Leaf rust, yellow (stripe) rust, common bunt, and tan spot are economically significant diseases affecting wheat (Triticum aestivum L.) production in Canada. In this study, we investigated the genetic relationship and population structure of 81 Canadian western spring wheat cultivars released primarily between 1963 and 2011 and identified genomic regions associated with resistance to the above four diseases and insensitivity to three Pyrenophora tritici‐repentis (Ptr) toxins (Ptr ToxA, Ptr ToxB and Ptr ToxC). The cultivars were evaluated for field reaction to the four diseases and for reaction to the three Ptr toxins in a greenhouse and were genotyped with a subset of 19,919 of the wheat 90K single‐nucleotide polymorphic array and 11 gene‐specific markers. There were large genetic differences among pairwise comparisons of cultivars, except six pairs that showed <0.05 genetic distance. The cultivars exhibited clear population structure, generally in agreement with the major western Canada spring wheat classes. Using a threshold of p ≤ 5 × 10−5 and a weighted mixed linear model, we identified 94 markers from seven chromosomes associated with all traits except Ptr ToxC. Two major‐effect genomic regions on chromosomes 5B (71–74 cM) and 1A (52–53 cM) were associated with Ptr ToxA, of which the former coincided with the Tsn1 gene. For Ptr ToxB, we identified two other major‐effect regions on chromosomes 2B and 5B. The genomic regions associated with common bunt mapped on 2B, 4B, and 7A, whereas those associated with leaf rust mapped at two positions on 2B. We were only able to uncover a single marker‐trait association for tan spot on 7B and for yellow rust on 2A.

Background MDR bacteria including carbapenem-resistant Pseudomonas aeruginosa are recognized as an important cause of hospital-acquired infections worldwide. This investigation seeks to determine the molecular characterization and antibiotic resistance genes associated with carbapenem-resistant P. aeruginosa. Methods We conducted WGS and phylogenetic analysis of 72 carbapenem-resistant P. aeruginosa isolated from hospital-acquired infection patients from August 2011 to March 2015 in three major hospitals in Hanoi, Vietnam. Results We identified three variants of IMP gene, among which blaIMP-15 was the most frequent (n = 34) in comparison to blaIMP-26 (n = 2) and blaIMP-51 (n = 12). We observed two isolates with imipenem MIC &gt;128 mg/L that co-harboured blaIMP-15 and blaDIM-1 genes and seven isolates (imipenem MIC &gt; 128 mg/L) with a blaKPC-1 gene from the same hospital. MLST data shows that these 72 isolates belong to 18 STs and phylogenetic tree analysis has divided these isolates into nine groups. Conclusions Our results provide evidence that not only blaIMP-26 but other IMP variants such as blaIMP-15 and blaIMP-51 genes and several STs (ST235, ST244, ST277, ST310, ST773 and ST3151) have been disseminating in healthcare settings in Vietnam. In addition, we report the emergence of two isolates belonging to ST1240 and ST3340 that harboured two important carbapenemase genes (blaIMP-15 and blaDIM-1) and seven isolates belonging to ST3151 of P. aeruginosa that carried the blaKPC-1 gene in Vietnam, which could potentially cause serious restricted availability of treatment options in healthcare settings.

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