Evolutionary histories and antimicrobial resistance in Shigella flexneri and Shigella sonnei in Southeast Asia

Chung The, Hao; Bodhidatta, Ladaporn; Pham, Duy Thanh; Mason, Carl J.; Ha Thanh, Tuyen; Voong Vinh, Phat; Turner, Paul; Hem, Sopheak; Dance, David A. B.; Newton, Paul N.; Phetsouvanh, Rattanaphone; Davong, Viengmon; Thwaites, Guy E.; Thomson, Nicholas R.; Baker, Stephen; Rabaa, Maia A.

doi:10.1038/s42003-021-01905-9

Download PDF

Article
Open access
Published: 19 March 2021

Evolutionary histories and antimicrobial resistance in Shigella flexneri and Shigella sonnei in Southeast Asia

Communications Biology volume 4, Article number: 353 (2021) Cite this article

3150 Accesses
17 Citations
5 Altmetric
Metrics details

Subjects

Bacterial genetics

Abstract

Conventional disease surveillance for shigellosis in developing country settings relies on serotyping and low-resolution molecular typing, which fails to contextualise the evolutionary history of the genus. Here, we interrogated a collection of 1,804 Shigella whole genome sequences from organisms isolated in four continental Southeast Asian countries (Thailand, Vietnam, Laos, and Cambodia) over three decades to characterise the evolution of both S. flexneri and S. sonnei. We show that S. sonnei and each major S. flexneri serotype are comprised of genetically diverse populations, the majority of which were likely introduced into Southeast Asia in the 1970s–1990s. Intranational and regional dissemination allowed widespread propagation of both species across the region. Our data indicate that the epidemiology of S. sonnei and the major S. flexneri serotypes were characterised by frequent clonal replacement events, coinciding with changing susceptibility patterns against contemporaneous antimicrobials. We conclude that adaptation to antimicrobial pressure was pivotal to the recent evolutionary trajectory of Shigella in Southeast Asia.

Mechanisms of SARS-CoV-2 entry into cells

Article 05 October 2021

Molecular mechanisms of antibiotic resistance revisited

Article 21 November 2022

Antibiotic resistance in the environment

Article 04 November 2021

Introduction

Shigella remains a common cause of dysentery in young children in developing countries, causing an estimated 160,000 deaths per year across all age groups globally^1,2. Though composed of four species (S. dysenteriae, S. boydii, S. flexneri, and S. sonnei), >90% of shigellosis cases globally are attributed to the latter two species³. Regional epidemiological surveillance in Southeast Asia (SEA) has been important in characterizing the burden and distribution of different Shigella species and serotypes^4,5,6,7. Such studies have highlighted the gradual decline of S. flexneri and emerging predominance of S. sonnei, particularly associated with multi-drug resistant (MDR) variants. However, conventional microbiological approaches cannot provide an in-depth understanding of the pathogens’ population structures and recent life histories.

The use of whole genome sequencing (WGS) provides unprecedented granularity for studying the circulation, population dynamics, and evolution of a specific pathogen. An early key genomic study on the global collection of extant S. sonnei revealed that the contemporary variant of this pathogen likely emerged in Europe at least 400 years ago⁸. Among the extant lineages (1–5), Lineage 3 has been the most successful, with global dissemination in the 1980s and frequent association with antimicrobial resistance (AMR). WGS and genomic analyses also detailed how Lineage 3 S. sonnei evolved and propagated following its introduction into Southern Vietnam⁹. This study also suggested that resistance to contemporaneous antimicrobials was crucial in shaping the clonal expansion of S. sonnei. Similarly, a genomic investigation of ~350 S. flexneri genomes delineated seven phylogenetic groups constituting the species¹⁰, excluding serotype 6 (which is phylogenetically closely related to Shigella boydii serotypes)¹¹. Notably, these phylogenetic groups are inconsistent with serotype-based groupings and arose on multiple occasions between the 14th and 19th centuries. The distinct accumulation of virulence factors and antimicrobial resistance (AMR) determinants in S. flexneri Lineage 3 likely account for enhanced virulence and the international dominance of serotype 2a, the predominant serotype in Lineage 3¹⁰.

Despite the discoveries made from these detailed molecular epidemiology studies, much remains unknown about the evolutionary history of S. sonnei and S. flexneri across SEA. Here, we aimed to better understand these relationships by performing WGS on a large historical collection of both S. sonnei and S. flexneri isolated across continental SEA. We aimed to investigate the population structures and evolution of these organisms, as well as to examine the establishment of AMR and the population dynamics of the two species in this region.

Results

Southeast Asian Shigella in global context

We compiled a collection of 1804 Shigella genome sequences from across mainland SEA (Thailand, Vietnam, Laos and Cambodia), including 803 S. sonnei and 1001 S. flexneri isolates. Figure 1 details the geographical distribution of these samples in the region, with Bangkok, Central Thailand, and Southern Vietnam accounting for over half of the collection (n = 915). The correlation between the proportion of species isolated over time to those sequenced in this study in the well-sampled urban area of Thailand (Bangkok and Central provinces) over three decades (normalised cross-correlation >0.95 for both S. flexneri and S. sonnei; Supplementary Fig. 1) suggests this collection is likely to be representative of the epidemiological patterns of Shigella across SEA countries. The isolation rate of S. flexneri in Thailand started to decline in the mid-1990s, which echoes the trend reported by a recent human shigellosis surveillance study (from 1993 to 2006) performed in Thailand¹². Similarly, the rapid increase of S. sonnei sequences from Vietnam since the mid-2000s (Supplementary Fig. 2) corresponds with epidemiological observations from Southern Vietnam¹³. These data reflect independent replacement events of Shigella species occurring in these two well-sampled countries. Since shigellosis is not a notifiable disease in these countries, the samples are sourced from multiple diarrhoeal surveillance studies conducted in Southeast Asia in different time frames. Thus, the temporal trend in Supplementary Fig. 2 may not fully represent the epidemiological history of the pathogen.

**Fig. 1: Overview of Southeast Asian *Shigella* genome sequences used in this study.**

Phylogenetic reconstruction of these data and globally sourced sequences demonstrated that the SEA S. flexneri samples isolated in the past three decades could be positioned in previously defined lineages (or phylogenetic groups, PGs), except for Lineages (Lin-) 5 and 6 (Fig. 2a). Based on the detection of specific combinations of the phage-borne serotype determining factors, gtr and oac variants, we overlaid the molecular serotype of all S. flexneri strains included in this study. In line with previous surveillance efforts, S. flexneri 2a (n = 431) was determined to be the predominant S. flexneri serotype in the region, followed by serotype 3a (n = 157)^12,13. As apparent in Fig. 2a, Lin-3 (N = 606) is the dominant circulating lineage and is mainly composed of serotype 2a (n = 429/606). This is followed by Lin-2 (N = 143, serotype 3a exclusively) and Lin-1 (N = 110, serotypes 1a, 1b, 1c). Sub-lineages were divided further for Lin-3 and Lin-2. Lin-3 was split into three sub-lineages (3Xv, 3.1, 3.2), with 3.1 and 3.2 appearing to be of greatest epidemiological significance. Clear geographical clustering was observed for Lin-2, with Lin-2.1 and 2.2 comprised only of South and Southeast Asian organisms and 2p mainly endemic in Africa. In addition to known lineages, our data showed the presence of a novel lineage, consisting exclusively of isolates from SEA, and most closely related to Lin-7. We defined this as Lin-8.

