Emergence of an Extensively Drug-Resistant <i>Salmonella enterica</i> Serovar Typhi Clone Harboring a Promiscuous Plasmid Encoding Resistance to Fluoroquinolones and Third-Generation Cephalosporins

Возникновение клона Salmonella enterica серовара Typhi с экстремальной лекарственной устойчивостью, несущего конъюгативную плазмиду, кодирующую устойчивость к фторхинолонам и цефалоспоринам третьего поколения
Elizabeth J. Klemm, Sadia Shakoor, Andrew J. Page, Farah Naz Qamar, Kim Judge, Dania Khalid Saeed, Vanessa Wong, Timothy J. Dallman, Satheesh Nair, Stephen Baker, Ghazala Shaheen, Shahida Qureshi, Mohammad Tahir Yousafzai, Muhammad Rehan Saleem, Zahra Hasan, Gordon Dougan, Rumina Hasan
2018-02-19

Extensively drug-resistant typhoidIncY plasmidSalmonella enterica serovar TyphiWhole-genome sequencingblaCTX-M-15 extended-spectrum beta-lactamase
ABSTRACT Antibiotic resistance is a major problem in Salmonella enterica serovar Typhi, the causative agent of typhoid. Multidrug-resistant (MDR) isolates are prevalent in parts of Asia and Africa and are often associated with the dominant H58 haplotype. Reduced susceptibility to fluoroquinolones is also widespread, and sporadic cases of resistance to third-generation cephalosporins or azithromycin have also been reported. Here, we report the first large-scale emergence and spread of a novel S . Typhi clone harboring resistance to three first-line drugs (chloramphenicol, ampicillin, and trimethoprim-sulfamethoxazole) as well as fluoroquinolones and third-generation cephalosporins in Sindh, Pakistan, which we classify as extensively drug resistant (XDR). Over 300 XDR typhoid cases have emerged in Sindh, Pakistan, since November 2016. Additionally, a single case of travel-associated XDR typhoid has recently been identified in the United Kingdom. Whole-genome sequencing of over 80 of the XDR isolates revealed remarkable genetic clonality and sequence conservation, identified a large number of resistance determinants, and showed that these isolates were of haplotype H58. The XDR S . Typhi clone encodes a chromosomally located resistance region and harbors a plasmid encoding additional resistance elements, including the bla CTX-M-15 extended-spectrum β-lactamase, and carrying the qnrS fluoroquinolone resistance gene. This antibiotic resistance-associated IncY plasmid exhibited high sequence identity to plasmids found in other enteric bacteria isolated from widely distributed geographic locations. This study highlights three concerning problems: the receding antibiotic arsenal for typhoid treatment, the ability of S . Typhi to transform from MDR to XDR in a single step by acquisition of a plasmid, and the ability of XDR clones to spread globally. IMPORTANCE Typhoid fever is a severe disease caused by the Gram-negative bacterium Salmonella enterica serovar Typhi. Antibiotic-resistant S . Typhi strains have become increasingly common. Here, we report the first large-scale emergence and spread of a novel extensively drug-resistant (XDR) S . Typhi clone in Sindh, Pakistan. The XDR S . Typhi is resistant to the majority of drugs available for the treatment of typhoid fever. This study highlights the evolving threat of antibiotic resistance in S . Typhi and the value of antibiotic susceptibility testing and whole-genome sequencing in understanding emerging infectious diseases. We genetically characterized the XDR S . Typhi to investigate the phylogenetic relationship between these isolates and a global collection of S . Typhi isolates and to identify multiple genes linked to antibiotic resistance. This S . Typhi clone harbored a promiscuous antibiotic resistance plasmid previously identified in other enteric bacteria. The increasing antibiotic resistance in S . Typhi observed here adds urgency to the need for typhoid prevention measures.
1
A novel extensively drug-resistant S. Typhi clone emerged and spread widely in Sindh, Pakistan, causing over 300 cases since November 2016.
2
A travel-associated case in the United Kingdom demonstrates the potential for this XDR typhoid clone to spread internationally.
3
Plasmid acquisition can transform MDR S. Typhi into XDR in a single step, further narrowing treatment options for typhoid.
4
The IncY plasmid shares high sequence identity with plasmids from enteric bacteria across geographically diverse locations.
5
The clone carries a chromosomal resistance region plus a promiscuous IncY plasmid encoding blaCTX-M-15 and qnrS resistance determinants.
6
The clone resists chloramphenicol, ampicillin, trimethoprim-sulfamethoxazole, fluoroquinolones, and third-generation cephalosporins.
7
Whole-genome sequencing of more than 80 isolates showed remarkable clonality, sequence conservation, and assignment to the H58 haplotype.

The extensively drug-resistant Salmonella enterica serovar Typhi H58 clone and its IncY resistance plasmid

The clone’s emergence, genetic clonality, dissemination, and acquisition of resistance to first-line antibiotics, fluoroquinolones, and third-generation cephalosporins

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2018-02-19
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Elizabeth J. Klemm
Sadia Shakoor
Andrew J. Page
Farah Naz Qamar
Kim Judge
Dania Khalid Saeed
Vanessa Wong
Timothy J. Dallman
Satheesh Nair
Stephen Baker
Ghazala Shaheen
Shahida Qureshi
Mohammad Tahir Yousafzai
Muhammad Rehan Saleem
Zahra Hasan
Gordon Dougan
Rumina Hasan
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