Journal of Global Infectious Diseases

: 2020  |  Volume : 12  |  Issue : 2  |  Page : 94--100

Phage types of Vibrio cholerae 01 biotype ELtor strains isolated from India during 2012–2017

Alok Kumar Chakrabarti1, Asim Biswas1, Devendra Nath Tewari1, Partha Pratim Mondal1, Shanta Dutta2,  
1 Division of Virology, ICMR - National Institute of Cholera and Enteric Diseases, Kolkata, West Bengal, India
2 Division of Bacteriology, ICMR - National Institute of Cholera and Enteric Diseases, Kolkata, West Bengal, India

Correspondence Address:
Dr. Alok Kumar Chakrabarti
Division of Virology and Vibrio Phage Reference Laboratory, ICMR-National Institute of Cholera and Enteric Diseases, P33, CIT Road, Scheme XM, Beliaghata, Kolkata - 700 010, West Bengal


Background: Cholera is a primordial disease caused by Vibrio cholerae which existed from centuries in different parts of the world and still shows its periodic, endemic and epidemic presence. Thousands of cholera cases are reported from different parts of India and the disease remains endemic throughout the year. At present, we do not have enough knowledge about the phenotypic nature of the circulating V. cholerae strains in this part of the world. Objectives: This study was carried out over a period of 6 years with the aim defer with the changes in the prevalence and distribution of biotypes, serotypes and phage types of V. cholerae clinical isolates from various endemic regions of the country to determine phenotypic characteristics of the circulating strains and also to predict the attributes of cholera strains responsible for causing significant outbreaks in future. Materials and Methods: A total of 1882 V.cholerae O1 isolates from different cholera endemic areas of India were included in this study. V.cholerae strains which were identified as O1 biotype ElTor further analyzed for serotype and phage types using the standard methodologies. Polyvalent O1 and monospecific Inaba and Ogawa antisera were used for serotyping. A panel of five phages of Basu and Mukherjee phage typing scheme and five phages from the new phage typing scheme were used for phage typing analysis following standard methodology. Results: Maximum numbers of strains were isolated from cholera-endemic states like Gujarat and Maharashtra. All the isolates were confirmed as V. cholerae O1 biotype ElTor and majority of them were serotype Ogawa (93.2%). New phage typing scheme resulted in almost 100% typeable V. cholerae O1 strains included in this study and phage type 27 was the predominant type. Although 80% of the strains used in this study were sensitive to all the vibrio phages, S5 phage was found most efficient in lysing cholera strains indicating its broader host range. Conclusion: The current study identified phage type 27 as the most dominant type and serotype Ogawa was found continuous in circulation throughout the year which has caused recent cholera outbreaks in India during the past years. Phage sensitivity data propose an alternative cost-effective approach to prevent cholera outbreak by therapeutic uses of typing phages irrespective of origin or clonality of the strains.

How to cite this article:
Chakrabarti AK, Biswas A, Tewari DN, Mondal PP, Dutta S. Phage types of Vibrio cholerae 01 biotype ELtor strains isolated from India during 2012–2017.J Global Infect Dis 2020;12:94-100

How to cite this URL:
Chakrabarti AK, Biswas A, Tewari DN, Mondal PP, Dutta S. Phage types of Vibrio cholerae 01 biotype ELtor strains isolated from India during 2012–2017. J Global Infect Dis [serial online] 2020 [cited 2020 Jun 6 ];12:94-100
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Cholera remains a significant global health burden and is endemic in many parts of the third world countries due to inadequate sanitation and safe drinking water resources mainly during the rainy season.[1]Vibrio cholerae, an extremely motile, halophilic, curved shaped, Gram-negative bacterium is known for causing profound acute secretory diarrhea, cholera. Although V. cholerae is a natural member of aquatic environments, only a small fraction of environmental strains are capable of causing the disease. Among the several known serogroups, only two serogroups, V. cholerae O1 and O139 can produce cholera toxin and V. cholerae O1 often accountable for causing the vast majority of the disease including recent cholera outbreaks throughout the world.[2] Serogroup O1 consists of biotypes ElTor and classical with distinct phenotypes. Both the biotypes carry two serotypes, Inaba and Ogawa with different disease characteristics.[3] Cholera has a long history; in the past 200 years, seven cholera pandemics have killed millions across the globe including the Indian subcontinent (specifically in Gangetic Bengal).[4] After several devastating pandemics in the different corners of the globe, the seventh pandemic which originated in Indonesia is still ongoing.[5],[6] Most recent cholera outbreaks caused by V. cholerae O1 occurred in Haiti, causing at least 8,183 deaths and above 665,000 cholera incidences till date ([7] Global estimates suggest that every year 1.3 million to 4.0 million cases of cholera are responsible for 21,000–143,000 deaths.[8] In India, 27,615 cholera cases were reported between 2010 and 2015, reflecting the sustained presence of V. cholerae O1 in the country and cholera is considered to be one of the underreported pathogens throughout the world.[9]