**Fig. 2: The global phylogenetic structure of *Shigella flexneri* and *Shigella sonnei*.**

The global phylogeny of S. sonnei reiterates that isolates from SEA mainly belong to the highly successful Lineage 3 (N = 765) (Fig. 2b). The whole genome phylogeny allowed delineation of this lineage into three sub-lineages. Two distinct sub-lineages were nested within Global 3 (the internationally disseminated major clone of S. sonnei Lin-3), and were named Global 3.1 (N = 455) and 3.2 (N = 202)⁸. These encompass the previously described S. sonnei expansions into Vietnam (IIIa and IIIb clones, respectively), with Global 3.1 shown to have undergone extensive clonal expansion across Vietnam⁹. The remaining sub-lineage, termed earlySEA (N = 101), circulated only in SEA, and was found to be most closely related to the South American expansion of S. sonnei in the 1950s⁸. A group of >30 SEA isolates were clustered within Lineage 1, which is unusual given that this lineage has only been associated with historical circulation of S. sonnei in Europe⁸.

For consistency, we refer to the aforementioned lineages and sub-lineages of SEA S. flexneri and S. sonnei as “lineages” herein (i.e. S. sonnei Lineage Global 3.1), and monophyletic clades within these lineages as “clades”.

The evolutionary history and geographical spread of Shigella in Southeast Asia

To enhance phylogenetic resolution and decipher the evolutionary history of SEA S. flexneri and S. sonnei within each lineage, we constructed individual maximum likelihood phylogenies for each examined lineage. All lineages, except for S. flexneri Lin-4, displayed a high correlation between sampling date and the phylogeny’s root-to-tip divergence (R² ranging from 0.5 to 0.95; linear regression), thus indicating that most Shigella populations shows a clock-like single nucleotide polymorphism (SNP) accumulation rate (Supplementary Figs. 3, 4). Estimated nucleotide substitution rates were comparable among Shigella lineages (5 × 10⁻⁷ to 9 × 10⁻⁷ substitutions per site per year) (Table 1), which is concordant with previous estimates from global studies of S. flexneri and S. sonnei^8,10,14. However, estimates for S. flexneri Lin-7 and Lin-8 and S. sonnei Lin-1 suggest that these organisms have significantly lower substitution rates (1.4 × 10⁻⁷ to 3.84 × 10⁻⁷ substitutions per site per year). These lineages also formed the root of the S. flexneri and S. sonnei global phylogeny, respectively, and were genetically distant to their more rapidly disseminating counterparts. It has been shown in S. sonnei that an elevated evolutionary rate is associated with successful global spread and clonal establishment⁸, which may facilitate adaptation in new environments. The slower molecular clocks of the aforementioned lineages (S. flexneri Lin-7 and Lin-8, S. sonnei Lin-1) may be associated with a corresponding reduction in fitness or adaptability, which may explain their lower than expected isolation rates in regional surveillance studies.

Table 1 Summary of findings from Bayesian phylogenetic inference for major Shigella lineages.

Full size table

Using these data, we estimated the times to most recent common ancestor (TMRCAs) of multiple SEA Shigella lineages, inferred individually via Bayesian phylogenetics (BEAST v1.8.3) (Table 1). Despite their overarching genetic differences, the majority of these lineages appeared to have emerged within or entered the region during the last century, between the 1970s and 1980s (Supplementary Figs. 5–9). Some lineages, such as S. sonnei early SEA, S. flexneri 3Xv (serotype Xv) and S. flexneri 2.1 (serotype 3a), were composed of a single clone and largely circulated exclusively within Thailand over a relatively short time period (<15 years from 1980 to 1995) with limited detection elsewhere in SE Asia (Supplementary Figs. 5–7). This suggests that these lineages could exhibit transient and restricted establishment in the region. In contrast, the phylogenies of other Shigella lineages showed a high degree of genetic diversity and a wider geographical and temporal distribution. S. flexneri Lin-3.1 and S. sonnei Global 3.1 contained exclusively SEA isolates, appearing as two substantial and extensive clonal expansion events that occurred throughout the region starting in the late 1970s (Supplementary Figs. 8, 9). Other lineages (S. flexneri Lin-1, 2.2, 3.2 and S. sonnei Global 3.2) in our dataset show wider geographical distributions, with SEA clades often interspersed with isolates from other continents. This observation indicates that these clades were likely introduced and established endemically circulating populations in SEA on three to five occasions (per lineage) after 1970. Once introduced, these lineages disseminated across the region (Supplementary Figs. 6–9). Geographical mapping conducted on lineages with highest recorded disease burdens (S. flexneri Lin-3.1 and 3.2, S. sonnei Global 3.1 and 3.2) demonstrated that the two species shared similar patterns of circulation in SEA (Supplementary Fig. 10). Intranational dissemination was frequent and characterised by Shigella transmission between major urban areas (i.e. Bangkok and Central Thailand; Southern Vietnam) and secondary population centres (Western and Northeastern Thai provinces; North-Central, and South-Central Vietnam), usually creating pan-regional Shigella populations. Specifically, inter-regional connectivity was most pronounced in Shigella lineages undergoing extensive clonal expansion across SEA (S. flexneri Lin-3.1, S. sonnei Global 3.1).

Further genomic interrogation found that serotype 4av was the most common, and likely the ancestral serotype for S. flexneri Lin-7 isolates (Supplementary Fig. 11). Frequent deletions of gtrIV and/or pSfYv prompt conversion to serotypes Yv, 4a, and Y. The TMRCA of Lin-7 was estimated to date back to the 15th century. However, circulations within SEA were founded by two major clades that likely emerged during the mid-1800s, with a lack of samples from outside of the region suggestive of in situ evolution and divergence of these two clades within SEA. S. flexneri Lin-8, for which the TMRCA was estimated to date back to the 1930s, is mostly comprised of serotypes Y and Yv (Supplementary Fig. 11). Previous surveillance studies have reported a low prevalence of these serotypes (4, Y, Yv) in the region, indicating the minor contributions of Lin-7 and Lin-8 to the clinical burden of shigellosis here^7,12,13. Alternatively, S. sonnei Lin-1 was estimated to have been introduced to SEA in the mid-1800s but has subsequently been largely restricted to Northern Vietnam, with only occasional isolates seen elsewhere in SEA (Supplementary Fig. 5). The most closely related organisms, as well as the immediate sister group, to these SEA Lin-1 were historical organisms isolated in France from 1940s to 1970s.

The antimicrobial resistance profile of Shigella in Southeast Asia

The diversity and dynamic interplay of different Shigella lineages within SEA pose questions concerning the underlying factors that govern their ecology. We hypothesised that changes in AMR were associated with dynamics of Shigella populations. Since antimicrobial susceptibility testing was only available for a subset of isolates, we profiled the resistome of all isolates, supported by the consistent agreement between phenotypic and genotypic results for Shigella¹⁵.

A high proportion of both S. sonnei and S. flexneri exhibited resistance to sulphonamides, tetracycline, and streptomycin (Fig. 3), evidencing the maintenance of these resistance types since as early as 1980. Resistance to these antimicrobials was conferred by a one-time acquisition of the spA plasmid (sul2, tetRA, strAB) in S. sonnei prior to the existence of the MRCA of CenAsiaIII, Global 3.1 and 3.2, but excluding earlySEA (Supplementary Fig. 12). Alternatively, earlySEA exclusively and stably harboured a genomic island that was almost identical to the Shigella Resistance Locus (SRL) (aadA, bla_OXA-1, tetB, and catA1) previously reported in S. dysenteriae serotype 1¹⁶. These events explain the distinctive resistance profile of earlySEA among S. sonnei (Fig. 3b and Supplementary Fig. 12). The SRL island (strAB, bla_OXA-1, tetB, and catA1) was also independently integrated into multiple S. flexneri lineages, except Lin-3Xv (Supplementary Fig. 13), in addition, granting S. flexneri ubiquitous resistance to ampicillin and chloramphenicol. The SRL was also subject to frequent modification, exemplified by the independent deletion of bla_OXA-1 and tetB in Lin-2.2 around 1990 (Figs. 3a, 4c).

