Browse Subject Areas

Click through the PLOS taxonomy to find articles in your field.

For more information about PLOS Subject Areas, click here.

  • Loading metrics

Reduced Gut Acidity Induces an Obese-Like Phenotype in Drosophila melanogaster and in Mice

  • Wei-Sheng Lin ,

    Contributed equally to this work with: Wei-Sheng Lin, Cheng-Wen Huang, You-Sheng Song

    Affiliations Graduate Institute of Brain and Mind Sciences, College of Medicine, National Taiwan University, Taipei, Taiwan, Department of Pediatrics, National Taiwan University Hospital Yun-Lin branch, Yun-Lin, Taiwan

  • Cheng-Wen Huang ,

    Contributed equally to this work with: Wei-Sheng Lin, Cheng-Wen Huang, You-Sheng Song

    Affiliations Graduate Institute of Brain and Mind Sciences, College of Medicine, National Taiwan University, Taipei, Taiwan, Institute of Biotechnology, National Tsing Hua University, HsinChu, Taiwan

  • You-Sheng Song ,

    Contributed equally to this work with: Wei-Sheng Lin, Cheng-Wen Huang, You-Sheng Song

    Affiliation Institute of Neuroscience, National Chengchi University, Taipei, Taiwan

  • Jui-Hung Yen,

    Affiliation Department of Microbiology and Immunology, Indiana University School of Medicine, Fort Wayne, Indiana, United States of America

  • Ping-Chang Kuo,

    Affiliation Department of Microbiology and Immunology, Indiana University School of Medicine, Fort Wayne, Indiana, United States of America

  • Sheng-Rong Yeh,

    Affiliation Graduate Institute of Brain and Mind Sciences, College of Medicine, National Taiwan University, Taipei, Taiwan

  • Hung-Yu Lin,

    Affiliation Institute of Biotechnology, National Tsing Hua University, HsinChu, Taiwan

  • Tsai-Feng Fu,

    Affiliation Department of Applied Chemistry, National Chinan University, Nantou, Taiwan

  • Ming-Shiang Wu , (PYW); (HDW); (MSW)

    Affiliation Department of Internal Medicine, National Taiwan University Hospital, National Taiwan University, Taipei, Taiwan

  • Horng-Dar Wang , (PYW); (HDW); (MSW)

    Affiliations Institute of Biotechnology, National Tsing Hua University, HsinChu, Taiwan, Institute of Systems Neuroscience, National Tsing Hua University, HsinChu, Taiwan, Department of Life Science, National Tsing Hua University, HsinChu, Taiwan

  • Pei-Yu Wang (PYW); (HDW); (MSW)

    Affiliation Graduate Institute of Brain and Mind Sciences, College of Medicine, National Taiwan University, Taipei, Taiwan

Reduced Gut Acidity Induces an Obese-Like Phenotype in Drosophila melanogaster and in Mice

  • Wei-Sheng Lin, 
  • Cheng-Wen Huang, 
  • You-Sheng Song, 
  • Jui-Hung Yen, 
  • Ping-Chang Kuo, 
  • Sheng-Rong Yeh, 
  • Hung-Yu Lin, 
  • Tsai-Feng Fu, 
  • Ming-Shiang Wu, 
  • Horng-Dar Wang


In order to identify genes involved in stress and metabolic regulation, we carried out a Drosophila P-element-mediated mutagenesis screen for starvation resistance. We isolated a mutant, m2, that showed a 23% increase in survival time under starvation conditions. The P-element insertion was mapped to the region upstream of the vha16-1 gene, which encodes the c subunit of the vacuolar-type H+-ATPase. We found that vha16-1 is highly expressed in the fly midgut, and that m2 mutant flies are hypomorphic for vha16-1 and also exhibit reduced midgut acidity. This deficit is likely to induce altered metabolism and contribute to accelerated aging, since vha16-1 mutant flies are short-lived and display increases in body weight and lipid accumulation. Similar phenotypes were also induced by pharmacological treatment, through feeding normal flies and mice with a carbonic anhydrase inhibitor (acetazolamide) or proton pump inhibitor (PPI, lansoprazole) to suppress gut acid production. Our study may thus provide a useful model for investigating chronic acid suppression in patients.


Aging and metabolic syndrome are among the major issues in contemporary medicine. Although the mechanisms underlying these health problems remain incompletely understood, it has been demonstrated that aging and metabolism are intimately related, and that gut homeostasis plays an important role in regulation of these processes [13]. Recent studies have suggested that chronic (at least 10 months), but not short term (4 months), PPI treatment is associated with undesirable weight gain [4, 5]. Similarly, a suboptimal weight loss after gastric bypass bariatric surgery was found in two separate cohorts of PPI users [6]. Acid homeostasis in the gut may thus play a critical role in metabolic regulation.

