynamics, ETC dysfunction, and aging research, we performed a survey of natural variation in fitness, physiological, and aging related phenotypes among C. briggsae isolates containing different proportions of ND5-deletion bearing mtDNA genomes. We found significant among-isolate variation in all phenotypes studied, some of which was statistically associated with isolate-specific ND5 deletion heteroplasmy level. Specifically, C. briggsae isolates containing a high proportion of ND5 deletion genomes tended to have reduced reproductive fitness and early-onset physical decline compared to isolates with low or zero deletion levels. However, the same isolates did not differ consistently with respect to lifespan, ATP content, or acute oxidative stress resistance. Additionally, although the C. briggsae isolate with the highest ND5 deletion frequency exhibited the highest levels of ROS as expected, we found a non-linear relationship between ND5 deletion and ROS level. These patterns may be explained by as yet unknown differences in physiological adaptations among C. briggsae isolates; e.g., ROS detoxification mechanisms and reliance on anaerobic energy metabolism.
Results and Discussion
Phenotypic variation among C. briggsa e isolates
31.99 surviving offspring
103.8 surviving offspring
135.7 surviving offspring
Intrinsic rate of increase (r)
4.499 nM/mg protein
224.20 relative fluorescence units
To further quantify natural phenotypic variation and to test whether the observed relationships between fitness-related life history traits and ND5 deletion levels may be mediated by mitochondrial ETC functioning, we quantified the relationship between ND5 deletion level and several aspects of animal physiology. Our expectation was that, as a result of reduced mitochondrial ETC efficiency, higher-ND5 deletion isolates would exhibit reduced levels of ATP and oxidative stress resistance, together with increased ROS production compared to lower or zero-ND5 deletion isolates.
We found significant among-isolate variation for oxidative stress resistance as measured by survival times of worms during acute paraquat exposure (Table 1). We predicted that, if higher-ND5 deletion isolates experience mitochondrial dysfunction leading to increased endogenous ROS levels, these isolates would be less able to survive attack from exogenous sources of ROS. A weak but significant negative relationship existed between this form of oxidative stress resistance and ND5 deletion frequency (Table 1). This pattern was largely driven by two low-ND5 deletion isolates (PB800 and JU726) with high oxidative stress resistance (data not shown). We currently have no information on whether C. briggsae isolates vary in their expression of antioxidant proteins and thus in their abilities to detoxify ROS, which would provide one possible explanation for the weak relationship between paraquat-induced oxidative stress resistance and ND5 deletion heteroplasmy level.
Finally, relative ROS levels measured for pharyngeal bulbs also varied significantly among C. briggsae isolates (Table 1; Figure 5B). We measured total levels of mitochondrial oxidants using MitoSOX Red (Invitrogen). MitoSOX Red is preferentially taken up by actively respiring mitochondria, and while it is nearly exclusively oxidized by superoxide [31, 32]--the most common form of mitochondrially generated ROS--it is considered an accurate and effective system for measuring total ROS levels in vivo . In contrast to our simple expectation that a positive, linear relationship would exist between ND5 deletion frequency and ROS level, we found a significant, non-linear relationship between these variables such that zero and high deletion isolates tended to exhibit higher superoxide levels than low deletion isolates (Figure 5B legend). The in vivo fluorogenic dye-based method used here gives a view of net ROS level in living tissue and therefore reflects both the rate at which ROS are generated by cells and the rate at which they are scavenged by superoxide dismutases and other antioxidant systems. Consequently, we do not yet know which of these sources of variability explain more of the variance in net ROS levels among isolates, which was considerable despite modest sample sizes (Table 1). This variation suggests that C. briggsae may provide a useful system in which to test whether endogenous ROS have a role in generating variability in spontaneous mutation rates .
Thus, while more work is required to understand whether and how the ND5 deletion directly affects mitochondrial functioning in C. briggsae, it is clear that there is no simple relationship between isolate-specific net ROS production and the detrimental phenotypes associated with high ND5 deletion heteroplasmy levels in nature. For example, both Japanese isolates, HK104 and HK105, exhibit low fitness (Figure 2) and pharyngeal pumping rates (Figure 4), but their relative levels of superoxide (and ATP) are quite different from one another (Figure 5). These results may indicate that C. briggsae isolates experience different forms of mitochondrial dysfunction [Figure 3 in ] that may or may not be related directly to the ND5 deletion.
