The gram-negative bacterium Vibrio cholerae is the causative agent of the diarrhoeal disease cholera and is responsible for seven recorded pandemics. Several factors are postulated to have led to the decline of 6th pandemic classical strains and the rise of El Tor biotype V. cholerae, establishing the current 7th pandemic. We investigated the ability of classical V. cholerae of the 2nd and 6th pandemics to engage their type six secretion system (T6SS) in microbial competition against non-pandemic and 7th pandemic strains. We report that classical V. cholerae underwent sequential mutations in T6SS genetic determinants that initially exposed 2nd pandemic strains to microbial attack by non-pandemic strains and subsequently caused 6th pandemic strains to become vulnerable to El Tor biotype V. cholerae intraspecific competition. The chronology of these T6SS-debilitating mutations agrees with the decline of 6th pandemic classical strains and the emergence of 7th pandemic El Tor V. cholerae.
Vibrio cholerae is a gram-negative bacterium and the causative agent of the diarrhoeal disease cholera. Throughout modern history, seven cholera pandemics have been reported, all caused by pandemic strains of the O1 serogroup. Understanding how these O1 pandemic strains evolved is hampered by the absence of available strains. Historical strains were not isolated until the germ theory became accepted in the late 1800s. Furthermore, V. cholerae colonises soft tissues and is noninvasive. Therefore, historical specimens for DNA extraction are rare. As a result, DNA sequences are available principally from the 6th pandemic (classical biotype strains, 1899–1923) and the ongoing 7th pandemic (El Tor biotype strains, 1961–today). A preserved intestine from an 1849 cholera victim belonging to the Mütter Museum collection in Philadelphia offers unprecedented insights into 2nd pandemic V. cholerae (Supplementary Fig. 7)1. The generation of a high-resolution genomic sequence allowed us to track the evolution of one V. cholerae virulence factor, the type-six secretion system (T6SS)2.
The T6SS is a bacterial nanomachine embedded in the envelope of gram-negative bacteria that mediates contact-dependent translocation of effector toxins into neighbouring cells2. Contraction of the T6SS outer sheath ejects an inner tube consisting of polymerised Hcp proteins, capped with effector proteins, into adjacent bacteria. These effectors are toxic unless inhibited by cognate immunity proteins in the attacked bacterium. Three distinct genetic loci across two chromosomes encode the T6SS in V. cholerae: auxiliary cluster 1, auxiliary cluster 2 and a large cluster, each harbouring an effector-immunity pair: tseL & tsiV1, vasX & tsiV2 and vgrG3 & tsiV3, respectively. Effector and immunity pairs must have evolved in tandem with a cognate immunity protein for each effector. Each immunity protein protects only against a single cognate effector because cross-resistance has not been observed3.
Based on the similarity of TsiV1, TsiV2 and TsiV3 at each locus in 6th and 7th pandemic strains, we initially classified all 6th pandemic strains into the same compatibility group as the AAA-7th pandemic strains3. Compatibility groups were named as follows: the first A refers to TsiV1 (Axx), the second A to TsiV2 (xAx) and the third A to TsiV3 (xxA). Divergent alleles at each locus were named in the order of discovery (A, B, C, D, etc.) for the auxiliary 1, 2 or large cluster, respectively, giving rise to 27 currently known compatibility groups in V. cholerae3. Compatibility groups were further classified into subfamilies to account for distinct TsiV1 amino acid sequences among the same modules: the 6th pandemic classical strains are represented by compatibility groups A1A1A1 (e.g. strain NIH41), A2A1A1 (e.g. strains CA401 and O395) and A3A1A1 (MZO-2); A4A1A1 (e.g. strain A59) was identified in this study. Members of the same compatibility group are immune to or compatible with each other3, as homologous immunity proteins define compatibility groups. In contrast, V. cholerae strains that do not encode the same effector and immunity genes will compete and are considered to be incompatible. Pandemic strains are subdivided into two biotypes; the seventh pandemic V. cholerae O1 El Tor biotype and the sixth pandemic O1 classical biotype, which evolved as distinct lineages4,5,6,7,8. The causes that led the 7th pandemic El Tors to replace classical strains as the source of pandemic cholera remains an intense research area. Three main hypotheses support classical biotype displacement: distinct virulence gene regulation, additional virulence factors encoded by El Tor V. cholerae, and biotype-specific phenotypic differences9,10,11. For example, El Tor and classical strains regulate ~1 in 8 genes differently, resulting in biotype-specific spatial-temporal expression of the main virulence factors, cholera toxin (CT) and toxin-coregulated pilus (TCP)9,10.