Gastric acid is produced by the parietal cells of the stomach, and not only facilitates digestion and absorption of nutrients, but also helps to prevent bacterial overgrowth and enteric infection. In the Drosophila digestive tract, the midgut region is considered to be the equivalent of the mammalian stomach/small intestine. Specialized acid-producing cells, the copper cells of the midgut, were originally identified by their orange florescence in copper-fed larvae and their ability to accumulate radioactively-labeled cooper [7]. Copper cells show several striking similarities to mammalian gastric parietal cells in morphological studies, and they also co-localize with the acidic region of Drosophila midgut [7, 8]. Moreover, acid secretion is not detectable in mutant flies with perturbed copper cell differentiation [9]. Copper cells of the fly midgut thus appear to be structurally and functionally related to mammalian parietal cells.

Unlike parietal cells of the mammalian stomach that rely on H+K+-ATPase (of the P-type H+ ATPase family, pha) for acid secretion, Drosophila copper cells use V-type H+ ATPase (vha) for acid secretion [10]. No pha has thus far been shown to be expressed in Drosophila. Vacuolar-type H+ ATPases are multisubunit proton pumps comprising two functional parts, an ATP catalytic V1 complex (subunits A to H), and a proton-translocating V0 complex (subunits a, c, d and e). vha is an ATP-hydrolyzing enzyme that can transfer energy to proton gradients across diverse biological membranes, thus permitting regulation of the acidity of an organelle or of the extracellular side of the membrane. Although it has been suggested that gut acidification in insects may work through vha [11], it remains to be shown whether vha is actively involved in acid production in the Drosophila midgut. Here, we report that vha16-1 is a critical component of acid production in the fly midgut. Genetic and pharmacological approaches for acid suppression in the fly and in mice both induced increased body weight and lipid accumulation, and in flies, were also accompanied by accelerated aging. Our results may have critical implications for the use of chronic acid suppression in a clinical setting.

Materials and Methods

Flies and life span assays

w1118, EP2372, P[Δ2–3], P112087, Cyo/sp;TM3,Ser/TM6, Cop-Gal4 (NP3270), daughterless-Gal4 and UAS-GFP fly stocks were obtained from the Bloomington Drosophila Stock Center. UAS-vha16-1 was generated from a full-length vha16-1 cDNA and subcloned into the pUAST vector as previously described [12]. All flies were raised on standard sucrose/yeast/cornmeal food and were backcrossed into the w1118 background for at least 5 generations, as described previously [13]. For the life span assays, flies that had eclosed within 48 hours (approximately 100 males and 100 females) were transferred to a 1-liter population cage and maintained in a humidified, temperature-controlled incubator with 12-hour on/off light cycle at 25°C [14]. Fresh food was provided every other day, and the number and sex of dead flies were scored. Fly food contained 5% dextrose, 5% yeast, 2% agar, and 0.23% Tegosept (Apex). 500uM lansoprazole (Takeda Pharmaceuticals Taiwan), acetazolamide (Sigma) or vehicle control was added to the foods described in the experiment.

Genetic screen for starvation resistance

The P-element-containing line P112087 was crossed to a constitutively expressed transposase source P[Δ2–3] in order to excise and transpose the P-element to other chromosomal locations in progeny. The transposase was then removed by crossing F1 progeny to a balancer line Cyo/sp;TM3,Ser/TM6. Individual flies having the P-element integrated on the 2nd or 3rd chromosome were established as stock lines. For starvation challenge, ten-day-old flies that had been maintained on regular food were transferred to vials containing 2% agar and the number of dead flies was counted every 3 to 4 hours.

Inverse PCR and mRNA quantification

To map the insertion site of the P-element, genomic DNA was isolated from more than 30 flies using WelPrep DNA isolation kit (Welgene). DNA was then digested with DpnII (NEB) and ligated with T4 DNA ligase (Fermentas). PGaw2 5’-CAGATAGATTGGCTTCAGTGGAGAC–3’, PGaw3 5’-CGCATGCTTGTTCGATAGAAGAC–3’, Plw3 5’-TAACCCTTAGCATGTCCGTGGGGTTTG–3’, and PRY4 5’-CAATCATATCGCTGTCTCACTCA -3’ primers were used to amplify the flanking regions of the P-element. A PCR product of approximately 2000 base pair was isolated and sequenced. The P-element was mapped to nucleotide 6632424 on the 2nd chromosome of Drosophila melanogaster. The P-element insertion was also verified by specific primers GT-F 5’-CCGCACGTAAGGGTTAATGTTTT–3’, GT-R 5’-TTTTGCACGGATGAATCTGAATG–3’, PGawB-F 5’-GTGATTGGTTTTGGGTGGGTAA -3’ and PGawB-R 5’-TGTTCAGATGCTCGGCAGATG–3’.

