Bacterial Respiration and Growth Rates Affect the Feeding Preferences, Brood Size and Lifespan of Caenorhabditis elegans.

Bacteria serve as live food and nutrients for bacterial-feeding nematodes (BFNs) in soils, and influence nematodes behavior and physiology through their metabolism. Five bacterial taxa (Bacillus amyloliquefaciens JX1, Variovorax sp. JX14, Bacillus megaterium JX15, Pseudomonas fluorescens Y1 and Escherichia coli OP50) and the typical BFN Caenorhabditis elegans were selected to study the effects of bacterial respiration and growth rates on the feeding preferences, brood size and lifespan of nematodes. P. fluorescens Y1 and E. coli OP50 were found to be more active, with high respiration and rapid growth, whereas B. amyloliquefaciens JX1 and B. megaterium JX15 were inactive. The nematode C. elegans preferred active P. fluorescens Y1 and E. coli OP50 obviously. Furthermore, worms that fed on these two active bacteria produced more offspring but had shorter lifespan, while inactive and less preferred bacteria had increased nematodes lifespan and decreased the brood size. Based on these results, we propose that the bacterial activity may influence the behavior and life traits of C. elegans in the following ways: (1) active bacteria reproduce rapidly and emit high levels of CO2 attracting C. elegans; (2) these active bacteria use more resources in the nematodes' gut to sustain their survival and reproduction, thereby reducing the worm's lifespan; (3) inactive bacteria may provide less food for worms than active bacteria, thus increasing nematodes lifespan but decreasing their fertility. Nematodes generally require a balance between their preferred foods and beneficial foods, only preferred food may not be beneficial for nematodes.

Introduction

Diet provides carbohydrates, fats, proteins and other nutrients to support the growth and daily activities of animals [1]. Diet also influences an animal's behavior and life traits such as fecundity and aging. Bacteria are food for bacterial-feeding nematodes (BFNs) in soils, and BFNs require numerous bacteria to sustain growth, as an individual worm requires as many as 103−105 bacteria per day [2]. Therefore, bacterial quality and metabolism play important roles in regulating BFNs feeding behavior and life traits.

In nature, animals must make decisions regarding what to eat [3]. The ability to locate and access food is critical for survival and reproduction. n class="Chemical">BFNs enpan>counter manpan>y types of bacteria inpan> soils ranpan>ginpan>g from benpan>eficial to harmful. They should therefore evaluate their prey before makinpan>g a feedinpan>g choice. In the lab, pan> class="Chemical">BFNs exhibit distinct feeding preferences for different bacteria [4-6]. For example, Salinas et al. [5] found that Cephalobus brevicauda strongly prefers gram-negative and small-celled bacteria. Shtonda and Avery [7] concluded that C. elegans searches for high quality food that best supports its growth and avoids unfavorable bacteria. Some experimental evidence has shown that C. elegans can distinguish between pathogenic and nonpathogenic bacteria and avoid the former [8-10]. However, other factors that affect BFNs feeding choices remain unclear. Many insect species use CO2 as an olfactory signal to locate food or hosts [11]; therefore, we hypothesize that the concentration of CO2 released through bacterial respiration could influence BFNs feeding behavior.

Bacteria can not only influence the feeding behavior of n class="Chemical">BFNs, but also regulate nematodes lifespanpan> anpan>d brood size accordinpan>g to bacteria availability [12,13]. Lifespanpan> anpan>d fertility are recognpan>ized as basic life traits of organpan>isms anpan>d diet has signpan>ificanpan>t effects onpan> organpan>ismal lifespanpan> anpan>d fertility [14-16]. pan> class="Species">C. elegans fed E. coli OP50 were found to have shorter lifespan than those fed E. coli HT115 [17]. MacNeil et al. [13] found that C. elegans fed the soil bacteria Comamonas DA1877 had lower reproduction and shorter longevity than worms fed E. coli OP50. In another study, the preferred bacteria of Cephalobus brevicauda resulted in the lowest reproduction of nematodes [5]. In addition, Coolon et al. [18] found that C. elegans preferred Pseudomonas sp. over B. megaterium but that worms lived longer on B. megaterium than on Pseudomonas sp. As bacteria are a live food, we hypothesize that bacterial activity may have direct or indirect effects on BFNs lifespan and brood size.

