taxonID	type	description	language	source
2D2AB30DFFD0FF93A93AFCE86DE9F90C.taxon	discussion	We hypothesized that the different bacteria encountered and eaten by C. elegans in the wild could affect its physiology, and in particular RS. To this end, we first isolated bacteria from rotting vegetation, substrates from which nematodes would often be found, from two national parks in Vietnam. We isolated 64 bacterial strains from 50 sampling sites in Cat Tien National Park and 45 strains from 44 sites in Cuc Phuong National Park (Tables S 2 and S 3). These 109 strains were qualitatively characterized based on colony size, color, thickness, and prevalence on the original screening plate (Table S 3). Next, we used a simple 1 - plate assay (see “ Methods ”) to screen all 109 isolates for an effect on RS of C. elegans in comparison to the E. coli OP 50 control. The RS of C. elegans on OP 50 was about 3 – 4 days. Qualitatively, 108 strains also had similar RS in the 3 - to 4 - day range. One strain, CFBb 37, seemed to extend RS to approximately 7 days. We note that we found a nematode, Caenorhabditis briggsae, co-occurring in the field sample containing CFBb 37 (Table S 2). We also noticed that this and six other bacterial strains reduced the body size and another delayed the onset of first brood production in C. elegans (Fig. S 1 and Table S 2). To determine their genus or species identity we sequenced the 16 S rDNA barcode for these eight bacterial strains as well as four others without obvious effects on C. elegans (Table S 2). This revealed that CFBb 37 is a Microbacterium sp., which is in the Actinobacteria phylum. Most of the other strains belonged to the phylum Proteobacteria (n = 8) while the rest were in the phyla Bacteroidetes (n = 1) or Firmicutes (n = 2). We focused on Microbacterium sp. CFBb 37 for the rest of this study.	en	Le, Tho Son, Nguyen, Thi Hong Gam, Ha, Bich Hong, Huong, Bui Thi Mai, Nguyen, Thi Thu Hang, Vu, Kim Dung, Ho, Tu Cuong, Wang, John (2022): Reproductive Span of Caenorhabditis elegans Is Extended by Microbacterium sp. Journal of Nematology 54 (1): 1-21, DOI: 10.2478/jofnem-2022-0010, URL: http://dx.doi.org/10.2478/jofnem-2022-0010
2D2AB30DFFD0FF93A93AFCE86DE9F90C.taxon	description	Confirmation of RS extension by Microbacterium sp. CFBb 37 To confirm the screening results, we determined more precisely the RS of C. elegans when fed with Microbacterium sp. CFBb 37, the control OP 50, and two additional identified strains (Acinetobacter sp. CFBb 9 and Serratia sp. CFBb 17). In this assay we moved pools of adults (n = 6 – 15) to fresh plates daily, which allowed determining both the presence of brood and counting the number of brood per day. The worms growing on OP 50 as well as Acinetobacter sp. CFBb 9 and Serratia sp. CFBb 17 had similar RS durations, which was 4 days (P <0.001; Table 1). In contrast, worms growing on Microbacterium sp. CFBb 37 had an RS of 8 days (P <0.001), confirming the RS extension from the screen. Qualitatively, average daily brood counts appeared to decline exponentially from day 2 onward (day 2, n = 47; day 7 and later, n <4) (Table 1). In the above assay, the number of parents per plate varied both within and among bacterial strains. While unlikely to be of major effect, we decided to eliminate the potential confounding effects of parental interactions and differing parental density by re-examining brood presence (and brood sizes, see below) using one parental worm per plate. We found that the average RS for worms growing on Microbacterium sp. CFBb 37 was 79 % greater than on OP 50 (7.29 ± 0.25 days; mean ± 1 standard error (SE) versus 4.08 ± 0.16; P <0.001; Fig. 1 A and S 1; Table 2). The combined data clearly indicate that CFBb 37 induces RS extension in C. elegans. Daily count of eggs in the uterus of C. elegans Our assays for RS above were sometimes difficult (e. g., looking for rare laid eggs near the end of the RS period) or required moving the worms to new plates everyday as well as waiting for the progeny to hatch. A simplification of the RS assay would be to directly look for eggs in the uteruses (“ uterus egg assay ”) of the focal adult worm at 400 × magnification under a DIC compound microscope each day. The presence of at least one egg would indicate fertility. The lack of eggs could indicate reproductive senescence or that any eggs were recently laid. Examining many adult worms each day should help distinguish between the two possibilities, although there would still be a bias for incorrectly scoring a batch of worms (i. e., day) as reproductively senescent. To test whether the uterus egg assay gives comparable results to our original RS assays, we placed C. elegans L 1 s on either CFBb 37 or OP 50 and raised them to adulthood. Then, each day we counted the number of eggs in the uterus of 29 – 37 worms. For each day, if this number of eggs was greater than zero (using a one-sample t - test), then we considered that day to be a fertile day (i. e., not reproductively senescent). Using this assay, the worms on CFBb 37 had an RS of 8 days while those on OP 50 had an RS of 4 days (Table S 5). The results from counting eggs in the uteruses were qualitatively concordant with the earlier brood-based assays (7.29 and 4.08 days, respectively; Table 2). Thus, although this approach has an inherent bias for reproductive senescence (i. e., scoring shorter RS), we suggest that the simpler uterus egg assay provides a reasonably good estimate for the RS, and can distinguish differences in RS, at least for those separated by several days. Reduction of brood size by Microbacterium sp. CFBb 37 While confirming the RS extension by