For mRNA quantification, total RNA was prepared from at least 30 flies using the NucleoSpin RNA Kit (Macherey-Nagel), and the RNA was converted to cDNA as described previously [15]. Quantitative polymerase chain reaction (qPCR) was carried out using a StepOnePlus Real-Time PCR System (Applied Biosystems), SYBR Green Master Mix (Fermentas), and gene-specific primers 5’-GGAACTCACGAAGCAAGTGTTGA–3’ and 5’-AAAACCGCACCATTGGATACAT–3’ for vha16-1, and 5’-AATGGGTGTCGCTGAAGAAGTC–3’ and 5’-GACGAAATCAAGGCTAAGGTCG–3’ for glyceraldehyde 3-phosphate dehydrogenase (GAPDH). A two-step PCR reaction was carried out with denaturation at 95°C for 15 seconds, annealing and extension combined at 60°C for 1 minute, in a total of 40 cycles. The mRNA expression level of each target gene compared to GAPDH was quantified by subtraction: Ct (specific gene)—Ct (GAPDH) = ΔCt. A difference of one PCR cycle equates to a two-fold change in mRNA expression level. The uniqueness of amplicons was confirmed using dissociation curves.

Gut acidity, total triglycerides, body weight, feeding and fecundity measurements in flies

To measure fly gut acidity, 10-day-old flies were fed with yeast paste containing 1% bromophenol blue for 24 hours, and midgut acidity was observed under a dissecting microscope. To measure total triglycerides, ten 10-day-old flies were homogenized in PBS containing 0.05% Tween 20 and centrifuged at 16,000 g. Total triglycerides were measured using a triglyceride test kit (Fortress Diagnostics). For body weight measurements, 10-day-old flies were anesthetized by CO2 and weighed immediately, using a microbalance (Sartorius). Female fecundity was determined by daily counting of eggs produced by 3 mating pairs. Flies were passed daily to new vials containing appropriate food, and the number of eggs laid was counted and recorded for the first 14 days of adult life. For the feeding assays, 10-day-old flies were transferred to fresh vials with regular food containing 0.5% FD&C no. 1 blue food dye. After 6 hours, 10 flies were homogenized in a single tube containing PBS, and the amount of ingested dye was determined by spectrophotometer for dye absorbance at 620nm.

Mouse experiments

All experimental protocols followed the local animal ethics regulations and approved by National Taiwan University College of Medicine and College of Public Health Institutional Animal Care and Use Committee (IACUC). C57BL/6 male mice were obtained from National Taiwan University College of Medicine Laboratory Animal Center and maintained in an animal room with controlled temperature at 22–24°C and humidity at 50–55% under 12 hr light/dark cycle. All mice were fed ad libitum with standard pelleted mice chow (LabDiet 5058, PicoLab). For chronic acid suppression, mice received a daily subcutaneous injection of lansoprazole for 3 to 4 months. Food intake, water consumption and change in body weight were monitored regularly. Blood from tails of mice was collected at different time points and serum total triglycerides and cholesterol were measured using commercial kits (Fortress Diagnostics). For stomach acidity measurements, the mouse stomach was removed and washed with 1ml PBS. Gastric contents were collected and pH of the collected gastric juice was measured using a pH meter (Sartorius).


All data are expressed as mean ± SEM. Survival curves were analyzed by the Kaplan-Meier procedure and log-rank test. Data for all other assays were analyzed using one-way ANOVA or Student’s t test.


Isolation of vha16-1 mutant flies

To identify novel genes involved in metabolic regulation, we set up a genetic screen for starvation resistance using P-element-mediated mutagenesis in D. melanogaster. A total of 696 mutant lines were generated, and a mutant, dubbed m2, was found to have prolonged survival under food-deprived conditions, and was homozygous viable and fertile (Fig 1a and Table 1). Inverse PCR followed by sequencing showed that the landing site of the P-element for this mutant is in the first intron of the vha16-1 gene (Fig 1b), which encodes the c subunit of vha. The insertion site of P[GawB] was further confirmed by PCR, which detected an approximately 350 base pair PCR product spanning the vha16-1 gene and a P[GawB] fragment (Fig 1b and 1c), and an approximately 120 base pair PCR product within the P[GawB]. This P-element insertion produces a hypomorphic mutation of the vha16-1 gene, since we detected approximately 40% down-regulation of vha16-1 mRNA in m2 homozygous mutant flies (Fig 1d).

