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Opposing plant community responses to warming with and without herbivores.

ABSTRACT: If controls over primary productivity and plant community composition are mainly environmental, as opposed to biological, then global change may result in large-scale alterations in ecosystem structure and function. This view appears to be favored among investigations of plant biomass and community responses to experimental and observed warming. In far northern and arctic ecosystems, such studies predict increasing dominance of woody shrubs with future warming and emphasize the carbon (C)-sequestration potential and consequent atmospheric feedback potential of such responses. In contrast to previous studies, we incorporated natural herbivory by muskoxen and caribou into a 5-year experimental investigation of arctic plant community response to warming. In accordance with other studies, warming increased total community biomass by promoting growth of deciduous shrubs (dwarf birch and gray willow). However, muskoxen and caribou reduced total community biomass response, and responses of birch and willow, to warming by 19%, 46%, and 11%, respectively. Furthermore, under warming alone, the plant community shifted after 5 years away from graminoid-dominated toward dwarf birch-dominated. In contrast, where herbivores grazed, plant community composition on warmed plots did not differ from that on ambient plots after 5 years. These results highlight the potentially important and overlooked influences of vertebrate herbivores on plant community response to warming and emphasize that conservation and management of large herbivores may be an important component of mitigating ecosystem response to climate change.

SUBMITTER: Post E

PROVIDER: S-EPMC2527915 | biostudies-literature |

REPOSITORIES: biostudies-literature

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Project description:BackgroundOne of the greatest impediments to cancer immunotherapy is the paucity of antigens that are tumor specific, sufficiently immunogenic, and shared among patients. Mucosa-restricted antigens that are expressed by tumor cells represent a novel class of vaccine targets that are characterized by immunologic privilege, which limits systemic tolerance to those antigens, and immunologic partitioning, which shields mucosae from systemic autoimmune responses. Here we defined the immunogenicity and antitumor efficacy of guanylyl cyclase C (GCC), a protein that is normally restricted to intestinal mucosa and universally expressed by metastatic colorectal cancer.MethodsBALB/c mice (n = 197) were immunized with recombinant GCC-expressing viral vectors before (prophylactic) or after (therapeutic) a lethal challenge of GCC-expressing mouse colon cancer cells, and antitumor efficacy was monitored by quantifying metastasis and survival. Induction of autoimmunity was monitored by histopathology. Induction of GCC-specific B-cell and CD4(+) and CD8(+) T-cell responses were determined by enzyme-linked immunosorbent assay and ELISpot, respectively. Tolerance to GCC was quantified by comparing responses in GCC-deficient (n = 45) and wild-type (n = 69) C57BL/6 mice. Statistical tests were two-sided.ResultsImmunization with GCC-expressing viral vectors reduced the formation of metastases to liver (control vs GCC: mean = 30.4 vs 3.55 nodules, difference = 26.9 nodules, 95% confidence interval [CI] = 8.47 to 45.3 nodules; P = .008) and lung (control vs GCC: mean = 263 vs 55.7 nodules, difference = 207, 95% CI = 163 to 251; P < .001) and extended the median survival of mice with established lung metastases following therapeutic immunization (control vs GCC: 29 vs 38 days, P = .024), without autoimmunity. Antitumor efficacy reflected asymmetrical tolerance that was characterized by CD8(+) T-cell, but not CD4(+) T-cell or antibody, responses.ConclusionsImmunologic partitioning together with immunologic privilege highlight the potential of mucosa-restricted antigens, particularly GCC, as therapeutic targets for metastatic cancer.

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Opposing plant community responses to warming with and without herbivores.

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