**Fig. 3: Trend of antimicrobial resistance (AMR) genotype in Southeast Asian *Shigella flexneri* and *Shigella sonnei*.**

**Fig. 4: Clonal replacement of *Shigella flexneri* in Southeast Asia.**

Trimethoprim resistance coincides with clonal replacement in Shigella

We observed a marked difference in resistance to trimethoprim pre- and post-1990 in S. flexneri, with the resistant genotype gradually becoming dominant in all populations (Fig. 3a). This apparent preference for trimethoprim resistance was evident in both the numbers of dfrA variants (eight genes) and the independent occasions upon which they were integrated into our S. flexneri collection (Supplementary Fig. 13). Specifically, the expansions of Lin-3.2, 3Xv, and part of 2.2 were all associated with the fixation of dfrA1, while independent acquisitions of a plasmid-borne dfrA14 were pervasive in other lineages (Lin-1, 3.1, 7, 8). This distinctive bla_TEM-1-strAB-sul2-dfrA14 AMR gene cluster was found to be co-transferred with a plasmid backbone highly similar to pRC960-1 (accession number: KY848295; 219/298 plasmid occasions), which was recently isolated from a S. flexneri Y of porcine-origin in China¹⁷. Independent acquisitions across multiple lineages in all examined countries resulted in the presence of the plasmid in ~300 S. flexneri isolates, commonly in organisms isolated from mid-1990s onwards. These results suggest a strong selective pressure favouring the maintenance of trimethoprim resistance in S. flexneri. We next sought to evaluate how S. flexneri population dynamics were altered in response to trimethoprim pressure. In order to limit the effects of pressure exerted by serotype-mediated immune escape, the analysis was conducted only for S. flexneri serotypes 2 (2a and 2b) and 3a. For serotypes 2 in Thailand and 3a across SEA, trimethoprim resistance increased rapidly in the 1980s and 1990s, nearly reaching fixation in both populations (Figs. 4a, 4c). This trend occurred concurrently with a shift in population structure, with Lin-3.1 replaced by Lin-3.2 (serotype 2), and Lin-2.1 replaced by Lin-2.2 (serotype 3a). Alternatively, an opposing trend was observed for serotype 2 in Vietnam, with trimethoprim resistance in gradual decline as Lin-3.1 began to predominate by 1996 (Fig. 4b).

Similarly, trimethoprim resistance accelerated dramatically in S. sonnei during 1980–1990, which occurred concurrently with the replacement of earlySEA by Global 3.2 and resulted in the predominance of the latter in SEA in the early 1990s. Trimethoprim resistance was mainly attributed to the stable inheritance of a class II integron (dfrA1) following its acquisition in the inferred MRCA of Global 3.1, 3.2, and CenAsiaIII (Supplementary Fig. 12). Moreover, other resistance mechanisms were also noted, including the integration of a class I integron (carrying aph3-ereA-dfrA5) into eight earlySEA isolates in 1989-90, and a 20 kbp MDR cassette (carrying dfrA12-aadA2-qacEΔ-sul1-mphA-merADE- bla_TEM-1) into Lineage 1 in five separate events. These lines of evidence point to a preference for trimethoprim resistance in several S. sonnei lineages in the 1980s and 1990s. In contrast, the diminishing role of earlySEA resulted in the reduction of resistance to chloramphenicol and ampicillin across the region.

Heightened resistance to quinolones and 3rd generation cephalosporin associated with recent endemic circulation in Southeast Asia

Quinolone resistance in Shigella emerged in the mid-1990s and became more prevalent in the 2000s (Figs. 3, 4, 5) due to the proliferation of clones bearing mutations in gyrA (S83L or D87Y), which was apparent for S. flexneri lineages with widespread circulation in SEA (Lin-2.2, Lin-3.1, and to a lesser extent in Lin-8) (Figs. 3a, 4b, 4c). This finding mirrors previously published data for S. sonnei in Vietnam, in which the establishment of local populations of S. sonnei Global 3.1 was preceded by fixations of gyrA mutations⁹.

**Fig. 5: Clonal replacement of *Shigella sonnei* in Southeast Asia.**

The most pronounced difference between the resistomes of S. flexneri and S. sonnei was their susceptibility to 3rd generation cephalosporins. Resistance to this antimicrobial was predicted for only 6/1001 S. flexneri in our collection, with all bla_CMY and bla_CTX-M variants appearing from the year 2000 onwards (Supplementary Fig. 13). It is also clear that macrolide resistance emerged sporadically in S. flexneri over the entire period of the study with no apparent fixation (Fig. 3a). Conversely, carriage of several ESBL plasmids bearing bla_CTX-M was noted in S. sonnei Global 3.1 isolated in Vietnam⁹ (Fig. 5, Supplementary Fig. 12). However, in the early 2010s, the newly introduced fluoroquinolone resistant CenAsiaIII rapidly superseded Global 3.1 to be the most commonly detected¹⁸, but this clonal replacement did not reverse the ongoing AMR trends. Alternatively, resistance to 3rd generation cephalosporins and macrolides continued to increase, as evidenced by CenAsiaIII S. sonnei’s ability to sample the local AMR gene pool¹⁹.

Discussion

Our work represents the most comprehensive genomic epidemiology study of Shigella in SEA to date. We employed an intensive sampling strategy to cover both temporal and spatial scales, resulting in a collection of >1800 genome sequences from four countries. Nevertheless, our interpretations remain subject to the uneven temporal distribution inherent to the collection. In particular, Thai isolates dominated from 1980 to 1995, while Vietnamese isolates were more common from 1995 onward. Organisms from Laos and Cambodia were scarce and only available from the last decade. These limitations, together with the over-representation of major urban Shigella populations in this collection, may bias interpretations. Specifically, the predominance of Thai isolates in the earlier period might have favoured the inference of directional transmissions originating from this country. Further, our collection was limited to clinical samples from the paediatric population, ignoring potential Shigella diversity that may arise in environmental reservoirs (for S. flexneri) and other shigellosis high-risk groups, such as the elderly or men-who-have-sex-with-men (MSM).

Notwithstanding these limitations, we were able to document the genetic diversity of various Shigella species and serotypes over the past three decades in SEA. S. sonnei was composed of several genetically distinct populations circulating over different timeframes. Within S. flexneri, a single serotype frequently consisted of several phylogenetically related but distinct clones, highlighting the limitation of inferring the genetic makeup of the species from serotyping¹⁰. Despite the diverse genetic composition of multiple Shigella lineages, we found that the majority of their progenitors were likely introduced into continental SEA around 1970s-90s. Evidence for regional transmission of Shigella was most pronounced in lineages undergoing extensive clonal evolution, such as S. flexneri Lin-3.1 and S. sonnei Global 3.1, likely driven by increased human movement in the region. Indeed, domestic migration increased as economic growth accelerated and migration costs lowered in the 1990s, resulting in the relocation of 4.5 million people within Vietnam (~6% total population)²⁰. Generally, we observed multiple introductions of Shigella lineages in the 20th century, except for two lineages (S. sonnei Lin-1 and S. flexneri Lin-7) having established regional endemic populations from the late 19th century. It is therefore intriguing that S. sonnei Lin-1 seems to have been maintained for more than a century, which stands in contrast to the relatively transient establishment of other S. sonnei populations observed in Southern Vietnam and Thailand. As this lineage is rarely found outside Europe, its distinctive epidemiology raises questions related to its exclusive success in Northern Vietnam. While most regions under consideration in these analyses (Central Thailand, Cambodia, Central and Southern Vietnam) experience a tropical climate throughout the year, Northern Vietnam belongs to the humid subtropical climate zone characterised by distinct seasonal temperature fluctuations. Meteorological factors have been associated with seasonal variation in shigellosis incidence in endemic countries²¹. Therefore, future research should examine how climatic differences affect the survival and transmission of S. sonnei, as well as the epidemiological significance of S. sonnei Lin-1.