Fig 1. vha16-1 mutation induces starvation resistance in flies.

(a) Enhanced survival of m2 homozygous (red) and EP2372 heterozygous (green) mutant flies on starvation challenge compared to control flies (w1118, blue). Statistical analysis is shown in Table 1. (b) Schematic diagram of vha16-1 gene illustrating the insertion site of P-elements. (c) The P[GawB] insertion in m2 mutant flies was further verified by specific primer sets. The GT primer set detected a PCR product spanning the vha16-1 gene and P[GawB] fragment, and P generated a PCR product within the P[GawB]. (d) vha16-1 mRNA is significantly down regulated in m2 homozygous mutant flies (red) and EP2372 heterozygous (green) mutant flies compared to control flies (w1118, blue). Experiments were done in triplicate and each replicate contained more than 30 flies for each group. *, P < 0.05, compared to the control group.

Table 1. The effects of acid suppression on starvation resistance and life span (LS) in Drosophila melanogaster.

For comparison, an additional vha16-1 mutant EP2372 was obtained from the Bloomington Drosophila stock center. EP2372 is homozygous lethal, but heterozygous mutant flies showed reduced vha16-1 mRNA expression and increased starvation resistance, similar to our results for m2 homozygous mutant flies (Fig 1a, 1b and 1c).

vha16-1 mutation reduces gut acidity in flies

Since m2 mutant flies carrying P[GawB] constitutively express the yeast transcription activator protein Gal4, we crossed them to mutant flies carrying a UAS-GFP construct. The progeny reporter flies displayed a high level of GFP expression in a circumscribed segment of the central midgut in adult flies (Fig 2a and 2b). This segment corresponds to the copper cell region, where vha is highly expressed in the apical plasma membrane, and is responsible for acidification of the midgut lumen [16, 17]. To evaluate whether midgut acidity is affected in vha16-1 mutants, flies were fed bromophenol blue (BPB, a pH indicator) for 24 hours. BPB changes color from yellow at pH = 3.0 to blue at pH = 4.6. We found that 56.06% of m2 homozygous mutant flies and 60.61% of EP2372 heterozygous mutant flies showed diminished midgut acidity, compared to 19.23% of control w1118 flies (Fig 2c–2g). Although vha16-1 overexpression specifically in copper cells did not affect midgut acidity of flies, it did effect recovery of midgut acidity of EP2372 heterozygous mutant flies to the normal level (Fig 2h). Moreover, a majority of w1118 control flies and vha16-1 mutant flies fed with acetazolamide or lansoprazole also exhibited diminished midgut acidity (Fig 2g). Lansoprazole is has been shown to inhibit gastric and vesicular acidity through inhibition of both vha and pha [18, 19].

Fig 2. vha16-1 mutation reduces gut acidity in flies.

(a and b) m2>UAS-GFP reporter flies showing that vha16-1 was highly expressed in the Drosophila midgut region. Scale bars = 100 μm. (c-f) Representative images showing that m2 homozygous mutant flies (e) displayed reduced midgut acidity compared to control flies (c, w1118). The midgut acidity can also be diminished by feeding both control flies (d) and m2 homozygous mutant flies (f) with carbonic anhydrase inhibitor (acetazolamide). Scale bars = 0.5 mm. The anterior and posterior regions of Drosophila midgut are marked as “A” and “P”, respectively. (g) Quantitative results showing that majority of m2 homozygous, EP2372 heterozygous mutant flies, and acetazolamide- or lansoprazole-treated flies had diminished midgut acidity compared to control flies. (h) vha16-1 overexpression specifically in copper cells (Cop-Gal4/;UAS-vha16-1) did not affect the midgut acidity of flies, but did recover the midgut acidity of EP2372 heterozygous mutant flies to normal level. (i) Effectiveness of the UAS-vha16-1 constructs used for vha16-1 overexpression was verified by crossing daughterless (Da)-Gal4 with UAS-vha16-1 flies. vha16-1 mRNA significantly increased in Da-Gal4;UAS-vha16-1 flies compared to control (UAS-vha16-1) flies. Experiments were done in triplicate and each replicate contained more than 30 flies for each group. *, P < 0.05, compared to the control group.