The type, size, pathogenicity and n class="Disease">toxicity of bacteria canpan> all affect pan> class="Chemical">BFNs. Moreover, bacterial respiration and growth rates can also affect BFNs. Some researchers have focused on the effects of bacterial respiration on the lifespan of C. elegans [19]. Bacterial respiration may be an indicator of bacterial activity and bacterial population size and thereby influence BFNs behavior and life traits. Bacteria respire to release CO2, which could influence BFNs sensitivity, and bacterial respiratory strength also affects their ability to colonize in the BFNs guts [19]. In this work, we selected five bacterial species (Bacillus amyloliquefaciens JX1, Variovorax sp. JX14, Bacillus megaterium JX15, Pseudomonas fluorescens Y1 and Escherichia coli OP50) and the typical model BFN C. elegans for experimentation. We aimed to (1) determine the feeding preferences of C. elegans and the effects of bacterial respiration and growth rates on nematode feeding preferences; (2) evaluate the effects of bacteria on the lifespan and brood size of C. elegans; (3) explore the relationships between bacterial activity and C. elegans feeding preferences, lifespan and brood size.

Materials and Methods

Preparation of bacteria

Soil bacteria were obtained from a sandy loam alluvial soil collected from Banqiao Town, Nanjing City, Jiangsu Province, China. No specific permissions were required for the described field studies. We confirmed that the location of the soil collection was not privately owned or protected in any way, and the field studies did not involve endangered or protected species. The bacteria were obtained by plating a serial dilution of soil suspension onto n class="Chemical">LB medium dishes (10 g L-1 tryptonpan>e, 5 g L-1 pan> class="Species">yeast extract, 10 g L-1 NaCl, and 17 g L-1 agar, pH 7.0); then, the bacteria were purified by picking up the single colony onto LB medium. Finally, we selected 4 representative species of bacteria for our experiments. All of these species were sequenced by 16S rRNA genes (Table 1). Additionally, the four bacteria, along with E. coli OP50 obtained from the CGC (Caenorhabditis Genetics Center, USA), were prepared in liquid LB medium freshly at a shaking speed of 180 rpm, and the bacterial OD600 values were normalized to 1.

Table 1

Descriptions of the bacteria used for the experiments.

Bacteria	Shape	Gram stain	Accession number
B. amyloliquefaciens JX1	rod	G+	JX424611
Variovorax sp. JX14	rod	G-	JX424612
B. megaterium JX15	rod	G+	JX424613
P. fluorescens Y1	rod	G-	KC962432
E. coli OP50	rod	G-	-

Preparation of nematodes

Caenorhabditis elegans N2 obtained from the CGC were cultivated on freshly prepared nematode growth medium (NGM) (3 g NaCl, 2.5 g peptone, 17 g agar and 975 ml H2O, autoclaved; cooled to 55°C, further added 1 ml 1 M CaCl2, 1 ml 5 mg/ml cholesterol in ethanol, 1 ml 1 M MgSO4 and 25 ml 1 M KPO4 buffer, and filtered through 0.22 μm filter). Petri plates seeded with E. coli OP50, a standard bacterial food source for C. elegans in the lab [20]. Any petri plates contaminated with fungi or other bacteria should be discarded.

