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Pandemics, pathogenicity and changing molecular epidemiology of cholera in the era of global warming
Annals of Clinical Microbiology and Antimicrobials volume 16, Article number: 10 (2017)
Vibrio cholerae, a Gram-negative, non-spore forming curved rod is found in diverse aquatic ecosystems around the planet. It is classified according to its major surface antigen into around 206 serogroups, of which O1 and O139 cause epidemic cholera. A recent spatial modelling technique estimated that around 2.86 million cholera cases occur globally every year, and of them approximately 95,000 die. About 1.3 billion people are currently at risk of infection from cholera. Meta-analysis and mathematical modelling have demonstrated that due to global warming the burden of vector-borne diseases like malaria, leishmaniasis, meningococcal meningitis, viral encephalitis, dengue and chikungunya will increase in the coming years in the tropics and beyond.
Cholera and climate
This review offers an overview of the interplay between global warming and the pathogenicity and epidemiology of V. cholerae. Several distinctive features of cholera survival (optimal thriving at 15% salinity, 30 °C water temperature, and pH 8.5) indicate a possible role of climate change in triggering the epidemic process. Genetic exchange (ctxAB, zot, ace, cep, and orfU) between strains and transduction process allows potential emergence of new toxigenic clones. These processes are probably controlled by precise environmental signals such as optimum temperature, sunlight and osmotic conditions. Environmental influences on phytoplankton growth and chitin remineralization will be discussed alongside the interplay of poor sanitary conditions, overcrowding, improper sewage disposal and global warming in promoting the growth and transmission of this deadly disease.
The development of an effective early warning system based on climate data could help to prevent and control future outbreaks. It may become possible to integrate real-time monitoring of oceanic regions, climate variability and epidemiological and demographic population dynamics to predict cholera outbreaks and support the design of cost-effective public health strategies.
Vibrio cholera (V. cholerae), which causes outbreaks resulting in massive disease burden, is a Gram-negative, non-spore-forming curved rod. V. cholerae is an autochthonous member of diverse aquatic ecosystems around the planet, and is often found in close association with a variety of algae and crustaceans . The World Health Organization estimates that officially reported cases of cholera represent only 5–10% of the actual case number occurring annually worldwide . A recent spatial modelling technique estimated that around 2.86 million cholera cases occur globally every year, and of them approximately 95,000 die . About 1.3 billion people are currently at risk of being infected with cholera .
The bacterium is classified by the composition of its major surface antigen (O) from lipopolysaccharide into serogroups, of which there are nearly 206 . Only two serogroups of V. cholerae, O1 and O139, have been considered causative agents of cholera . The V. cholerae O1 strain is further divided into two biotypes named El Tor and classical, on the basis of biochemical differences and bacteriophage susceptibility (Fig. 1). It is generally accepted that seven distinct cholera pandemics have occurred since the onset of the first report in 1817 and the seventh one in 1961 in Egypt . It reappeared dramatically and unexpectedly in January 1991 in Latin America as a continuation of seventh pandemic after a hiatus in that region of more than a century . The appearance in late 1992 in southern India of an epidemic strain of V. cholerae, O139 Bengal has caused global concern [7, 8]. This concern was probably unwarranted as the prevalence of O139 cases seems to be receding. It has been hypothesised that the serological switching and genetic diversity of strains between pandemics and epidemics may be influenced by climate variations, with global warming making the environment favourable for cholera outbreaks by switching of virulence factors. This hypothesis is supported by studies of V. cholerae outbreaks in India , Bangladesh  and China , as well as a literature review of the influence of environmental factors on V. cholerae presence . Furthermore, experimental studies have demonstrated variation with changes in environmental conditions in expression of ChiA2 and TfoX, key regulators of V. cholerae horizontal gene transfer . Warmer conditions also provide enriched food sources and ecological protection for the organism by causing algae blooms and making availability of chitin. The delta region of the Ganges and the Brahmaputra have been identified as cholera’s ‘native habitat’ for centuries, and the source for periodic pandemic spread . Of the 36 countries that reported cholera in the seventh pandemic, 28 were newly affected countries and 16 were in Africa . Outbreaks or cases have since been reported in Pakistan, Nepal, China, Thailand, Kazakhstan, Afghanistan, and Malaysia, Sierra Leone, The Democratic Republic of Congo, Nigeria, Angola and Zimbabwe [16–20]. Since the beginning of the century the cholera prevalence has massively expanded on the African continent. In 2015 the majority of cholera cases and mortality were reported from sub-Saharan Africa . Imported cases have been reported in the United Kingdom and United States amongst other countries and in Haiti after the massive earthquake [17, 22–24].