Gut acid suppression increases lipid accumulation and body weight in flies

Starvation resistance in animals is generally associated with altered metabolism. For instance, animals having increased lipid accumulation or body weight are often resistant to food deprivation because of their greater nutrient storage [13, 20]. We examined triglycerides and body weight in flies as a measure of nutrient storage and ability to resist starvation. We found that m2 homozygous mutant flies have an elevated level of triglycerides and increased body weight compared to control w1118 flies (Fig 3a and 3b). Intriguingly, chronic acid suppression by lansoprazole also induced these phenotypes, similar to what is seen in m2 homozygous mutant flies (Fig 3a and 3b).

Fig 3. Midgut acid suppression induces an obese-like phenotype in flies.

(a and b) m2 homozygous mutant flies (red) and lansoprazole-treated flies (orange) show increased triglyceride accumulation (a) and body weight (b) compared to control flies (w1118, blue). (c and d) Food intake and female fecundity are not altered in m2 homozygous mutant flies (red) compared to control flies (w1118, blue). Data were collected from 8–10 replicates for each group. Each replicate contained 10 flies for triglyceride (a), body weight (b) and feeding assays (c), and 3 mated pairs for female fecundity measurements (d). *, P < 0.05, compared to the control group.

Increased nutrient storage upon gut acid suppression was not associated with alterations in feeding behavior, since the feeding rate for m2 homozygous mutant flies was comparable to that of control w1118 flies (Fig 3c). Although female fecundity is also linked to energy availability in animals, this is not a factor in m2 homozygous mutant flies, as normal egg production was observed in the first 2 weeks of female adult life (Fig 3d).

Gut acid suppression reduces life span in flies

Because metabolism is considered to be a central component of life span regulation, it is therefore crucial to determine how life span is affected in flies that have decreased midgut acidity. We found that median and maximal life span were significantly decreased in both m2 and EP2372 mutants, as well as in lansoprazole-treated flies, compared to control w1118 flies (Fig 4a and 4b and Table 1).

Fig 4. Midgut acid suppression shortens life span in flies.

(a) Shortened life spans in m2 homozygous mutant flies (red) and EP2372 heterozygous mutant flies (green) compared to control flies (w1118, blue). (b) Shortened life spans in lansoprazole-treated flies (orange) compared to control flies (w1118, blue). Statistical analysis is shown in Table 1.

Gut acid suppression induced an obese-like phenotype in mice

We further verified whether acid suppression in mice could induce a similar phenotype to that observed in flies. We treated mice with lansoprazole for 3 to 4 months, and found that stomach acidity was significantly reduced in a dosage-dependent manner (Fig 5a). Over the course of lansoprazole treatment, we found that serum triglycerides and cholesterol gradually increased for mice on higher doses of lansoprazole (5 and 25 mg/kg) but not on the lower dose of lansoprazole (1 mg/kg). Levels of serum triglycerides and cholesterol were significantly higher 60 days after receiving lansoprazole (Fig 5e and 5f). Moreover, body weight was also increased in mice treated with higher doses of lansoprazole (Fig 5d). Neither food intake nor water consumption was altered in mice treated with lansoprazole (Fig 5b and 5c).

Fig 5. Gastric acid suppression induces an obese-like phenotype in mice.

(a) Increased stomach pH in mice receiving lansoprazole treatment. (b and c) Chronic lansoprazole treatments do not affect food intake (b) or water consumption (c) of mice. (d-f) Chronic lansoprazole treatments gradually induce increased body weight, and elevated levels of serum triglycerides and cholesterol. Data were collected from 7 mice for each group. *, P < 0.05, compared to the saline group.


Our study demonstrates that flies and mice consistently exhibit an obese-like phenotype, that is accompanied by accelerated aging in flies, when gut acid production is suppressed by either genetic or pharmacologic means. On the other hand, the resulting elevated store of triglycerides probably confers starvation resistance upon these flies [21, 22]. The relationships among fat storage, starvation resistance, and life span are complex and sometimes counterintuitive. Obesity and increased stores of triglycerides can be associated with either increased or decreased starvation resistance, likely depending on whether triglycerides stored in lipid droplets can be mobilized. For example, flies with the Brummer lipase gene loss-of-function mutation are obese and starvation sensitive [23], while overexpression of Lsd–2 (encoding a perilipin protein), leads to an obese and starvation-resistant phenotype, reminiscent of our flies with deficient midgut acidity [24]. Furthermore, increased weight or lipid content is not necessarily linked to decreased life span. The methuselah mutant fly is heavier, and starvation resistant, but also long-lived [25]. A recent study by Lee [26] also showed a positive (and almost linear) correlation between lipid content and life span in female flies fed diets having various protein:carbohydrate ratios. Nonetheless, excessive lipid storage may still increase the risk of mortality in insects [27].

