Microevolution within a clonal population of pathogenic bacteria: recombination, gene duplication and horizontal genetic exchange in the opa gene family of Neisseria meningitidis

1994 ◽  
Vol 12 (2) ◽  
pp. 171-180 ◽  
Author(s):  
Marcia M. Hobbs ◽  
Andrea Seiler ◽  
Mark Achtman ◽  
Janne G. Cannon
1989 ◽  
Vol 9 (3) ◽  
pp. 1224-1232 ◽  
Author(s):  
W F Ng ◽  
F Sarangi ◽  
R L Zastawny ◽  
L Veinot-Drebot ◽  
V Ling

Overproduction of P-glycoprotein is intimately associated with multidrug resistance. This protein appears to be encoded by a multigene family. Thus, differential expression of different members of this family may contribute to the complexity of the multidrug resistance phenotype. Three lambda genomic clones isolated from a hamster genomic library represent different members of the hamster P-glycoprotein gene family. Using a highly conserved exon probe, we found that the hamster P-glycoprotein gene family consists of three genes. We also found that the P-glycoprotein gene family consists of three genes in mice but has only two genes in humans and rhesus monkeys. The hamster P-glycoprotein genes have similar exon-intron organizations within the 3' region encoding the cytoplasmic domains. We propose that the hamster P-glycoprotein gene family arose from gene duplication. The hamster pgp1 and pgp2 genes appear to be more closely related to each other than either gene is to the pgp3 gene. We speculate that the hamster pgp1 and pgp2 genes arose from a recent gene duplication event and that primates did not undergo this duplication and therefore contain only two P-glycoprotein genes.


2021 ◽  
Vol 11 (1) ◽  
Author(s):  
Katie Emelianova ◽  
Andrea Martínez Martínez ◽  
Lucia Campos-Dominguez ◽  
Catherine Kidner

AbstractBegonia is an important horticultural plant group, as well as one of the most speciose Angiosperm genera, with over 2000 described species. Genus wide studies of genome size have shown that Begonia has a highly variable genome size, and analysis of paralog pairs has previously suggested that Begonia underwent a whole genome duplication. We address the contribution of gene duplication to the generation of diversity in Begonia using a multi-tissue RNA-seq approach. We chose to focus on chalcone synthase (CHS), a gene family having been shown to be involved in biotic and abiotic stress responses in other plant species, in particular its importance in maximising the use of variable light levels in tropical plants. We used RNA-seq to sample six tissues across two closely related but ecologically and morphologically divergent species, Begonia conchifolia and B. plebeja, yielding 17,012 and 19,969 annotated unigenes respectively. We identified the chalcone synthase gene family members in our Begonia study species, as well as in Hillebrandia sandwicensis, the monotypic sister genus to Begonia, Cucumis sativus, Arabidopsis thaliana, and Zea mays. Phylogenetic analysis suggested the CHS gene family has high duplicate turnover, all members of CHS identified in Begonia arising recently, after the divergence of Begonia and Cucumis. Expression profiles were similar within orthologous pairs, but we saw high inter-ortholog expression variation. Sequence analysis showed relaxed selective constraints on some ortholog pairs, with substitutions at conserved sites. Evidence of pseudogenisation and species specific duplication indicate that lineage specific differences are already beginning to accumulate since the divergence of our study species. We conclude that there is evidence for a role of gene duplication in generating diversity through sequence and expression divergence in Begonia.


1991 ◽  
pp. 159-164
Author(s):  
Li Xinwu ◽  
Hu Xujing ◽  
Gao Lihui ◽  
Xi Wenlong ◽  
Ji Yinduo ◽  
...  

Author(s):  
Kimberley V. Sukhum ◽  
Sophonie Jean ◽  
Meghan Wallace ◽  
Neil Anderson ◽  
Carey-Ann D. Burnham ◽  
...  

Neisseria meningitidis (Nm) and Neisseria gonorrhoeae (Ng) are pathogenic bacteria that can cause human infections. While Nm infections are associated with bacterial meningitis and bacteremia, a strain of Nm, isolated from the urogenital system, has recently been associated with urethritis. As this strain is becoming prominent as an emerging pathogen, it is essential to assess identification tools for Nm and Ng urogenital isolates. Consecutive Nm isolates recovered from urogenital cultures of symptomatic patients with presumptive diagnoses of gonorrhea and a random selection of Ng isolates recovered from the same population within the same time frame were characterized with routine identification systems, antimicrobial susceptibility testing, and whole genome sequencing. MALDI-ToF MS, multilocus sequence typing, 16S rRNA gene sequence, and average nucleotide identity methods accurately identified 95% (18/19) of Nm and Ng isolates. 30% (3/10) of Nm isolates were misidentified as Ng with Aptima Combo 2 CT/NG but no misidentifications were found with the Xpert CT/NG NAAT. Phylogenetic core genome and SNP-based grouping analyses showed that urogenital Nm isolates were highly related, and phylogenetically distinct from Ng and respiratory Nm isolates but similar to urogenital Nm isolates from patients with urethritis in the US. Urogenital Nm isolates were predominantly azithromycin resistant while Ng isolates were azithromycin susceptible. These data indicate that urogenital isolates of Nm can cause false-positive detections with Ng diagnostic assays. Misidentification of urogenital Nm isolates may confound public health-related activities for gonorrhea and future studies are needed to understand the impact on clinical outcome of Nm urogenital infection.


2009 ◽  
Vol 191 (12) ◽  
pp. 3861-3868 ◽  
Author(s):  
Allison Jones ◽  
Miriam Geörg ◽  
Lisa Maudsdotter ◽  
Ann-Beth Jonsson

ABSTRACT Pathogenic bacteria have evolved numerous mechanisms to evade the human immune system and have developed widespread resistance to traditional antibiotics. We studied the human pathogen Neisseria meningitidis and present evidence of novel mechanisms of resistance to the human antimicrobial peptide LL-37. We found that bacteria attached to host epithelial cells are resistant to 10 μM LL-37 whereas bacteria in solution or attached to plastic are killed, indicating that the cell microenvironment protects bacteria. The bacterial endotoxin lipooligosaccharide and the polysaccharide capsule contribute to LL-37 resistance, probably by preventing LL-37 from reaching the bacterial membrane, as more LL-37 reaches the bacterial membrane on both lipooligosaccharide-deficient and capsule-deficient mutants whereas both mutants are also more susceptible to LL-37 killing than the wild-type strain. N. meningitidis bacteria respond to sublethal doses of LL-37 and upregulate two of their capsule genes, siaC and siaD, which further results in upregulation of capsule biosynthesis.


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