ABSTRACT
Neocaridina davidi is a caridean shrimp that has gained popularity in recent years as an ornamental species. Using geometric morphometrics, we investigated sexual dimorphism in carapace and second abdominal segment shape of N. davidi. Adult females displayed a more elongated carapace and a longer rostrum than males. However, male carapace shape was similar to that of juvenile females. The second abdominal pleura was more elongated and wider in adult females than in males. Significant differences were found in centroid size for the carapace and the second abdominal segment between sexes, which is consistent with sexual size dimorphism. These results support the hypothesis of a "pure search" mating system in N. davidi, where small males search actively for receptive females, and after insemination they continue searching.
Subject(s)
Decapoda/anatomy & histology , Decapoda/classification , Animal Shells/anatomy & histology , Animals , Female , Fresh Water , Male , Principal Component Analysis , Sex Characteristics , Species SpecificityABSTRACT
Methicillin-resistant Staphylococcus aureus (MRSA) is the causal agent of multiple nosocomial infections worldwide, including catheter-associated bacteremia in hemodialysis patients. The purposes of this work were to genetically characterize a group of MRSA isolates from catheter-related infections of ambulatory Mexican hemodialysis patients and to determine whether the strains are the same as those carried by the patients in their anterior nares. Sixteen pairs of MRSA isolates from the catheter (cat) and anterior nares (N) of hemodialysis patients were compared using pulsed-field gel electrophoresis (PFGE), PCR detection of adhesion genes and other virulence markers, and an antibiogram. Three pairs of N/cat MRSA isolates (18.7 %) with identical resistograms also showed the same combination of PCR-detected markers and PFGE pattern; one additional pair showed only an identical electrophoretic PFGE pattern. Of the MRSA isolates, 75 % (n = 24) were resistant to ≥ 7 antibiotics, 4 isolates were resistant to 11 antibiotics, and 7 isolates were resistant to the 12 antibiotics tested. The most frequent virulence marker combination found was spa, clfA, clfB, cna, bbp, ebps, map/eap, sdrC, sdrD, sdrE, ica, agr (65.6 %, n = 21). The SCCmec alleles of the 32 MRSA isolates were IV (n = 20), I (n = 7), II (n = 4), and V (n = 1), and no SCCmec type III MRSA was found. The genotypic characterization of the MRSA isolates studied in this work will contribute to a better understanding of the virulence gene makeup of catheter-colonizing S. aureus strains and will help to lower the infection risk in these patients.