Parallel change in life span and stress resistance (starvation resistance, in particular) has often been noted in Drosophila studies [28]. For instance, flies with loss of the Apolipoprotein D (ApoD) homolog exhibit reduced life span and lowered starvation resistance [29], while overexpression of the ApoD homolog leads to life span extension and starvation resistance (without alteration of lipid content) [30]. Other examples include the methuselah mutant and female flies with loss of chico, both being long-lived and starvation resistant [25, 31]. Furthermore, starvation resistance has been successfully used as a screening strategy for identification of longevity genes [32]. However, our study makes the case that the two can be decoupled, and that caution should be exercised in using one to infer the other.

An aspect of digestion that is conserved between flies and mammals is the role of an acidified gut compartment. Even yeast, a unicellular organism in which the vacuoles serve as digestive organelles could be seen as conserving this strategy. Interestingly, vha is also responsible for vacuolar acidification, and suppression of vacuolar acidity in yeast affects nutrient signaling, leading to shortened replicative life span [33]. Together with our findings, these observations suggest the intriguing possibility that the relationship between digestive organ/organelle acidity and life span may be evolutionarily conserved.

In addition to supporting the robustness of findings observed in genetic models, another benefit of using pharmacological models in our study derives from the fact that suppression of midgut acidity is limited to adult fly life. This helps to exclude the possibility that suppression of larval midgut acidity could contribute to some of the phenotypes observed in the genetic models, although a previous study has suggested that larval midgut acidity may be dispensable [34]. Importantly, pharmacological models have direct clinical relevance since acid suppression is a commonly used treatment for both peptic ulcer disease and gastroesophageal reflux disease in human patients. Indeed, long-term treatment with PPI was shown to be associated with altered intestinal microflora [35, 36] and with undesirable weight gain [4], the latter being consistent with our finding in flies. These previous reports, along with our findings, raise serious questions, and call for careful studies of the potential risks that may be associated with acid suppression therapy in humans.

In conclusion, our study adds to the organismal-level understanding of the inter-relationships between gut homeostasis, metabolism, and aging, in which gut acidity plays a role. Flies and mice with deficient gut acidification recapitulate features of metabolic syndrome, and thus could be candidates for disease modeling. Further study is needed to elucidate precisely how gut acidity acts to modulate various aspects of gut homeostasis and metabolism, and it would be of great interest to test whether preservation of gut acidity, if feasible, can extend life span.


This study was supported by grants from Ministry of Science and Technology (MOST, 102-2311-B-007-008-MY3) to Dr. Horng-Dar Wang, National Taiwan University Hospital (UN102-029 and UN103-055) and MOST (100-2311-B-002-017-MY3 and 103-2321-B-002-093-) to Drs. Ming-Shiang Wu and Pei-Yu Wang, and National Taiwan University Hospital Yun-Lin branch (NTUHYL.103.S006) to Dr. Wei-Sheng Lin. We thank Mr. Chuan-Hao Lai, Mr. Hao-Wei Wang, Mr. Shi-Yow Yang and Mr. You-Qing Wu (National Taiwan University) for technical assistance. We thank Fly Core in Taiwan for fly stocks and reagents.

Author Contributions

Conceived and designed the experiments: WSL CWH YSS HYL MSW HDW PYW. Performed the experiments: WSL CWH YSS SRY. Analyzed the data: WSL CWH YSS PYW. Contributed reagents/materials/analysis tools: JHY PCK TFF. Wrote the paper: WSL PYW.