The Haiti outbreak in 2010 was thought to be imported from South Asia by United Nations peace keeping forces [24–26]. Analysis of local climatic variables suggested that following importation, other factors contributed to propagation of the outbreak. The average air temperature and rainfall preceding the outbreak in Haiti was significantly above the long term average of that region . In addition, destruction of sanitary infrastructure and lack of safe water made the situation more vulnerable for the habitant . The cholera outbreak in Haiti supports the suggested role of climatic factors in the transmission of cholera. This review will explore the interplay between environmental influences, changing virulence factors and the molecular epidemiology of cholera.
Variation of strain (serotype and biotype) during epidemic and pandemic
The V. cholerae strain type causing the first four pandemics are unknown. The fifth and sixth pandemics were caused by the classical biotype of O1 strains whereas the seventh was due to the El Tor biotype. In 1992 an epidemic clone of a non-O1 strain with serogroup O139 Bengal caused a large cholera outbreak in Bangladesh and neighbouring countries [8, 28]. At the beginning of the outbreak, the O139 strain displaced the V. cholerae O1 strains, including both classical and El Tor biotypes, which coexisted only in Bangladesh. The subsequent emergence of a new clone of V. cholerae O1 El Tor that transiently displaced the O139 strains during 1994 and 1995, and the re-emergence in 1996 of V. cholerae O139 as the main cause of cholera in Calcutta and its coexistence with the O1 El Tor strains demonstrated temporal changes in the epidemiology of cholera [29, 30]. These clones are genetically (different ctx genotype and ribotype) different compared to other co-existing global clones (the Mexican Gulf coast clone, and the Australian clone) .
If we consider these events from a different angle, this heterogeneity of clones might not be due to serological switching but emergence of a new toxigenic strain. Transient appearance and disappearance of more than six ribotypes of classical Vibrios [32–34], at least five ribotypes of El Tor Vibrios , and three different ribotypes of V. cholerae O139 [35, 36] during epidemics between 1961 and 1996 in Bangladesh have been demonstrated. Genetic diversity among clinical and environmental isolates during and between epidemics over the past 20 years were also found [34, 37]. All these studies indicate that there has been a continual emergence of new clones of toxigenic V. cholerae replacing existing clones. The question is what factors contribute to this shifting? We hypothesize that the clonal shifting in V. cholerae is driven chiefly by environmental variations rather than by human-borne dissemination.