Numerous additional virulence factors encoded within El Tor genomes are either absent or differentially regulated in classical Vibrio cholerae strains, including the Vibrio seventh pandemic island 1 (VSP-I) and 2 (VSP-II), HlyA, PilE, MSHA and RTX. Phenotypically, the El Tor biotype displays increased biofilm production and motility compared to classical strains8,9,10,11. Lastly, lytic phages are specific to either of the two biotypes, inviting the hypothesis that phage population fluctuations could have contributed to the biotype replacement7,12,13. El Tor strains cause a less virulent form of cholera accompanied by a more extended period of bacterial shedding14,15,16, likely due to the considerable differences between the biotypes described above, thereby benefiting the pathogen by increasing dissemination time16.
We investigated differences in the DNA sequences encoding T6SS genes of classical and El Tor biotype V. cholerae to improve understanding of how bacterial competition plays in cholera’s pathogenesis. In this work, we examined three aspects of competitiveness across pandemic cholera strains: the ability to engage in T6SS battle with commensal bacteria, compete with non-pandemic strains and compete with other pandemic strains.
2nd and 6th pandemic classical V. cholerae encode polymorphic T6SS
The draft genome of the 2nd cholera pandemic classical strain PA1849 isolated from a preserved intestine stored at the Mütter Museum in Philadelphia was recently sequenced1. Because the sequencing effort was not designed to provide sufficient sequencing depth to cover the entire T6SS gene clusters, we designed specific booster probes for the enrichment and adequate coverage of these loci. Re-sequencing the microbial content from the same Mütter Museum specimen provided an average coverage depth of ~300x across the T6SS gene clusters (Fig. 1).
An earlier analysis of the three T6SS genetic loci of the 6th pandemic classical V. cholerae strain O395 (isolated in India in 1965) revealed frameshift mutations in the large gene cluster17. Therefore, we conducted a comparative analysis of the re-sequenced T6SS clusters from the 2nd pandemic strain PA1849 and the 6th pandemic classical strain O395. T6SS sequences from each genome were aligned with those of the El Tor reference strain C6706. The 2nd and the 6th classical pandemic strains PA1849, and O395 encode a 12-nucleotide deletion (Δ293-304) in VCA0109 renamed vasN. In addition, the 6th pandemic classical strain O395 harbours an 8-nucleotide frameshift mutation (Δ514-521) in the structural gene vasK (VCA0120), one single-nucleotide polymorphism (SNP) in the effector tseL, and another SNP in its cognate immunity gene tsiV1 (Fig. 1). Evaluation of available 6th pandemic classical strain T6SS sequences showed that additional frameshift mutations in the large cluster’s vipA (VCA0107) and vasE (VCA0114) genes are shared among all 6th pandemic strains (Supplementary Fig. 1). Next, we investigated the impact of these mutations on T6SS activity in classical biotype strains.
The T6SS of 2nd and 6th pandemic classical strains is disabled
VipA–VipB complexes constitute the contractile outer sheath of the T6SS18. Similarly, VasK (TssM in Escherichia coli) links the outer membrane protein TssJ with the inner membrane protein TssL, forming the membrane core complex of the T6SS19. Deletions of vipA, vasE or vasK in strain V52, which constitutively expresses the T6SS, abolish Hcp secretion (the hallmark of a functional T6SS) and abrogate T6SS-mediated killing2,20. Therefore, the mutations highlighted in Fig. 1 and Supplementary Fig. 1 result in truncations of these genes and are prone to disable T6SS activity. Furthermore, the vasN in-frame deletion removes four amino acids in VasN, a structural protein essential for Hcp secretion and T6SS function in general20.
To test whether these polymorphisms restrict the ability of 2nd and 6th pandemic strains to outcompete microbial opponents, we introduced the classical alleles from PA1849 into V. cholerae strain V52 with an El Tor T6SS (the V52 T6SS structural components share 99.2% amino acid identity with 7th pandemic El Tor strains such as C670617). This experiment allowed us to determine whether the mutations found in classical strains interfere with T6SS activity while bypassing potential strain-specific regulatory differences21. Streptomycin-resistant V. cholerae V52 with the vasKΔ514-521 allele from the 6th pandemic classical strains or with the vasNΔ293-304 allele from 2nd and 6th pandemic classical strains were incubated with rifampicin-resistant E. coli (see ‘Methods’ for details). The vasK Δ514-521 and the vasNΔ293-304 V52 strains lost T6SS activity and did not kill E. coli comparably to the ΔvasK mutant control (Fig. 2). As reported for previous experiments21, wild-type V52 yielded ~1000-fold killing of E. coli. The deleted Arginine, Valine, Leucine and Valine residues in the classical vasNΔ293-304 allele is adjacent to a residue essential for VasN function in Pseudomonas aeruginosa22 (Supplementary Fig. 2). In V. cholerae, these four amino acids are located within a β-strand and are likely to disrupt its secondary structure (Supplementary Fig. 2).
