The leaf‐eared mouse, Phyllotis xanthopygus (Waterhouse 1837) is a widely distributed sigmodontine rodent in South America, with populations ranging from central Peru to southern Argentina and Chile. Previous morphological and molecular contributions have suggested that P. xanthopygus represents a species complex. In order to characterize and disclose this cryptic species complex, we perform a molecular genetic/phylogenetic analysis of representative samples across its geographical distribution. Phylogenetic analyses were based on sequences of cytochrome‐b gene (801 base pairs; n = 114 specimens) and analysed by maximum likelihood and Bayesian approaches. We also employed a Bayesian implementation of the Poisson tree processes (bPTP) as a unilocus species delimitation method. Results from our phylogenetic analyses retrieve eight well‐supported clades. Five of these clades belong to populations known as P. xanthopygus s.l., which were paraphyletic to the closely related species P. bonariensis, P. caprinus, and P. limatus, displaying strong genetic divergences (>8%). The (bPTP) analyses recovered ten species within P. xanthopygus s.l. plus related forms (i.e. P. bonariensis, P. caprinus, and P. limatus). Our results, coupled with chromosomal and morphological evidences, support the recognition of these clades at the species level and provide a new framework to characterize the leaf‐eared mice complex. Our study highlights the importance of integrative approaches in disentangling the biodiversity of Neotropical rodents.

This paper informs the characterization by 16SrDNA partial sequence analysis of an endophytic diazotrophic bacterium isolated from roots of the halophyte shrub Prosopis strombulifera. The bacterium produced ABA, IAA, GA 1 , GA 3 and jasmonic acid in chemicallydefined culture medium as assessed by GC-EIMS. The results emphasize the role of phytohormones produced by endophytic bacteria in the association host-beneficial microorganisms, especially under conditions of adverse environments.

Background Leptospirosis is a zoonotic disease that can be transmitted by contact with the urine of infected mammals. Rodents play a mayor role in the transmission of leptospires to humans. The province of Santa Fe reports the greatest number of cases in Argentina. Yet, in this region, there are still knowledge gaps regarding the diversity of rodent species that may be hosts of pathogenic leptospires. The aims of this study were to evaluate the presence of leptospiral antibodies in rodents from three riverside communities of Santa Fe, and to identify factors associated with leptospiral infection. Methodology/Principal findings Each community was divided into three environmental settings based on the level of human disturbance, and sampled during two springs (Sep-Oct 2014 and 2015) and one autumn (Mar-Apr 2015). Serum samples of captured sigmodontine and murine rodents were tested for leptospiral antibodies by enzyme-linked immunosorbent assay (ELISA), and microagglutination test (MAT) was used to assess the infecting serovar in seropositive individuals. Factors influencing seropositivity were analyzed using logistic regression models. We caught 119 rodents, of which 101 serums were suitable for analysis. Most frequently trapped species were Scapteromys aquaticus, Akodon azarae and Oligoryzomys spp., with seroprevalences of 41.3%, 42.9% and 55% respectively. Seropositivity was higher in individuals with an average body condition score and in those that were sexually mature, but in the latter the differences were marginally significant.

To investigate the molecular bases of postzygotic hybridization barriers in tuber-bearing Solanums, the wild species Solanum commersonii Dunal ex Poir. (cmm, 2n = 2x = 24, 1EBN) and Solanum acaule Bitter (acl, 2n = 4x = 48, 2EBN) were crossed in intra- and interspecific genotypic combinations, and the transcriptome of immature seeds was analyzed by using the cDNA-AFLP technique. From a total of 423 analyzed cDNA fragments, 107 (25.3%) were differentially regulated in the compatible (acl × acl and cmm × cmm) versus incompatible (acl × cmm) crosses. DNA sequence data were obtained from 21 fragments and RT-PCR analyses were carried out with five fragments to validate the cDNA-AFLP differential pattern. Sequence analysis suggested a possible role for the differentially expressed sequences in cytokinesis, cell cycle, secondary and hormonal metabolism, biodegradation, and transport. In situ hybridization experiments with fragments encoding an ubiquitin-fold modifier 1 precursor and a possible vesicle transport protein revealed expression of these genes in the embryo and endosperm. The results suggest that the collapse of the embryo and endosperm in incompatible crosses may be related to alterations in cell cycle and cytokinesis.