TY - JOUR
T1 - Comparison of Sample Extraction and Storage Methods across Time for Fecal Progesterone Metabolite Analysis in Female Verreaux’s Sifaka
AU - Hays, Allison
AU - Birr, Madalena
AU - Peñaherrera-Aguirre, Mateo
AU - Cook, Erica
AU - Lewis, Rebecca J.
AU - Tecot, Stacey
N1 - Publisher Copyright:
© 2025 The University of Chicago. All rights reserved.
PY - 2025/5/1
Y1 - 2025/5/1
N2 - Researchers commonly collect fecal samples from wild animals to monitor steroid metabolites and associate them with ecology and behavior. This method requires that we develop and validate species-specific methods that are appropriate for various field conditions and compatible with laboratory resources. We compared multiple extraction and storage methods for analyzing fecal progesterone metabolites (fPms) in wild female Verreaux’s sifaka (Propithecus verreauxi). We created a subset of samples from a single homogenized fecal pool. We preserved samples by freezing, desiccation, and suspension on four different brands of solid-phase extraction (SPE) cartridges and extracted or eluted samples under each condition at 0-, 90-, 180-, and 270-d intervals for subsequent enzyme immunoassay. Mean progesterone metabolite levels varied across conditions ((Formula presented.) to (Formula presented.) ng/g). Frozen samples generally yielded the highest fPm levels; post hoc comparisons, with Bonferroni correction, indicated that samples that were desiccated and samples that were suspended on Alltech Maxi-Clean SPE cartridges were the most similar to frozen samples overall ((Formula presented.)). Alltech SPE cartridges produced the most consistent results within and across time points. We were unable to suspend or elute sample extracts using SPE cartridges from two brands that were not developed for long-term storage. Based on samples from the remaining four conditions, fPm levels did not vary from time point 1, except for an increase in time point 4 ((Formula presented.), (Formula presented.), (Formula presented.), (Formula presented.)), suggesting long-term stability to at least 180 d. However, no consistent trend across time was apparent within any condition. Overall, we found that freezing, desiccation, and field extraction using Alltech SPE cartridges are reliable methods for measuring fPms in Propithecus edwardsi. We provide guidance for choosing methods under certain field and laboratory conditions, as well as detailed protocols that can help guide protocol development for analyzing fecal steroid metabolites in other species.
AB - Researchers commonly collect fecal samples from wild animals to monitor steroid metabolites and associate them with ecology and behavior. This method requires that we develop and validate species-specific methods that are appropriate for various field conditions and compatible with laboratory resources. We compared multiple extraction and storage methods for analyzing fecal progesterone metabolites (fPms) in wild female Verreaux’s sifaka (Propithecus verreauxi). We created a subset of samples from a single homogenized fecal pool. We preserved samples by freezing, desiccation, and suspension on four different brands of solid-phase extraction (SPE) cartridges and extracted or eluted samples under each condition at 0-, 90-, 180-, and 270-d intervals for subsequent enzyme immunoassay. Mean progesterone metabolite levels varied across conditions ((Formula presented.) to (Formula presented.) ng/g). Frozen samples generally yielded the highest fPm levels; post hoc comparisons, with Bonferroni correction, indicated that samples that were desiccated and samples that were suspended on Alltech Maxi-Clean SPE cartridges were the most similar to frozen samples overall ((Formula presented.)). Alltech SPE cartridges produced the most consistent results within and across time points. We were unable to suspend or elute sample extracts using SPE cartridges from two brands that were not developed for long-term storage. Based on samples from the remaining four conditions, fPm levels did not vary from time point 1, except for an increase in time point 4 ((Formula presented.), (Formula presented.), (Formula presented.), (Formula presented.)), suggesting long-term stability to at least 180 d. However, no consistent trend across time was apparent within any condition. Overall, we found that freezing, desiccation, and field extraction using Alltech SPE cartridges are reliable methods for measuring fPms in Propithecus edwardsi. We provide guidance for choosing methods under certain field and laboratory conditions, as well as detailed protocols that can help guide protocol development for analyzing fecal steroid metabolites in other species.
KW - enzyme-linked immunosorbent assay
KW - primate
KW - progesterone metabolites
KW - solid-phase extraction
UR - https://www.scopus.com/pages/publications/105011062128
UR - https://www.scopus.com/pages/publications/105011062128#tab=citedBy
U2 - 10.1086/736425
DO - 10.1086/736425
M3 - Article
C2 - 40749203
AN - SCOPUS:105011062128
SN - 2993-7973
VL - 98
SP - 182
EP - 195
JO - Ecological and Evolutionary Physiology
JF - Ecological and Evolutionary Physiology
IS - 3
ER -