Surveillance data have shown that S. sonnei is replacing S. flexneri as the major aetiological agent of shigellosis in most developing countries, including those in SEA^12,13,22. However, there is little understanding of the intraspecific population dynamics of S. sonnei and S. flexneri. Importantly, our findings highlight the regularity of clonal replacement within this genus, as observed in both S. sonnei and major S. flexneri serotypes 2 and 3a. These ecological successions are often coupled with changes in resistance to contemporaneous antimicrobials, most notably to trimethoprim as outlined by resistome profiling in this study. This observation strongly suggests that response to antimicrobial usage is a key adaptive strategy in both species. Indeed, the deployment of co-trimoxazole for shigellosis treatment in the 1980s was quickly met with rapid increases in trimethoprim resistance by the mid-1980s across SEA²³. Similarly, the current reliance on ciprofloxacin for shigellosis treatment has clearly instigated the global spread of fluoroquinolone resistant S. sonnei, which originated from South Asia around 2007¹⁴. In a separate scenario, clonal replacement has been noted in the recent shigellosis epidemiology of the MSM community in the United Kingdom. S. flexneri 3a was the predominant aetiology from the mid 2000s to early 2010s, and its propagation was linked with the acquisition of the pKSR100 plasmid encoding for resistance to azithromycin, an antimicrobial frequently prescribed for sexually transmitted infections in the MSM community²⁴. Subsequently, the horizontal transfer of pKSR100 into other Shigella genotypes has similarly and repeatedly fuelled the emergence of novel variants in this population²⁵, culminating in the recent dominance of dual ciprofloxacin and azithromycin resistant S. sonnei (of CenAsiaIII sub-lineage) since 2017²⁶. It is generally seen that intensified antimicrobial usage coupled with increased human mobility at the global scale may allow Shigella to exploit its high degree of genetic variability, at times favouring the establishment of newly introduced but highly resistant clones. Thus, changes in antimicrobial treatment in one locale could have far-reaching regional or global implications.

The epidemiology of S. sonnei is driven by intercontinental spread and recent local establishment of pandemic clones⁸; this trend is apparent in SEA, exemplified by the local expansion of Global 3.1 and multiple introductions of Global 3.2. In contrast, previous genomic epidemiology research has suggested that longer-term local establishment of lineages in endemic regions dominate the epidemiology of S. flexneri populations, in which a high degree of genetic diversity is frequently maintained in a single location¹⁰. This notion is supported by the occasional recovery of environmental S. flexneri and the epidemiological association between this bacterial species and contaminated water^27,28. Moreover, the virulence plasmid of S. sonnei is unstable at environmental temperatures, whereas S. flexneri’s counterpart is not²⁹. S. sonnei also exclusively possesses a Type VI secretion system (T6SS) to overcome E. coli-established colonization resistance³⁰, as well as a plasmid-borne O-antigen and capsule granting resistance to complement-mediated killing³¹, phagocytosis³², and phagolysosomal degradation³³. These lines of evidence suggest that S. sonnei may have adapted specifically for person-to-person transmission, while S. flexneri retains a more generalist lifestyle. However, our analysis offers a different perspective on S. flexneri evolution in SEA. While the population diversity of S. flexneri has been maintained by the simultaneous existence of multiple lineages, these were generally established from the 1950s onwards. This observation indicates that long-term circulation is uncommon for the majority of S. flexneri lineages in SEA. The emergence of new S. flexneri clones in the region could be attributed to either: (1) foreign introductions with or without local establishment or (2) successful expansions of specific clones from native S. flexneri populations. Recent clonal emergence and the admixture of regional and global isolates in a single lineage lend more support to the former postulation. Thus, we speculate that the introduction-local expansion mechanism supported the evolution of Lineages 1, 2.1, 2.2, 3Xv, 3.1, and 3.2, while the ancestral Lin-7 and Lin-8 represent a scenario where long-term local circulation may play a more prominent role. These results resonate with those recently described for Vibrio cholerae. In this pathogen, a single bacterial lineage responsible for the seventh cholera pandemic was shown to have been introduced into Africa on twelve distinct occasions, with the later and increasingly drug resistant waves replacing the pre-existing antimicrobial susceptible populations³⁴. These introductions began in the 1970s, with the authors arguing that intense human migration and contact during the few decades of globalization resulted in inter- and intra-continental cholera transmission. This finding also downplays the role of aquatic V. cholerae in the pandemic’s epidemiology. We speculate that although species diversity in both S. flexneri and V. cholerae are sustained via occupation of respective environmental niches, the majority of existent clinical burden could be attributed to expansions of specific clones, probably owing in part to increased human mobility and contact following globalization.

Collectively, our findings indicate that the evolutionary histories of both S. flexneri and S. sonnei in SEA were shaped by frequent clonal replacement events, which are linked to changing patterns of resistance to contemporaneous antimicrobials. However, antimicrobial resistance alone does not necessarily guarantee the continuing dominance of the Shigella species in the human population. The aetiological landscape of childhood diarrhoea in one of Vietnam’s urban centres, for example, now mirrors that of developed settings, with decreasing isolation rates of Shigella and increasing non-typhoid Salmonella burden³⁵. This is likely due to improved hygiene and sanitation, changing diet, or other factors tied to economic development. While our work focused on the impact of antimicrobial resistance, other factors could potentially contribute to the observed population dynamics in Shigella. These include stochasticity and population bottlenecks, as well as differences in population size or virulence potential at the sub-lineage level, which are difficult to quantify using only genomic data. Nevertheless, our work highlights the importance of continuous surveillance of shigellosis, preferably using high-resolution genomic techniques, to better inform public health measures and future intervention studies.