Taken together, these results suggest that the deletion in vasN present in both 2nd and 6th pandemic strains disabled the T6SS, permitting the accumulation of additional T6SS-disabling mutations, including a premature stop codon in vasK (vasKΔ514-521) in 6th pandemic strains.
A subset of 6th pandemic classical V. cholerae strains is sensitive to T6SS-mediated attack by bacteria belonging to the same compatibility group
Compatibility groups comprise V. cholerae strains encoding the same T6SS effector and immunity alleles, rendering them immune to reciprocal T6SS-mediated attack and permitting coexistence3. Comparative sequence analysis of compatibility groups revealed that TsiV2 and TsiV3 of 6th pandemic strains are identical to their counterparts in C6706 (Supplementary Fig. 3B, C). Comparison of classical TsiV1 amino acid sequences with those of El Tor strains revealed an overall sequence identity of 98.8%. Visualisation of the alignment in a radial tree differentiated four clades of TsiV1 sequences (Fig. 3A). The four polymorphic TsiV1 amino acid sequences vary at positions Leu4Phe, Ile163Phe and Ala237Thr in four different permutations (Fig. 3B) based on single nucleotide substitutions T12G, A487T or G709A in tsiV1, giving rise to compatibility groups A1–A4, respectively.
We compared V. cholerae TseL (Supplementary Fig. 3A) to determine whether the polymorphisms observed in TsiV1 amino acid sequences are matched in the cognate effector because immunity protein TsiV1 inhibits TseL effector-mediated T6SS killing3,23. The alignment reveals that four TseL alleles are present in the analysed classical V. cholerae genomes: 10 out of the 26 strains encode an identical TseL to the allele found in C6706, 14 out of 26 strains differ by a single Tyr528His amino acid substitution, 1 out of 26 differs by both Tyr528His and an additional Ala98Gly substitution and 1 out of 26 is uniquely truncated. Therefore, TseL has undergone sequential mutations over time: no change from PA1849 to CA401, Tyr528His introduced at A57 and the additional Ala98Gly mutation in A279. These results suggest that the mutation of TseL accompanied the mutation of TsiV1 in 6th pandemic strains examined here.
Whether strains with immunity proteins of the same family (e.g. A) but different subfamilies (e.g. A1, A2) are immune to each other was experimentally determined next. To test the ability of 6th pandemic V. cholerae to coexist with other strains of the AAA compatibility family, O395 (A2A1A1), CA401 (A2A1A1) and NIH41 (A1A1A1) were competed against strain V52 (A1A1A1) or V52∆vasK (Fig. 3C). T6SS activity of V52 led to an ~10-fold decrease in the number of surviving O395 and CA401 bacteria; in contrast, NIH41 was recovered in equal numbers regardless of exposure to wild-type V52 or V52∆vasK, indicating full immunity against T6SS-mediated attack by other members of the A1A1A1 compatibility group. Similar numbers of compatible C6706 (A1A1A1) survived exposure to V52 or V52∆vasK resulting in a competitive index of ~1. The competitive index of incompatible AM-19226 (C1D4F1) that survive exposure to V52 was ~104-fold lower, and the competitive index of AM-19226 surviving exposure to V52∆vasK was ~103-fold higher (Fig. 3C).
Next, we evaluated TsiV1 immunity gene expression profiles to determine whether the observed sensitivity of A2A1A1 classical V. cholerae to T6SS-mediated attack by strains of the A1A1A1 compatibility group is due to transcriptional variation. TsiV1 expression levels determined by qPCR in select strains did not explain the difference in susceptibility; for example, although O395’s immunity is compromised (Fig. 3C), this strain displayed the highest tsiV1 transcript levels (Supplementary Fig. 4).
