Background: High-altitude ecosystems are extreme environments that generate specific physiological, morphological, and behavioral adaptations in ectotherms. The shifts in gut microbiota of the ectothermic hosts as an adaptation to environmental changes are still largely unknown. We investigated the food ingested and the bacterial, fungal, and protistan communities in feces of the lizard Sceloporus grammicus inhabiting an altitudinal range using metabarcoding approaches. Results: The bacterial phyla Bacteroidetes and Firmicutes, and the genera Bacteroides and Parabacteroides dominated the core fecal bacteriome, while Zygomycota and Ascomycota, and the species Basidiobolus ranarum and Basidiobolus magnus dominated the core fecal mycobiome. The diet of S. grammicus included 29 invertebrate families belonging to Arachnida, Chilopoda, and Insecta. The diversity and abundance of its diet decreased sharply at high altitudes, while the abundance of plant material and Agaricomycetes was significantly higher at the highest site. The composition of the fecal microbiota of S. grammicus was different at the three altitudes, but not between females and males. Dietary restriction in S. grammicus at 4150 m might explain the high fecal abundance of Akkermansia and Oscillopira, bacteria characteristic of long fasting periods, while low temperature favored B. magnus. A high proportion of bacterial functions were digestive in S. grammicus at 2600 and 3100, while metabolism of aminoacids, vitamins, and key intermediates of metabolic pathways were higher at 4150 m. Different assemblages of fungal species in the lizard reflect differences in the environments at different elevations. Pathogens were more prevalent at high elevations than at the low ones. Conclusions: Limiting food resources at high elevations might oblige S. grammicus to exploit other food resources and its intestinal microbiota have degradative and detoxifying capacities. Sceloporus grammicus might have acquired B. ranarum from the insects infected by the fungus, but its commensal relationship might be established by the quitinolytic capacities of B. ranarum. The mycobiome participate mainly in digestive and degradative functions while the bacteriome in digestive and metabolic functions.
The potential of Pseudomonas putida KT2440 to act as a plant-growth promoter or as a bioremediator of toxic compounds can be affected by desiccation. In the present work, the bacterial survival ratio (BSR) in response to air desiccation was evaluated for P . putida KT2440 in the presence of different protectors. The BSR in the presence of nonreducing disaccharides, such as trehalose, was high after 15 days of desiccation stress (occurring at 30°C and 50% relative humidity), whereas in the absence of a protector the bacterial counts diminished to nondetectable numbers (ca 2.8 log CFU/mL). The LIVE/DEAD staining method showed that bacteria protected with trehalose maintained increased numbers of green cells after desiccation while cells without protection were all observed to be red. This indicated that nonprotected bacteria had compromised membrane integrity. However, when nonprotected bacteria subjected to 18 days of desiccation stress were rehydrated for a short time with maize root exudates or for 48 h with water (prolonged rehydration), the bacterial counts were as high as that observed for those not subjected to desiccation stress, suggesting that the cells entered the viable but nonculturable (VBNC) state under desiccation and that they returned to a culturable state after those means of rehydration. Interestingly an increase in the green color intensity of cells that returned to a culturable state was observed using LIVE/DEAD staining method, indicating an improvement in their membrane integrity. Cellular activity in the VBNC state was determined. A GFP-tagged P . putida strain expressing GFP constitutively was subjected to desiccation. After 12 days of desiccation, the GFP-tagged strain lost culturability, but it exhibited active GFP expression, which in turn made the cells green. Furthermore, the expression of 16S rRNA, rpoN (housekeeping), mutL , mutS (encoding proteins from the mismatch repair complex), and oprH (encoding an outer membrane protein) were examined by RT-PCR. All evaluated genes were expressed by both types of cells, culturable and nonculturable, indicating active molecular processes during the VBNC state.
Summary Land‐use change has been identified as the most severe threat to biodiversity. Soils are important biodiversity reservoirs, but to what extent conversion of high‐altitude temperate forest to arable land affects taxonomic and functional soil biodiversity is still largely unknown. Shotgun metagenomics was used to determine the taxonomic and functional diversity of bacteria, archaea and DNA virus in terms of effective number of species in high‐altitude temperate oak and pine‐oak forest and arable soils from Mexico. Generally, the soil ecosystem maintained its microbial species richness notwithstanding land‐use change. Archaea diversity was not affected by land‐use change, but the bacterial diversity decreased with 45–55% when the oak forest was converted to arable land and 65–75% when the pine‐oak forest was. Loss in bacterial diversity as a result of land‐use change was positively correlated (R2 = 0.41) with the 10–25% loss in functional diversity. The archaeal communities were evener than the bacterial ones, which might explain their different response to land‐use change. We expected a decrease in DNA viral communities as the bacterial diversity decreased, i.e. their potential hosts. However, a higher viral diversity was found in the arable than in the forest soils. It was found that converting high altitude oak and pine‐oak forests to arable land more than halved the bacterial diversity, but did not affect the archaeal and even increased the viral diversity.
BackgroundTerrestrial ecosystems play a significant role in carbon (C) storage. Human activities, such as urbanization, infrastructure, and land use change, can reduce significantly the C stored in the soil. The aim of this research was to measure the spatial variability of soil organic C (SOC) in the national park La Malinche (NPLM) in the central highlands of Mexico as an example of highland ecosystems and to determine the impact of land use change on the SOC stocks through deterministic and geostatistical geographic information system (GIS) based methods.MethodsThe soil was collected from different landscapes, that is, pine, fir, oak and mixed forests, natural grassland, moor and arable land, and organic C content determined. Different GIS-based deterministic (inverse distance weighting, local polynomial interpolation and radial basis function) and geostatistical interpolation techniques (ordinary kriging, cokriging and empirical Bayes kriging) were used to map the SOC stocks and other environmental variables of the top soil layer.ResultsAll interpolation GIS-based methods described the spatial distribution of SOC of the NPLM satisfactorily. The total SOC stock of the NPLM was 2.45 Tg C with 85.3% in the forest (1.26 Tg C in the A horizon and 0.83 Tg C in the O horizon), 11.4% in the arable soil (0.23 Tg in the A horizon and only 0.05 Tg C in the O horizon) and 3.3% in the high moor (0.07 Tg C in the A horizon and <0.01 Tg C in the O horizon). The estimated total SOC stock in a preserved part of the forest in NPLM was 4.98 Tg C in 1938 and has nearly halved since then. Continuing this trend of converting all the remaining forest to arable land will decrease the total SOC stock to 0.52 Tg C.DiscussionDifferent factors explain the large variations in SOC stocks found in this study but the change in land use (conversion of forests into agricultural lands) was the major reason for the reduction of the SOC stocks in the high mountain ecosystem of the NPLM. Large amounts of C, however, could be stored potentially in this ecosystem if the area was used more sustainable. The information derived from this study could be used to recommend strategies to reverse the SOC loss in NPLM and other high-altitude temperate forests and sequester larger quantities of C. This research can serve as a reference for the analysis of SOC distribution in similar mountain ecosystems in central part of Mexico and in other parts of the world.
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