Microbacterium sp. CFBb 37 on pools of C. elegans, we noticed that this bacterial strain reduced the average total brood size compared with OP 50 (141.6 vs 251.2; P <0.001; Table 1). As above, to remove the potential confounding effects of pooled worms, we recounted the brood sizes using one parental worm per plate. We found that the average total brood size on Microbacterium sp. CFB 37 was less than on OP 50 (137.63 mean ± 5.74 SE versus 266.28 ± 6.42; P <0.001, Table 2). Partitioning the data into daily brood sizes over the first 8 days (i. e., the number of days with data for both bacterial strains, Table 2) revealed that worms fed with OP 50 had greater brood sizes than those fed with Microbacterium sp. CFB 37 during the first 3 days (29 – 125 more eggs / day) while the opposite (2 – 19 fewer eggs / day) occurred during the last 5 days (all P <0.001, Table 2). Although there were more days where worms growing on CBFb 37 had greater brood sizes than OP 50, the magnitude of the differences was smaller during these 5 days, explaining the lower average total brood sizes for Microbacterium sp. CFB 37. Lifespan extension by Microbacterium sp. CFBb 37 Bacterial diet has been shown to affect the (somatic) lifespan of C. elegans in many cases (Zhang et al., 2017; Kumar et al., 2020). Thus, we tested whether Microbacterium sp. CFBb 37 could also alter the C. elegans lifespan. We found that worms fed with Microbacterium sp. CFBb 37 lived longer than those fed with OP 50 (26.77 ± 0.86 days, mean ± 1 SE, versus 17.26 ± 0.57; P <0.001; Fig. 2 and Table S 4). aFirst, an average brood number per individual was calculated per pool, then the average of the pools was reported. bN, number of pools tested; n, total numbers of individuals tested. cAverage brood size per worm in pools is the sum of all the daily brood sizes. dRS is the number of days with average daily individual brood counts> 0 based on one-sample t - test. RS, reproductive span. To determine at what general “ time period ” lifespan extension was occurring, we partitioned the total lifetime into the time spent in the larval, reproductive, and post-reproductive periods. For Microbacterium sp. CFBb 37, C. elegans spent an average of 2.89 days as larvae, 7.29 days as reproductive adults, and 16.59 days as post-reproductive adults. On OP 50, these durations were 2.05, 4.08, and 11.13 days, respectively. Thus, worms fed with CFBb 37 spent longer periods of time in all three stages. This suggests that the total lifespan of the worms on CFBb 37 was likely a combination of slower growth as larvae plus lifespan extension during reproductive and post-reproductive stages. Extension of RS in closely related species The extension of RS by Microbacterium sp. CBFb 37 (compared with E. coli OP 50) in C. elegans could be a species-specific effect. Alternatively, Microbacterium sp. CBFb 37 may also extend RS in other worm species. We tested this by examining RS using both the uterus egg assay and the presence of brood assay for two additional Caenorhabditis species (C. briggsae CFB 233 and C. tropicalis BRC 20400) and another Rhabditidae family species, Protorhabditis sp. CFB 231. C. briggsae CFB 233 and Protorhabditis sp. CFB 231 were isolated from two different field samples that were each also the source of two bacterial strains (Tables S 2 and S 3). The sexual system of Protorhabditis sp. CFB 231 could be self-fertile hermaphrodites, because their spermathecae contain sperm (Fig. S 2). However, other parthenogenetic Protorhabditis species also produce sperm (Fradin et al., 2017; Grosmaire et al., 2019), so additional genetic analysis will be needed to determine the sexual system of this species. For all three species and for both assays, we found that feeding on Microbacterium sp. BCFb 37 extended the RS compared with OP 50 (all P <0.001, log-rank test; Figures 1 B – D and S 1; Tables 2 and S 5). For C. briggsae the RS extension was 1.64 additional days (+ 41 %), for C. tropicalis 2.59 days (+ 109 %), and for Protorhabditis sp. 3.09 days (+ 86 %). Together, these results suggest that Microbacterium sp. CBFb 37 can likely extend RS broadly across the Caenorhabditis genus and perhaps, at least, across the Rhabditidae family. (Continued) an, the total number of tested individuals in each test. bAverage brood size per worm was the total brood of all hermaphrodites (n) divided by n. cAverage RS. N. A., not applicable. RS, reproductive span; SE, standard error. Brood sizes of closely related species on Microbacterium sp. CFBb 37 The extension of RS in C. elegans by Microbacterium sp. CBFb 37 was associated with a decrease in brood size. We next examined whether the extension of RS in the three other species was also associated with a consistent decrease in brood size. We found that the brood sizes of both C. briggsae (16.00 ± 1.88 Microbacterium sp. CBFb 37 versus 65.40 ± 7.09 E. coli OP 50; P <0.001; Table 2) and Protorhabditis sp. (22.08 ± 2.26 versus 161.38 ± 10.05; P <0.01; Table 2) on Microbacterium sp. CFBb 37 was less than on E. coli OP 50. However, C. tropicalis brood size on Microbacterium sp. CFBb 37 was more than on E. coli OP 50 (25.25 ± 3.59 versus 10.78 ± 1.90; P <0.01; Table 2). Together, these results suggest that the interaction between Microbacterium sp. CFBb 37 and the nematodes is not simple.	en	Le, Tho Son, Nguyen, Thi Hong Gam, Ha, Bich Hong, Huong, Bui Thi Mai, Nguyen, Thi Thu Hang, Vu, Kim Dung, Ho, Tu Cuong, Wang, John (2022): Reproductive Span of Caenorhabditis elegans Is Extended by Microbacterium sp. Journal of Nematology 54 (1): 1-21, DOI: 10.2478/jofnem-2022-0010, URL: http://dx.doi.org/10.2478/jofnem-2022-0010
