In higher dimensional models where the gauge and gravity fields live in the bulk and the matter fields only in a brane, we point out the importance of the brane (transverse) coordinate modes, which are the Nambu-Goldstone bosons appearing as a result of spontaneous breaking of the translation symmetry. The brane recoil effect suppresses the couplings of higher Kaluza-Klein modes to the matter, and gives a natural resolution to the divergence problem caused by the exchange of infinitely many Kaluza-Klein modes. *
Escherichia coli sequence type 131 (ST131) is a pandemic clonal lineage that is responsible for the global increase in fluoroquinolone resistance and extendedspectrum--lactamase (ESBL) producers. The members of ST131 clade C, especially subclades C2 and C1-M27, are associated with ESBLs. We developed a multiplex conventional PCR assay with the ability to detect all ST131 clades (A, B, and C), as well as C subclades (C1-M27, C1-nM27 [C1-non-M27], and C2). To validate the assay, we used 80 ST131 global isolates that had been fully sequenced. We then used the assay to define the prevalence of each clade in two Japanese collections consisting of 460 ESBL-producing E. coli ST131 (2001-12) and 329 E. coli isolates from extraintestinal sites (ExPEC) (2014). The assay correctly identified the different clades in all 80 global isolates: clades A (n ϭ 12), B (n ϭ 12), and C, including subclades C1-M27 (n ϭ 16), C1-nM27 (n ϭ 20), C2 (n ϭ 17), and other C (n ϭ 3). The assay also detected all 565 ST131 isolates in both collections without any false positives. Isolates from clades A (n ϭ 54), B (n ϭ 23), and C (n ϭ 483) corresponded to the O serotypes and the fimH types of O16-H41, O25b-H22, and O25b-H30, respectively. Of the 483 clade C isolates, C1-M27 was the most common subclade (36%), followed by C1-nM27 (32%) and C2 (15%). The C1-M27 subclade with bla CTX-M-27 became especially prominent after 2009. Our novel multiplex PCR assay revealed the predominance of the C1-M27 subclade in recent Japanese ESBL-producing E. coli isolates and is a promising tool for epidemiological studies of ST131.
Pneumococcal infection in children is a major public health problem worldwide, including in Japan. The pneumococcal conjugate vaccine 7 (PCV7) was licensed for use in Japan in 2010 followed by PCV13 in 2013. This report includes the results of a nationwide surveillance of invasive pneumococcal disease (IPD) and non-IPD in paediatric patients from January 2012 to December 2014. We collected 343 isolates from 337 IPD patients and 286 isolates from 278 non-IPD patients. Of the IPD isolates, the most identified serotypes included 19A, 24F, and 15A. The prevalence of non-PCV13 serotype isolates increased significantly from 2012 to 2014 (51.6-71.4%, p=0.004). Serotypes 19A, 15A and 35B were highly non-susceptible to penicillin, and the rates of non-susceptible isolates from IPD patients to penicillin and cefotaxime significantly declined during the study period (p=0.029 and p=0.013, respectively). The non-susceptible rate to meropenem increased, particularly for serotype 15A. The IPD isolates comprised clonal complex (CC) 3111 (93.8% was serotype 19A) followed by CC2572 (81.5% was serotype 24F) and CC63 (97.1% was serotype 15A). CC3111, CC63 and CC156 (33.3% was serotype 23A, 28.6% was serotype 6B, and 14.3% was serotype 19A) were highly non-susceptible to penicillin. Of the non-IPD isolates, the most identified serotypes included 19A, 15A, and 3. In conclusion, the introduction of PCV7 and PCV13 resulted in increasing non-PCV13 serotypes and clones, including antimicrobial resistant serotypes 15A and CC63 (Sweden(15A)-25 clone).
Puberty in mammals is timed by an increase in gonadotropin-releasing hormone (GnRH)
secretion. Previous studies have shown involvement of the two neuropeptides,
kisspeptin and neurokinin B (NKB), in controlling puberty onset. Little is known
about the role of the other key neuropeptide, dynorphin, in controlling puberty
onset, although these three neuropeptides colocalize in the arcuate kisspeptin
neurons. The arcuate kisspeptin neuron, which is also referred to as the KNDy neuron,
has recently been considered to play a role as an intrinsic source of the GnRH pulse
generator. The present study aimed to determine if attenuation of inhibitory
dynorphin-kappa-opioid receptor (KOR) signaling triggers the initiation of puberty in
normal developing female rats. The present study also determined if stimulatory
NKB-neurokinin 3 receptor (NK3R) signaling advances puberty onset. Female
Wistar-Imamichi rats were weaned and intraperitoneally implanted with osmotic
minipumps filled with nor-binaltorphimine (nor-BNI), a KOR antagonist, or senktide, a
NK3R agonist, at 20 days of age. Fourteen days of intraperitoneal infusion of nor-BNI
or senktide advanced puberty onset, manifested as vaginal opening and the first
vaginal estrus in female rats. Frequent blood sampling showed that nor-BNI
significantly increased luteinizing hormone (LH) pulse frequency at 29 days of age
compared with vehicle-treated controls. Senktide tended to increase this frequency,
but its effect was not statistically significant. The present results suggest that
the inhibitory input of dynorphin-KOR signaling plays a role in the prepubertal
restraint of GnRH/LH secretion in normal developing female rats and that attenuation
of dynorphin-KOR signaling and increase in NKB-NK3R signaling trigger the onset of
puberty in female rats.
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