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Barriers to prevent spawning migrations of sea lampreys Petromyzon marinus remain an important component of an integrated sea lamprey management program in the Laurentian Great Lakes. Concerns about effects on nontarget fishes have led to the construction of specially designed vertical‐slot trap‐and‐sort fishways to mitigate potential barrier effects. To improve passage at these fishways, we used passive integrated transponder technology to assess the performance of two fishways located on low‐head sea lamprey barriers. Fishways on the Big Carp River (which flows into Lake Superior) and Cobourg Brook (which flows into Lake Ontario) were assessed for attraction efficiency, trap attraction and retention, and passage efficiency. Based on the results of these assessments, fishways were modified by increasing the trap volume and altering the funnel characteristics to reduce escapement from the trap and then reassessed. Attraction efficiency for all tagged fish was high (≥80%) at both sites in all years. Fishway modifications improved passage from 35% in 2003 to 88% and 64% in 2004 and 2005, respectively, at the Big Carp River. As expected, white suckers Catostomus commersonii, an obligate migrant, had higher attraction and passage efficiency, fewer passage attempts, and shorter migration delay than did rock bass Ambloplites rupestris, a facultative migrant. No improvements were seen at Cobourg Brook, where passage efficiency remained low (7% in 2003, 10% in 2005), probably because of the loss of attraction flow. At both fishways, individual fish averaged 3‐10 attempts to pass through the fishways and had their migrations delayed 1‐2 weeks. The observed improvements to the Big Carp River fishway, which resulted in high fishway attraction and passage rates for white suckers, suggest that vertical‐slot fishways can help mitigate the effects of low‐head barriers for some species. Our study provides a rigorous quantifiable approach to assessing fishway performance that can be employed widely and successfully to assess initial fishway design and subsequent modifications.

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AbiG is an abortive infection (Abi) mechanism encoded by the conjugative plasmid pCI750 originally isolated from Lactococcus lactis subsp. cremoris UC653. Insensitivity conferred by this Abi manifested itself as complete resistance to 712 (936 phage species) with only partial resistance to c2 (c2 species). The mechanism did not inhibit phage DNA replication. The smallest subclone of pCI750 which expressed the Abi phenotype contained a 3.5-kb insert which encoded two potential open reading frames. abiGi (750 bp) and abiGii (1,194 bp) were separated by 2 bp and appeared to share a single promoter upstream of abiGi. These open reading frames showed no significant homology to sequences of either the DNA or protein databases; however, they did exhibit the typical low G؉C content (29 and 27%, respectively) characteristic of lactococcal abi genes. In fact, the G؉C content of a 7.0-kb fragment incorporating the abiG locus was 30%, which may suggest horizontal gene transfer from a species of low G؉C content. In this context, it is notable that remnants of IS elements were observed throughout this 7.0-kb region.

BACKGROUND: Imatinib is a direct and potent inhibitor of the constitutively active tyrosine kinase, breakpoint cluster region-Abelson (Bcr-Abl), which is central to the pathogenesis of chronic myeloid leukaemia (CML) patients. As such, imatinib has become the frontline treatment for CML patients. However, the recent emergence of imatinib resistance, commonly associated with point mutations within the kinase domain, has led to the search for alternative drug treatments and combination therapies for CML. METHODS: In this report, we analyse the effects of representative members of the novel pro-apoptotic microtubule depolymerising pyrrolo-1,5-benzoxazepines or PBOX compounds on chemotherapy-refractory CML cells using a series of Bcr-Abl mutant cell lines, clinical ex vivo patient samples and an in vivo mouse model. RESULTS: The PBOX compounds potently reduce cell viability in cells expressing the E225K and H396P mutants as well as the highly resistant T315I mutant. The PBOX compounds also induce apoptosis in primary CML samples including those resistant to imatinib. We also show for the first time, the in vivo efficacy of the pro-apoptotic PBOX compound, PBOX-6, in a CML mouse model of the T315I Bcr-Abl mutant. CONCLUSION: Results from this study highlight the potential of these novel series of PBOX compounds as an effective therapy against CML.

In the Laurentian Great Lakes, sea lamprey Petromyzon marinus is an invasive species controlled primarily through application of selective toxicants (lampricides) to tributaries expected to contain the most large larvae (>100 mm). Current assessment techniques make the assumption that larvae occupy all stream habitats in the same proportion irrespective of size or life history stage. Testing this assumption relies on the availability of a marking method to determine individual animal movement between habitats over time. To evaluate the feasibility of using passive integrated transponder (PIT) technology to detect sea lamprey larvae in situ, we implanted two sizes of PIT tags (8 and 9 mm) in larvae of less than 120-mm average length to assess survival, tag loss, behavior, and detectability in situ. Larval mortality and tag loss were lower when smaller tags were used, but mortalities were still high (60%) due to the small body cavity severely restricting internal tag implantation. Burrowing performance of 8-mm PIT-tagged larvae and untagged larvae was compared, and tagged larvae spent significantly more time moving (35 vs. 21 s) and more total time (71 vs. 31 s) to completely burrow into the substrate than untagged larvae. Detectability of those 8- and 9-mm PIT-tagged larvae in situ was evaluated by releasing them in a simulated stream and using a portable PIT tag antenna on three occasions to relocate them at a detection rate that ranged from 47 to 100%. Feasibility of tracking individual larval sea lamprey movements was evaluated by tagging larvae with either 9-mm PIT tags, visible implant alpha tags, or visible implant elastomer tags; releasing them in a natural stream; and relocating them by PIT antenna or recapturing them by electrofishing. In the natural stream, a total of 36% of 9-mm PIT-tagged larvae were relocated in situ during the study period, whereas less than 7% of larvae tagged with other tag types were recaptured. The smallest currently available PIT tags are not suitable for tracking movements of individual sea lamprey larvae less than 120 mm in average length because of the significant effects of tagging on behavior and survival rates. We are unaware of other tagging technologies currently available to track individual sea lamprey larvae of this size range in situ over time.