TsiV1 of O395 and CA401 differs from TsiV1 of the fully protected strain NIH41 by a single amino acid substitution, Ile163Phe. We, therefore, replaced tsiV1 in CA401 with a chromosomally FLAG-tagged copy of the tsiV1163Phe (A2) or tsiV1163Ile (A1) allele to further evaluate the phenotype of this amino acid substitution. The CA401 strain harbouring the tsiV1163Ile allele was fully protected from the V52 T6SS, while CA401 expressing the tsiV1163Phe allele experienced a significant reduction in viability analogous to the CA401 WT allele (TsiV1163Phe = A2) (Fig. 3D). Deleting tsiV1 in the same native CA401 background compromised survival by 3 logs as expected (Fig. 3D). Western blot analysis of the two prey strains indicated that CA401 produces approximately 5-fold higher levels of TsiV1163Ile than TsiV1163Phe despite being expressed from the same promoter. This result suggests that the 163Ile El Tor allele is more stable than the classical TsiV1 version or that the classical 163Phe TsiV1 protein is conformationally compromised. Different half-lives may explain why TsiV1 encoded by the A1 allele is more protective than the A2 version.
Non-AAA V. cholerae outcompete 6th pandemic classical strains
We previously showed that V. cholerae belonging to distinct T6SS compatibility groups compete against each other. Those of the AAA genotype are predominately human pathogens that outcompete all other non-AAA strains tested thus far3. We hypothesised that 6th pandemic classical strains would be outcompeted by non-AAA strains because of the T6SS disabling deletions in vasNΔ293-304 and vasKΔ514-521 —regardless of their tsiV1 allele as long the non-AAA strain does not represent an Axx compatibility group (e.g. groups AAB (strain MZO-2) or group ABK (strain YB2A12). Classical 6th pandemic V. cholerae were competed against non-AAA environmental isolates DL4211 (CEE), DL4215 (CEC), V51 (CDA) or 1587 (CDC) at a 1:1 ratio. Non-AAA strains outcompeted CA401 and NIH41 between 103 and 104 fold compared to controls (Supplementary Fig. 5). These results indicate that CA401 and NIH41 are sensitive to killing by non-AAA V. cholerae, likely placing classical 6th pandemic strains at a disadvantage in intraspecific competition with environmental V. cholerae. The subtypes A1 and A2 do not contribute to a difference in T6SS sensitivity, providing additional support for our compatibility hypothesis.
Gain, loss and exchange of T6SS mutations in classical V. cholerae strains model
Figures 1–3 demonstrate that the T6SS gene clusters of 2nd and 6th pandemic classical strains accumulated mutations affecting their ability to assemble a functional T6SS and, therefore, engage in interbacterial competition. Furthermore, we report that AAA and non-AAA strains outcompete 6th pandemic classical V. cholerae tested here.
Next, we compared available T6SS sequences between classical and El Tor strains with a focus on vipA, vasE, vasK and vasN, as well as amino acid substitutions in TsiV1 (Fig. 4A). Comparative sequence analysis of PA1849 and twenty-six 6th pandemic classical strains isolated over 50 years (1940–1990) highlighted how the classical T6SS changed over time throughout multiple pandemics. The 12-nucleotide vasN deletion is conserved in all 26 classical strains, and 24 of them also encode the 8-nucleotide deletion in vasK. The 2nd pandemic PA1849 and its closest phylogenetic relative, the 6th pandemic M29 strain, retained the wild-type allele of vasK. All analysed 6th pandemic V. cholerae other than 2nd pandemic PA1849 (i.e. 25 of 26 classical sequences) harboured the additional two nucleotide insertion in vasE and one nucleotide insertion in vipA (Fig. 4A and Supplementary Fig. 1).
Next, representative strains of each T6SS genotype were chosen to reconstruct the sequential order of mutations acquired within the T6SS gene clusters of classical V. cholerae (Fig. 4B). According to this model, the 2nd pandemic strain PA1849 codes only one of the multiple mutations found in 6th pandemic strains, namely the 12-nucleotide deletion in vasN. Strain M29 forms an ancestral bridge between PA1849 and the 6th pandemic strains. In addition to the vasN mutation, M29 acquired the 2 bp insertion in vasE and the 1 bp insertion in vipA. Next, all subsequent 6th pandemic classical V. cholerae examined here acquired the 8 bp deletion in vasK. The nucleotide substitution A487T in tsiV1 replaced isoleucine with phenylalanine at position 163 of TsiV1, giving rise to strains analogous to CA401 and O395 susceptible to intraspecific T6SS-mediated attack within the same compatibility group, AAA. The additional G709A nucleotide substitution in strains such as A59 gave rise to the Ala237Thr TsiV1 allele.
In summary, our model suggests that classical strains acquired debilitating mutations in their T6SS gene clusters in multiple, sequential steps. Individual mutations were likely inherited vertically from a common ancestor and propagated through the classical population, conferring some form of advantage or, conversely, not having detrimental effects on V. cholerae fitness until the emergence of 7th pandemic El Tor strains.