The worms were cultured at 20°C for 10 days, rinsed with M9 buffer (5 g NaCl, 3 g KH2PO4, 6 g Na2HPO4, 1 mL 1 M MgSO4, H2O to 1 L autoclaved) and collected by the modified Baermann funnel method using sterile beakers and tissue papers. The nematodes were transferred to capped, sterile 10 mL centrifuge tubes at room temperature and washed 5 times with M9 buffer to remove the E. coli OP50 from the nematode cuticle. The worms were then transferred to capped, sterile 5 mL centrifuge tubes containing 3 mL M9 buffer and they should be starved for 24 h at 20°C. For the feeding preferences experiment, nematodes mixed with adult and juvenile worms were concentrated in the collection tubes to a density of 1500 nematodes per 20 μL in M9 buffer.

Healthy gravid 3-day-old adult nematodes were harvested by rinsing the surfaces of the Petri dishes with n class="Chemical">M9 buffer at room temperature anpan>d thenpan> tranpan>sferred to 10 mL cenpan>trifuge tubes, usinpan>g 2–3 mL pan> class="Chemical">M9 buffer per plate. M9 buffer was added to a total volume of 8 mL, and most of the bacteria were removed from worms after washing 3 times at 5000 g for 3 minutes at 4°C. Next, 6 mL sterile H2O and 2 mL bleach (mixed with 1:2 v/v of 5 M NaOH and 5% NaClO solution) were added to the tubes. The tubes were shaken for a few seconds per minute for a total of 8 minutes. The liquid was discarded after centrifugation at 5000 g for 3 minutes at 4°C. The sediment was then washed 4 times with M9 buffer. This process killed the gravid adult worms and released the eggs, which remained intact and surface-sterilized. The eggs were cultured in M9 buffer overnight at 20°C for hatching, and the hatched larvae were transferred to freshly prepared NGM plates, which had been seeded with one of the five bacteria (Table 1). The dishes were then placed in a dark environment at 20°C for the nematodes rearing. Each week, worms were transferred to newly prepared NGM plates with the corresponding bacterium to ensure that the nematodes and their offspring could stay under the same and fresh conditions. These nematodes were prepared to use for the lifespan and brood size assays.

Feeding preferences experiment

This experiment was conducted to determine the preferences of n class="Species">C. elegans for differenpan>t bacteria, usinpan>g 90 mm diameter Petri dishes filled with NGM. Each dish was divided inpan>to five equal sectionpan>s conpan>tainpan>inpan>g a 15-mm diameter dot-circle that was 20 mm from a cenpan>ter circle where the worms were placed (Fig 1). In each sectionpan>, the dot-circle was definpan>ed as the ‘bacterial zonpan>e’, anpan>d the remainpan>der of the sectionpan> was definpan>ed as the ‘nonpan>-bacterial zonpan>e’. The five bacterial suspenpan>sionpan>s (20 μL) were ranpan>domly placed onpan> the bacterial zonpan>e respectively. Approximate 1500 inpan>dividual nematodes were placed onpan> the cenpan>ter circle, with 10 replicates. All dishes were placed at ranpan>dom inpan> a dark inpan>cubator at 20°C. The number of nematodes that migrated to each bacterial zonpan>e anpan>d nonpan>-bacterial zonpan>e was recorded pan> class="Species">at 1, 2, 4, 8, 12, 24, 36, and 48 hours under a stereomicroscope at 50 × magnification.

Fig 1

Feeding preferences experiment.

At time point 0, nematodes were placed in the center of the dish and the bacteria were placed on the surrounding circles; the dishes were then stored in the dark at 20°C. Over time, the worms moved away from the center and toward the bacterial zone (indicated by the five circles with dots) and non-bacterial zone (the remainder of the dish). The worms in the bacterial and non-bacterial zones were counted at 1, 2, 4, 8, 12, 24, 36, 48 hours.

At time point 0, nematodes were placed in the center of the dish and the bacteria were placed on the surrounding circles; the dishes were then stored in the dark at 20°C. Over time, the worms moved away from the center and toward the bacterial zone (indicated by the five circles with dots) and non-bacterial zone (the remainder of the dish). The worms in the bacterial and non-bacterial zones were counted n class="Species">at 1, 2, 4, 8, 12, 24, 36, 48 hours.