Several serotypes of V. cholerae strains harbor variety of bacteriophages, and these are beneficial from the clinical viewpoint with the command to control the bacterial population leading to controlling the disease.[10],[11],[12] Vibrio phage plays a critical role in the evolution of pathogenic V. cholerae by mediating horizontal transfer of clusters of virulence genes, genomic rearrangements, as well as by bactericidal selection.[13] Lysogenic filamentous phage, CTXϕ, is capable of transferring cholera toxin genes to nontoxigenic strains leading to the conversion of nontoxigenic strains to toxigenic strain.[14],[15],[16] The presence of cholera bacteriophages was found inversely associated with the occurrence of viable V. cholerae in the aquatic environment which was found in correlation with the number of locally reported cholera cases.[12] Lysogenic phage present in some environmental V. cholerae strains of both epidemic and nonepidemic serogroups has the power to kill the epidemic strains and thus contributes to the control of the disease.[16]

Different bacteriophages have been used to distinguish pathogenic strains of bacteria from clinical isolates based on their phage susceptibility. Due to their natural specificity, ease of maintenance and straightforward production, phage owns several desirable characteristics which makes them especially suited as bacterial strains discriminator. Since the late 1960s when molecular and modern methods were not widely available, lytic phages of V. cholerae have been used for typing of V. cholerae O1 which remained primary choice for classification of V. cholerae strains. Basu and Mukherjee initially proposed a phage typing scheme for V. cholerae O1 biotype ElTor in 1968, which was considered as a primary choice and a gold standard approach for differentiating V. cholerae biotype ElTor strains in the past.[17] Six phage types were identified by Basu and Mukherjee to characterize V. cholerae O1 biotype ElTor strains, among them phage type 2 and 4 are predominant whereas types 1, 3, 5, and 6 are not in circulation due to some unknown reason, investigation of which may require a separate study. A fundamental feature of the phage typing of V. cholerae was its usefulness in differentiating strains into several types as well as for differentiating classical and ElTor biotypes. Phage typing schemes for V. cholerae O1 and O139 were developed form NICED over the last few decades.[17],[18],[19],[20]

Apart from the importance of cholera bacteriophages to discriminate cholera strains, phages have been used as an alternative to antibiotic therapy to circumvent the burden of antibiotic resistance.[21],[22] An earlier study has found that V. cholerae isolates from Kolkata, India are strongly correlated with resistance to some antibiotics such as streptomycin, tetracycline, and trimethoprim–sulfamethoxazole.[23] Other studies conducted in Nepal on V. cholerae strains isolated from cholera patients have found that 6.45% of the strains were multidrug resistant.[24],[25] These studies suggest that antibiotic-resistant strains of V. cholerae in the Indian subcontinent are on the rise.[26],[27],[28] Horizontal gene transfer is an widely accepted methods of antibiotics resistance spreads.[29]

To use bacteriophages for therapeutic application in cholera, phage candidate or phage cocktal must have a broad host range and minimum effect on commensal organisms. A recent epidemiological study had identified the cholera hot spot region in India, but data on the phenotypic nature of presently circulating vibrio strains are missing in this part of the world. In this study, we have not only characterized the V. cholerae strains but did a comparative analysis on the host range of these phages for future therapeutic applications. Phenotypic characteristics including their susceptibility to vibrio phages described in this study are beneficial to keep the scientific community better equipped with the knowledge about the nature of circulating strains and the capability of phages to kill circulating V.cholerae strains to subvert future epidemic.