Methods

Organism collection and whole genome sequencing

In order to explore the evolutionary history of Shigella in Southeast Asia, we gathered a collection of 1433 Shigella isolates from continental Southeast Asian countries, including Thailand, Vietnam, Laos and Cambodia. Shigella isolates were retrieved from multiple collaborative institutions in the region, including: Armed Forces Research Institute of Medical Sciences (AFRIMS) Thailand, N = 1,239; Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit (LOMWRU), N = 43; Cambodia-Oxford Medical Research Unit (COMRU), N = 19; Institut Pasteur Cambodia, N = 19; Oxford University Clinical Research Unit (OUCRU) Ho Chi Minh City, N = 113. The bacterial isolates and data for this investigation originated from clinical studies approved by the scientific and ethical committees of The Hospital for Tropical Diseases (HTD) in Ho Chi Minh City, Vietnam, all other participating hospitals, the Institutional Review Board of the Walter Reed Army Institute of Research (Thailand data) and the Oxford Tropical Research Ethics Committee (OXTREC) in the United Kingdom. The study also included the characterization of bacterial isolates submitted for routine diagnostic purposes. Study participants or parents of young participants were required to provide written informed consent for the collection of samples and subsequent analyses, except when samples were collected as part of routine care. All of these Shigella were isolated from patients, predominantly young children, with dysenteric diarrhoea during diarrhoeal surveillance studies performed in the respective countries. For all of these isolates, genomic DNA was extracted from pure bacterial culture by staff scientists of the corresponding institutions, using the Wizard Genomic DNA Extraction Kit (Promega, Wisconsin, USA). DNA was stored at −20 ^oC until shipment to the Wellcome Trust Sanger Institute (WTSI) for whole genome sequencing on an Illumina HiSeq2000 platform to produce paired-end reads of 125 bp in length. In addition, these data were appended with sequences available from previous studies, including 119 S. flexneri and 252 S. sonnei collected at OUCRU from previous diarrhoea surveillance research⁹. In summary, the compiled collection includes 1804 sequences (803 S. sonnei and 1001 S. flexneri), which covers multiple locations in the area, as detailed in Fig. 1 and Supplementary Table 1. These consist of S. flexneri of all reported phenotypic serotypes, except for serotype 6, as it is genetically more closely related to S. boydii. The collection times range from 1980 to 2013, but the timing of sample collections varies geographically.

Shigella flexneri molecular serotyping

Though S. flexneri serotyping was performed by collaborating institutes using commercial antisera (Denka Seiken, Japan), this was not available for all isolates and could not cover all S. flexneri epitopes arising from bacteriophage-mediated O-antigen modification. We sought to exhaustively identify serotype-determining genetic elements from S. flexneri whole genome sequences, adopting the methodology developed previously^36,37. Genomic derived serotyping has shown a high concordance (>90%) with phenotypic serotyping, with the majority of discrepancies in serotype resulting from disruptive genetic mutations¹⁵. ARIBA v2.12.0 was used to identify serotype-specific determinants, including gtrI, gtrII, gtrIV, gtrIc, gtrV, gtrX, oacA, oacB, oacD, and opt (pSFXv_2). ARIBA outputs from each isolate were then compiled and curated. Genes that contained any deletion, frameshift, or nonsense mutations were deemed non-functional and counted as being absent from the isolate. Genomic serotype was defined based on specific combinations of these elements, as detailed in Supplementary Table 2.

Short read mapping and phylogenetic reconstruction

S. sonnei and S. flexneri sequencing reads were mapped to either the reference Ss046 (accession NC_007384) or Sf2a strain 301 (accession NC_004337), respectively, using the hash-indexing mapping tool SMALT (version 0.7.4)³⁸. Candidate single nucleotide polymorphisms (SNPs) were called against the reference and filtered using SAMtools v1.8 (mpileup option) and bcftools v1.8³⁹. Low quality SNPs were removed if they met any of the following criteria: consensus quality <50, mapping quality <30, ratio of SNPs to read at a position <75%, read depth <4, or number of reads per strand <2.

Phylogenetic reconstructions were performed independently for S. flexneri and S. sonnei. To provide phylogenetic context, we combined the SEA S. flexneri collection with >300 sequences from the species global evolution study¹⁰. Regions pertaining to mobile and recombinogenic genetic elements were detected and removed by Gubbins v1.4.5⁴⁰, as were alignments columns with at least 2% indeterminate bases or gaps. This created a 51,616 bp SNP alignment across 1323 S. flexneri taxa, which was input into RAxML v8.2.4 for maximum likelihood phylogenetic reconstruction under the GTRCAT model, with 100 bootstrap replicates⁴¹. Phylogenetic groups (lineages) were defined as previously proposed, including Lineages 1, 2, 3, 4, 5, 6, and 7¹⁰. To identify the most appropriate root for the S. flexneri species tree, we constructed a maximum likelihood phylogeny based on a core genome SNP alignment of 111 representative sequences. These include ten random samples from each of the defined lineages (1, 2.1, 2.2, 3Xv, 3.1, 3.2, 4, 5, 6, 7, 8) and a S. flexneri serotype 6 isolate (phylogenetically closely related to S. boydii, and used as an outgroup). The core genome alignment was built using Roary v3.12.0, which utilised the annotations of de novo assemblies (see below)⁴². The resultant phylogeny indicated that the inferred common ancestor of Lineages 7 and 8 sits basal within the S. flexneri species phylogeny, so this inferred common ancestor was chosen as the most appropriate root. Maximum likelihood phylogenies were then generated independently in a similar manner for lineages containing substantial numbers of Southeast Asian sequences, including Lineages 1, 2, 3Xv, 3.1, 3.2, 4, 7, and 8.

For S. sonnei, we combined our SEA collection with 190 representative sequences from the species global evolution study^8,43. Using the aforementioned procedures, a 14,241 bp SNP alignment of 993 sequences was generated and used for phylogenetic reconstruction in RAxML under a GTRCAT model, with 100 bootstrap replicates. Phylogenetic nomenclatures followed those established previously in the global study, and we subsequently constructed individual maximum likelihood phylogenies for the following groups: Lineage 1, Lineage 3 earlySEA, Lineage 3 Global 3.1, and Lineage 3 Global 3.2. A previous global study of S. sonnei showed that Lineage 1 sits basal within the species phylogeny⁸; thus, we rooted our S. sonnei phylogeny using Lineage 1. The S. flexneri and S. sonnei species global trees were visualised with associated metadata using the web-based interactive Tree of Life (iTOL) v4⁴⁴.

Temporal structure analysis and Bayesian phylogenetic inferences

We conducted temporal structure analyses and Bayesian phylogenetic inferences separately for each of the major Shigella lineages (S. flexneri Lineages 1, 2.1, 2.2, 3Xv, 3.1, 3.2, 4, 7, 8; S. sonnei Lineage 1, earlySEA, Global 3.1, and Global 3.2). To limit sampling bias, a maximum of five isolates per year per region were included for each lineage. Table 1 provides detailed information on the input for analysis of each lineage. Maximum likelihood phylogenies of the subset taxa were constructed independently for each lineage, following the aforementioned procedures. TempEst v1.5.1 was used to estimate the linear relationship between root-to-tip divergence of the input phylogeny and the isolates’ attached date (sampling date in month/year)⁴⁵. The most suitable substitution model for each input alignment was determined using the fast ModelFinder implemented in IQ-TREE v1.6.7^46,47. BEAST v1.8.3 was used to infer evolutionary dynamics, including estimation of substitution rates and TMRCAs of SEA sequences for each Shigella lineage⁴⁸. To identify the best-fit model for each dataset, multiple BEAST runs were conducted on combinations of the appropriate substitution model (Table 1), and a strict, random local or relaxed lognormal clock model in conjunction with a constant or Bayesian skyline demographic model. Each of these analyses was performed in triplicate using a continuous 50–200 million generation MCMC chain, with samples taken every 5000–20,000 generations, respectively. Tracer v1.6 was used to visually assess the parameter convergence of each run (ESS > 200). For robust model selection, both path sampling and stepping-stone sampling approaches were applied to each BEAST run to estimate marginal likelihoods^49,50, and the best model was selected based on comparison of Bayes factors. For the best model, triplicate runs were combined using LogCombiner v1.8.3, with removal of 20% burn-in.