Bacterial respiration experiment

Liquid NGM medium was autoclaved, and 25 mL of this medium was transferred to the sterilized 130 mL saline bottles. The bacteria (100 μL) with OD600 values normalized to 1 were added to the liquid NGM, and then the bottles were sealed with soft air-tight lids and cultured in the dark at 20°C. The CO2 concentration was measured at 1, 2, 4, 8, 12, 24, 36, and 48 hours by gas chromatography (GC, Agilent 7890A, USA).

Bacterial growth rate experiment

Liquid n class="Chemical">NGM medium was autoclaved anpan>d 50 mL of the medium was tranpan>sferred to the sterilized 150 mL trianpan>gular flasks. The bacteria (500 μL) with OD600 values normalized to 1 were added to these trianpan>gular flasks, with 6 replicates per strainpan>. Thenpan>, the flasks were cultured inpan> the dark at 20°C with a shakinpan>g speed of 180 rpm. We counted the number of colonpan>y-forminpan>g units (CFUs) at each hour for the first 8 hours anpan>d thenpan> every two hours up to 48 hours. Each sample was diluted to a suitable conpan>cenpan>trationpan>, anpan>d 100 μL of the diluted samples was spread onpan>to anpan> LB pan> class="Chemical">agar plate, followed by incubation at 30°C for 12–18 hours. The number of colonies formed was counted. To compare the growth rates of the different bacteria, we calculated the doubling time as where t1 and t2 represent two different times during the mid-exponential phase and W1 and W2 represent the number of colonies at t1 and t2, respectively [21].

Nematode lifespan experiment

The survival analysis of worms cultured on the different tested bacteria was carried out at 20°C. On day 0, ten L1 stage nematodes (P0) were transferred to their corresponding n class="Chemical">NGM medium plates with fresh bacteria. Ten replicates were performed for each different bacterial strain. Surviving P0 worms were counted and transferred to fresh dishes daily until all of the worms had died. A worm was considered dead when it ceased moving and did not respond to a gentle touch with a platinum wire.

Nematode brood size experiment

The brood size analysis of worms cultured on the different bacteria was performed in the analog condition with the survival analysis described above. One L4 stage nematode was randomly selected from each bacterial plate (n class="Chemical">NGM medium) and placed to a fresh plate with the corresponding bacterium as food. Ten replicates per strain were used. The worms were transferred to fresh dishes daily until they stopped laying eggs, and the number of eggs was recorded every day. The nematode brood size was determined based on the sum of total eggs laid by individual n class="Disease">hermaphrodites.

Statistical analysis

One-way analysis of variance (ANOVA) was used to analyze the following items: (1) the numbers of nematodes remaining in the bacterial and non-bacterial zones at each time point, (2) the bacterial growth rate and n class="Chemical">CO2 conpan>cenpan>trationpan> released by bacterial respirationpan>, anpan>d (3) the brood size anpan>d lifespanpan> of pan> class="Species">C. elegans cultured with the five different bacteria. Duncan’s test (p < 0.05) was used to assess significant differences among the means. All statistical analysis was conducted using SPSS 16.0.

Results

Feeding preferences

n class="Species">C. elegans exhibited pronpan>ounced feedinpan>g preferenpan>ces inpan> our experimenpan>t. The number of pan> class="Species">C. elegans that moved to the five bacterial zones increased initially, particularly toward the P. fluorescens and E. coli lawns. However, the number of nematodes on the B. amyloliquefaciens and B. megaterium lawns decreased at 4 h and 8 h, respectively. The number of C. elegans remaining in the bacterial and non-bacterial zones showed an opposite trend after 4 hours (Fig 2), with more C. elegans in the bacterial zone than in the non-bacterial zone (Fig 2).