Virulence factor and transduction
Naturally occurring strains of toxigenic V. cholerae O1 and O139 contain the virulent enterotoxin cholera toxin (CT). The genes encoding CT (ctxAB) are part of a larger genetic element (CTX genetic element) consisting of at least six genes (ctxAB, zot, ace, cep, and orfU) . The entire CTX element constituted the genome of a filamentous bacteriophage (CTXф) . Genetic exchange in the environment allows the potential emergence of new toxigenic clones by lysogenic (self-replicating element) conversion with a filamentous bacteriophage (CTXф). CTXф encodes cholera toxin including its receptor, and the toxin-co regulated Pilus (TCP), another important virulence factor . CTXф confers increased evolutionary fitness to its host and hence to its own nucleic acids. With growing immunity in the host population against certain toxigenic clones of V. cholera, new toxigenic clones emerge and replace existing clones by a process of natural selection. Novel clone emergence may also happen by transduction. Transduction is the process by which DNA is transferred from one bacterium to another by a bacteriophage. Genes for both TCP and CTX (virulence factor) can be readily transduced into recipient strains via temperate phages . Induction of CTXф lysogens is probably controlled by precise environmental signals such as optimum temperature, sunlight, and osmotic conditions . Exposure to sunlight is a key factor in the induction of CTX prophase from the host and subsequent propagation of the phage particle [27, 29, 39]. The continual emergence of new strains of toxigenic V. cholera and their selective enrichment during cholera outbreaks constitute an essential component of the ecosystem for their survival. Goel et al. investigated two subsequent epidemics in India by genomic finger printing analysis. They have identified heavy rainfall as the plausible cause of genotype switching between O1 and O139 type strain. The duration between two peaks and switching was only 2 weeks . Koelle et al. also showed in Bangladesh through a phenotypical modelling that shifting in V. cholerae serotype is driven chiefly by environmental variations rather than by human-borne dissemination . The reason behind is the pathogen’s sensitivity to environmental fluctuations. El Tor, a seasonal generalist, seems to gain an advantage over the classical strain, a seasonal specialist, when monsoon rainfall becomes more extreme . This is because El Tor is known to be more fit then classical type because of the expression of vibrio polysaccharide (vps) gene which provide a protection to them against climatic variables . This molecular difference therefore establishes the trade-off between maximum transmission and sensitivity to climatic fluctuations between the serotypes .
Presence of virulence factors in environmental strain
Another alarming feature for cholera control is the presence of these virulence factors in environmental or non-toxigenic strains (non O1 and non-O139) of V. cholerae. Ghosha et al. identified the presence of virulence-associated genes like ctxA, tcpA, toxR and the repetitive sequence (RS element) in both non O1 and non-O139 strains . They suggested that a new toxigenic strain could evolve from these strains in favourable conditions. Kirschner et al. also observed rapid growth of non O1 and non-O139 strain in the presence of dissolved organic carbon and water temperature . It is therefore a major challenge to determine the role of these seemingly innocuous inhabitants in the development of new pathogenic strains capable of causing outbreaks.
Favourable environmental conditions
Vibrio cholerae thrive in 15% salinity, 30 °C water temperature, and pH 8.5 . In the absence of these optimal conditions it is difficult to isolate toxigenic strains from previously endemic regions. By contrast, epidemic periods occur during warmer water temperatures in combination with elevated pH and plankton blooms, and it becomes easy to isolate toxigenic strains . Montilla et al. found conversion from non 01 to 01 and vice versa in all microcosms of both artificial sea water and natural water at various temperatures . They concluded that seroconversion from non-O1 to O1 occurred earliest (within 5 days) at a salinity of ~10% and temperatures near 35 °C . A study in Bangladesh revealed that the highest number of clinical cases occur when the air temperature is more than 28.66 °C and sunshine is more than 4.13 h/day . Increased environmental water temperatures decrease multiplication time and hastened growth along with an increased detection rate of V. cholera . This suggested a triggering factor which may be responsible for enhancing the number of organisms under certain environmental conditions . V. cholerae O1 El Tor and O139 are able to form a three-dimensional biofilm on surfaces, providing a microenvironment . Within the biofilm, the organisms can survive during inter-epidemic periods. Biofilm formation is dependent on the expression of an exopolysaccharide (EPS). Expression of the vps synthesis genes, encoded in two gene clusters on the larger chromosome (vpsA-K and vpsL-Q), is required for the synthesis of EPS . These gene clusters show higher expression at the time of increased salinity and water temperature . Lu et al. in China also found that, spatiotemporal serotype shifts (Ogawa, Inaba and O139) generally correlated with the variations in the pulsed-field gel electrophoresis patterns (PIV, PIIIc, PIa, PIIIb, PIIIa, PIb, and PII) . These patterns largely influenced by seasonal variations particularly rainfall due to formation of bio film .
