Due to the resistance of Streptococcus pneumoniae to β-lactams, macrolides, and tetracyclines, treatment alternatives have become increasingly limited worldwide. We aim to describe the characterization of erythromycin-resistant S. pneumoniae (ERSP) strains in northeastern China over a period of 20 years. A total of 1,240 ERSP strains were collected and classified into five groups based on the ages of the patients. Etest strips and Kirby-Bauer disk diffusion were performed for drug susceptibility testing. The capsule swelling test was used for capsule typing. The phenotype of drug resistance was detected by the erythromycin and clindamycin double-disk method. The , , , and genes were detected by PCR. Among the 1,240 ERSP strains, 510 were invasive isolates, and 730 were noninvasive isolates. The results of drug susceptibility testing showed that the rates of resistance to penicillin, amoxicillin, cefotaxime, ceftriaxone, meropenem, tetracycline, trimethoprim-sulfamethoxazole, and chloramphenicol varied among the different age groups. 19F, 19A, 23F, 14, and 6B were the serotypes that were commonly found among ERSP strains. Among all strains, 99.03% (1,228/1,240) exhibited an MLSB (macrolide-lincosamide-streptogramin B) resistance phenotype, of which 1,221 strains displayed a constitutive MLSB (cMLSB) phenotype and 7 strains showed an inducible MLSB (iMLSB) phenotype. All of these strains carried the gene. In contrast, only 0.97% of strains of M phenotypes were found to carry the gene. Both the and genes were detected in 704 strains that exhibited multidrug resistance, whereas the gene was not detected. Furthermore, 1,185 tetracycline-resistant strains were found to carry the gene. Macrolide antimicrobial drugs should be used cautiously for the empirical treatment of S. pneumoniae infections. This study presents a retrospective analysis using 1,240 clinical erythromycin-resistant Streptococcus pneumoniae (ERSP) isolates collected in northeastern China between January 2000 and December 2019. The serotype distribution, corresponding vaccine coverage, as well as resistance phenotypes, genes, and mechanisms to macrolide and tetracycline of these isolates were systematically described, analyzed, and discussed. We hope that this study will inform clinicians in their respective regions when selecting antimicrobial agents. We also hope that this study is useful for researchers in related fields. Finally, we emphasize in this study that vaccination is the best preventive measure for S. pneumoniae infection considering its resistance to commonly used antibiotics. The determination of the S. pneumoniae serotype distribution also provides valuable empirical evidence for local health authorities when introducing appropriate vaccines in a specific area.
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http://dx.doi.org/10.1128/spectrum.00546-22 | DOI Listing |
Microbiol Resour Announc
March 2024
Gastro-Intestinal Microbiology and Biotechnology Unit, Agricultural Research Council-Animal Production, Irene, Pretoria, South Africa.
Rep Biochem Mol Biol
July 2023
Department of Pathobiology, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran.
Background: The number of erythromycin-resistant has significantly increased around the world. The present study aimed to determine the serotype distribution and molecular epidemiology of the erythromycin-resistant (ERSP) isolated from patients with invasive disease.
Methods: A total of 44 isolates were tested for susceptibility to several antimicrobial agents.
Microbiol Resour Announc
November 2023
Gastro-Intestinal Microbiology and Biotechnology Unit, Agricultural Research Council-Animal Production , Irene, Pretoria, South Africa.
We present draft genome sequences of 12 strains from feces isolated from cow rectums in the North West province, South Africa. The genome sizes ranged from 4.43 to 5.
View Article and Find Full Text PDFMicrobiol Spectr
October 2022
Department of Laboratory Medicine, Shengjing Hospital of China Medical University, Liaoning Clinical Research Center for Laboratory Medicine, Shenyang, China.
Acta Neuropathol Commun
April 2017
Center for Cognitive Neurology and Departments of Neurology, Pathology and Psychiatry, New York University School of Medicine, Alexandria ERSP, 450 East 29th Street, New York, 10016, NY, USA.
Studies in vivo and in vitro have suggested that the mechanism underlying Alzheimer's disease (AD) neuropathogenesis is initiated by an interaction between the cellular prion protein (PrP) and amyloid-β oligomers (Aβo). This PrP-Aβo complex activates Fyn kinase which, in turn, hyperphosphorylates tau (P-Tau) resulting in synaptic dysfunction, neuronal loss and cognitive deficits. AD transgenic mice lacking PrP accumulate Aβ, but show normal survival and no loss of spatial learning and memory suggesting that PrP functions downstream of Aβo production but upstream of intracellular toxicity within neurons.
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