Fig 2

Numbers of C. elegans in the bacterial zone and non-bacterial zone with different bacteria.

a, b, c, d, and e represent B. amyloliquefaciens JX1, Variovorax sp. JX14, B. megaterium JX15, P. fluorescens Y1 and E. coli OP50, respectively. Error bars represent standard errors.

At the first hour, the number of n class="Species">C. elegans movinpan>g to the pan> class="Species">Variovorax sp. lawn was significantly higher than the number of worms moving to the other four bacterial lawns (p < 0.05, Fig 3a). However, the nematodes changed their choices shortly thereafter, with P fluorescens becoming the most preferred bacteria of C. elegans at 4 h, followed closely by E. coli; both bacteria were preferred over Variovorax sp., followed by B. megaterium and B. amyloliquefaciens (Fig 3c). This trend continued until the end of the experiment (Fig 3h). At 24 h, we observed an increase in the number of nematodes moving to the Variovorax sp. lawn, but there were still far fewer worms on Variovorax sp. than on either P. fluorescens or E. coli (Fig 3f).

Fig 3

Variations in the number of C. elegans in the bacterial zone at different time points.

Results are shown as box plots. a, b, c, d, e, f, g, and h represent 1, 2, 4, 8, 12, 24, 36, and 48 hours, respectively. B. a, V. s, B. m, P. f, E. c denotes B. amyloliquefaciens JX1, Variovorax sp. JX14, B. megaterium JX15, P. fluorescens Y1 and E. coli OP50, respectively (these abbreviations used in the following figures show the same meaning).

Overall, C. elegans exhibited a hierarchy of food preferences, with P. fluorescens being the most preferred isolate, followed by E. coli, Variovorax sp. and B. megaterium; B. amyloliquefaciens was the least preferred (Fig 3).

Bacterial respiration

The n class="Chemical">CO2 conpan>cenpan>trationpan>s released by the five bacteria were signpan>ificanpan>tly differenpan>t (p < 0.05, Fig 4). In the first 4 hours, pan> class="Species">E. coli produced the highest concentration of CO2 (Fig 4a–4c). Thereafter, the respiration of P. fluorescens was significantly (p < 0.05) higher than that of E. coli, followed by Variovorax sp., B. amyloliquefaciens and B. megaterium (Fig 4d). Over time, the bacteria produced increasing amounts of CO2 (Fig 4e–4h). From 8 hours to 48 hours, P. fluorescens released significantly more CO2 than the other four bacteria, except at 24 hours (Fig 4d–4h). We also used a Clark-type electrode (Hansatech, UK) to measure the respiration of the bacteria on vented solid NGM plates resuspended in 1 mL of sterilized water. There were no significant differences observed between these two methods (data not shown).

Fig 4

Bacterial respiration measured as CO2 released.

Error bars represent standard errors, and letters over the error bars represent significant differences in bacterial respiration (p<0.05). a, b, c, d, e, f, g, and h represent 1, 2, 4, 8, 12, 24, 36, and 48 hours, respectively. The ordinate of Fig 4a–4d differs from the ordinate of Fig 4e–4h.

Bacterial growth rates

We found that P. fluorescens had the fastest growth rate, and B. megaterium had the slowest (Table 2). There was a strong correlation between bacterial respiration and bacterial growth rates (Table 2 and Fig 4). Considering the respiration and growth rates of the bacteria, we defined those bacteria with relatively high respiration rates and rapid growth as active bacteria and those with relatively weak respiration and slow growth as inactive bacteria. Accordingly, P. fluorescens and E. coli were categorized as active bacteria, whereas B. amyloliquefaciens and B. megaterium were categorized as inactive bacteria.

Table 2

Bacterial growth rates.

Bacteria	Doubling time (h)
B. amyloliquefaciens JX1	1.78±0.10b
Variovorax sp. JX14	1.35±0.08b
B. megaterium JX15	2.44±0.29a
P. fluorescens Y1	0.42±0.00c
E. coli OP50	1.44±0.03b

Values are the means of the bacterial doubling time ± standard error.