Plankton load and role of chitin
Sunlight, temperature, and nutrients all influence the growth of phytoplankton (green, red and blue-green) and aquatic plants, which in turn raise the pH of the surrounding water to favour growth of V. cholera . Blue-green algae are a reservoir of V. cholera . Heavy loads of phytoplankton produce food for zooplankton in the next level of the food chain. Various chitinous organisms (whose exoskeleton is formed by the polysaccharide chitin), e.g. copepods, amphipods, and other crustaceans (crabs, lobsters and shrimp) are prevalent among zooplankton populations . Chitin is thin and provides flexibility to these organisms . If chitin is not degraded, high levels of carbon and nitrogen remain insoluble and inaccessible to most organisms . Using chitinase, marine bacteria including Vibrio spp. play a significant role in chitin remineralisation, so very little chitin can be detected in aquatic sediments . In addition to providing a food source for Vibrios and enhancing survival under starvation conditions, chitin also offers protection to V. cholerae at low temperatures and under acidic conditions such as the human gut. This could be important if copepods carrying V. cholerae are ingested in drinking water . Such protection is likely to play an important role in the expanding and changing epidemiology of cholera.
Recent studies suggest that chitin facilitates and regulates competence-mediated horizontal gene transfer in V. cholera by expressing Chi A2 and TfoX [13, 46]. The seroconversion between O1 El Tor and O139 Bengal during the 1992 epidemic in Bangladesh and India could be due to this factor . The activity of Chi A2 and the expression of TfoX gene could be influenced by environmental conditions such as high salinity and water temperature .
Other environmental factors
Other influences under investigation include sea surface height, river discharge, climate variables that affect water levels and salinity . Cholera is primarily a waterborne disease. Sanitation facilities, provision of safe drinking water and good infrastructure for sewage treatment in industrialized nations has made cholera extremely rare. Outbreak studies done in Odisha, India found a clear relationship between sewage contaminated water and cholera epidemics . Several field surveys in West Bengal and Gujrat revealed cholera outbreaks related to sewage leaks from municipality pipelines and local overpopulation [49–51]. In Africa, water source contamination due to weak sanitary infrastructure is considered the main risk factor for cholera . It is inevitable that poor sanitary conditions, overcrowding with the majority of people living below the poverty line, lack of proper sewage disposal systems and improper water supply, all provide ideal transmission conditions for cholera once it is introduced into a community. In future as an effect of global warming these conditions could worsen in many parts of the world.
Prevention by vaccine
An extensive review of vaccines is beyond the scope of this review, but the benefits of vaccinations merit highlighting. Although the ideal vaccine is yet to be developed, some promising vaccines have been licensed. Among them oral killed cholera vaccines (OCVs) are particularly helpful in the control and prevention of outbreaks. A systematic meta-analysis found the overall vaccine efficacy was 52% during the first year and 62% during the second year with less protectiveness in children under 5 years of age . Other limitations to this approach are the necessity of multiple doses, limited evidence of long term protection, production costs etc. . Single dose administration of oral vaccine is also protective and can reduce the logistic requirements for mass vaccination campaigns . A single dose of the inactivated/killed oral vaccine, ‘Shanchol’ was found to be efficacious in older children (≥5 years of age) and in adults in Bangladesh which is a high cholera endemic setting . Though the currently available and licensed cholera vaccines do not confer life-long 100% protection they are increasingly recognised as valuable tools in the containment of cholera outbreaks. New funding mechanisms and the creation of the international cholera vaccine stockpile are helping to make OCVs globally available .
Recent research has focused on alternative delivery systems such as micro particles, proteoliposomes, LPS subunit, DNA vaccine and rice seeds containing toxin subunits . Although a fully ideal vaccine has yet to be designed, these new approaches show promise.
