Mismatch Amplification Mutation Assay (MAMA) PCR Reveals Altered El Tor Vibrio Cholerae O1 Circulating in Delhi, India

Int. J. Life. Sci. Scienti. Res., 2(6): 678-681 NOVEMBER- 2016
http://ijlssr.com Copyright © 2015-2016 International Journal of Life-Sciences Scientific Research Page 678
Mismatch Amplification Mutation Assay (MAMA)
PCR Reveals Altered El Tor Vibrio Cholerae O1
Circulating in Delhi, India
Dhirendra Kumar1
, Preety Sinha2
, Naresh Chand Sharma3*
1
Research Scholar, PG Department of Zoology, A. N. College, Patna, India
2
Professor, PG Department of Zoology, A. N. College, Patna, India
3
Consultant Bacteriologist, Laboratory Department, Maharishi Valmiki Infectious Diseases Hospital, Delhi, India
*
Address for Correspondence: Dr. Naresh Chand Sharma, Consultant Bacteriologist, Laboratory Department,
Maharishi Valmiki Infectious Diseases Hospital, Kingsway Campus, Delhi, India
Received: 17 Sept 2016/Revised: 28 Sept 2016/Accepted: 19 Oct 2016
ABSTRACT- The acute diarrheal disease cholera is caused by Vibrio cholerae, a major public health problem in Asia,
Africa and Latin America. V. cholerae has more than 200 known serotypes but not all the strains are pathogenic. In recent
years, it has been seen that the emergence of new variants of V. cholerae O1 have carried characteristics of both classical
and El Tor biotypes and these variants of V. cholerae O1 are called as ‘atypical El Tor’. These strains might have evolved
from El Tor variants that acquired certain characteristics from classical genome. 30 V. cholerae O1 isolates (Table 1) were
revived from stock cultures maintained at Laboratory Department in Maharishi Valmiki Infectious Diseases Hospital
(MVIDH), Delhi during 2012-2014. Mismatch amplification mutation assay was used for classifying the strains into
prototype El Tor, hybrid, or El Tor variant biotype based on their ctxB gene. All isolates were biochemically identified as
V. cholerae biotype El Tor and serologically O1 Ogawa. All isolates were amplified with classical specific primers.
Cholera continues to be endemic in large number of states in the eastern, western, northern and southern parts of India and
there were 38 cholera outbreak reports published in India during 2007 to 2013. These Indian outbreaks have been
associated with new El Tor variant.
Key-words- V. cholerae O1, El Tor, MAMA PCR, ctxB
-------------------------------------------------IJLSSR-----------------------------------------------
INTRODUCTION
The acute diarrheal disease cholera is caused by Vibrio
cholerae, a major public health problem in Asia, Africa and
Latin America1
. According to the World Health Organisation
(WHO) estimates there were 3-5 million cholera cases and
1,00,000- 1,20,000 deaths each year throughout the world2
. V.
cholerae has more than 200 known serogroups but not all the
strains are pathogenic. Among them, O1 and O139 antigens
are highly pathogenic and acknowledged to cause epidemic
and pandemic disease3
. The symptom of the acute cholera is
rice water stools.
Access this article online
Quick Response Code:
Website:
www.ijlssr.com
DOI: 10.21276/ijlssr.2016.2.6.6
Clinical manifestations of the disease range from mild
symptoms such as abdominal cramps, nausea and vomiting,
to more severe symptoms such as dehydration, shock and
death4
. A devastating cholera outbreak, that had occurred in
Haiti since October 2010, involved 6, 98, 893 cases and
8,540 deaths5
. V. cholerae serogroup O1 is classified into
two biotypes, which are termed ‘classical’ and ‘El Tor’6
.
The current seventh pandemic of cholera is caused by the
El Tor biotype was originated in 1961 from Celebes Islands
in Indonesia7
. Spread of this biotype was recorded for the
first time during 1964 in India and it made its first
appearance in Delhi during June, 19658
. In recent years, it
has been seen that the emergence of new variants of V.
cholerae O1 have carried characteristics of both classical
and El Tor biotypes and these variants of V. cholerae O1 are
called as ‘atypical El Tor’. These strains might have
evolved from El Tor variants that acquired certain
characteristics from classical genome9
. In this study, we
focused on type of CT genotype existing among V. cholerae
Research Article (Open access)