 Materials and Methods

Bacterial strains

V. cholerae O1 biotype ElTor strain MAK 757 (ATCC 51352) was used as the standard propagating strain or as the host for the propagation of V. cholerae O1 phages. We received clinical and environmental samples used in this study from different parts of the country. We included a total of 1882 V. cholerae O1 strains isolated from different cholera endemic areas in India between 2012 and 2017 in this study. We also included V. cholerae O139 strain NPR-4, classical biotype strains V. cholerae 154 and 569B which were used as negative control. Bacterial strains used in the recent study were grown in selected media (TCBS) using the standard methodology.[30]


The panel of five phages of Basu and Mukherjee phage typing scheme (Gr 1 to Gr V) and five phages from the new phage typing scheme (i.e., N4, S5, S20, M4, and D10] were used for phage typing study. These phages are in regular use in our laboratory which were reported earlier as different from each other and biotype specific.[18],[19] All the phages were purified from the stock by successive single-plaque isolation against the respective standard propagating strain.

Propagation of bacteriophages

Standard broth lysis procedure was used to prepare phage lysates. Nutrient broth inoculated with 1% (vol/vol) cell suspension from the overnight grown culture of MAK757 and grown at 37°C for 4–6 h in a shaker incubator. Mid-logarithmic-phase cultures of V. cholerae MAK757 were infected with respective phages at a multiplicity of infection of 0.1, and the infected cultures were incubated with shaking at 37°C until complete lysis occurred. After complete lysis of the culture solution, few drops of chloroform was added in the lysate, mixed well and centrifuged at 10,000 rpm for 20 min at 4°C. Phage lysate was collected and stored at 40 C followed by centrifugation. For concentrating, phage lysate was centrifuged at 30,000 rpm for 2 h at 4°C using a Beckman 50.2 Ti rotor to pellet down the phage particles, resuspended in 0.05 M Tris [pH 7.5] with 0.02 M MgCl2 and kept at 4°C.[19] Broth lysis was used for preparation of larger stock. However, to get small volume high titer stock of phages, alternate to the above lysis method, plate lysis procedure was used for phage propagation following the standard methodology.[19] Bacteriophages used in the present study were purified using cesium chloride density (1.3–1.7 g/ml) gradient as per the standard protocol.[18],[19]


Serological identification was carried out with each strain by using polyvalent O1 and consequently monospecific Inaba and Ogawa antisera (Difco, Detroit, Mich., USA) according to the WHO guideline (World Health Organization (1993): Guidelines for Cholera Control. World Health Organization, Geneva).

Determination of routine test dilution and Phage typing

Phage typing was carried out based on the standard technique regularly performed in our laboratory.[18],[19] A panel of the typing phages were used to type all the 1882 V. cholerae O1 biotype ElTor strains used in this study. Briefly, a single colony of V. cholerae strain grown in nutrient agar media was inoculated in nutrient broth and incubated under static conditions for 4–5 h at 37°C. An aliquot of the fresh culture (0.1 ml) was mixed with molten 0.8% soft agar (3.5 ml, maintained at 42°C) and poured onto a nutrient agar plate to prepare a uniform lawn of bacteria. Routine test dilutions (RTDs) of the phages were determined by the method as described by Chattopadhyay et al.[18] In brief, bacteriophage stock was serially diluted and the dilutions were spotted onto the lawn of the standard propagating host strain. Lowest dilution which was capable to lyse or react positively (appearance of at least five plaques) was considered as RTD and used for phage typing.[18],[19]

Phage typing was performed as per the standard protocol of our laboratory.[19] Mid logarithmic phase young culture of V. cholerae (0.1 ml.) was mixed with molten soft agar and poured onto a nutrient agar plate. The plates were then kept to dry at room temperature (20–30 min) followed by the application of small drops of all the typing phages at the respective RTD dilutions. The drops on the plates were allowed to dry at room temperature for around 10 min and incubated at 37°C for 16–18 h. V. cholerae MAK757 was used in each set of an experiment as a positive control due to the ability of all the typing phages to lyse MAK757. Presence of a clear lytic zone or appearance of at least five or more plaques for individual phage drop was considered as positive reaction.