Analysis of global temperature data led the Inter-Governmental Panel for Climate Change to the conclusion that the average global temperature over land and ocean surfaces has risen by 0.85 °C (0.65–1.06) in the period from 1880 to 2012 . They predicted that global surface temperature will rise by 1.5 °C relative to 1850 by the end of the twenty-first century (2081–2100) . Climatologists also estimate that the sea level has risen by about 1 mm/year in recent decades, caused by thermal expansion . These events will change the diversity of cholera epidemiology throughout the world in the future. Spontaneous seroconversion and rapid transduction between environmental and toxigenic strains giving rise to the emergence of new epidemic strains could become a global issue. How this happens, and what the impact of climate change will be is a matter of ongoing debate. The potential risk of the presence of virulence factors in different environmental (non-toxigenic) strains as well as the possible role of global warming is an important area for future research.
Cholera cannot be imminently eradicated as it is a native species of the aquatic eco system. It is found in close association with various algae and crustaceans which are also natural inhabitants of water. But the disease is preventable with implementation of public health measures to ensure adequate sanitation and safe water supply. Climate change is challenging the health sector. Meta-analysis and mathematical model have demonstrated that the burden of vector borne diseases like malaria, leishmaniasis, meningococcal meningitis, viral encephalitis, dengue, chikungunya, giardiasis, toxoplasmosis etc. will increase in coming years in the tropics and beyond [59, 60]. The licensing of several oral cholera vaccines has added a promising tool to the traditional cholera control strategies namely safe water, sanitation and hygiene improvements.
With changing climate patterns more countries may become at risk of cholera, and there is a high risk of further pandemics. Interdisciplinary analysis and integrated prevention strategies are mandatory. Mathematical modelling of the disease in relation to climate offers a first step to identify the key environmental and climate parameters associated with disease variability. The development of an effective early warning system based on climate data could help to prevent and control future outbreaks. It may become possible to integrate real-time monitoring of oceanic regions, climate variability and epidemiological and demographic population dynamics to predict cholera outbreaks and support the design of cost-effective public health strategies.
- V. cholerae :
toxin co-regulated pilus
oral cholera vaccines
exo poly saccharide
Colwell RR, Huq A. Environmental reservoir of Vibrio cholerae. The causative agent of cholera. Ann NY Acad Sci. 1994;740:44–54.
Ali M, Lopez AA, You YA, Kim YE, Sah B, Maskery B, Clemens J. The global burden of cholera. Bull World Health Organ. 2012;90:209–218A.
Ali M, Nelson AR, Lopez AL, Sack DA. Updated global burden of cholera in endemic countries. PLoS Negl Trop Dis. 2015;9(6):e0003832.
Sharma NC, Mandal PK, Dhillon R, Jain M. Changing profile of Vibrio cholerae O1, O139 in Delhi and its periphery (2003–2005). Indian J Med Res. 2007;125:633–40.
Centers for Disease Control and Prevention (CDC). Imported cholera associated with a newly described toxigenic Vibrio cholerae O139 strain—California, 1993. Morb Mortal Wkly Rep. 1993;42(26):501–3.
Gil AI, Louis VR, Rivera IN, Lipp E, Huq A, Lanata CF, et al. Occurrence and distributionof Vibrio cholerae in the coastal environment of Peru. Environ Microbiol. 2004;6(7):699–706.
Kaper J, Lockman H, Colwell RR, Joseph SW. Ecology, serology, and enterotoxin production of Vibrio cholerae in Chesapeake Bay. Appl Environ Microbiol. 1979;37:91–103.
Ramamurthy T, Garg S, Sharma R, Bhattacharya SK, Nair GB, Shimada T, et al. Emergence of a novel strain of Vibrio cholerae with epidemic potential in southern and eastern India. Lancet. 1993;341:703–4.
Goel AK, Jiang SC. Association of heavy rainfall on genotypic diversity in V. cholerae Isolates from an outbreak in India. Int J Microbiol. 2011;2011:230597. doi:10.1155/2011/230597.