V. cholerae of the classical biotype was responsible for the first six reported cholera pandemics. How El Tor strains replaced classical V. cholerae as the sole source of contemporary pandemic cholera remains unclear. This study investigated competitive differences between the two biotypes to understand whether the T6SS might have contributed to this replacement. While El Tor strains reach higher cell densities, they express approximately 5-fold less CT and TCP and cause milder disease symptoms than classical V. cholerae24. We propose that classical V. cholerae did not require the T6SS to be successful pathogens through at least five pandemics. Still, they were outcompeted by the emergence of El Tor biotype strains that, despite lower CT and TCP expression, encode additional virulence factors, engage in T6SS-mediated combat and reach higher cell densities.
Pradhan and colleagues reported that in mixed cultures, El Tor strains outnumber classical V. cholerae during stationary growth phase and speculated that this phenotype is associated with utilisation of amino acids at higher efficiency in alkaline conditions25. Additionally, in contrast to classical V. cholerae, growth of El Tor biotype strains is enhanced by the production of 2,3-butanediol, a neutral fermentation end product that prevents the accumulation of organic acids permitting increased El Tor growth rates8. These observations suggest that El Tor biotype V. cholerae exhibits higher frugality with energetic resources than classical biotype strains, consistent with the view that selective pressure favours pathogens better adapted to capitalise on host resources.
Our work suggests that classical V. cholerae lost their ability to employ their T6SS to attack and defend themselves. Consequently, classical strains do not perform effectively in inter- and intraspecific competition with El Tor and other non-classical rivals. Classical strains lost the ability to engage in T6SS attacks as early as the second pandemic, preventing them from killing other prokaryotic cells, and thereby reducing competitiveness compared to V. cholerae expressing a functional T6SS.
Figure 5A–C presents a model of T6SS-mediated microbial competition for 2nd through 7th pandemic strains hypothesised to occur in any given ecological or host niche26,27. The 2nd pandemic strain PA1849 and its closest 6th pandemic relative M29 could not engage their T6SS due to the disabling vasNΔ293-304 deletion. Shared immunity genes protected these early classical strains from attack by pre-7th pandemic El Tor biotype strains27 T6SS, but not from environmental (non-AAA) V. cholerae (Fig. 5A). Further, TsiV1 Ile163Phe conversion from subfamily A1 to A2 left 6th pandemic strains sensitive to T6SS-mediated attack by El Tor biotype V. cholerae (Fig. 5B). In contrast, the current 7th pandemic El Tor biotype strains are compatible with bacterial kin. Thus, they outcompete environmental (non-AAA) V. cholerae and heterologous prey (Fig. 5C)28.
Deletions in vasN and subsequently vasK affect the ability to produce a functional T6SS and predate the single nucleotide substitutions in the immunity gene tsiV1. The A2 allele of tsiV1 compromises protection from T6SS-mediated attack by A1A1A1 V. cholerae (Fig. 4B). According to this model, in the absence of El Tor strains, selection against 2nd and 6th pandemic classical V. cholerae’s inability to engage their T6SS would occur exclusively upon interaction with non-AAA strains (Fig. 5A). One explanation for classical V. cholerae having caused five pandemics without an active T6SS may be the existence of a yet-to-be-identified mechanism to outcompete non-AAA competitors during the initial phases of outbreaks when pathogenic V. cholerae colonise the small intestine as a mixed population. Subsequently, a short aquatic life phase of classical strains between hosts would further reduce interactions with non-AAA competitors.
Pandemic and environmental strains interpret external cues in the environment and host, adding to the complexity of interbacterial interactions. For example, chitin is required for maximal killing by El Tor strains allowing them to remain competitive against non-AAA V. cholerae that are far more likely to express T6SS constitutively during encounters in environmental niches27. Conversely, another report demonstrated that intestinal mucins induce expression, and bile acids further modulate the activity of T6SS in pandemic El Tor strains26. These reports contribute towards our understanding of the tight regulation T6SS of pandemic strains.
Synergy among V. cholerae strains capable of coexisting with other members of their species sharing the same T6SS compatibility group includes sharing exchanged toxins and structural tube proteins29. In contrast, toxin exchange between non-kin cells leads to cell death without the possibility to recycle T6SS components. T6SS duelling contributes to kin selection and enhances the ability of kin bacteria to colonise environmental and host niches3,28.