Values with the same letter within a column indicate no significant difference (p>0.05).

Nematode lifespan and brood size

Compared to n class="Species">E. coli, all the other four soil bacteria were found to prolonpan>g the lifespanpan> of pan> class="Species">C. elegans (Fig 5a). Nematode lifespan is generally measured as the time to death for 50% of the worms [18, 22, 23]. The bacteria that most increased the lifespan of C. elegans was B. amyloliquefaciens, increasing it up to 80% (p < 0.01), followed by Variovorax sp., B. megaterium, and P. fluorescens (Fig 5a). In contrast to their effects on lifespan, these four soil bacteria strongly decreased the brood size of C. elegans relative to E. coli (Fig 5b). Moreover, the impacts of these four soil bacteria on worm brood size were significantly different (p < 0.05, Fig 5b). Except for B. amyloliquefaciens, the bacteria had seemingly opposite effects on C. elegans lifespan and brood size, extending the former but decreasing the latter.

Fig 5

Effects of different bacteria on lifespan and brood size of C. elegans.

(a) A survival curve showing the proportion of surviving worms in different bacterial environments at different times. Error bars represent standard errors. (b) Brood size indicates the ability of C. elegans to produce offspring in association with different bacterial isolates. Error bars represent standard errors, and letters over error bars represent significant differences in brood size.

(a) A survival curve showing the proportion of surviving worms in different bacterial environments at different times. Error bars represent standard errors. (b) Brood size indicates the ability of n class="Species">C. elegans to produce offspring in association with different bacterial isolates. Error bars represent standard errors, and letters over error bars represent significant differences in brood size.

Discussion

n class="Chemical">BFNs consume a diverse variety of bacteria in soils, regulating the community, population, activity and phenotype of bacteria [24-29]. In turn, bacteria also affect the feeding behavior, lifespan and brood size of n class="Chemical">BFNs [19, 30–32].

It is possible that the bacterial cells or their metabolism release a food signal that attracts the worms [33]. In the feeding preferences experiment, we found that n class="Species">C. elegans exhibited marked food preferenpan>ces for pan> class="Species">P. fluorescens Y1 and E. coli OP50 (Figs 2 and 3). When starved C. elegans encountered the five different bacteria, they initially showed random movement, presumably because they needed time to make decisions [34]. Subsequently, most of the worms moved to P. fluorescens Y1, which grew the fastest and emitted the highest concentration of carbon dioxide of the bacteria tested (Table 2, Figs 3 and 4). Thus, the CO2 gas released by bacterial respiration may be the food signal that attracted the starved C. elegans. Dusenbery [35] proposed that CO2 in basic solutions attracts C. elegans. Rasmann et al. [36] also suggested that CO2 is universally used as a cue to attract nematodes. However, other studies have demonstrated that C. elegans displays acute avoidance of CO2 under some conditions [37, 38]. These studies have also acknowledged that starved nematodes exhibit reduced CO2 avoidance [38], because C. elegans olfactory discrimination and acuity are enhanced during starvation [39]. Higher CO2 concentrations could indicate a larger and fresher bacterial population, an interpretation consistent with the results of our bacterial growth rate experiment (Table 2 and Fig 4); as a result, active bacteria, which release more CO2 and offer more food than inactive bacteria, attract C. elegans. Based on these ideas, we postulated that bacterial activity has significant effects on the feeding preferences of starved nematodes (Table 2, Figs 3 and 4). Additionally, gram-negative bacteria were much preferred by C. elegans over gram-positive bacteria (Figs 2 and 3). This result is consistent with previous studies showing that soil bacterial-feeding organisms prefer gram-negative bacteria over gram-positive bacteria [5, 40, 41].