Int. J. Life. Sci. Scienti. Res., VOL 2, ISSUE 6
O1 isolated from the patients who were admitted in
MVIDH, Delhi during 2012-2014.
MATERIALS AND METHODS
Collection and processing of samples
30 V. cholerae O1 isolates were revived from stock cultures
were maintained at Laboratory Department in MVIDH,
Delhi during 2012-2014. These samples were revived and
transferred to alkaline peptone water (APW, pH-8.6) and
incubated at 37°C for 4-6 hrs. After incubation, the
enriched cultures were further inoculated to the
thiosulphate-citrate-bile-salts-sucrose (TCBS) agar and bile
salt agar (BSA, pH-8.6) (Hi-Media, Mumbai)10
.
Confirmation of V. cholerae
Typical colonies appearing on TCBS/BSA were confirmed
by standard biochemical tests10
. These isolates were further
tested serologically11
with commercially available V.
cholerae O1 polyvalent and monovalent and O139
antiserum (BD, USA and Denka Seiken, Ltd. Japan).
Genomic DNA preparation
Genomic DNA from each isolate was extracted using
protocol described previously12
.
PCR assays for detection of ctxB genotype
Mismatch amplification mutation assay was used for
classifying the strains into prototype El Tor, hybrid, or El
Tor variant biotype based on their ctxB gene13
. In this PCR,
the common forward primer for both classical and El Tor
alleles was used. Two allele specific primers Re-Cla and
Re-Elt were used respectively. The PCR conditions and
cycles were described previously13
. V. cholerae O1 strains
569B (classical) and N16961 (El Tor) were used as control
strains. The primers used were synthesized by Invitrogen,
India and dNTPs, Taq polymerase, 10X Taq buffer used in
this study were obtained from Genei, Bangalore. The
primer sequences were used in this PCR is given in Table 2.
RESULTS
Characterisation of isolates
A total of 30 V. cholerae O1 isolates were revived from
maintained isolates during 2012-2014 (Table 1). All isolates
were biochemically confirmed as V. cholerae biotype El
Tor and serologically confirmed with polyvalent O1 and
then agglutination with monovalent Ogawa.
Table 1: Showing types of ctxB in Delhi isolates during
2012-2014
No. of
isolates
Year Serogroup/Serotype ctxB
10 2012 O1/Ogawa Classical
Table 2: Primer sequences were used in MAMA PCR
Gene (S) Primer Sequence
Ampli-
con
Size
(bp)
Ref.
ctxB FW ACTATCTTCAGCATATGCACATGG 13
Re-El CTGGTACTTCTACTTGAAACA 186bp 13
Re-Cla CTGGTACTTCTACTTGAAACG 186bp 13
Confirmation of ctxB gene by MAMA PCR
All 30 isolates were screened for ctxB gene by MAMA
PCR with two allele specific primers, one for Classical and
other for El Tor. All isolates were amplified with classical
specific primers (Fig. 1). Only control strain N16961 were
amplified with El Tor specific primers (Fig. 2).
Figure 1: MAMA PCR assay of agarose gel
electrophoresis of ctxB yielded 186bp amplicon size
fragment when using primer pair FW-Com with
Re-Cla. Lane M, 100bp molecular weight marker,
lane1-569B Positive Control, lane
2- N16961 Control strain for El Tor, lane
3- Negative Control and lane 4-15 test strains shown
positive band