The disadvantages of lacking T6SS activity include the inability to battle intra- and interspecific competitors and, consequently, the decreased uptake of exogenous DNA30,31,32, reduced resistance to conjugation33 and the failure to deploy anti-eukaryotic effectors2. One significant advantage from the loss of T6SS activity among classical strains is the energetic investment that biosynthesis of structural components demands on cell metabolism at the expense of motility and virulence factor production. The absence of Hcp protein synthesis among 6th pandemic V. cholerae supports this hypothesis (Supplementary Fig. 6). Lack of T6SS activity may also contribute towards immune avoidance of secreted antigens, thereby facilitating colonisation persistence24. Furthermore, a strain unable to engage its T6SS triggers fewer retaliatory events from competing bacteria (a phenomenon known as tit-for-tat), thereby increasing chances for survival in select interspecific encounters34.
The loss of T6SS immunity (Fig. 5B) was not selected against until the emergence of El Tor V. cholerae (Fig. 5C, E). The deletions that incapacitated T6SS engagement removed the pressure to maintain full immunity among kin strains, permitting the mutations to debilitate T6SS immunity genes without immediate consequence (Fig. 5D). Perhaps not coincidentally, El Tor strains became pandemic after classical V. cholerae progressively lost their ability to express the T6SS apparatus and further became susceptible to T6SS-mediated attack by A1A1A1 kin such as those of the El Tor biotype. It is tempting to speculate that these events and other biotype-specific features contributed to the observed reduction in classical strains isolated, as their persistence in environmental niches is hampered by their inability to engage and defend against T6SS attacks by any other V. cholerae. Collectively, these factors may have supported the emergence and persistence of El Tor strains as the cause of pandemic cholera (Fig. 5E).
Our study support the idea that intraspecific microbial competition and compatibility among bacterial strains is critical for understanding the succession of pathogenic agents of the same species.
Strains and culture conditions
Vibrio cholerae and E. coli strains were grown in Lysogeny broth (LB) (1% tryptone, 0.5% yeast extract, 0.5% NaCl) at 37 °C shaking or on LB agar plates (supplemented with 1.5% agar). Bacteria were grown in the presence of 100 µg/mL ampicillin, 100 μg/mL streptomycin or 50 µg/mL rifampicin. The strains used in this study are described in Table 1.
The in-frame deletion mutant CA401∆tsiV1 was constructed as described previously using pWM91-based knockout constructs35. Knock-in versions of PA1849 alleles of vasK and vasN were made using the same approach. Table 2 lists the primers employed to construct all mutant strains.
Competition assays were performed as described previously21. Briefly, two V. cholerae strains or a V. cholerae strain and E. coli MG1655 were mixed at indicated ratios and incubated on pre-dried LB agar plates. After a 4 h incubation at 37 °C, bacteria were harvested, serially diluted and plated onto LB agar plates supplemented with selective antibiotics to enumerate surviving V. cholerae or E. coli bacteria. The next day, colony-forming units (CFUs) were counted.
Western blot analysis
Samples for western blots were prepared by growing bacteria in LB to the mid-logarithmic phase of growth, harvesting cells and normalising the OD600 to 1.0. Cell pellets from mid-logarithmic growth phase bacterial cultures were resuspended in PBS/2X lysis buffer, boiled and centrifuged. Supernatants were loaded and electrophoresed in either 12% or 15% acrylamide SDS-PAGE at 120 V before transfer to nitrocellulose. After blocking in dry milk/1X TBST for 1 h, blots were probed with primary antibodies diluted to 1:5000 (anti-FLAG), 1:500 (anti-Hcp) or 1:10,000 (anti-DnaK) followed by probing with fluorescently labelled secondary antibodies diluted at 1:10,000. Images were captured with a LICOR Odyssey scanner and analysed using Image Studio Lite software (Supplementary Fig. 11).
RNA isolation, cDNA synthesis and RT-PCR
RNA from bacterial cultures grown to the mid-logarithmic phase of growth was extracted using TRIzol reagent (Invitrogen), treated with DNase I (Invitrogen) and transcribed into cDNA using the SuperScript III Reverse Transcriptase (Invitrogen). Quantitative real-time PCR (qPCR) was performed with the SensiFAST SYBR No-ROX Kit (FroggaBio) using the CFX96 Real-Time System (Biorad). Thermocycling parameters were as follows: 95 °C for 2 min hot start, 40 cycles at 95 °C for 15 s, and 60 °C for 1 min followed by a melting curve. Primers to genes of interest were designed using PrimerQuest software from Integrated DNA Technologies (IDT). Primers were tested for performance in qPCR with a cDNA concentration gradient, and those with slopes between −3.3 and −3.7, the efficiency of ∼1.0 and R2 of ∼1.0 were used in the qPCR studies. All primers employed here are listed in Table 2. Expression of tsiV1 relative to 16 s rRNA control was determined by the 2−ΔΔCT method using the CFX Manager Software (Biorad). The resulting relative quantification (RQ) values of all samples were normalised against expression of strain C6706.