Koelle K, Pascual M, Yunus M. Pathogen adaptation to seasonal forcing and climate change. Proc Biol Sci. 2005;272(1566):971–7.
Lü H, Yuan Y, Sun N, Bi Z, Guan B, Shao K, Wang T, Bi Z. Characterization of Vibrio cholerae isolates from 1976 to 2013 in Shandong Province China. Braz J Microbiol. 2017;48(1):173–9.
Sedas VT. Influence of environmental factors on the presence of Vibrio cholerae in the marine environment: a climate link. J Infect Dev Ctries. 2007;1(3):224–41.
Mondal M, Chatterjee NS. Role of Vibrio cholerae exochitinase ChiA2 in horizontal gene transfer. Can J Microbiol. 2016;62(3):201–9.
Koelle K. The impact of climate on the disease dynamics of Cholera. Clin Microbiol Infect. 2009;15 (Suupl I):29–31.
Escobar L, Ryan SJ, Stewart-Ibarra AM, Finkelstein JL, King CA, Qiao H, et al. A global map of suitability for coastal Vibrio cholerae under current and future climate conditions. Acta Trop. 2015;149:202–11.
Rashed SM, Iqbal A, Mannan SB, Islam T, Rashid MU, Johura FT, et al. Vibrio cholerae O1 El Tor and O139 Bengal strains carrying ctxB (ET). Bangladesh. Emerg Infect Dis. 2013;19(10):1713–5.
Hoqe CW, Bodhidatta L, Echeverria P, Deesuwan M, Kitporka P. Epidemiologic study of Vibrio cholerae O1 and O139 in Thailand: at the advancing edge of the eighth pandemic. Am J Epidemiol. 1996;143(3):263–8.
Mutreja A, Kim DW, Thomson NR, Connor TR, Lee JH, Kariuki S, et al. Evidence for several waves of global transmission in the seventh cholera pandemic. Nature. 2011;477(7365):462–5.
Harris JB, Larocque RC, Charles RC, Mazumder RN, Khan AI, Bardhan PK. Cholera’s western front. Lancet. 2010;376(9757):1961–5.
Reyburn R, Deen JL, Grais RF, Bhattacharya SK, Sur D, Lopez AL, et al. The case for reactive mass oral cholera vaccinations. PLoS Negl Trop Dis. 2011;5(1):e952.
World Health Organization. Weekly epidemiological record, Cholera 2014. http://www.who.int/wer/2015/wer9040.pdf?ua=1. Accessed 10 May 2016.
Swerdlow DL, Ries AA. Vibrio cholerae non-O1—the eighth pandemic? Lancet. 1993;342:382–3.
Nair GB, Faruque SM, Bhuiyan NA, Kamruzzaman M, Siddique AK, Sack DA. New variants of Vibrio cholerae O1 biotype El Tor with attributes of the classical biotype from hospitalized patients with acute diarrhea in Bangladesh. J Clin Microbiol. 2002;40(9):3296–9.
Chunara R, Andrews JR, Brownstein JS. Social and news media enable estimation of epidemiological patterns early in the 2010 Haitian cholera outbreak. Am J Trop Med Hyg. 2012;86(1):39–45.
Chin C, Sorenson J, Harris JB, Robins WP, Charles RC, Jean-Charles RR, et al. The origin of the Haitian cholera outbreak strain. N Eng J Med. 2011;364:33–42.
Enserink M. Haiti’s cholera outbreak, Cholera linked to UN forces, but questions remain. Science. 2011;332:776–7.
Jutla A, Whitcombe E, Hasan N, Haley B, Akanda A, Huq A, et al. Environmental factors influencing epidemic cholera. Am J Trop Med Hyg. 2013;89(3):597–607.
Climate change 2007: The physical science basis. Contribution of Working Group I to the fourth assessment report of the Intergovernmental Panel on Climate Change (IPCC). http://sswww.ipcc.ch/ipccreports/ar4-wg1.htm. Accessed 5 Feb 2015.