The limited molecular population genetic structuring of C. briggsae [, but see ] belies the striking phenotypic variation among isolates reported here, the latter of which suggests an immense capacity for evolution of aging and life-history phenotypes. Together with previous findings of geographic variation in mitochondrial genome content among C. briggsae isolates  and of elevated spontaneous mutation rates in some isolates relative to the C. elegans N2 lab strain [6, 19, 20], the findings from this paper suggest that C. briggsae will provide an opportunity to understand the linkages between mitochondrial function (e.g., ROS production), mutation processes, and aging. And importantly, because C. briggsae contains naturally-occurring mtDNA variation that is likely to affect organismal fitness, this system offers a major advantage for studying the evolutionary dynamics of mtDNA mutations over C. elegans where the majority of mtDNA mutant strains have been isolated from laboratory mutagenesis screens.
Although we found no straightforward relationship between ND5 deletion frequency and relative ROS levels, our accumulated findings are consistent with the notion that the natural mitochondrial genetic variation observed among C. briggsae isolates is detrimental to the organism. This is particularly true in light of recent studies that show high mutation rates in high-ND5 C. briggsae isolates [6, 19, 20], Nevertheless, two issues prevent us from demonstrating that the ND5 deletion is the root cause of the detrimental phenotypes: 1) ND5 deletion level is clearly confounded with phylogenetic relationship (e.g., two of our three "high-deletion" isolates are sister taxa from Japan; Figure 1), and 2) we cannot disentangle the effects of among-isolate variation in ND5 deletion level from among-isolate nuclear variation on the phenotypes studied here. However, the ability to generate inbred lines and mitochondrial-nuclear hybrid strains in which mitochondria from natural C. briggsae isolates with different ND5 deletion heteroplasmy levels may be evaluated on uniform nuclear genetic backgrounds  will be a major advantage of this nematode system. (A large-scale analysis of such hybrid strains will be reported elsewhere.) A congener of the well-known model nematode, C. elegans, C. briggsae has a similar life-history and mating system, and offers many of the same advantages as C. elegans as an animal genetic model system . Together with the ample among-isolate variation in ND5 deletion heteroplasmy level (Figure 1B)  and aging-related phenotypes, we contend that the C. briggsae system offers a powerful and versatile model for understanding the interplay between mitochondrial dysfunction and aging in an evolutionary context, as well as the basic biology underlying mtDNA deletion genetics. This study lays the necessary groundwork to rigorously test these and other questions in aging biology and life history theory [e.g., ].
Nematode strains and culture conditions
As described in , the ΨND5-2 pseudogene directly upstream of ND5 (Figure 1A) is required for the ND5 deletions to occur within C. briggsae. Directly repeated nucleotide sequences occur within ND5 and ΨND5-2 that promote direct repeat-associated deletion events. Isolates in the "Kenya" clade (Figure 1B) provide natural outgroup controls because they lack ΨND5-2 and are thus inherently unable to experience the ND5 deletions. The among-isolate variability in average heteroplasmy level is thought to also be partly accounted for by the presence of compensatory sequences within the mtDNA of certain populations (Figure 1B legend). These sequences, present at the ΨND5-2 direct repeat associated with the deletions, appear to prevent the deletion by reducing sequence homology between ΨND5-2 and ND5 and to thereby place an upper limit on the proportion of ND5-deletion bearing genomes able to accumulate within individuals . We chose to use a subset of nine natural C. briggsae isolates studied by  that captured the full range of ND5 deletion heteroplasmy level (Figure 1, Additional file 1, Table S1). All nematodes were grown under standard laboratory conditions on 15 mm plates with NGM and Escherichia coli strain HB101. All nine natural isolates were included in each analysis.
Isolate-specific fecundities were estimated for each natural isolate following . ''Early fecundity'' is the number of offspring produced on the first two days of reproduction combined; ''late fecundity'' is the number of offspring produced on the third and fourth days of reproduction. We also calculated total lifespan as the number of days lived from the egg stage. We calculated intrinsic rate of increase, r, for each natural isolate by solving Σe*** l(x) m(x) for r, where l(x) is the proportion of worms surviving to day x and m(x) is the fecundity on day x. We also quantified average correlations among life history traits across C. briggsae isolates to investigate whether the magnitude or pattern of these trait associations would change with increasing ND5 deletion frequency.