PA1849 DNA extraction
We analysed tissue collected from a single intestinal sample (specimen 3090.13) taken from a cholera patient in Philadelphia in 1849 and archived by the Mütter Museum in Philadelphia, PA, USA. The Mütter Museum approved sampling and analysing this sample. All tissue handling and library preparation (before indexing amplification) were performed in a positive-pressurised ancient DNA-appropriate laboratory at Arbor Biosciences in which no human or cholera tissue handling or library preparation had previously been performed. We employed field-appropriate standards of anti-contamination technique, including the use of full-body suits, frequent bleach-based work surface and tool decontamination, and blank extraction reactions containing only reagents without template.
Two 5 × 5 mm squares (Supplementary Fig. 7) were cut from the intestinal specimen using decontaminated tweezers and unused razor blades and placed in 2 mL microcentrifuge tubes. An open tube was kept near the processing area during this sub-sampling procedure to serve as another extraction blank.
Each sample was digested with 750 μL solution comprised of 2.5 mM EDTA, 5 mM Tris-Cl, 0.5% SDS, 0.25 ng/μL Proteinase K, which exhibited a final pH of 8.5 after introduction to the dried tissue specimen. After 17 h of incubation at 37 °C, each sample was placed at 4 °C for 4 h, and then 500 μL of the resulting fluid was taken to purification using method B from Glocke & Meyer, 201736, with final eluates of 100 μL TET buffer.
Roughly 36 ng total tissue DNA extract (15 μL) was taken to library preparation and indexing amplification using the Swift Biosciences (Ann Arbor Michigan) Accel-NGS(R) Methyl-Seq DNA Library Kit following the manufacturer’s standard procedure. The library was index-amplified 10 cycles using dual 8 bp-indexing primers.
Two distinct probe sets were designed for this project, one designed to enrich the entire cholera genome, and another targeting only the three T6SS clusters. The whole-genome kit tiled 80 nt probes every 20 nt across both V. cholerae O395 genome reference chromosomes (NCBI Accessions NC_009456 and NC_009457) following soft-masking regions annotated as repeat elements. Where probes overlapped regions of known SNPs in PA1849, probes containing those SNPs were also included (n = 203). Any probe candidate that overlapped 20 nt or more with annotated repeat regions, or that had multiple strong hybrid sites in the genome were eliminated from the design. This resulted in a final set of 186,228 probes. A similar procedure was used for the T6SS probe set, starting with the V. cholerae T6SS auxiliary 1, auxiliary 2 and large loci as references for probe design, and probes for putative PA1849 SNPs included as well (n = 2). This final set comprised 2876 probes.
Target enrichment used a combination of whole-genome and T6SS probes at a mass ratio of 99% whole-genome, 1% T6SS or exclusively T6SS probes. Depending on library availability, between 75 and 1000 ng of sample, or 2 and 500 ng of extraction blank library, were taken to enrichment using the myBaits protocol version 3.0. This involved a first round of overnight hybridisation at 60 °C and a single Wash Buffer 2 hot wash, followed by post-capture amplification of 80% of the resulting volume of bead-bound enriched libraries for 14 cycles prior to purification. Then the enriched libraries were taken to a second round of enrichment using identical conditions as the first, except three washes were used during cleanup. Half of the available volume of bead-bound library was taken to 8 cycles of amplification prior to purification. These double-enriched libraries were then submitted for sequencing. Enriched and non-enriched versions of each library were then sequenced using PE100 protocol on a HiSeq 2500 lane, demultiplexed by dual 8 bp barcodes.
Construction of PA1849 genome
The following analyses were performed on sequencing reads produced with (SL264753) and without (SL264742) target enrichment. Enriched sequencing reads (SL264753) were used to generate consensus sequences and identify variant loci due to significantly increase coverage over the T6SS clusters.