Stochastic mapping of geographical traits

For major SEA Shigella lineages (S. flexneri Lin-3.1 and Lin-3.2; S. sonnei Global 3.1 and 3.2), we aimed to reconstruct the ancestral geographical states of each isolate using the maximum likelihood phylogeny, as previously described¹⁴. We treated geographical source (as documented in Supplementary Table 1) of the organisms as discrete characters. To control for biased sampling, for each lineage, we sub-sampled the input phylogeny to include an equal number of isolates (N ranging from 11 to 18) from each character state, generating 500 subsampled trees. Stochastic mapping, implemented as the function make.simmap in the R package phytools v0.6.0, was applied to quantify transition events between geographical characters, separately for each subsampled tree⁵¹. The analysis was performed under an asymmetric model of character change (ARD) with the rate matrix sampled from the posterior probability distribution using MCMC (Q = mcmc) for 100 simulations⁵².

De novo assembly and determination of accessory genomes

De novo sequence assembly for each isolate was performed using Velvet v1.2.03, with optimal k-mer size determined by VelvetOptimizer by varying its size between 66% and 90% of read length⁵³. Sequence assemblies also followed the procedure described by the WTSI’s Pathogen Genomic Bacteria Assembly pipeline, which facilitates robust and improved high-throughput prokaryote assembly⁵⁴. Contigs with size <300 bp were removed, and read pairs were mapped back to the improved assembly using SMALT to assess the assembly quality. Annotation was determined for each assembly using Prokka⁵⁵. ARIBA, an approach to detect genetic elements of choice from short reads, was implemented to identify the presence of antimicrobial (AMR) genes and plasmid incompatibility types, based on the reliably curated ResFinder and PlasmidFinder database, respectively^56,57,58. The resulting resistome served as the isolates’ AMR profiles for downstream analyses, supported by the consistent agreement between phenotypic and genotypic AMR findings for Shigella¹⁵.

The resistance profile for each isolate was summarised based on the following detected determinants: 3rd generation cephalosporins (bla_CTX-M, bla_CMY, bla_DHA), aminoglycoside (strAB, aadA, aac(3)-IIa, aph(3’)), beta-lactam (bla_TEM, bla_OXA-1), macrolide (ermB, mefB, ereA, mphA), phenicol (cmlA1, floR, catA, cat3), quinolone (qnrS1, qnrB, gyrA codons S83 or D87 mutations), sulphonamide (sul), tetracycline (tet), trimethoprim (dfrA variants), and fluoroquinolone (gyrA codons S83 and D87, and parC S80 mutations). The resistance profile for each antimicrobial was summarised for each S. flexneri and S. sonnei lineage, during a defined five- to six-year period (from 1980 to 2016). We additionally included 71 Southeast Asian CenAsiaIII lineage isolates in this analysis, sampled mostly from Vietnam after 2013, to provide an up-to-date overview on trends in AMR and clonal replacement. For analysis of S. flexneri serotype 3a, twelve Lin-2.2 isolates (all isolated from a hospital in Bangkok in 1983) were found to be genetically closely related (pairwise SNP difference ranging from 0 to 5). This suggests a presumptive shigellosis outbreak and is not representative of Shigella regional circulation. Thus, we only included one isolate from this 1983 outbreak to the AMR and clonal replacement analysis.

Statistics and reproducibility

General data summary, analysis, and visualization were conducted using R⁵⁹ (version 3.6.1) and RStudio⁶⁰ (version 1.1.383), including the package phytools v0.6.0⁵². Maximum likelihood phylogenies were constructed with at least 100 rapid bootstrap replicates, and Bayesian phylogenetic inference was performed in triplicate for each tested model specification. Stochastic mapping was performed on 500 subsampled phylogenies for each of the examined Shigella lineages.

Reporting summary

Further information on research design is available in the Nature Research Reporting Summary linked to this article.

Data availability

Raw sequence data are available in the NCBI Sequence Read Archive (project PRJEB5281: Phylogeography of Shigella spp. in Southeast Asia). Data are available from the corresponding author on request. Source data for figures are provided in Supplementary Data 1.