Phage sensitivity

We have calculated individual phage sensitivity by dividing the total number of strains sensitive for specific phage with the total number strain studied.[18],[20]


Bacteriophage and host range

A total of ten bacteriophages which are in routine use for phage typing in Vibrio phage reference laboratory were used in this study to determine phenotypic characterization of V. cholerae strains circulating in India. V. cholerae O1 biotype ElTor strain MAK757 (ATCC 51352) was found sensitive to all the ten bacteriophages but V. cholerae O1 classical biotype strain 569B and V. cholerae 154 were found resistant to these ten ElTor phages. Strains of common enteropathogens such as Salmonella, Shigella, and enteropathogenic Escherichia coli were not sensitive to these phages.

Biotyping and serotyping

All the 1882 strains used in this study were characterized and confirmed as V. cholerae. Our result showed that all the strains included in this study belonged to V. cholerae O1 biotype ElTor [Table 1]. This result is indicative of complete replacement of classical biotypes by ElTor and revealed that V. cholerae O1 biotype ElTor is the only circulating pathogenic strain in India.{Table 1}

Based on cholera strains O1 antigen seroreactivity V. cholerae O1 strains can be divided into three groups, Inaba, Ogawa, and Hikojama. 1882 strains of V. cholerae O1 biotype ElTor were serotyped in our laboratory. Results indicated 1754 (93.2%) strains belonged to serotype Ogawa. Only 128 (6.8%) strains were found as serotype Inaba. We did not found any Hikojima serotype in our analysis [Table 1].

Phage typing

A total of 1882 V. cholerae O1 biotype ElTor strains isolated from different cholera endemic areas in India were used for phage typing with the set of typing phages available in the Vibrio Phage Reference Laboratory. Out of the ten phages, five phages were from Basu and Mukherjee scheme and five were from the new phage typing scheme.

Basu and Mukherjee phage typing

Five phages of the Basu and Mukherjee phage typing scheme was used to discriminate the ElTor strains and our results indicated that the strains were typed into two different phage types, phage type 2 (T-2) and phage type 4 (T-4). It was found that 1529 (81.25%) strains were grouped as T-2 and 334 (17.75%) were grouped as T-4. Almost 1% strains were found untypeable (UT) [Table 1].

New phage typing

Along with the Basu and Mukherjee typing phages, new phage typing[18] scheme was simultaneously used to classify the 1882 V. cholerae O1 isolates. In contrast to Basu and Mukherjee's scheme, new phage typing scheme, developed in our institute has a better discriminatory power and is capable of differentiating V.cholerae O1 biotype ElTor strains into 27 different types. Phage typing analysis based on the lytic reaction with the phages from the new phage typing scheme [Table 1] indicated 100% type ability of V. cholerae O1 biotype El Tor strains. Analysis revealed that V. cholerae O1 biotype ElTor strains were distributed into several different phage tapes of which (Types 27, 26, 23.24,13,21 and 25) were the major types that represented almost 81% of the total typed strains in this study [Table 2]. Majority of the 1882 strains belonged to phage type 27 (60.41 %). Phage type 26 (8.66%) was the next major phage type followed by type 23 (4.94%), type 24 (4.41%), type 13 (3.82%), type 21 (3.08%) and type 25 (2.92%) [Table 1]. It was found that the V. cholerae O1 biotype ElTor strains belonging to phage type 27 were widely and almost equally distributed in all the nine states from where strains were selected for the present study.{Table 2}

Identification of candidate phage for an alternative therapy

Sensitivity of the circulating V. cholerae strains against the five phages of the new phage typing scheme was calculated and it was found that all the phages have the ability to lyse at least 80% of the circulating strains in India. As shown in [Table 3], phage N4 can lyse 91.17% strains, phage S20 can lyse 83.95%, phage M4 can lyse 86.29% of strains and phage D10 can lyse 80.49%. However, phage S5 has shown highest lethality which can kill or lyse 94% of the circulating V. cholerae O1 biotype El Tor strains.{Table 3}


We are using phage typing as one of the primary methods in monitoring the V. cholerae strains responsible for cholera infection in India at Vibrio Phage Typing Reference Laboratory. Besides potential application of phage typing scheme to distinguish cholera strains, our study will definitely contribute to an improved understanding of possible application of the phages as biocontrol agents during cholera outbreak.