  1. 1. Lim DH, Oh CT, Lee L, Hong JS, Noh SH, Hwang S, et al. The endogenous siRNA pathway in Drosophila impacts stress resistance and lifespan by regulating metabolic homeostasis. FEBS letters. 2011;585(19):3079–85. pmid:21889502.
  2. 2. Wang L, Karpac J, Jasper H. Promoting longevity by maintaining metabolic and proliferative homeostasis. The Journal of experimental biology. 2014;217(Pt 1):109–18. pmid:24353210; PubMed Central PMCID: PMC3867494.
  3. 3. Erkosar B, Leulier F. Transient adult microbiota, gut homeostasis and longevity: novel insights from the Drosophila model. FEBS letters. 2014;588(22):4250–7. pmid:24983497.
  4. 4. Yoshikawa I, Nagato M, Yamasaki M, Kume K, Otsuki M. Long-term treatment with proton pump inhibitor is associated with undesired weight gain. World Journal of Gastroenterology. 2009;15(38):4794–8. WOS:000270841600010. pmid:19824113
  5. 5. Syu YF, Huang HH, Chen CY. Do proton pump inhibitors contribute to weight gain? Obesity surgery. 2015;25(6):1071–2. pmid:25845352.
  6. 6. Ward EK, Schuster DP, Stowers KH, Royse AK, Ir D, Robertson CE, et al. The effect of PPI use on human gut microbiota and weight loss in patients undergoing laparoscopic Roux-en-Y gastric bypass. Obesity surgery. 2014;24(9):1567–71. pmid:24849914.
  7. 7. Strasburger M. Bau, Funktion und variabilitat des darmtractus von Drosophila melanogaster. Zeitschrift fur Wissenchaft Zoologie. 1932;140:539–649.
  8. 8. Filshie BK, Poulson DF, Waterhouse DF. Ultrastructure of the copper-accumulating region of the Drosophila larval midgut. Tissue Cell. 1971;3(1):77–102. pmid:18631544.
  9. 9. Dubreuil RR, Frankel J, Wang P, Howrylak J, Kappil M, Grushko TA. Mutations of alpha spectrin and labial block cuprophilic cell differentiation and acid secretion in the middle midgut of Drosophila larvae. Dev Biol. 1998;194(1):1–11. pmid:9473327.
  10. 10. Phillips MD, Thomas GH. Brush border spectrin is required for early endosome recycling in Drosophila. Journal of Cell Science. 2006;119(7):1361–70. WOS:000236763900016.
  11. 11. Wieczorek H, Putzenlechner M, Zeiske W, Klein U. A vacuolar-type proton pump energizes K+/H+ antiport in an animal plasma membrane. The Journal of biological chemistry. 1991;266(23):15340–7. Epub 1991/08/15. pmid:1831202.
  12. 12. Huang CW, Wang HD, Bai H, Wu MS, Yen JH, Tatar M, et al. Tequila Regulates Insulin-Like Signaling and Extends Life Span in Drosophila melanogaster. J Gerontol A Biol Sci Med Sci. 2015. pmid:26265729.
  13. 13. Wang PY, Neretti N, Whitaker R, Hosier S, Chang C, Lu D, et al. Long-lived Indy and calorie restriction interact to extend life span. Proceedings of the National Academy of Sciences of the United States of America. 2009;106(23):9262–7. pmid:19470468; PubMed Central PMCID: PMCPMC2685744.
  14. 14. Lin WS, Chen JY, Wang JC, Chen LY, Lin CH, Hsieh TR, et al. The anti-aging effects of Ludwigia octovalvis on Drosophila melanogaster and SAMP8 mice. Age. 2014;36(2):689–703. Epub 2013/12/18. pmid:24338263.
  15. 15. Chou HJ, Lai DM, Huang CW, McLennan IS, Wang HD, Wang PY. BMP4 is a peripherally-derived factor for motor neurons and attenuates glutamate-induced excitotoxicity in vitro. PLoS One. 2013;8(3):e58441. pmid:23472198; PubMed Central PMCID: PMCPMC3589418.
  16. 16. Royet J. Epithelial homeostasis and the underlying molecular mechanisms in the gut of the insect model Drosophila melanogaster. Cell Mol Life Sci. 2011;68(22):3651–60. pmid:21964927.
  17. 17. Shanbhag S, Tripathi S. Epithelial ultrastructure and cellular mechanisms of acid and base transport in the Drosophila midgut. The Journal of experimental biology. 2009;212(Pt 11):1731–44. Epub 2009/05/19. pmid:19448082.
  18. 18. Spugnini EP, Baldi A, Buglioni S, Carocci F, de Bazzichini GM, Betti G, et al. Lansoprazole as a rescue agent in chemoresistant tumors: a phase I/II study in companion animals with spontaneously occurring tumors. Journal of translational medicine. 2011;9:221. pmid:22204495; PubMed Central PMCID: PMC3264547.