Figure 2: MAMA PCR assay of agarose gel
electrophoresis of ctxB yielded 186bp amplicon size
fragment when using primer pair FW-Com with Re-Elt.
Lane M, 100bp molecular weight marker, lane1-N16961
Positive Control, lane
2- 569B Control strain for Classical, lane
3- Negative Control and 4-15 test strains shown negative
band
DISCUSSION
Cholera continues to be endemic in large number of states
in the eastern, western, northern and southern parts of India
and there were 38 cholera outbreak reports published in
India during 2007 to 201314
. These Indian outbreaks have
been associated with new El Tor variant15
. Classical and El
Tor biotypes differ in not only their phenotypic and
genotypic characteristics, but also their pathogenic
potentials, survivalness and diseases causing ability in their
human hosts16
. El tor strains are associated more frequently
with asymptomatic infections and lower fatalities rate,
better survival in the environment and in the human hosts
and more efficient host-to-host transmission as compared
with classical strains where as classical strains is more
severe than El Tor biotype and fatality rate is high as
compared to El tor biotype16-17
. In 2006, first naturally
occurring atypical El Tor variants observed by Nair 18
among stool samples of hospitalized patients strains of V.
cholerae O1 isolated between 1991 and 1994 in Matlab,
Bangladesh. In the present study, we found all the isolates
carried ctxB gene of classical biotype i.e. ctxBCla
(ctxB1). It
revealed that atypical El Tor is circulating in Delhi since
200812
.
CONCLUSION
In the present study, all isolates are phenotypically El Tor
but carried ctxB gene of classical biotype and known as
altered El Tor. Altered El Tor is more pathogenic than El
Tor because it harboured ctxB gene of classical biotype and
better survival in the environment. More molecular study is
needed to understand the changing epidemiology of V.
cholerae O1 infections and better planning to control
cholera disease in this part of the country.
REFERENCES
[1] Farque SM and Nair GB (2002). Molecular Ecology of
Toxigenic Vibrio Cholerae. Microbiol Immunol 46: 59-66.
[2] Taylor DL, Kahawita TM, Cairncross S, Ensink JHJ (2015)
The Impact of Water, Sanitation and Hygiene Interventions
to Control Cholera: A system Review. PLoS ONE 10: 1-19,
DOI:10.1371/journal.pone.0135676.
[3] Reidl J and Klose KE (2002) Vibrio cholerae and cholera:
out of the water and into the host. FEMS Microbiol Rev 26:
125-139.
[4] Weir E and Haider S (2004) Cholera outbreaks continue.
CMAJ 170: 1092-1093.
[5] UN FACT SHEET (2014) Combatting Cholera in Haiti.
www.un.org/news/dh/infocus/haiti/Cholera_UN_Factsheet_2
4%20Feb_2014. Accessed on 24.6.2015.
[6] Samadi AR, Huq MI, Shahid N, Khan MU, Eusof A,
Rahman AS et al., (1983) Classical Vibrio cholerae
biotype displaces EL tor in Bangladesh. Lancet 1:
805-807.
[7] Faruque SM, Albert MJ, and Mekalanos JJ (1998)
Epidemiology, genetics, and ecology of toxigenic Vibrio
cholerae. Microbiol Mol Biol Rev 62: 1301-1314.
[8] Singh J, Bora D, Sharma RS, Khanna KK, Verghese T
(1995) Epidemiology of cholera in Delhi-1992. J Trop
Pediatr 4l: 139-42.
[9] Safa A, Nair GB and Kong RYC (2009) Evolution of new
variants of Vibrio cholerae O1. Trends in Microbiol 18:
46-53.
[10]World Health Organization (2003) Manual for the laboratory
identification and antimicrobial susceptibility testing of
bacterial pathogens of public health importance in the
developing world. Centre for Disease Control and
Prevention, Atlanta Georgia USA. USAID/WHO/CDC
141-159.
[11]Kay BA, Bopp CA, Wells JG (1994).Isolation and
identification of Vibrio Cholerae O1 from fecal specimens.
In: Wachsmuth Ik, Blake PA, Olsvik O, editors. Vibrio
cholerae and cholera: Molecular to global perspectives.
Wahington DC, USA: ASM Press; p.3-25.
[12]Singh P, Kumar D, Prasad Y, Ramamurthy T, Sarkar BL,
Sharma NC (2015). Prevalence of multidrug resistant altered
Vibrio cholerae O1 isolates among Diarrhoeal patients in
Delhi during 2008-2012. Indian J Appl Res 5: 624-628.
[13]Morita M, Ohnishi M, Arakawa E, Bhuiyan NA, Nusrin S,
Alam M et al., (2008) Development and validation of a
mismatch amplification mutation PCR assay to monitor the
dissemination of an emerging variant of Vibrio cholerae O1
biotype El Tor. Microbiol Immunol 52:314-317.

[14]Ramamurthy T and Sharma NC (2014) Cholera Outbreaks in
India. Current Topics in Microbiology and Immunology 379:
49-85.
[15]Kanungo S, Sah BK, Lopez AL, Sung JS, Paisly AM, et al.
(2010) Cholera in India: an analysis of reports, 1997-2006.
Bull World Health Organ 88: 185-191.
[16]Kaper JB, Morris JG Jr., and Levine MM (1995) Cholera.
Clin Microbiol Rev 8: 48-86.
[17]Sack DA, Sack RB, Nair GB, Siddique AK (2004) Cholera.
Lancet 363: 223-233.
[18]Nair GB, Qadir F, Holmgren J, Svennerholm AM, Safa A,
Bhuiyan NA et al., (2006) Cholera due to altered El Tor
strains of Vibrio cholerae O1 in Bangladesh. J Clin
Microbiol 44: 4211-3.
International Journal of Life-Sciences Scientific Research (IJLSSR)
Open Access Policy
Authors/Contributors are responsible for originality, contents, correct
references, and ethical issues.
IJLSSR publishes all articles under Creative Commons
Attribution- Non-Commercial 4.0 International License (CC BY-NC).
https://creativecommons.org/licenses/by-nc/4.0/legalcode
How to cite this article:
Kumar D, Sinha P, Sharma NC: Mismatch Amplification Mutation Assay (MAMA) PCR Reveals Altered El Tor Vibrio
Cholerae O1 Circulating in Delhi, India. Int. J. Life. Sci. Scienti. Res., 2016; 2(6): 678-681. DOI:10.21276/ijlssr.2016.2.6.6
Source of Financial Support: Nil, Conflict of interest: Nil

Mismatch Amplification Mutation Assay (MAMA) PCR Reveals Altered El Tor Vibrio Cholerae O1 Circulating in Delhi, India

More Related Content

What's hot (20)

Viewers also liked (18)

Similar to Mismatch Amplification Mutation Assay (MAMA) PCR Reveals Altered El Tor Vibrio Cholerae O1 Circulating in Delhi, India (20)

More from SSR Institute of International Journal of Life Sciences (20)

Recently uploaded (20)

Mismatch Amplification Mutation Assay (MAMA) PCR Reveals Altered El Tor Vibrio Cholerae O1 Circulating in Delhi, India