Most of the cholera cases during the period from 2010 to 2015 in India were reported from West Bengal, Karnataka, Assam, Madhya Pradesh, Maharastra, Gujrat, and Punjab.[9] We incorporated V. cholerae strains in our present study which were received from these cholera endemic states of India as shown in [Table 1]. West Bengal reported 5,914 cholera cases in this time frame and other states were also considered to be cholera endemic due to the frequent cholera outbreaks in recent past.[7]

We have characterized and confirmed all the strains used in this study as V. cholerae O1 biotype ElTor. The frequency of serogroup O139 has declined significantly over the past few years consistent with our findings as well. Analysis of serotype distribution in our present study indicates the dominance of Ogawa serotype among the circulating V. cholerae O1 strains in India irrespective of demography and period which matches well with the earlier findings in India.[20],[31] The capability of the strains belonging to Inaba serotype to convert into Ogawa serotype may explain the dominance of Ogawa serotype in our present study.[32],[33] Clinical symptoms of patients infected with Ogawa or Inaba serotype of V. cholerae showed different disease pattern as explained elsewhere.[34] Infection with Ogawa strains are associated with shorter duration of diarrhea with more frequent abdominal pain, vomiting and need for more intravenous fluids when compared with infection with Inaba strain of V. cholerae.[34] Recent Cholera outbreaks in Haiti indicates that toxigenic V. cholerae O1 serotype Ogawa can rapidly change into Inaba serotype with the potential to cause disease in individuals who have acquired immunity against Ogawa serotype which supports the hypothesis that periodic shift may occur due to a consequence of host immunity against different serotypes of V. cholerae O1.[32] Findings of our present study may challenge the previous hypothesis of cyclic shift of V. cholerae O1 serotype due to induction of population-level immunity against dominant strain during an outbreak season. In India, so far, there is no report available regarding the shift in serotypes during different outbreak seasons irrespective of the geography or ethnicity of the infected host indicating equilibrium may have achieved between Ogawa and Inaba strains which require further investigation on responsible host factors associated with dominating serotypes to fine-tune the earlier proposed hypothesis.

Phage typing is a classical method to discriminate bacterial strains into different phage types based on the sensitivity pattern of a panel of typing phages with the bacterial host of the same species. It is a phenotypic characterization method of bacterial strains; much used in the microbiological community and has been around for several decades. The method itself requires that the different phages are available and therefore can generally only be performed at reference laboratories. Vibrio phage Reference Laboratory is involved in phage typing study over the decades using different phage typing schemes. Although Basu and Mukherjee scheme can classify V. cholerae O1 strains into six different types, over the years only two dominating types was found in circulation, reasons for abolition of other four types may demand a different study. In the current study, all of the 1882 strains clustered into two phage types only (either type 2 or type 4) when phage typing was performed using Basu and Mukerjee's scheme [Table 1]. Moreover 1% of the isolates remained untypeable. An earlier study also reported existence of significant number of untypable strains of V. cholerae O1 biotype ElTor when phage typing was performed using Basu and Mukherjee's scheme.[20] Another drawback of this scheme is that the finer distinction is missing and our result indicates that this scheme lacks true identification of origin or clonality of the disease dissemination. Therefore, a different scheme with better discrimination power and better typeability was essential. New phage typing scheme which was developed based upon phages isolated from NICED, Kolkata can distinguish V. cholerae O1 strains into 27 different types and is useful to achieve more type distinction and improved discrimination within the biotype ElTor strains to get a better idea on the origin and clonality route of the outbreak.[18] The present study has shown that type 27 is the dominant phage type in every state with maximum percentage [80%] from West Bengal [Figure 1], indicating the dissemination of cholera outbreak may have occurred from common precursor strain. These observations reveal a common origin and probably the pathogenic strains of cholera belong to the same clone. O1 strains from Maharashtra, Andhra Pradesh and Gujarat exhibited the maximum number of phage types where chorea is endemic over last 5 years. Co-occurrence type 27 and incidence of cholera indicates that V. cholerea O1 strains belonging to phage type 27 might be primarily responsible for outbreaks in recent past in India.{Figure 1}

