The role of environmental, structural and anthropogenic variables on underpass use by African savanna elephants (Loxodonta africana) in the Tsavo Conservation Area

Wildlife crossing structures are effective interventions for mitigating fragmentation of habitats by linear infrastructure. The 2017 construction of a new railway cutting through the Tsavo Con- servation Area (TCA), home to the largest elephant population in Kenya, affected wildlife movement and habitat connectivity. Although numerous studies have investigated the use of wildlife crossing structures by a wide range of species, few have focused on their use by mega- herbivores. In this study, we examined use of 41 wildlife crossing structures by African savanna elephants (Loxodonta africana) along a 133 km section of new railway in Tsavo, Kenya. We used a generalized linear mixed modeling approach to assess the relationship between elephant crossing rate over 28 months between July 2017 to April 2021 and explanatory factors including crossing structure attributes, livestock presence and proximity to highways, water points and human settlement. We found that structural attributes of crossing structures were most strongly associ- ated with the elephant crossing rate, particularly height and its interaction with type of crossing structure (bridges, wildlife underpasses and culverts). Higher crossing structures were associated with higher crossing rate, with the largest influence of height at culverts and wildlife underpasses. Although bridges comprised only 19.5 % of the 41 available crossing structures, they accounted for a disproportionately high number of elephants crossing events (56 %). The results demon- strated the importance of bridges over designated crossing structures for elephants, with pre- dicted seasonal counts of elephant crossings being 0.31 for average sized culverts, 2.88 for wildlife underpasses and 5.86 for bridges. The environmental and anthropogenic variables were not strongly associated with elephant crossing rate. Our findings have direct application for future siting and design of crossing structures across elephant rang

Intestinal Epithelial Serum Amyloid A Modulates Bacterial Growth In Vitro and Pro-Inflammatory Responses in Mouse Experimental Colitis

<p>Abstract</p> <p>Background</p> <p>Serum Amyloid A (SAA) is a major acute phase protein of unknown function. SAA is mostly expressed in the liver, but also in other tissues including the intestinal epithelium. SAA reportedly has anti-bacterial effects, and because inflammatory bowel diseases (IBD) result from a breakdown in homeostatic interactions between intestinal epithelia and bacteria, we hypothesized that SAA is protective during experimental colitis.</p> <p>Methods</p> <p>Intestinal SAA expression was measured in mouse and human samples. Dextran sodium sulfate (DSS) colitis was induced in SAA 1/2 double knockout (DKO) mice and in wildtype controls. Anti-bacterial effects of SAA1/2 were tested in intestinal epithelial cell lines transduced with adenoviral vectors encoding the CE/J SAA isoform or control vectors prior to exposure to live <it>Escherichia coli</it>.</p> <p>Results</p> <p>Significant levels of SAA1/SAA2 RNA and SAA protein were detected by in situ hybridization and immunohistochemistry in mouse colonic epithelium. SAA3 expression was weaker, but similarly distributed. SAA1/2 RNA was present in the ileum and colon of conventional mice and in the colon of germfree mice. Expression of SAA3 was strongly regulated by bacterial lipopolysaccharides in cultured epithelial cell lines, whereas SAA1/2 expression was constitutive and not LPS inducible. Overexpression of SAA1/2 in cultured epithelial cell lines reduced the viability of co-cultured <it>E. coli</it>. This might partially explain the observed increase in susceptibility of DKO mice to DSS colitis. SAA1/2 expression was increased in colon samples obtained from Crohn's Disease patients compared to controls.</p> <p>Conclusions</p> <p>Intestinal epithelial SAA displays bactericidal properties in vitro and could play a protective role in experimental mouse colitis. Altered expression of SAA in intestinal biopsies from Crohn's Disease patients suggests that SAA is involved in the disease process..</p