Lipp EK, Huq A, Colwell RR. Effects of global climate on infectious disease: the cholera model. Clin Microbial Rev. 2002;15:757–70.
Albert MJ, Siddique AK, Islam MS, Faruque AS, Ansaruzzaman M, Faruque SM, et al. Large outbreak of clinical cholera due to Vibrio cholerae non-O1 in Bangladesh. Lancet. 1993;341:704.
Faruque SM, Ahmed KM, Abdul ARA, Qadri F, Siddique AK, Albert MJ. Emergence of a new clone of toxigenic Vibrio cholerae O1 biotype ElTor displacing V. cholerae O139 Bengal in Bangladesh. J Clin Microbiol. 1997;35:624–30.
Garza DR, Thompson CC, Loureiro EC, Dutilh BE, Inada DT, Junior EC, et al. Genome-wide study of the defective sucrose fermenter strain of Vibrio cholerae from the Latin American cholera epidemic. PLoS ONE. 2012;7(5):e37283.
Faruque SM, Alim ARMA, Rahman MM, Siddique AK, Sack RB, Albert MJ. Clonal relationships among classical Vibrio cholerae O1 strains isolated between 1961 and 1992 in Bangladesh. J Clin Microbiol. 1993;31:2513–6.
Faruque SM, Roy SK, Alim ARMA, Siddique AK, Albert MJ. Molecular epidemiology of toxigenic V. cholerae in Bangladesh studied by numerical analysis of rRNA gene restriction patterns. J Clin Microbiol. 1995;33:2833–8.
Mukhopadhyay AK, Basu A, Garg P, Bag PK, Ghosh A, Bhattacharya SK, et al. Molecular epidemiology of reemergent Vibrio cholerae O139 Bengal in India. J Clin Microbiol. 1998;36:2149–52.
Faruque SM, Ahmed KM, Siddique AK, Zaman K, Alim ARMA, Albert MJ. Molecular analysis of toxigenic Vibrio cholerae O139 Bengal isolated in Bangladesh between 1993 and 1996: evidence for the emergence of a new clone of the Bengal vibrios. J Clin Microbiol. 1997;35:2299–306.
Siddique AK, Cash R. Cholera outbreaks in the classical biotype era. Curr Top Microbiol Immunol. 2014;379:1–16.
Faruque SM, Asadulghani, Alim AR, Albert MJ, Islam KM, Mekalanos JJ. Induction of the lysogenic phage encoding cholera toxin in naturally occurring strains of toxigenic Vibrio cholerae O1 and O139. Infect immun. 1998;66(8):3752–7.
Faruque SM, Asadulghani, Rahman MM, Waldor MK, Sack DA. Sunlight-induced propagation of the lysogenic phage encoding cholera toxin. Infect immun. 2000;68(8):4795–801.
Ghosha C, Nandya RK, Dasguptaa SK, Nairb GB, Hallc RH, Ghosea AC. A search for cholera toxin (CT), toxin co regulated pilus (TCP), the regulatory element ToxR and other virulence factors innon-O1/non-O139 Vibrio cholerae. Microb Pathog. 1997;22:199–208.
Kirschner AK, Schlesinger J, Farnleitner AH, Hornek R, Süss B, Golda B, et al. Rapid growth of planktonic Vibrio cholerae non-O1/non-O139 strains in a large alkaline lake in Austria: dependence on temperature and dissolved organic carbon quality. Appl Environ Microbiol. 2008;74(7):2004–15.
Montilla R, Chowdhury MA, Huq A, Xu B, Colwell RR. Serogroup conversion of Vibrio cholerae non-O1 to Vibrio cholerae O1: effect of growth state of cells, temperature, and salinity. Can J Microbial. 1996;42:87–93.
Islam MS, Sharker MAY, Rheman S, Hossain S, Mahmud ZH, Islam MS, et al. Effects of local climate variability on transmission dynamics of cholera in Matlab, Bangladesh. Trans R Soc Trop Med Hyg. 2009;103:1165–70.