We measured the decline of pharyngeal pumping rate with age among C. briggsae isolates. Caenorhabditid nematodes ingest soil bacteria using rhythmic contractions of the pharynx - a neuromuscular organ comprising 20 muscle cells and 20 neurons. As in humans, muscle organization and function in nematodes deteriorates with chronological age. The rate of pharyngeal pumping is known to decline steadily with age in C. elegans as a result of contraction-related cellular injury [27, 40]. Pharyngeal pumping was quantified for the same 10 to 20 individuals per isolate beginning two days after the L4 stage, and every other day until death. Daily pharyngeal pumping rates were taken as the average of three 5-second counts, converted to pumps per minute.
ATP content was measured using a protocol adapted from [, B. Braeckman, pers. comm.] for 8-10 independent, age-synchronous samples of young adult nematodes from each isolate. ATP content was determined for 50 uL of supernatant using the ATP Bioluminescence Assay Kit CLS II (Roche) and following the manufacturer's instructions. ATP measurements were standardized by total protein content using a BCA Kit (Pierce).
Oxidative stress resistance
We measured resistance of C. briggsae to acute paraquat exposure following . Age-synchronized populations of post-reproductive (8 day old) worms were generated for each natural isolate. Sixteen individuals per isolate were exposed to 300 mM paraquat in S-basal and scored for survival every 5 minutes. Worms that remained completely unresponsive after three taps with a glass prod were scored as dead.
Relative superoxide production
We followed the basic approach of  to quantify relative ROS levels among C. briggsae isolates. Briefly, age-synchronized worms were incubated for 24 hours in 10 uM MitoSOX Red (Invitrogen) before being transferred as young adults to fresh NGM plates seeded with non-labeled HB101 E. coli. They were allowed to feed for 1 hour, and paralyzed using a drop of 5M levamisole prior to imaging. Images were acquired using a high resolution wide field Core DV system (Applied Precision™), equipped with an Olympus IX71 inverted microscope mounted with a Nikon Coolsnap ES2 HQ camera (Advanced Light Microscopy Core Facility, Oregon Health and Science University, Portland, OR). Fluorescent, z-stack images of the mitochondrial-rich pharynx with a 1.0 second exposure time were captured at 60X magnification. Images were deconvolved prior to analysis. Terminal pharyngeal bulbs were manually circled to quantify mean fluorescence intensity of the area in exposed and unexposed (control) animals for each strain using ImageJ software (NIH). The final pharyngeal bulb intensity values were calculated as the difference between intensity values for exposed and control worms.
Although the use of mitochondria-specific dyes has become a widely used and accepted method for measuring a variety of mitochondrial traits in vivo, a caveat is that differential dye uptake between samples could lead to inaccurate interpretation of fluorescence differences. There is currently no means of determining the extent to which this occurs . However, great care was taken to minimize all other sources of error. For example, we exposed only one sample at a time to the microscope light source and used the shortest exposure time possible to avoid introducing variation due to breakdown of the dye.
We analyzed among-isolate variation using separate one-way analyses of variance (ANOVA) for each phenotype measured. To test for differences between pairs of isolates, least-squares contrasts (Tukey's HSD for all pairwise comparisons; ) were performed on the data for each trait. To test for associations between traits and ND5 deletion levels, we calculated Pearson correlation coefficients between trait values and isolate-specific ND5 deletion percentages, and applied one-way ANOVA to data categorized as being from high, low, or zero-ND5 deletion isolates (see Figure 1B legend). Finally, we characterized correlations among life-history characters measured on the same individuals by calculating Spearman rank correlation coefficients between each pair of traits following .
We are deeply appreciative of the K. Garlid lab for willingness to share protocols and equipment, and of A. Snyder (Advanced Light Microscopy Core Facility, OHSU) and the B. Braekman lab for generous technical advice and assistance. We also thank H. Bui, S. Anderson, and T. Polley for laboratory assistance, and D. Howe and three anonymous reviewers for helpful suggestions on the manuscript. This work was supported by NSF grant DEB-0743871 (SE and DRD), PSU Faculty Enhancement Grant (SE), and PSU Undergraduate Scholarly and Creativity Grants (ACH and JK).
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