References

Kotloff, K. L. et al. Burden and aetiology of diarrhoeal disease in infants and young children in developing countries (the Global Enteric Multicenter Study, GEMS): a prospective, case-control study. Lancet 382, 209–222 (2013).
Article PubMed Google Scholar
Troeger, C. et al. Estimates of global, regional, and national morbidity, mortality, and aetiologies of diarrhoeal diseases: a systematic analysis for the Global Burden of Disease Study 2015. Lancet Infect. Dis. 3099, 1–40 (2017).
Google Scholar
Gu, B. et al. Comparison of the prevalence and changing resistance to nalidixic acid and ciprofloxacin of Shigella between Europe-America and Asia-Africa from 1998 to 2009. Int. J. Antimicrob. Agents 40, 9–17 (2012).
Thompson, C. N. et al. A prospective multi-center observational study of children hospitalized with diarrhea in Ho Chi Minh City, Vietnam. Am. J. Trop. Med. Hyg. 92, 1045–1052 (2015).
Article PubMed PubMed Central Google Scholar
Bodhidatta, L. et al. Bacterial enteric pathogens in children with acute dysentery in thailand: increasing importance of quinolone-resistant Campylobacter. Southeast Asian J. Trop. Med. Public Health 33, 752–757 (2002).
CAS PubMed Google Scholar
Meng, C. Y. et al. Etiology of diarrhea in young children and patterns of antibiotic resistance in Cambodia. Pediatr. Infect. Dis. J. 30, 331–335 (2011).
Article PubMed Google Scholar
von Seidlein, L. et al. A multicentre study of Shigella diarrhoea in six Asian countries: disease burden, clinical manifestations, and microbiology. PLoS Med 3, e353 (2006).
Article Google Scholar
Holt, K. E. et al. Shigella sonnei genome sequencing and phylogenetic analysis indicate recent global dissemination from Europe. Nat. Genet. 44, 1056–1059 (2012).
Article CAS PubMed PubMed Central Google Scholar
Holt, K. E. et al. Tracking the establishment of local endemic populations of an emergent enteric pathogen. Proc. Natl Acad. Sci. USA. 110, 17522–17527(2013).
Article CAS PubMed PubMed Central Google Scholar
Connor, T. R. et al. Species-wide whole genome sequencing reveals historical global spread and recent local persistence in Shigella flexneri. Elife 4, 1–16 (2015).
Article Google Scholar
The, H. C., Thanh, D. P., Holt, K. E., Thomson, N. R. & Baker, S. The genomic signatures of Shigella evolution, adaptation and geographical spread. Nat. Rev. Microbiol. (2016). https://doi.org/10.1038/nrmicro.2016.10
Bangtrakulnonth, A. et al. Shigella from humans in Thailand during 1993 to 2006: spatial-time trends in species and serotype distribution. Foodborne Pathog. Dis. 5, 773–784 (2008).
Article PubMed Google Scholar
Vinh, H. et al. A changing picture of shigellosis in southern Vietnam: shifting species dominance, antimicrobial susceptibility and clinical presentation. BMC Infect. Dis. 9, 204 (2009).
Article PubMed PubMed Central Google Scholar
Chung The, H. et al. Dissecting the molecular evolution of fluoroquinolone-resistant Shigella sonnei. Nat. Commun. 10, 4828 (2019).
Article PubMed PubMed Central CAS Google Scholar
Sadouki, Z. et al. Comparison of phenotypic and WGS-derived antimicrobial resistance profiles of Shigella sonnei isolated from cases of diarrhoeal disease in England and Wales, 2015. J. Antimicrob. Chemother. 72, 2496–2502 (2017).
Article CAS PubMed Google Scholar
Njamkepo, E. et al. Global phylogeography and evolutionary history of Shigella dysenteriae type 1. Nat. Microbiol. 16027 (2016). https://doi.org/10.1038/nmicrobiol.2016.27
Liang, B. et al. Transferable plasmid-borne mcr-1 in a colistin resistant Shigella flexneri isolate. Mbio. 84, 1–10 (2018).
Google Scholar
Chung The, H. et al. South Asia as a reservoir for the global spread of ciprofloxacin resistant Shigella sonnei. PLoS Med 13, 1–12 (2016).
Article Google Scholar
Pham, T. D. et al. Commensal Escherichia coli are a reservoir for the transfer of XDR plasmids into epidemic fluoroquinolone-resistant Shigella sonnei. Nat. Microbiol. 5, 1–9 (2020).
CAS Google Scholar
Phan, D. & Coxhead, I. Inter-provincial migration and inequality during Vietnam’s transition. J. Dev. Econ. 91, 100–112 (2010).
Article Google Scholar
Zhao, Y., Zhu, Y., Zhu, Z. & Qu, B. Association between meteorological factors and bacillary dysentery incidence in Chaoyang city, China: an ecological study. BMJ Open 6, e013376 (2016).
Article PubMed PubMed Central Google Scholar
Thompson, C. N., Duy, P. T. & Baker, S. The rising dominance of Shigella sonnei: an intercontinental shift in the etiology of bacillary dysentery. PLoS Negl. Trop. Dis. 9, e0003708 (2015).
Article PubMed PubMed Central CAS Google Scholar
Niyogi, S. K. Increasing antimicrobial resistance-an emerging problem in the treatment of shigellosis. Clin. Microbiol. Infect. 13, 1141–1143 (2007).
Article CAS PubMed Google Scholar
Baker, K. S. et al. Intercontinental dissemination of azithromycin-resistant shigellosis through sexual transmission: a cross-sectional study. Lancet Infect. Dis. 3099, 1–9 (2015).
Google Scholar
Baker, K. S. et al. Horizontal antimicrobial resistance transfer drives epidemics of multiple Shigella species. Nat. Commun. 9, 1462 (2018).
Article PubMed PubMed Central CAS Google Scholar
Bardsley, M. et al. Persistent transmission of shigellosis in England is associated with a recently emerged multidrug-resistant strain of shigella sonnei. J. Clin. Microbiol. 58, e01692–e01719 (2020).
Article CAS PubMed PubMed Central Google Scholar
He, F. et al. Shigellosis outbreak associated with contaminated well water in a rural elementary school: Sichuan Province, China, June 7-16, 2009. PLoS One 7, 16–19 (2012).
Article Google Scholar
Rahman, M. Z. et al. Recovery and characterization of environmental variants of Shigella flexneri from surface water in Bangladesh. Curr. Microbiol. 63, 372–376 (2011).
Article CAS PubMed Google Scholar
McVicker, G. & Tang, C. M. Deletion of toxin–antitoxin systems in the evolution of Shigella sonnei as a host-adapted pathogen. Nat. Microbiol. 2, 16204 (2016).
Article CAS PubMed Google Scholar
Anderson, M. C., Vonaesch, P., Saffarian, A., Marteyn, B. S. & Sansonetti, P. J. Shigella sonnei encodes a functional T6SS used for interbacterial competition and niche occupancy. Cell Host Microbe 21, 769–776.e3 (2017).
Article CAS PubMed Google Scholar
Caboni, M. et al. An O antigen capsule modulates bacterial pathogenesis in Shigella sonnei. PLOS Pathog. 11, e1004749 (2015).
Article PubMed PubMed Central CAS Google Scholar
Watson, J. L. et al. Shigella sonnei O-antigen inhibits internalization, vacuole escape, and inflammation activation. MBio. 10, 1–14 (2019).
Article CAS Google Scholar
Torraca, V. et al. Shigella sonnei infection of zebrafish reveals that O-antigen mediates neutrophil tolerance and dysentery incidence. PLoS Pathog. 15, 1–26 (2019).
Article CAS Google Scholar
Weill, F. et al. Genomic history of the seventh pandemic of cholera in Africa. Science 789, 785–789 (2017).
Article CAS Google Scholar
Duong, V. T. et al. No Clinical benefit of empirical antimicrobial therapy for pediatric diarrhea in a high-usage, high-resistance setting. Clin. Infect. Dis. 66, 504–511 (2018).
Article CAS PubMed Google Scholar
Sun, Q. et al. Development of a multiplex PCR assay targeting O-antigen modification genes for molecular serotyping of Shigella flexneri. J. Clin. Microbiol. 49, 3766–3770 (2011).
Article CAS PubMed PubMed Central Google Scholar
Gentle, A., Ashton, P. M., Dallman, T. J. & Jenkins, C. Evaluation of molecular methods for serotyping Shigella flexneri. J. Clin. Microbiol. 54, 1456–1461 (2016).
Article CAS PubMed PubMed Central Google Scholar
Ponsting, H. & Ning, Z. SMALT—A new mapper for DNA sequencing reads. F1000Posters 1 (2010). https://doi.org/10.7490/F1000RESEARCH.327.1
Li, H. et al. The sequence alignment/map format and SAMtools. Bioinformatics 25, 2078–2079 (2009).
Article PubMed PubMed Central CAS Google Scholar
Croucher, N. J. et al. Rapid phylogenetic analysis of large samples of recombinant bacterial whole genome sequences using Gubbins. Nucleic. Acids. Res. 44, 1–13 (2014).
Google Scholar
Stamatakis, A. RAxML version 8: a tool for phylogenetic analysis and post-analysis of large phylogenies. Bioinformatics 30, 1312–1313 (2014).
Article CAS PubMed PubMed Central Google Scholar
Page, A. J. et al. Roary: rapid large-scale prokaryote pan genome analysis. Bioinformatics 31, 3691–3693 (2015).
Article CAS PubMed PubMed Central Google Scholar
Chung The, H. et al. Introduction and establishment of fluoroquinolone resistant Shigella sonnei into Bhutan. Microb. Genomics 1, 1–11 (2015).
Article Google Scholar
Letunic, I. & Bork, P. Interactive tree of life (iTOL) v3: an online tool for the display and annotation of phylogenetic and other trees. Nucleic. Acids. Res. 44, W242–W245 (2016).
Article CAS PubMed PubMed Central Google Scholar
Rambaut, A., Lam, T. T., Max Carvalho, L. & Pybus, O. G. Exploring the temporal structure of heterochronous sequences using TempEst (formerly Path-O-Gen). Virus Evol. 2, vew007 (2016).
Article PubMed PubMed Central Google Scholar
Nguyen, L. T., Schmidt, H. A., Von Haeseler, A. & Minh, B. Q. IQ-TREE: a fast and effective stochastic algorithm for estimating maximum-likelihood phylogenies. Mol. Biol. Evol. 32, 268–274 (2015).
Article CAS PubMed Google Scholar
Kalyaanamoorthy, S., Minh, B. Q., Wong, T. K. F., von Haeseler, A. & Jermiin, L. S. ModelFinder: fast model selection for accurate phylogenetic estimates. Nat. Methods 14, 587–589 (2017).
Article CAS PubMed PubMed Central Google Scholar
Drummond, A. J. & Rambaut, A. BEAST: bayesian evolutionary analysis by sampling trees. BMC Evol. Biol. 7, 214 (2007).
Article PubMed PubMed Central CAS Google Scholar
Baele, G. et al. Improving the accuracy of demographic and molecular clock model comparison while accommodating phylogenetic uncertainty. Mol. Biol. Evol. 29, 2157–2167 (2012).
Article CAS PubMed PubMed Central Google Scholar
Baele, G., Li, W. L. S., Drummond, A. J., Suchard, M. A. & Lemey, P. Accurate model selection of relaxed molecular clocks in Bayesian phylogenetics. Mol. Biol. Evol. 30, 239–243 (2013).
Article CAS PubMed Google Scholar
Bollback, J. P. SIMMAP: stochastic character mapping of discrete traits on phylogenies. BMC Bioinforma. 7, 88 (2006).
Article CAS Google Scholar
Revell, L. J. phytools: an R package for phylogenetic comparative biology (and other things). Methods Ecol. Evol. 3, 217–223 (2012).
Article Google Scholar
Zerbino, D. R. & Birney, E. Velvet: algorithms for de novo short read assembly using de Bruijn graphs. Genome. Res. 18, 821–829 (2008).
Article CAS PubMed PubMed Central Google Scholar
Page, A. J. et al. Robust high-throughput prokaryote de novo assembly and improvement pipeline for Illumina data. Microb. Genomics. 2, 1–7 (2016).
Article Google Scholar
Seemann, T. Prokka: rapid prokaryotic genome annotation. Bioinformatics 30, 2068–2069 (2014).
Article CAS PubMed Google Scholar
Hunt, M. et al. ARIBA: rapid antimicrobial resistance genotyping directly from sequencing reads. Microb. Genomics. 3, 1–11 (2017).
Article Google Scholar
Zankari, E. et al. Identification of acquired antimicrobial resistance genes. J. Antimicrob. Chemother. 67, 2640–2644 (2012).
Article CAS PubMed PubMed Central Google Scholar
Carattoli, A. et al. In Silico detection and typing of plasmids using plasmidfinder and plasmid multilocus sequence typing. Antimicrob. Agents Chemother. 58, 3895–3903 (2014).
Article PubMed PubMed Central CAS Google Scholar
R Core Team. R: a language and environment for statistical computing. (2016).
Team Rs. RStudio: integrated development for R. (2020).