However, nematodes feeding on the preferred, highly active bacteria n class="Species">P. fluorescens Y1 anpan>d pan> class="Species">E. coli OP50 had significantly shorter lifespan than those feeding on the less preferred, weakly active bacteria (Fig 5a). This suggests that bacterial activity may be harmful to BFNs. Bacterial activity affects bacterial colonization in the gut of nematodes, and bacterial colonization and proliferation in the intestine are considered to be major contributors to the death of nematodes [30]. Increases in CO2 concentration released by bacterial respiration have been found to be accompanied by decreases in O2 concentration [42]. Bacteria living around BFNs or within the BFNs intestine compete with BFNs for O2 and utilize resources within the BFNs intestine. Therefore, bacterial respiration and population growth in the nematodes gut may significantly affect nematodes lifespan. Portal-Celhay et al. [32] proposed that an intensively negative relationship between the lifespan of C. elegans and bacterial populations exists in the nematode’s intestine. The lifespan of C. elegans can be significantly increased by a diet lacking coenzyme Q [12, 43]. Similarly, Gomez et al. [19] reported that the longevity of C. elegans fed diets of respiratory deficient E. coli was dramatically enhanced compared to those fed E. coli OP50. Gomez et al. [19] also postulated that respiring E. coli utilize D-lactic acid and other metabolites in the nematodes guts as fuel for proliferation. In light of these studies, our findings suggest that P. fluorescens Y1 and E. coli OP50, both of which demonstrated high respiration and rapid reproductive rates, consumed more resources and metabolites in the intestine of nematodes than the other bacteria, thereby decreasing the lifespan of C. elegans (Table 2, Figs 4 and 5a). Thus, the most preferred food may not be the healthiest food for nematodes.

Compared to the active bacteria n class="Species">P. fluorescensY1 anpan>d pan> class="Species">E. coli OP50, the inactive bacteria increased the lifespan of C. elegans (Fig 5a) but significantly decreased the brood size (Fig 5b). Our results also show a negative correlation between lifespan and brood size in C. elegans (Fig 5), which may be related to their life strategies. It is well known that r-strategist nematodes usually produce large numbers of eggs and have a short life cycle, whereas k-strategist nematodes have a low reproductive rate and a long life cycle [44-46]. Recently, more studies have focused on the relationship between lifespan and reproduction [47-49]. Partridge et al. [50] suggested that longevity and reproduction have a negative relationship with each other in model organisms. Barnes et al. [51] stated that increased reproduction was accompanied by a decreased lifespan in various organisms. Furthermore, dietary restriction, which is a popular study subject, might increase lifespan but inhibit reproduction in organisms [52]. When cultured with less favorable bacteria, nematodes ate fewer of them, increasing their lifespan but decreasing their reproduction, similar to dietary restriction. Food plays an important role in determining how reproduction affects lifespan [52]. In an unfavorable environment, organisms reduce their reproduction and increase their lifespan until the environment improves [53]. However, Salinas et al. [5] found that Cephalobus brevicauda had the lowest reproductive rate when fed its preferred bacteria. However, our brood size experiment demonstrated that C. elegans cultured with its preferred bacteria P. fluorescens Y1 and E. coli OP50 produced many more eggs than nematodes cultured with their less preferred bacteria (Figs 3 and 5). On low quality food, BFNs decrease their fecundity, employing resources reallocation to support lifespan processes [54]. In a less favorable bacterial environment, C. elegans decreased its brood size, allocating resources to support lifespan processes. This reallocation may be why less preferred bacteria extended the lifespan of C. elegans but decreased its brood size.

In conclusion, bacterial activity, including bacterial growth rate and bacterial respiration, directly and positively affect the feeding preferences and brood size of n class="Species">C. elegans, but they negatively inpan>fluenpan>ce the worms’ lifespanpan>. The most preferred food may not be the most benpan>eficial food for pan> class="Species">C. elegans, and therefore, worms may need to balance their consumption of preferred vs. beneficial bacteria.