Islam MS, Islam MS, Mahmud ZH, Cairncross S, Clemens JD, Collins AE. Role of phytoplankton in maintaining endemicity and seasonality of cholera in Bangladesh. Trans R Soc Trop Med Hyg. 2015;109:572–8.
Sheen JP. Chitin. http://www.encyclopedia.com/topic/chitin.aspx. Accessed 7 Apr 2016.
Metzger LC, Blokesch M. Regulation of competence-mediated horizontal gene transfer in the natural habitat of Vibrio cholera. Curr Opin Microbiol. 2016;30:1–7.
Pascual M, Chaves LF, Cash B, Rod X, Yunus M. Predicting endemic cholera: the role of climate variability and disease dynamics. Clim Res. 2008;36:131–40.
Ramamurthy T, Sharma NC. Cholera outbreaks in India. Curr Top Microbiol Immunol. 2014;379:49–85.
Bhunia R, Ramakrishnan R, Hutin Y, Gupte MD. Cholera outbreak secondary to contaminated pipe water in an urban area, West Bengal, India, 2006. Indian J Gastroenterol. 2009;28:62–4.
Mukherjee R, Halder D, Saha S, Shyamali R, Subhranshu C, Ramakrishnan R, et al. Five pond-centred outbreaks of cholera in villages of West Bengal, India: evidence for focused interventions. J Health Popul Nutr. 2011;29:421–8.
Shah HD, Shah VP, Desai AN. An epidemic outbreak of Vibrio cholerae El Tor O1 serotype Ogawa biotype in a Lalpur town, Jamnagar, India. J Postgrad Med. 2012;58:14–8.
Mengel MA, Delrieu I, Heyerdahl L, Gessner BD. Cholera outbreaks in Africa. Curr Top Microbiol Immunol. 2014;379:117–44.
Sinclair D, Abba K, Zaman K, Qadri F, Graves PM. Oral vaccines for preventing cholera. Cochrane Database Syst Rev. 2011;3:CD008603.
Kabir S. Critical analysis of compositions and protective efficacies of oral killed cholera vaccines. Clin Vaccine Immunol. 2014;21(9):1195–205.
Qadri F, Wierzba TF, Ali M, Chowdhury F, Khan AI, Saha A, et al. Efficacy of a single-dose, inactivated oral cholera vaccine in Bangladesh. N Engl J Med. 2016;374(18):1723–32.
Abubakar A, Azman AS, Rumunu J, Ciglenecki I, Helderman T, West H, et al. The first use of the global oral cholera vaccine emergency stockpile: lessons from South Sudan. PLoS Med. 2015;12(11):e1001901.
Pastor M, Pedraz JL, Esquisabel A. The state-of-the-art of approved and under-development cholera vaccines. Vaccine. 2013;31(38):4069–78.
Inter-Governmental Panel on Climate Change (IPCC). Climate change 2014 synthesis report summary for policy makers.http://www.ipcc.ch/pdf/assessment-report/ar5/syr/AR5_SYR_FINAL_SPM.pdf. Accessed 25 Jan 2016.
McMichael AJ, Lindgren E. Climate change and health. J Intern Med. 2011;270:401–13.
Evengard B, Sauerborn R. Climate change influences infectious diseases both in the Arctic and the tropics: joining the dots. Glob Health Action. 2009;11:2. doi:10.3402/gha.v2i0.2106.
FRC and SD conceived the idea. FRC, ZN and NH wrote the preliminary draft. SD and LVS revised the manuscript. All authors read and approved the final manuscript.
The authors declare that they have no competing interests.
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Chowdhury, F.R., Nur, Z., Hassan, N. et al. Pandemics, pathogenicity and changing molecular epidemiology of cholera in the era of global warming. Ann Clin Microbiol Antimicrob 16, 10 (2017) doi:10.1186/s12941-017-0185-1
- Climate change
- Global warming