Download references

Acknowledgements

H.C.T. is a Wellcome International Training Fellow (218726/Z/19/Z). S.B. is a Wellcome Senior Research Fellow (215515/Z/19/Z). D.T.P. is a leadership fellow funded through the Oak Foundation. Whole genome sequencing was funded by S.B. and N.R.T. The work of LOMWRU was funded by Wellcome (grant number 106698/Z/14/Z), and we are grateful to all the patients and staff of the Microbiology Laboratory and wards who helped with the collection of isolates, to Bounthaphany Bounxouei, former Director of Mahosot Hospital; Chanphomma Vongsamphan, former director of the Department of Health Care, Ministry of Health; and Bounkong Syhavong, Minister of Health, Lao People’s Democratic Republic, for their very kind help and support.

Author information

Deceased: Rattanaphone Phetsouvanh.

Authors and Affiliations

Oxford University Clinical Research Unit, Ho Chi Minh City, Vietnam
Hao Chung The, Duy Thanh Pham, Tuyen Ha Thanh, Phat Voong Vinh, Guy E. Thwaites & Maia A. Rabaa
Department of Enteric Diseases, Armed Forces Research Institute of Medical Sciences, Bangkok, Thailand
Ladaporn Bodhidatta & Carl J. Mason
Centre for Tropical Medicine and Global Health, Nuffield Department of Clinical Medicine, University of Oxford, Oxford, UK
Duy Thanh Pham, Paul Turner, David A. B. Dance, Paul N. Newton, Rattanaphone Phetsouvanh, Guy E. Thwaites & Maia A. Rabaa
Cambodia-Oxford Medical Research Unit, Angkor Hospital for Children, Siem Reap, Cambodia
Paul Turner
Medical Biology Unit, Institut Pasteur du Cambodge, Institut Pasteur International Network, Phnom Penh, Cambodia
Sopheak Hem
Lao-Oxford-Mahosot Hospital-Wellcome Trust Research Unit, Microbiology Laboratory, Mahosot Hospital, Vientiane, Laos
David A. B. Dance, Paul N. Newton, Rattanaphone Phetsouvanh & Viengmon Davong
London School of Hygiene and Tropical Medicine, London, UK
David A. B. Dance, Paul N. Newton & Nicholas R. Thomson
The Wellcome Trust Sanger Institute, Hinxton, Cambridge, UK
Nicholas R. Thomson
The Department of Medicine, University of Cambridge, Cambridge, UK
Stephen Baker

Authors

Hao Chung The
View author publications
You can also search for this author in PubMed Google Scholar
Ladaporn Bodhidatta
View author publications
You can also search for this author in PubMed Google Scholar
Duy Thanh Pham
View author publications
You can also search for this author in PubMed Google Scholar
Carl J. Mason
View author publications
You can also search for this author in PubMed Google Scholar
Tuyen Ha Thanh
View author publications
You can also search for this author in PubMed Google Scholar
Phat Voong Vinh
View author publications
You can also search for this author in PubMed Google Scholar
Paul Turner
View author publications
You can also search for this author in PubMed Google Scholar
Sopheak Hem
View author publications
You can also search for this author in PubMed Google Scholar
David A. B. Dance
View author publications
You can also search for this author in PubMed Google Scholar
Paul N. Newton
View author publications
You can also search for this author in PubMed Google Scholar
Rattanaphone Phetsouvanh
View author publications
You can also search for this author in PubMed Google Scholar
Viengmon Davong
View author publications
You can also search for this author in PubMed Google Scholar
Guy E. Thwaites
View author publications
You can also search for this author in PubMed Google Scholar
Nicholas R. Thomson
View author publications
You can also search for this author in PubMed Google Scholar
Stephen Baker
View author publications
You can also search for this author in PubMed Google Scholar
Maia A. Rabaa
View author publications
You can also search for this author in PubMed Google Scholar

Contributions

H.C.T. performed data analysis and interpretation of the results under the scientific guidance of N.R.T., S.B., and M.A.R. H.C.T. drafted and edited the paper, with S.B. and M.A.R. revising and structuring the paper. L.B., D.T.P., C.J.M., T.H.T., P.V.V., P.T., S.H., D.A.B.D., P.N.N., V.D. and R.P. contributed to sample collection, storage, DNA extraction and sequencing. N.R.T. provided access to sequencing and bioinformatic analysis facilities. G.T., D.T.P., S.B., D.A.B.D., P.T. and N.R.T. contributed to the editing of the paper. All authors with the exception of RP (deceased) read and approved the final draft.

Corresponding author

Correspondence to Maia A. Rabaa.

Ethics declarations

Competing interests

The authors declare no competing interests.

Additional information

Publisher’s note Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.

Supplementary information

Peer Review File

Supplementary Information

Description of Additional Supplementary Files

Supplementary Data 1

Reporting Summary

Rights and permissions

Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

Reprints and permissions

About this article

Cite this article

Chung The, H., Bodhidatta, L., Pham, D.T. et al. Evolutionary histories and antimicrobial resistance in Shigella flexneri and Shigella sonnei in Southeast Asia. Commun Biol 4, 353 (2021). https://doi.org/10.1038/s42003-021-01905-9

Download citation

Received: 04 September 2020
Accepted: 10 February 2021
Published: 19 March 2021
DOI: https://doi.org/10.1038/s42003-021-01905-9

This article is cited by

The genomic epidemiology of shigellosis in South Africa
- George E. Stenhouse
- Karen H. Keddy
- Kate S. Baker
Nature Communications (2023)

Comments

By submitting a comment you agree to abide by our Terms and Community Guidelines. If you find something abusive or that does not comply with our terms or guidelines please flag it as inappropriate.