Raw PA1849 FASTQ files were QC validated with FastQC (v0.11.9) to assess Phred quality score and nucleotide distribution over reads. The forward adapter (AGATCGGAAGAGCACACGTCTGAACTCCAGTCA) and the reverse adapter (AGATCGGAAGAGCGTCGTGTAGGGAAAGAGTGT) were removed from paired-end read files, and ends were trimmed with a Phred quality score cut-off of 30 using cutadapt (v1.16). Reads below a minimum length cut-off of 30 nucleotides were removed. Overlapping paired-end reads from the trimmed FASTQ files were merged into single-end reads with NGmerge (v0.2)37. Merged reads were aligned to a reference FASTA with the Burrows-Wheeler Aligner (bwa v0.7.17) MEM algorithm38. For analysis of the T6SS loci, reference FASTA files were constructed by concatenating genomic islands extracted from C6706 (PacBio sequence of laboratory stock) or O395 (PacBio sequence of laboratory stock) with 100 nucleotide spacers between each region. For phylogenetic analysis, reads were mapped to the whole-O395-genome. SAM files produced were then sorted and marked for duplicates with Picard Tools (v2.17.11) to generate sorted, unique BAM files, which were indexed with Picard Tools39. Variants were called against the constructed reference FASTA, and consensus sequences were generated with Pilon (v1.22)40. For analysis of the T6SS loci, PA1849 consensus sequences were aligned to C6706 and O395 reference sequences using the progressive MAUVE algorithm (v1.1.1) algorithm in Geneious (v2019.0.4), assuming colinear genomes. Genome coverage plots were generated from sorted, unique BAM files uploaded to the Integrative Genomics Viewer (v2.9.4).
Assessing damage profile of PA1849 reads
Mapped reads from the sorted, unique BAM files were assessed for fragment length distribution (Supplementary Fig. 8). The median fragment length of >150 bp is higher than the 40 bp length from Devault et al.1, because of a difference in Illumina chemistry, lack of sonication of the tissue and enrichment with our updated T6SS probes. Nucleotide substitution patterns characteristic of ancient DNA samples (Supplementary Fig. 9) with mapDamage (v2.0)41. Canonical damage patterns typical of ancient DNA (C > T substitutions at the 5′ fragment end and G > A substitutions and the 3′ fragment end) were not observed for these samples. A low frequency of C > T substitutions can be seen at either end of the mapped reads (Supplementary Fig. 9).
Core-genome phylogeny and genomic alignments
Core-genome-based phylogenetic trees were constructed as follows: Genomic FASTA files for tree building were obtained from the PATRIC database or NCBI (Table 3) and annotated using Prokka (v1.12)42. A core genome was extracted from Prokka-output GFF3 files using Roary (v3.11.2)43 with a minimum blastp percentage identity of 95% for calling core genes. Roary extracted and aligned 688 core genes (present in >99% of analysed strains). The core-genome alignment was reduced to only loci harbouring polymorphisms using SNP sites (v2.4.1)44. A total of 6,225 distinct SNP sites were extracted from the 688 core genes. A Maximum Likelihood phylogenetic tree was built using the RAxML (v8.2.12) GTR model. Model was selected using jModelTest (v0.1.6)45. Statistical branch support was obtained from 100 bootstrap repeats. Phylogenetic trees were visualised from RAxML-generated newick files using TreeGraph 2 (v2.15.0-887 beta)46. Branches with bootstrapping support values <70 were collapsed. Alignments of amino acid sequences were performed with MUSCLE (v3.8.425)47 and alignments of the nucleotide sequences of whole-gene clusters were performed using the progressive MAUVE algorithm48 in Geneious (Geneious Prime v2019.0.4). To display the diversity of amino acid sequences as a radial tree, aligned sequences were analysed using RAxML (nucleotide model: GTR Gamma, Algorithm: Rapid hill-climbing)49 and displayed with Geneious Prime (v2019.0.4). Some genomes were poorly assembled over the T6SS clusters, and thus corresponding read files from SRA (Table 3) were aligned to the O395 and C6706 T6SS cluster reference sequences in Geneious Prime (v2019.0.4) to determine consensus sequences and identify polymorphisms.
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Work in the laboratory of S.P. has been supported by the National Institutes of Health R01 grant AI139103-01A1 and the Canadian Institutes of Health Research Operating Grants MOP-84473, MOP-137106. D.U. was funded by a Graduate Student Scholarship from Alberta Innovates Health Solutions. B.K. was a recipient of an NSERC PGS-D. D.P is supported by NIH grant AI137972-01. We gratefully acknowledge Ms Olga Eitel’s technical assistance. We also thank Jacob M. Enk and Alison M. Devault for their bioinformatic analysis.
The authors declare no competing interests.
Peer review information Nature Communications thanks Brian Hammer and the other, anonymous, reviewer(s) for their contribution to the peer review of this work.
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Kostiuk, B., Santoriello, F.J., Diaz-Satizabal, L. et al. Type VI secretion system mutations reduced competitive fitness of classical Vibrio cholerae biotype. Nat Commun 12, 6457 (2021). https://doi.org/10.1038/s41467-021-26847-y
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