  19. 19. De Milito A, Iessi E, Logozzi M, Lozupone F, Spada M, Marino ML, et al. Proton pump inhibitors induce apoptosis of human B-cell tumors through a caspase-independent mechanism involving reactive oxygen species. Cancer research. 2007;67(11):5408–17. pmid:17545622.
  20. 20. Sieber MH, Thummel CS. The DHR96 nuclear receptor controls triacylglycerol homeostasis in Drosophila. Cell Metab. 2009;10(6):481–90. Epub 2009/12/01. pmid:19945405; PubMed Central PMCID: PMC2803078.
  21. 21. Djawdan M, Chippindale AK, Rose MR, Bradley TJ. Metabolic reserves and evolved stress resistance in Drosophila melanogaster. Physiological zoology. 1998;71(5):584–94. Epub 1998/10/01. pmid:9754535.
  22. 22. Rion S, Kawecki TJ. Evolutionary biology of starvation resistance: what we have learned from Drosophila. Journal of evolutionary biology. 2007;20(5):1655–64. Epub 2007/08/24. pmid:17714282.
  23. 23. Gronke S, Mildner A, Fellert S, Tennagels N, Petry S, Muller G, et al. Brummer lipase is an evolutionary conserved fat storage regulator in Drosophila. Cell Metab. 2005;1(5):323–30. Epub 2005/08/02. pmid:16054079.
  24. 24. Gronke S, Beller M, Fellert S, Ramakrishnan H, Jackle H, Kuhnlein RP. Control of fat storage by a Drosophila PAT domain protein. Current biology: CB. 2003;13(7):603–6. pmid:12676093.
  25. 25. Lin YJ, Seroude L, Benzer S. Extended life-span and stress resistance in the Drosophila mutant methuselah. Science. 1998;282(5390):943–6. Epub 1998/10/30. pmid:9794765
  26. 26. Lee KP. Dietary protein:carbohydrate balance is a critical modulator of lifespan and reproduction in Drosophila melanogaster: A test using a chemically defined diet. Journal of insect physiology. 2015;75:12–9. Epub 2015/03/03. pmid:25728576.
  27. 27. Na J, Musselman LP, Pendse J, Baranski TJ, Bodmer R, Ocorr K, et al. A Drosophila model of high sugar diet-induced cardiomyopathy. PLoS Genet. 2013;9(1):e1003175. pmid:23326243; PubMed Central PMCID: PMCPMC3542070.
  28. 28. Rose MR, Vu LN, Park SU, Graves JL Jr. Selection on stress resistance increases longevity in Drosophila melanogaster. Experimental gerontology. 1992;27(2):241–50. Epub 1992/01/11. pmid:1521597.
  29. 29. Sanchez D, Lopez-Arias B, Torroja L, Canal I, Wang X, Bastiani MJ, et al. Loss of glial lazarillo, a homolog of apolipoprotein D, reduces lifespan and stress resistance in Drosophila. Current biology: CB. 2006;16(7):680–6. Epub 2006/04/04. pmid:16581513.
  30. 30. Walker DW, Muffat J, Rundel C, Benzer S. Overexpression of a Drosophila homolog of apolipoprotein D leads to increased stress resistance and extended lifespan. Current biology: CB. 2006;16(7):674–9. Epub 2006/04/04. pmid:16581512.
  31. 31. Clancy DJ, Gems D, Harshman LG, Oldham S, Stocker H, Hafen E, et al. Extension of life-span by loss of CHICO, a Drosophila insulin receptor substrate protein. Science. 2001;292(5514):104–6. Epub 2001/04/09. pmid:11292874.
  32. 32. Wang HD, Kazemi-Esfarjani P, Benzer S. Multiple-stress analysis for isolation of Drosophila longevity genes. Proceedings of the National Academy of Sciences of the United States of America. 2004;101(34):12610–5. pmid:15308776; PubMed Central PMCID: PMCPMC515105.
  33. 33. Hughes AL, Gottschling DE. An early age increase in vacuolar pH limits mitochondrial function and lifespan in yeast. Nature. 2012;492(7428):261–5. Epub 2012/11/23. pmid:23172144; PubMed Central PMCID: PMC3521838.
  34. 34. Dubreuil RR, Grushko T, Baumann O. Differential effects of a labial mutation on the development, structure, and function of stomach acid-secreting cells in Drosophila melanogaster larvae and adults. Cell Tissue Res. 2001;306(1):167–78. pmid:11683178.
  35. 35. Canani RB, Terrin G. Gastric acidity inhibitors and the risk of intestinal infections. Current opinion in gastroenterology. 2010;26(1):31–5. Epub 2009/11/13. pmid:19907324.
  36. 36. Compare D, Pica L, Rocco A, De Giorgi F, Cuomo R, Sarnelli G, et al. Effects of long-term PPI treatment on producing bowel symptoms and SIBO. European journal of clinical investigation. 2011;41(4):380–6. Epub 2010/12/07. pmid:21128930.