Apart from the phages characterized in our laboratory to distinguish V. cholerae O1, naturally occurring similar kind of lytic phages may play an essential role in controlling the spread of cholera infection. In the recent past, a model was proposed to understand how equilibrium exists between vibriophages and its host contributing to an outbreak. In an outbreak, increase load of V. cholerae leads to an increase in vibriophage population, which subsequently results in declining of vibrio population and helps in controlling outbreak.[35] A recent study suggests that a cholera patient having vibriophages in their stool less likely to transmit cholera infection through household contact when compared with patients without any vibrophage in their stool.[36] Later it was found that phage positive vibrio samples are non-motile under dark field microscope supporting the role bacteriophages in controlling and spread of an outbreak.

Bacteriophages are a cost effective alternative to antibiotics and sometimes may be used for therapeutic purposes to treat multi drug resistance (MDR) bacteria with limited success.[37],[38],[39],[40],[41] In India, the history of phage therapy dates back to 1930s when vibriophages had been successfully used to treat cholera infection in the pre-antibiotic era.[42],[43],[44]

Phage therapy remained a standard part of the healthcare systems in Eastern Europe and the USSR since the second half of the 20th century.[45] However, it was largely neglected in the other part of the world due to easy availability of antibiotics for treatment. Widespread use of antibiotics resulted in the development of MDR bacteria which is a major problem in healthcare units today. Increase in multidrug resistance phenotype of V. cholerae O1 biotype ElTor makes the population vulnerable to a new pandemic.[46],[47] To overcome the problem of MDR phenotypes of V. cholerae, phage therapy may be a better option. Earlier studies have shown that cocktail of the five bacteriophages reduced the V. cholerae load in a rabbit model of infection when administered 6 or 12 h after the pathogen challenge.[48] In other similar studies virulent vibriophages were used to control diseases in the animal model.[10],[21] We found that typing phages are highly reactive to circulating ElTor strains [Table 2]. Our analysis revealed that the ability of the phages to cause lysis of V.cholerae strains ranges between 80%–94%, signifying their probable usages as candidate for phage cocktail for therapeutic uses. Moreover, as 94% of the circulating strains are susceptible to S5 phage, vibriophage S5 alone may also be used as an ideal candidate for phage therapy. Therefore a cocktail of these vibriophages or vibriophage S5 in combination with lytic phages of other diarrhea causing organisms may be considered as an universal cocktail for the prophylaxis of diarrheal diseases.[41],[49],[50],[51] Hopefully future studies will be helpful to ascertain the decisive use of phages to treat diarrheal diseases. Cholera typing phages used in this study were found nonreactive (inability to cause bacterial lysis) to other commensals which makes them more suitable than antibiotics to manage cholera outbreak.


We have demonstrated that phage typing is still an internationally recognized method of choice for characterizing circulating strains. The present study has identified and characterized dominant cholera strains circulating in India throughout the year. This knowledge will be helpful to design a novel strategy to manage cholera outbreak in different parts of the country. Moreover, this study indirectly supports the use of phages as a cost-effective alternative to control the disease and antibiotic resistance burden of V. cholerae strains. We also advocate the use of these typing phages by directly applying them to water bodies and drinking water supply systems to reduce the burden of cholera incidence in the cholera hot spot region in India or anywhere in the world.


We would like to thank Dr. B. L Sarkar for his enthusiastic support, guidance and helpful advice in preparation of this manuscript. We are thankful to Mr. Motilal Gupta for technical support. This study was supported by the Indian Council of Medical Research as an Institutional service project.

Financial support and sponsorship

This study was funded by ICMR-NICED institutional grant.

Conflicts of interest

There are no conflicts of interest.


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